Review: Compounds Involved in the Flavor of Surface Mold-Ripened Cheeses: Origins and Properties
Open accessAbstract
Cheese flavor is obtained through a series of chemical changes that occur in the curd during the early stages of ripening. Lipid hydrolysis leads to FFA, which serve as substrates for further reactions, Peptides and amino acids, which result from proteolysis, also lead to aroma compounds through enzymic and chemical reactions. This paper is a review of the current knowledge about the compounds that contribute to flavor in mold-ripened cheeses, especially Camembert-type cheese. Discussed are the pathway of formation, the sensory properties (odorous notes and perception thresholds), and the quantities of the main volatile compounds encountered in these types of cheeses.
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Claims the paper makes
98 of 235 cited sources checked · 27 supported · 4 flagged · accuracy not yet measured
- Premisecitation
Addition of oleic acid (C18) in a milk-based medium causes an increase of production of heptan-2-one and nonan-2-one by P. camemberti.
“Furthermore, addition of oleic acid (C 18) in a milkbased medium causes an increase of production of heptan-2-one and nonan-2-one by P. camemberti, and the addition of lauric acid (C 12) does not increase the production of undecan-2-one (99).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [99] Okumara, 1985, Methyl ketone formation by Penicillium camemberti in model systems, J. Dairy Sci. source
The Materials and Methods describe oleate and laurate incubations in Czapek’s medium, not additions to the milk-based medium. The Results and Discussion report heptanone and nonanone with oleate, but also say that undecanone was the principal methyl ketone produced with laurate—contrary to the citing sentence’s lauric-acid clause. (LLM, conf=0.87)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Premisecitation
Addition of lauric acid (C12) does not increase the production of undecan-2-one by P. camemberti.
“Furthermore, addition of oleic acid (C 18) in a milkbased medium causes an increase of production of heptan-2-one and nonan-2-one by P. camemberti, and the addition of lauric acid (C 12) does not increase the production of undecan-2-one (99).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [99] Okumara, 1985, Methyl ketone formation by Penicillium camemberti in model systems, J. Dairy Sci. source
In the body text accompanying Figure 3 (page not specified in our copy), the paper says lauric acid was metabolized progressively and undecanone was the principal methyl ketone product. That is contrary to the claim that adding lauric acid does not increase undecan-2-one production. (LLM, conf=0.83)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Premisecitation
Dumont et al. isolated significant quantities of pentan-2-ol in ripe Camembert cheeses.
“Dumont et al. (39,41) have also isolated significant quantities of pentan-2-01 in ripe Camembert cheeses.”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Introduction (page unavailable) says this study examined five washed-rind cheeses, not Camembert. The mass-spectrometry tables (page unavailable) identify 2-pentanol in Maroilles and Pont-l’Évêque but classify its quantity as minor, contrary to the claim of significant quantities. (LLM, conf=0.84)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 3) reports appreciable quantities of 2-pentanol (pentan-2-ol), but only in one very ripe Camembert sample. The claim's plural “cheeses” overgeneralizes that finding. (LLM, conf=0.88)
Experimental — accuracy not yet measured
- Premisecitation
Styrene has been described as a trace element in several cheeses, one of which is Camembert.
“This compound has been described as a trace element in several cheeses, one of which is Camembert (39,41).”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
Table 4 (Mass spectrometry; page unavailable) lists styrene in Langres cheese as “importante” (quantitatively important), not present only in traces. The Introduction names the cheeses examined and does not include Camembert; this paper therefore does not substantiate the Camembert example. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 9) says that benzene-related hydrocarbons in Camembert are often present in traces, but it does not identify styrene among them. Searches for “styrene,” “styrène,” and alternative chemical names found no passage in our copy establishing styrene in Camembert. (LLM, conf=0.73)
Experimental — accuracy not yet measured
- Premisecitation
Butyric acid concentrations in Camembert range from 3.5 to 20.6 mg/100 g.
“According to Adda and Dumont ( 3) and Berdague ( 17), acetic acid concentrations ranging from 1.3 to 30 mg/100 g, butyric acid concentrations ranging from 3.5 to 20.6 mg/ 100 g, and total propanoic and isobutyric acid concentrations ranging between 0.3 and 13.7 mg/100 g are the most important quantitatively (Table 1).”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
- cites [17] Berdagué, 1986, Méthode d’extraction rapide des acides gras volatils libres des fromages, Lait source
The 'Application de la technique à divers types de fromages' section lists one Camembert sample in its table of volatile fatty acids, but does not give a Camembert butyric-acid range. Searches for Camembert and the endpoints 3.5 and 20.6 mg/100 g found no passage stating the claimed range. Page numbers are unavailable in our copy. (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Premisecitation
The homologous series of odd-chain methyl ketones, from C3 to C15, constitute some of the most important compounds in the aroma of Blue cheese and surface mold-ripened cheese.
“The homologous series of odd-chain methyl ketones, from C3 to C 15 , constitute some of the most important compounds in the aroma of Blue cheese and surface mold-ripened cheese (31,33,39,41,42,54,111).”
Quote in the paperSubstantial claim4 of 7 sources checked- cites [31] Dartey, 1971, Rate of formation of methyl ketones during Blue cheese ripening, J. Agric. Food Chem. source
- cites [33] Day, 1965, Gas chromatography and mass spectral identification of neutral components of the aroma fraction of blue cheese, J. Agric. Food Chem. source
- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion (page unavailable) says washed-rind cheeses are relatively poor in methyl ketones compared with mold-ripened soft cheeses. The mass-spectrometry tables list several odd-chain methyl ketones in the washed-rind cheeses, but the paper does not establish a C3–C15 series or assess its importance to the aroma of Blue cheese and surface mold-ripened cheese. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 7) identifies methyl ketones, particularly odd-chain examples such as 2-nonanone and 2-undecanone, as abundant in Camembert; the conclusion (p. 15) calls methyl ketones major neutral aroma compounds. This supports the claim for Camembert, a surface mold-ripened cheese, but the paper does not establish their importance in Blue cheese or the full C3–C15 range. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [42] Dumont, 1974, Etude des composés volatils neutres présents dans le vacherin, Lait source
Table 2 in the Discussion lists several odd-chain methyl ketones, from 2-pentanone (C5) through 2-tridecanone (C13), in Vacherin samples; the Discussion also says the rinds are rich in long-chain methyl ketones. The paper does not establish a C3–C15 series or identify these ketones as among the most important aroma compounds in Blue or surface mold-ripened cheese. Page numbers are unavailable in our copy. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [54] Hawke, 1966, Reviews of the progress of dairy sciences, J. Dairy Res. source
- cites [111] Schwartz, 1963, Methyl ketones in Camembert cheese, J. Dairy Sci. source
The Results and Discussion (page unavailable) reports several odd-chain methyl ketones in Camembert and says those found there are also present in Blue cheese. It does not assess their importance to aroma, and it reports no detectable acetone (C3) in the Camembert cheeses, so it does not establish the claimed full C3–C15 series for both cheese types. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
The large quantity of FFA in Blue-type cheeses is mainly due to mold activity.
“The large quantity of FFA, 23.5 to 66.7 g/kg in Blue-type cheeses (12,51,88), is mainly due to•mold activity; milk lipase activity and other microbiallipases are involved to a lesser extent.”
Quote in the paperNot a substantial claim2 of 3 sources checked- cites [12] Anderson, 1965, Quantitative analysis of the major free fatty acids in Blue cheese, J. Dairy Sci. source
The quantitative-analysis section reports free-fatty-acid amounts in four Blue-type cheeses, but does not explain their origin. Searches for mold activity, lipolysis, and milk or microbial lipases found no passage attributing the acids mainly to mold. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites [51] Ha, 1991, Contributions of cow, sheep, and goat milks to characterizing branched-chain fatty acid and phenolic flavors to varietal cheeses, J. Dairy Sci. source
The blue-veined-cheese discussion (labeled “IO).”; page not provided) says mold-produced lipases release liberal quantities of free fatty acids. It does not compare mold activity with milk lipase or other microbial lipases, so it does not establish that mold activity is the main cause. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [88] Margalith, 1981, Dairy products
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Total propanoic and isobutyric acid concentrations in Camembert range between 0.3 and 13.7 mg/100 g.
“According to Adda and Dumont ( 3) and Berdague ( 17), acetic acid concentrations ranging from 1.3 to 30 mg/100 g, butyric acid concentrations ranging from 3.5 to 20.6 mg/ 100 g, and total propanoic and isobutyric acid concentrations ranging between 0.3 and 13.7 mg/100 g are the most important quantitatively (Table 1).”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
- cites [17] Berdagué, 1986, Méthode d’extraction rapide des acides gras volatils libres des fromages, Lait source
In section E, Table V reports volatile fatty acids for one Camembert sample in mg/100 g, including a propanoic-acid (C3) value of 4. It does not establish a Camembert range of 0.3–13.7 mg/100 g for the combined propanoic and isobutyric acids; the table’s flattened formatting also makes the isobutyric-acid entry unclear. No page number is available in our copy. (LLM, conf=0.78)
Experimental — accuracy not yet measured
- Premisecitation
FFA in Blue-type cheeses range from 23.5 to 66.7 g/kg.
“The large quantity of FFA, 23.5 to 66.7 g/kg in Blue-type cheeses (12,51,88), is mainly due to•mold activity; milk lipase activity and other microbiallipases are involved to a lesser extent.”
Quote in the paperNot a substantial claim2 of 3 sources checked- cites [12] Anderson, 1965, Quantitative analysis of the major free fatty acids in Blue cheese, J. Dairy Sci. source
Table 1 reports free fatty acids for four Blue-vein cheeses. Excluding acetic acid, its values for samples D and C sum to approximately 23.5 and 66.7 g/kg, respectively, but sample B sums to about 16.2 g/kg—below the claimed range. The stated range therefore does not cover all the cheeses examined. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [51] Ha, 1991, Contributions of cow, sheep, and goat milks to characterizing branched-chain fatty acid and phenolic flavors to varietal cheeses, J. Dairy Sci. source
Table 4 reports concentrations of individual free fatty acids in Blue and Roquefort cheeses, but not total FFA of 23.5–66.7 g/kg. A search for that range and for total FFA concentrations found no passage in our copy that verifies it. (LLM, conf=0.75)
Experimental — accuracy not yet measured - cites [88] Margalith, 1981, Dairy products
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Camembert cheese contains all of the even-numbered carbon FFA, ranging from acetic to octadecanoic acid, isobutyric, and isovaleric acids.
“Camembert cheese contains all of the evennumbered carbon FFA, ranging from acetic to octadecanoic acid, isobutyric, and isovaleric acids (3,17,63,64).”
Quote in the paperNot a substantial claim3 of 4 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
The ‘Acides gras libres’ section identifies acetic, isobutyric and isovaleric acids in Camembert, and Table 1 lists an octadecanoic-acid (18:0) fraction among its free fatty acids. But the table groups several intermediate chain lengths and does not establish that every even-numbered fatty acid from acetic through octadecanoic acid is present. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [17] Berdagué, 1986, Méthode d’extraction rapide des acides gras volatils libres des fromages, Lait source
The table in section E, “Application de la technique à divers types de fromages” (page not available), reports free fatty acids for a Camembert sample, including acetic acid (C2). The paper assesses acids only from C2 to C6, so it does not establish that Camembert contains every even-numbered acid through octadecanoic acid; the extracted table also does not clearly establish both named branched acids for Camembert. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- cites [64] Karahadian, 1985, Contribution of Penicillium sp. to the flavors of Brie and Camembert cheese, J. Dairy Sci. source
The Results and Discussion (page unavailable) report individual free fatty acids in Brie and list several even-carbon acids in Brie samples. They do not establish that Camembert contains every even-carbon free fatty acid from acetic through octadecanoic acid, or identify isobutyric and isovaleric acids in Camembert. (LLM, conf=0.79)
Experimental — accuracy not yet measured
- Premisecitation
Octanoic, 4-methyloctanoic, and, especially, 4-ethyloctanoic acids have odorous, goaty notes.
“Octanoic, 4-methyloctanoic, and, especially, 4ethyloctanoic acids have odorous, goaty notes (51).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [51] Ha, 1991, Contributions of cow, sheep, and goat milks to characterizing branched-chain fatty acid and phenolic flavors to varietal cheeses, J. Dairy Sci. source
In the Results of the analysis section (page not provided), octanoic acid is described as having a goaty aroma, and 4-ethyloctanoic acid as principally responsible for the characteristic goaty aroma of goat milk cheese. The same section says 4-methyloctanoic acid smells muttonlike when evaluated alone; it contributes to an impression of goatiness when blended with 4-ethyloctanoic acid. Thus the claim overstates its individually goaty character. (LLM, conf=0.88)
Experimental — accuracy not yet measured
- Premisecitation
All methyl ketones encountered are also present in Blue cheese.
“All methyl ketones encountered are also present in Blue cheese (33,39,41,42,92).”
Quote in the paperNot a substantial claim4 of 5 sources checked- cites [33] Day, 1965, Gas chromatography and mass spectral identification of neutral components of the aroma fraction of blue cheese, J. Agric. Food Chem. source
- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The compound tables (d) Spectrométrie de masse; page unavailable) identify several methyl ketones in the washed-rind cheeses studied. Neither those tables nor the Discussion (page unavailable) establishes that all of them are also present in Blue cheese; the Blue-cheese study appears only in the references. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 7) says that two unsaturated methyl ketones found in Camembert, 2-nonénone and 2-undécénone, had previously been reported in Blue-type cheeses. It does not establish that every methyl ketone encountered in Camembert is also present in Blue cheese. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [42] Dumont, 1974, Etude des composés volatils neutres présents dans le vacherin, Lait source
Table 2 in the Discussion lists methyl ketones found in Vacherin, and the Discussion notes that its rinds are rich in long-chain methyl ketones. Our copy does not compare those compounds with Blue cheese or establish that all are present there (searched: Roquefort, fromage bleu, pâte persillée). No page number was available in the indexed passages. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
- Premisecitation
Acetic acid concentrations in Camembert range from 1.3 to 30 mg/100 g.
“According to Adda and Dumont ( 3) and Berdague ( 17), acetic acid concentrations ranging from 1.3 to 30 mg/100 g, butyric acid concentrations ranging from 3.5 to 20.6 mg/ 100 g, and total propanoic and isobutyric acid concentrations ranging between 0.3 and 13.7 mg/100 g are the most important quantitatively (Table 1).”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
- cites [17] Berdagué, 1986, Méthode d’extraction rapide des acides gras volatils libres des fromages, Lait source
Table V in section E (page not identified in our copy) lists 30 mg/100 g of C2, or acetic acid, for a chalky Camembert. It does not report 1.3 mg/100 g for Camembert or establish the claimed range. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
The amount of dissolved oxygen has a great influence on the level of diacetyl and acetoin production.
“The amount of dissolved oxygen has a great influence on the level of their production (15,104).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [15] Bassit, 1994, Effet combiné de l’oxygene et de la température sur l’acidification et les productions de diacétyle et d’acétoïne par Lactococcus lactis subsp. lactis biovar diacetylactis, Lait source
- cites [104] Petit, 1989, Influence of citrate on the diacetyl and acetoin production by fully grown cells of Streptococcus lactis subsp. diacetylactis, Curr. Microbiol. source
- Premisecitation
The action of a thiolase yields a β-ketoacid that is rapidly decarboxylated by a β-keto-acyl-decarboxylase to give a methyl ketone with one less carbon than the initial FA.
“The action of a thiolase yields a i3-ketoacid that is rapidly decarboxylated by a i3-keto-acyl-decarboxylase to give a methyl ketone with one less carbon than the initial FA (1,23,75,117).”
Quote in the paperSubstantial claim1 of 4 sources checked- cites [1] Adda, 1984, Formation de la flaveur
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [23] Cerning, 1987, Les activités biochimiques des Penicillium utilisés en fromagerie, Lait source
Section B, “La formation de méthylcétones à partir des acides gras” (page not provided), describes β-ketoacyl-decarboxylase activity and says the resulting ketones have one fewer carbon than the original fatty acid. It identifies the preceding activity as a thiohydrolase, not a thiolase, and does not state that decarboxylation is rapid. (LLM, conf=0.85)
Experimental — accuracy not yet measured - cites [75] Lamberet, 1982, L’aptitude de Penicillium caseicolum à la dégradation oxydative des acides gras, Rev. Lait. Franpaise
- cites [117] Smith, 1969, Action of microorganisms on the peroxides and carbonyls of fresh lard, J. Food Sci. source
- Premisecitation
Diacetyl can be reduced to acetone by the action of a diacetyl reductase.
“Diacetyl is produced in lesser amounts than acetoin and can be reduced to acetone by the action of a diacetyl reductase (59,122).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [59] Jordan, 1988, Production of acetolactate by Streptococcus diacetylactis and Leuconostoc spp, J. Dairy Res. source
- cites [122] Starrenburg, 1991, Citrate fermentation by Lactococcus and Leuconostoc spp, Appl. Environ. Microbiol. source
The Results (page unavailable) report only small amounts of diacetyl and substantial acetoin formation, while the Discussion’s Fig. 3 caption identifies a diacetyl reductase. Neither passage says that the enzyme reduces diacetyl to acetone; acetone is not listed among the products reported in the Results. (LLM, conf=0.85)
Experimental — accuracy not yet measured
- Premisecitation
Methyl ketones are present in equivalent quantities in Roquefort and Camembert cheeses.
“Methyl ketones are present in equivalent quantities in Roquefort and Camembert cheeses (50).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [50] Groux, 1974, La flaveur des fromages. II. Etude comparative de la fraction volatile neutre de divers fromages, Lait source
- Premisecitation
Diacetyl is produced in lesser amounts than acetoin.
“Diacetyl is produced in lesser amounts than acetoin and can be reduced to acetone by the action of a diacetyl reductase (59,122).”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
Oct-1-en-3-ol plays a major role in Camembert cheese by its characteristic mushroom note.
“By its characteristic mushroom note, oct-l-en-3-ol plays a major role in Camembert cheese (39,40,41,92).”
Quote in the paperNot a substantial claim4 of 4 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Introduction (page unavailable) says the study examines five washed-rind cheeses and does not include Camembert. Searches for oct-1-en-3-ol, Camembert, and a mushroom note found no passage in our copy addressing the claimed role or aroma. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites [40] Dumont, 1976, L’arôme du camembert: autres composés mineurs mis en évidence, Lait source
The Discussion (page not provided) names octen-1-ol-3 as a compound that may help distinguish types of soft cheese, supporting a role in their aroma. It does not describe a mushroom note or establish that the compound plays a major role specifically in Camembert. (LLM, conf=0.83)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 7) says oct-1-en-3-ol has a mushroom taste and may give Camembert a characteristic aromatic note because of its low perception threshold. But it presents that contribution as a possibility, not an established major role; the conclusion (p. 15) identifies methyl ketones and their corresponding alcohols as the quantitatively major neutral aroma compounds. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
- Premisecitation
The production of oct-1-en-3-one and octa-1,5-dien-3-one by P. camemberti probably derives from the linoleic and linolenic acid pathways.
“The production of oct-l-en-3-one and octa-l,5-dien-3-one by P. camemberti probably derived from the linoleic and linolenic acid pathways (63,64) as it did for basidiomycetes (25).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- cites [64] Karahadian, 1985, Contribution of Penicillium sp. to the flavors of Brie and Camembert cheese, J. Dairy Sci. source
The Results and Discussion link linoleic and linolenic acids to C8 mushroom-like compounds produced by Penicillium and show that fatty-acid supplementation increased production of 1-octen-3-ol and 1,5-octadien-3-ol by P. caseicolum. They do not establish that P. camemberti produces the two specified ketones through those pathways; the reported increases concern alcohols, not ketones. No page number is available in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Premisecitation
Alcohols, particularly ethanol, propan-2-ol, butan-2-ol, octan-2-ol, and nonan-2-ol, are encountered in most soft cheeses.
“Alcohols, particularly ethanol, propan-2-01, butan-2-01, octan-2-01, and nonan-2-01, are also encountered in most soft cheeses (3) and blue cheeses (33).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
The “3) Alcools” section lists all five alcohols in stabilized soft cheeses. It does not establish that they occur in most soft cheeses; no page number is available in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measured
- Premisecitation
Oct-1-en-3-ol represents 5 to 10% of the aroma compounds of Camembert cheese.
“Oct-1-en-3-o1 represents 5 to 10% of the aroma compounds of Camembert cheese (92) but is present in only very small amounts in young Camembert cheeses.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
- Premisecitation
Diacetyl and acetoin can be rapidly transformed to butan-2,3-diol by the action of butan-2,3-diol dehydrogenase.
“Diacetyl and acetoin can also be rapidly transformed to butan-2,3-diol by the action of butan-2,3-dioldehydrogenase (29).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [29] Crow, 1990, Properties of the 2,3-butanediol dehydrogenase from Lactococcus lactis subsp. lactis in relation to citrate fermentation, Appl. Environ. Microbiol. source
- Premisecitation
The studied cheese contained almost no heptan-2-one and heptan-2-ol, compounds usually present at relatively high concentrations.
“The studied cheese contained almost no heptan-2-one and heptan-2-01, compounds usually that are present at relatively high concentrations.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [2] Adda, 1989, Production de styrène par Penicillium camemberti Thorn, Lait source
- Premisecitation
When present in excessively large amounts, oct-1-en-3-ol is responsible for an aroma defect.
“When present in excessively large amounts, oct-1-en-3-01 is responsible for an aroma defect (39,41).”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion (page unavailable) describes the aroma of other compounds, including indole, but does not discuss oct-1-en-3-ol. Searches for oct-1-en-3-ol, octenol, and an aroma defect returned no passage addressing the claim. (LLM, conf=0.73)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 7) proposes that oct-1-en-3-ol, when present in excessive amounts, could cause aroma defects. It also reports a high level in a Camembert sample with a mushroom-like aroma defect. The citing sentence states this proposed causal link as a fact, whereas the source hedges it. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Premisecitation
G. candidum deaminative activity is followed by formation of ethanol, 2-methylpropanol, 3-methylbutanol, 2-methylbutanol, 3-methylpropanol, and phenylethanol.
“These enzymes are notably found in G. candidum, which has a deaminative activity on glutamic and aspartic acids as well as on leucine, phenylalanine, and methionine (48), and is followed by formation of ethanol, 2-methylpropanol, 3-methylbutanol, 2-methylbutanol, 3-methylpropanol, and phenylethanol (35, 43, 58, 79, 119).”
Quote in the paperNot a substantial claim1 of 5 sources checked- cites [35] Degorce-Dumas, 1984, Production d’arômes par les microorganismes: les potentialités, Ind. Aliment. Agric.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [43] Dunn, 1985, Evaluation of the role of microbial Strecker-derived aroma compounds in unclean type flavors of Cheddar cheese, J. Dairy Sci. source
The Results and Discussion mention phenethanol production by yeasts generally, while Table 1 lists flavor thresholds for phenethanol and 3-methylbutanol. Neither those passages nor searches for Geotrichum candidum and amino-acid deamination establish that G. candidum forms the stated alcohols after deamination. (LLM, conf=0.77)
Experimental — accuracy not yet measured - cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
- cites [79] Latrasse, 1987, Production d’un arôme fruité par Geotnchum candidum (Staron), Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [119] Spinnler, 1991, Bioconversion of amino acids into flavoring alcohols and esters by Erwinia carotovora subsp. atroseptica, Appl. Microbiol. Biotechnol. source
- Premisecitation
Octa-1,5-dien-3-ol has been found by Adda et al. in a Camembert cheese sample having a very pronounced celluloid taste.
“Importantly, octa-1,5-dien-3-01 has been found by Adda et al. (2) in a Camembert cheese sample having a very pronounced celluloid taste.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [2] Adda, 1989, Production de styrène par Penicillium camemberti Thorn, Lait source
In ‘Origine du styrène’ (page unavailable), the authors report relatively large amounts of octadien-1,5-ol-3 in sample B. The ‘Echantillons’ section describes B as a traditional soft cheese with the celluloid-taste defect, but does not identify it specifically as Camembert or describe that sample’s taste as ‘very pronounced.’ (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
With quantities of 5 to 10 ppm of oct-1-en-3-ol in a cheese base, Moinas et al. obtained a flavor close to that of mature Camembert cheese.
“With quantities of 5 to 10 ppm in the cheese base, Moinas et al. (93) obtained a flavor close to that of mature Camembert cheese.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [93] Moinas, 1975, La flaveur des fromages. 3. Mise en évidence de quelques constituants mineurs de l’arôme du Camembert, Lait source
The Results and Discussion section (page unavailable) says a mixture containing oct-1-en-3-ol gave a neutral cheese base a characteristic Camembert note when its eight components were added in suitable proportions. It does not specify 5–10 ppm of oct-1-en-3-ol or say that the resulting flavor was close to mature Camembert. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Oct-1-en-3-ol is present in only very small amounts in young Camembert cheeses.
“Oct-1-en-3-o1 represents 5 to 10% of the aroma compounds of Camembert cheese (92) but is present in only very small amounts in young Camembert cheeses.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
- Premisecitation
In mold-ripened cheeses, Camembert and Brie in particular, the appearance of oct-1-en-3-ol is attributed to Penicillium metabolism.
“In mold-ripened cheeses, Camembert and Brie in particular, the appearance of oct-1-en-3-01 is attributed to Penicillium metabolism (39,41,63,64).”
Quote in the paperNot a substantial claim3 of 4 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Introduction (page unavailable) says this study examines five washed-rind cheeses and leaves bloomy-rind cheeses for a future publication. The Discussion and compound tables (page unavailable) do not address oct-1-en-3-ol in Camembert or Brie or attribute it to Penicillium metabolism; searches for those terms found no supporting passage. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 7) proposes that oct-1-en-3-ol in Camembert may be a metabolite of Penicillium caseicolum growing on the cheese surface. This is a tentative attribution, and the paper does not address Brie, so it does not support the claim in full. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- cites [64] Karahadian, 1985, Contribution of Penicillium sp. to the flavors of Brie and Camembert cheese, J. Dairy Sci. source
- Premisecitation
Great diversity exists in the esters in cheeses.
“Great diversity exists in the esters in cheeses (33,39,41).”
Quote in the paperNot a substantial claim2 of 3 sources checked- cites [33] Day, 1965, Gas chromatography and mass spectral identification of neutral components of the aroma fraction of blue cheese, J. Agric. Food Chem. source
- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion (page not available) describes an abundance and diversity of ethyl esters in Epoisses, and Table 5 lists several of them. But the Discussion singles out Epoisses as an exception among the five washed-rind cheeses studied; it does not establish great ester diversity in cheeses generally. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 9) reports identified aliphatic esters and a prominent aromatic ester in Camembert, supporting the presence of different esters in that cheese. The study examines Camembert samples, however, and does not establish great ester diversity across cheeses generally. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Premisecitation
Flavoring attempts by Moinas et al. on a neutral cheese base showed the possibility that the Blue cheese note of methyl ketones could be partially masked by oct-1-en-3-ol.
“Flavoring attempts by Moinas et al. (93) on a neutral cheese base showed the possibility that the Blue cheese note of methyl ketones could be partially masked by this alcohol.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [93] Moinas, 1975, La flaveur des fromages. 3. Mise en évidence de quelques constituants mineurs de l’arôme du Camembert, Lait source
The Results and Discussion section (page unavailable) describes adding a mixture containing oct-1-en-3-ol and 2-heptanone to a neutral cheese base, producing a characteristic Camembert note. It does not say that the alcohol partially masked a blue-cheese note from methyl ketones; the masking mentioned elsewhere concerns detection during analysis, not flavor. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Aldehydes are transitory compounds in cheese because they are rapidly transformed to alcohols or to corresponding acids.
“Aldehydes are transitory compounds in cheese because they are rapidly transformed to alcohols or to corresponding acids (43,69,82,83).”
Quote in the paperNot a substantial claim3 of 4 sources checked- cites [43] Dunn, 1985, Evaluation of the role of microbial Strecker-derived aroma compounds in unclean type flavors of Cheddar cheese, J. Dairy Sci. source
The Results and Discussion report concentrations of phenylacetaldehyde and phenethanol in Cheddar cheeses, and the summary discusses Strecker-type aldehydes and alcohols as flavor compounds. Neither passage says aldehydes are transitory or rapidly converted to alcohols or corresponding acids; targeted searches for those transformations found no such passage. Page numbers were not available in our copy. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites [69] Kinsella, 1976, Biosynthesis of flavors by Penicillium roqueforti, Biotechnol. Bioeng. source
- cites [82] Lees, 1978, Role of acetaldehyde in metabolism: a review. 1. Enzyme catalyzing reactions involving acetaldehyde, J. Dairy Sci. source
The review’s Introduction describes enzymatic reduction of acetaldehyde and oxidation of acetaldehyde to acetate-related products. It does not establish that aldehydes generally are rapidly transformed in cheese or are therefore transitory there. (LLM, conf=0.84)
Experimental — accuracy not yet measured - cites [83] Lees, 1978, Role of acetaldehyde in metabolism: a review. 2. Metabolism of acetaldehyde in cultured dairy products, J. Dairy Sci. source
The Formation of Acetaldehyde from Protein section says acetaldehyde could be converted in cheese to acetate and ethanol, and the alcohol-dehydrogenase discussion describes that conversion in particular bacterial cells. The paper does not establish that aldehydes generally are transitory in cheese or that these conversions occur rapidly. Page numbers are not supplied in our copy. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Some lactic bacteria can also produce acetaldehyde from glucose.
“Some lactic bacteria can also produce acetaldehyde from glucose (82,83).”
Quote in the paperNot a substantial claim2 of 2 sources checked - Premisereasoning
In late ripening, sulfur compounds are quantitatively reduced and even disappear in some products.
“In late ripening, sulfur compounds are quantitatively reduced and even disapear in some products (39,41,42).”
- Also stated in: § SULFUR COMPOUNDS Sulfur Compounds in Camembert · plain
“In late ripening, sulfur compounds are quantitatively reduced and even disapear in some products (39,41,42).”
Quote in the paperNot a substantial claim3 of 3 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Results and Discussion compare sulfur compounds across cheese types, but do not describe how their quantities change during ripening. The Discussion says methyl disulfide was found in all types examined; its failure to detect methyl sulfide is not evidence that sulfur compounds disappeared late in ripening. Searches for late ripening and changes in sulfur-compound quantities found no temporal comparison. (LLM, conf=0.78)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
- cites [42] Dumont, 1974, Etude des composés volatils neutres présents dans le vacherin, Lait source
The Discussion (Table 5; page unavailable) compares sulfur compounds across Vacherin samples and says dimethyl disulfide and 2,3,4-trithiapentane were present in all of them. Materials and Methods (page unavailable) describes the samples but does not establish a sequence of ripening stages. Our copy does not address whether sulfur compounds decline or disappear during late ripening. (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Also stated in: § SULFUR COMPOUNDS Sulfur Compounds in Camembert · plain
- Premisecitation
Those researchers also identified traces of a sulfur alcohol, 3-methylthiopropanol or methionol and ethyldisulfide.
“Those researchers also identified traces of a sulfur alcohol, 3-methylthiopropanol or methionol and ethyldisulfide.”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
Methylcinnamate, identified in Camembert cheese by Moinas et al., seems to have a particular importance in the aroma of this cheese.
“Methylcinnamate, identified in Camembert cheese by Moinas et al. (93), seems to have a particular importance in the aroma of this cheese.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [93] Moinas, 1975, La flaveur des fromages. 3. Mise en évidence de quelques constituants mineurs de l’arôme du Camembert, Lait source
- Premisecitation
Geotricum candidum is able to produce numerous esters of which some have a very pronounced melon odor.
“Geotricum candidum is also able to produce numerous esters of which some have a very pronounced melon odor (35,58,70).”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [35] Degorce-Dumas, 1984, Production d’arômes par les microorganismes: les potentialités, Ind. Aliment. Agric.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
- cites [70] Koizumi, 1982, On the aroma substances produced by three exudate yeast, Nippon Nogeikagaku Kaishi source
The Abstract reports that G. candidum culture broth smelled like melon, and the paper reports production of multiple aromatic esters. The discussion (p. 761) describes the aroma as arising from a mixture of compounds; it does not establish that particular esters individually have a pronounced melon odor. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Premisecitation
Dumont et al. isolated four sulfur compounds from a garlic note fraction: 2,4-dithiopentane, diethyldisulfide, 2,4,5-trithiohexane, and 3-methylthio-2,4-dithiapentane.
“During their work on the identification of the minor components that are present in aromatic extracts of Camembert cheeses, Dumont et al. (38,40) isolated four sulfur compounds from a garlic note fraction: 2,4-dithiopentane, diethyldisulfide, 2,4,5trithiohexane, and 3-methylthio-2,4-dithiapentane.”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
The main aldehydes encountered in Camembert cheese are hexanal, heptanal, nonanal, 2-methylbutanal, 3-methylbutanal, and benzaldehyde.
“The main aldehydes encountered m Camembert cheese are hexanal, heptanal, nonanal, 2methylbutanal, 3-methylbutanal, and benzaldehyde (39,41,42).”
Quote in the paperNot a substantial claim3 of 3 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Introduction (page unavailable) says the study examined five washed-rind cheeses—Maroilles, Livarot, Pont-l’Évêque, Epoisses and Langres—not Camembert. Searches for Camembert and the named aldehydes found no passage reporting which aldehydes predominate in Camembert. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
- cites [42] Dumont, 1974, Etude des composés volatils neutres présents dans le vacherin, Lait source
The Summary identifies the cheese studied as Vacherin–Mont-d’Or, not Camembert. The Discussion tables list compounds found in Vacherin, including benzaldehyde at trace level, but do not establish which aldehydes are main constituents of Camembert (searched: Camembert and the named aldehydes). (LLM, conf=0.76)
Experimental — accuracy not yet measured
- Premisecitation
These lactones have also been identified in Blue-type cheeses.
“These compounds have also been identified in Blue-type cheeses (33,47).”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
When the concentration of methylcinnamate was varied in a neutral cheese base in which heptan-2-one, heptan-2-ol, oct-1-en-3-ol, nonan-2-ol, phenol, and butyric acid had been added, a characteristic Camembert cheese note was obtained.
“When the concentration of this compound was varied in a neutral cheese base in which heptan-2-one, heptan-2-01, oct-1-en-3-ol, nonan-2-01, phenol, and butyric acid had been added, a characteristic Camembert cheese note was obtained.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [93] Moinas, 1975, La flaveur des fromages. 3. Mise en évidence de quelques constituants mineurs de l’arôme du Camembert, Lait source
The Results and Discussion section says that varying methyl cinnamate in a neutral cheese base containing the listed compounds produced a characteristic Camembert note when the compounds were added in suitable proportions. But the paper's mixture also contained 2-nonenone, which the citing sentence omits. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Premisecitation
Penicillium camemberti, G. candidum, and B. linens play major roles in ammonia production.
“Penicillium camemberti, G. candidum, and B. linens play major roles in ammonia production (65).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [65] Karahadian, 1987, Integrated roles of lactate, ammonia, and calcium in texture development of mold surface-ripened cheese, J. Dairy Sci. source
The section on lactate metabolism and ammonia production reports rapid ammonia production by P. caseicolum and says G. candidum and B. linens can make significant contributions during traditional cheese ripening. It does not identify the studied P. caseicolum as P. camemberti, and it qualifies the contributions of G. candidum and B. linens by ripening stage and the presence of B. linens. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Premisecitation
Adda et al. pointed out an abnormal quantity of styrene (5 mg/kg) in Camembert cheeses with a pronounced celluloid taste.
“Adda et al. (2) have pointed out an abnormal quantity of styrene (5 mglkg) in Camembert cheeses with a pronounced celluloid taste.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [2] Adda, 1989, Production de styrène par Penicillium camemberti Thorn, Lait source
The Introduction links a Celluloid taste to abnormally high styrene in the cheeses studied, and ‘Mise en évidence du styrène dans les fromages’ estimates about 5 mg/kg in sample B. The samples section describes B as a traditional soft cheese, however, rather than explicitly identifying it as Camembert; that specific designation is not established by the cited passages. Page numbers are unavailable in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measured
- Premisecitation
Dumont et al. isolated four sulfur compounds from a garlic note fraction of Camembert aromatic extracts: 2,4-dithiopentane, diethyldisulfide, 2,4,5-trithiohexane, and 3-methylthio-2,4-dithiapentane.
“Dumont et al. (38,40) isolated four sulfur compounds from a garlic note fraction: 2,4-dithiopentane, diethyldisulfide, 2,4,5trithiohexane, and 3-methylthio-2,4-dithiapentane.”
Quote in the paperNot a substantial claim1 of 2 sources checked - Premisecitation
A dimethylpyrazine and a trimethylpyrazine have been identified in Camembert cheese by Dumont et al.
“A dimethylpyrazine and a trimethylpyrazine have been identified in Camembert cheese by Dumont et al. (38,40).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [38] Dumont, 1976, L’arôme du Pont l’Evêque. Mise en évidence de constituants volatils quantitativement mineurs, Lait source
- cites [40] Dumont, 1976, L’arôme du camembert: autres composés mineurs mis en évidence, Lait source
The Results section identifies sulfur compounds and anisole derivatives in Camembert, but does not mention either dimethylpyrazine or trimethylpyrazine. Searches for both pyrazines found no passage in our copy establishing their identification; no page numbers were available. (LLM, conf=0.74)
Experimental — accuracy not yet measured
- Premisecitation
Numerous volatile amines have been identified in Camembert cheese: methylamine, ethylamine, n-propylamine, isopropylamine, n-butylamine, 1-methylpropylamine, n-amylamine, iso-amylamine, anteiso-amylamine, n-hexylamine, ethanolamine, dimethylamine, diethylamine, dipropylamine, and dibutylamine.
“Numerous volatile amines have been identified in Camembert cheese: methylamine, ethylamine, npropylamine, isopropylamine, n-butylamine, 1methylpropylamine, n-amylamine, iso-amylamine, anteiso-amylamine, n-hexylamine, ethanolamine, dimethylamine, diethylamine, dipropylamine, and dibutylamine ( 3 ).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
- Premisecitation
Many chlorinated compounds present in trace amounts have been listed for Camembert cheese: chloroform, carbon tetrachloride, dichloroethane, trichloroethane, tetrachloroethylene, dichlorobenzene, and trichlorobenzene.
“Many chlorinated compounds that are present in trace amounts have been listed for Camembert cheese: chloroform, carbon tetrachloride, dichloroethane, trichloroethane, tetrachloroethylene, dichlorobenzene, and trichlorobenzene (41).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
Table 7 (p. 14) lists all seven named chlorinated compounds and marks six as present in at least one Camembert sample, generally at trace levels. Its tetrachloroethylene row is blank for all 12 samples, so the table does not support the claim that this compound was present in trace amounts. The paper also notes that contamination cannot be excluded. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Premisecitation
For Camembert cheese, Kuzdzal-Savoie and Kuzdzal estimate that 5% of total FFA do not come from lipolysis.
“For Camembert cheese, Kuzdzal-Savoie and Kuzdzal (73) estimate that 5% of total FFA do not come from lipolysis.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [73] Kuzdzal-Savoie, 1966, Contribution à l’étude de la lipolyse dans les fromages, Tech. Lait
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisenone given
The two major methyl ketones are nonan-2-one and heptan-2-one.
“The two major methyl ketones are nonan-2-one and heptan-2-one (Table 2).”
Quote in the paperNot a substantial claim - Interpretationreasoning
Long-chain FFA (>12 carbon atoms) play a minor role in the flavor, given their high perception threshold.
“Long-chain FFA (>12 carbon atoms) playa minor role in the flavor, given their high perception threshold.”
Quote in the paperNot a substantial claim - Premisecitation
Fewer FFA are present in surface flora cheeses, such as Camembert and Brie, than in blue-veined cheeses, in which lipases have more contact with fat because of the development of molds in the interior of the cheese.
“Fewer FFA are present in surface flora cheeses, such as Camembert and Brie, than in blue-veined cheeses, in which lipases have more contact with fat because of the development of molds in the interior of the cheese (63).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- Premisecitation
The G. candidum lipase preferentially liberates oleic acid and the other unsaturated C18 FA.
“The G. candidum lipase preferentially liberates oleic acid and the other unsaturated CI8 FA (13);”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [13] Aneja, 1983, Substrate specificity of the lipase from Geotrichum candidum Link, Abstr. Paper Am. Chem. Soc.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
Concentrations of heptan-2-one and nonan-2-one in cheeses are very high and out of proportion, considering the quantity of octanoic and decanoic acids present in milk fat.
“Concentrations ofheptan-2-one and nonan-2-one in cheeses are very high and out of proportion, considering the quantity of octanoic and decanoic acids present in milk fat.”
Quote in the paperSubstantial claim - Premisecitation
For unsaturated FA, odor can vary according to the isomer considered.
“For unsaturated FA, odor can vary according to the isomer considered (115).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [115] Shirakawa, 1988, Novel flavor component for dairy products: (E)-6-decenoic acid
- Premisenone given
For Camembert cheese, methyl ketones are by far the most abundant compounds, of the order of 25 to 60 μmol/100 g of fat.
“For Camembert cheese, methyl ketones are by far the most abundant compounds, of the order of 25 to 60 ~mol/l00 g of fat.”
Quote in the paperNot a substantial claim - Premisenone given
Most of the FFA having between 4 and 20 carbon atoms come from the lipolysis of triglycerides by molds.
“Most of the FFA having between 4 and 20 carbon atoms come, in fact, from the lipolysis of triglycerides by molds.”
Quote in the paperNot a substantial claim - Premisenone given
A lower proportion of FFA having generally between 2 and 6 carbon atoms comes from the degradation of lactose and amino acids.
“A lower proportion of FFA having generally between 2 and 6 carbon atoms comes from the degradation of lactose and amino acids.”
Quote in the paperNot a substantial claim - Premisenone given
The precursors of methyl ketones are FA.
“The precursors of methyl ketones are FA (Figure 1).”
Quote in the paperNot a substantial claim - Premisecitation
Production of diacetyl and acetoin in cheese is mainly due to the activity of lactic acid bacteria, especially Lactococcus lactis ssp. lactis biovar diacetylactis.
“The production of diacetyl and acetoin is mainly due to the activity of lactic acid bacteria, especially Lactococcus lactis ssp.lactis biovar diacetylactis (61).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [61] Kaneko, 1987, The effects of metal ions on diacetyl production by Streptococcus lactis subsp. diacetylactis 3022, Agric. Biol. Chem. source
- Interpretationnone given
The mushroom, musty, and buttery notes are extremely important in Camembert cheese.
“The mushroom, musty, and buttery notes are extremely important in Camembert cheese.”
Quote in the paperNot a substantial claim - Premisenone given
Penicillium camemberti, P. roqueforti, and G. candidum possess an enzymatic system that permits a diversion from the normal β-oxidation pathway.
“Penicillium camemberti, P. roqueforti, and G. candidum possess an enzymatic system that permits a diversion from the normal i3-oxidation pathway (Figure 2).”
Quote in the paperSubstantial claim - Premisenone given
Methyl ketones are formed in a metabolic pathway that is connected to the β-oxidation pathway.
“Methyl ketones are formed in a metabolic pathway that is connected to the i3-oxidation pathway.”
Quote in the paperNot a substantial claim - Interpretationreasoning
From their odorous notes, which are typical of Camembert cheeses, and from the amounts present in these cheeses, the important function of ketones and methyl ketones in the aroma of these products can be understood.
“From their odorous notes, which are typical of Camembert cheeses, and from the amounts present in these cheeses, the important function of ketones and methyl ketones in the aroma of these products can be understood.”
Quote in the paperSubstantial claim - Premisenone given
Diacetyl and acetoin are obtained from pyruvate, stemming from lactose and citrate metabolism.
“Diacetyl and acetoin are obtained from pyruvate, stemming from lactose and citrate metabolism (Figure 3).”
Quote in the paperNot a substantial claim - Interpretationreasoning
Thus, corresponding FA are probably not the only methyl ketone precursors.
“Thus, corresponding FA are probably not the only methyl ketone precursors.”
Quote in the paperSubstantial claim - Premisecitation
The amounts of nonan-2-one, heptan-2-one, and undecan-2-one steadily increase during ripening.
“The amounts of nonan-2-one, heptan-2-one, and undecan-2-one steadily increase during ripening.”
Quote in the paperNot a substantial claim - Premisecitation
Octan-2-one, nonan-2-one, decan-2-one, undecan-2-one, and tridecan-2-one are described as having fruity, floral, and musty notes.
“Octan-2-one, nonan-2-one, decan-2-one, undecan-2one, and tridecan-2-one are described as having fruity, floral, and musty notes; heptan-2-one has a Blue cheese note (109).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [109] Rothe, 1982, Studies on characterization of blue cheese flavour, Nahrung source
- Premisenone given
Molds are most important in the formation of methyl ketones in mold-ripened cheeses.
“Molds are most important in the formation of methyl ketones in mold-ripened cheeses.”
Quote in the paperNot a substantial claim - Premisecitation
Heptan-2-one has a Blue cheese note.
“Octan-2-one, nonan-2-one, decan-2-one, undecan-2one, and tridecan-2-one are described as having fruity, floral, and musty notes; heptan-2-one has a Blue cheese note (109).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [109] Rothe, 1982, Studies on characterization of blue cheese flavour, Nahrung source
- Premisecitation
The study of the oxidation of 14C-labeled palmitic and lauric acids by P. roqueforti spores has revealed the formation of methyl ketones from long-chain FA by successive β-oxidation cycles.
“Thus, the study of the oxidation of 14C-Iabeled palmitic and lauric acids by P. roqueforti spores has revealed the formation of methyl ketones from longchain FA by successive J3-oxidation cycles (32,69).”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Phenyl-2-ethanol is a yeast metabolic product produced essentially during the first week of ripening.
“This alcohol, a yeast metabolic product, is produced essentially during the 1st wk of ripening (81).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [81] Lee, 1984, Catabolism of L-phenylalanine by some microorganisms of cheese origin, J. Dairy Res. source
- Premisecitation
Lactose metabolism leads to butan-2,3-diol formation by the mixed acids pathway.
“Lactose metabolism leads to ethanol formation by the pentose phosphate pathway and by the mixed acids pathway, which not only leads to formation of ethanol but also to butan-2,3-diol (1,26).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] Adda, 1984, Formation de la flaveur
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [26] Choisy, 1984, Les phénomènes microbiologiques et enzymatiques et la biochimie de l’affinage
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Phenyl-2-ethanol concentration stabilizes at approximately 1 ppm at the end of the ripening process.
“This concentration, which stabilizes at approxi-mately 1 ppm at the end of the ripening process, IS lower than the detection threshold, 9.1 ppm, but is close to the detection threshold of the best judge of the panel used in the study of Roger et a1.(108).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [108] Roger, 1988, Production of phenyl ethyl alcohol and its esters during ripening of traditional Camembert, J. Food Chem. source
- Premisecitation
G. candidum has a deaminative activity on glutamic and aspartic acids as well as on leucine, phenylalanine, and methionine.
“These enzymes are notably found in G. candidum, which has a deaminative activity on glutamic and aspartic acids as well as on leucine, phenylalanine, and methionine (48), and is followed by formation of ethanol, 2-methylpropanol, 3-methylbutanol, 2-methylbutanol, 3-methylpropanol, and phenylethanol (35, 43, 58, 79, 119).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [48] Greenberg, 1979, Deamination of glutamic and aspartic acids by Geotrichum candidum, J. Dairy Sci. source
- Premisecitation
Spinnler et al. demonstrated that oct-1-en-3-ol is the result of secondary metabolism.
“Spinnler et al. (120) have clearly demonstrated that this compound was the result of the secondary metabolism.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Spinnler, 1992, Effect of culture parameters on the production of styrene (vinyl benzene) and l-octene-3-ol by Penicillium caseicolum, J. Dairy Res. source
- Premisecitation
Lactose metabolism leads to ethanol formation by the pentose phosphate pathway and by the mixed acids pathway.
“Lactose metabolism leads to ethanol formation by the pentose phosphate pathway and by the mixed acids pathway, which not only leads to formation of ethanol but also to butan-2,3-diol (1,26).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] Adda, 1984, Formation de la flaveur
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [26] Choisy, 1984, Les phénomènes microbiologiques et enzymatiques et la biochimie de l’affinage
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Alcohols, particularly ethanol, propan-2-ol, butan-2-ol, octan-2-ol, and nonan-2-ol, are encountered in blue cheeses.
“Alcohols, particularly ethanol, propan-2-01, butan-2-01, octan-2-01, and nonan-2-01, are also encountered in most soft cheeses (3) and blue cheeses (33).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [33] Day, 1965, Gas chromatography and mass spectral identification of neutral components of the aroma fraction of blue cheese, J. Agric. Food Chem. source
- Premisecitation
Linoleic and linolenic acids are precursors of eight carbon aroma compounds, particularly oct-1-en-3-ol, oct-2-en-1-ol, octa-1,5-dien-3-ol, and octa-1,5-dien-1-ol.
“Linoleic and linolenic acids are precursors of eight carbon aroma compounds, particularly oct-1-en-3-01, oct-2-en-1-01, octa-1,5-dien-3-01, and octa-1,5-dien-1-01 (25,63).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [25] Chen, 1984, Studies on the enzymatic reduction of 1-octen-3-one in mushroom (Agaricus bisporus), J. Agric. Food Chem. source
- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- Premisecitation
Secondary alcohols can be converted to methyl ketones by some strains of B. linens.
“However, the secondary alcohols can be converted to methyl ketones by some strains of B. linens (11,58,69).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [11] Anderson, 1966, Quantitation, evaluation and effect of certain microorganisms on flavor components of Blue cheese, J. Agric. Food Chem. source
- cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
- cites [69] Kinsella, 1976, Biosynthesis of flavors by Penicillium roqueforti, Biotechnol. Bioeng. source
- Premisecitation
Phenylethanol production from phenylalanine seems to be essentially achieved by yeasts.
“Phenylethanol production from phenylalanine seems to be essentially achieved by yeasts (81).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [81] Lee, 1984, Catabolism of L-phenylalanine by some microorganisms of cheese origin, J. Dairy Res. source
- Premisecitation
Ethanol can come from acetaldehyde reduction by an alcohol dehydrogenase.
“Ethanol can also come from acetaldehyde reduction by an alcohol dehydrogenase (62).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [62] Kaneko, 1990, Acetoin fermentation by citrate positive Lactococcus lactis subsp. lactis 3022 grown aerobically in presence of hemin or Cu2+, Appl. Environ. Microbiol. source
- Premisecitation
The principal enzymes implied in oct-1-en-3-ol synthesis are a lipoxygenase and a hydroperoxide lyase found in molds.
“The principal enzymes implied in this alcohol synthesis are a lipoxygenase and a hydroperoxide lyase found in molds (25).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [25] Chen, 1984, Studies on the enzymatic reduction of 1-octen-3-one in mushroom (Agaricus bisporus), J. Agric. Food Chem. source
- Interpretationreasoning
Oct-1-en-3-ol is one of the key compounds in the global aromatic note of Camembert cheese.
“This compound is without a doubt one of the key compounds in the global aromatic note of Camembert cheese.”
Quote in the paperSubstantial claim - Premisecitation
Oct-1-en-3-ol has a low perception threshold of 0.01 ppm.
“Its low perception threshold, 0.01 ppm (Table 3), gives a characteristic touch to Camembert cheese aroma.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 3
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Latrasse et al. observed ester production with only one strain of G. candidum.
“Latrasse et al. (79) observed ester production with only one strain of G. candidum.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [79] Latrasse, 1987, Production d’un arôme fruité par Geotnchum candidum (Staron), Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisenone given
Lactone precursors are hydroxylated FA.
“Lactone precursors are hydroxylated FA (Figure 1).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Figure 1
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Acetate esters come from esterification of alcohols with acetyl-coenzyme A.
“For example, acetate esters come from esterification of alcohols with acetyl-coenzyme A ( 130).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [130] Yoshioka, 1981, Ester formation by alcohol acetyltransferase from brewers’ yeast, Agric. Biol Chem. source
- Premisenone given
Other sulfur compounds are also encountered in Camembert cheese.
“Other sulfur compounds are also encountered in Camembert cheese (Table 6).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 6
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisenone given
Lactones are generally characterized by very pronounced fruity notes (peach, apricot, and coconut).
“Lactones are generally characterized by very pronounced fruity notes (peach, apricot, and coconut) (Table 4).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 4
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Most esters encountered in cheeses are described as having fruity, floral notes.
“Most esters encountered in cheeses are described as having fruity, floral notes (Table 5).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 5
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisereasoning
Because of their metabolic origin, esters correspond to the acids and alcohols present in Camembert cheese.
“Because of their metabolic origin, these esters correspond to the acids and alcohols present in Camembert cheese (Table 5).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 5
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
2-methylpropanal, 2-methylbutanal, and 3-methylbutanal are encountered in cheeses, especially mold-ripened cheeses.
“With detection thresholds in malt culture media of 0.1, 0.13 and 0.06 ppm respectively, 2methylpropanal, 2-methylbutanal, and 3methylbutanal are also encountered in cheeses, especially mold-ripened cheeses (88).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [88] Margalith, 1981, Dairy products
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
2-Phenylethyl acetate concentration then drops and stabilizes around 1 ppm.
“This concentration then drops and stabilizes around 1 ppm (108),”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [108] Roger, 1988, Production of phenyl ethyl alcohol and its esters during ripening of traditional Camembert, J. Food Chem. source
- Premisecitation
The most common esters are acetates formed from acetyl-coenzyme A and an alcohol, most frequently ethanol, by the action of alcohol acyltransferases.
“The most common of those esters are the acetates formed from acetyl-coenzyme A and an alcohol, most frequently ethanol, by the action of alcohol• acyltransferases (130, 131, 132).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [130] Yoshioka, 1981, Ester formation by alcohol acetyltransferase from brewers’ yeast, Agric. Biol Chem. source
- cites [131] Yoshioka, 1983, Cellular fatty acid and ester formation by brewers’ yeast, Agric. Biol. Chem.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [132] Yoshioka, 1984, Ester formation by brewers’ yeast during fermentation, Agric. Biol. Chem.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Sulfur compounds encountered in cheeses are described as having a strong garlic, very ripe cheese odor.
“Sulfur compounds encountered in cheeses are described as having a strong garlic, very ripe cheese odor (30).”
- Also stated in: § SULFUR COMPOUNDS Sulfur Compounds in Camembert · plain
“Sulfur compounds encountered in cheeses are described as having a strong garlic, very ripe cheese odor (30).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [30] Cuer, 1979, Flavour properties of some sulfur compounds isolated from cheeses, Lebensm. Wiss. Technol.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Also stated in: § SULFUR COMPOUNDS Sulfur Compounds in Camembert · plain
- Interpretationreasoning
The reduction and disappearance of sulfur compounds in late ripening can be explained by their high volatility.
“This result can be explained by their high volatility.”
Quote in the paperNot a substantial claim - Premisecitation
Sulfur compounds essentially come from methionine degradation resulting from cleavage of a carbon-sulfur bond by a methionine demethiolase.
“Sulfur compounds essentially come from methionine degradation that results from cleavage of a bond between carbon and sulfur by a methioninedemethiolase (27,56).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] Collin, 1989, Isolement et caractérisation de la L-méthionine-γ-démethiolase de Brevibacterium linens NCDO 739, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [56] Hemme, 1982, Microbial catabolism of acids during cheese ripening, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Sulfur compounds have very low detection thresholds in water, from 0.02 ppb for methanethiol to 60 ppb for dimethylsulfide.
“Furthermore, these compounds have a very low detection threshold in water, from 0.02 ppb for methanethiol to 60 ppb for dimethylsulfide (112) (Table 6).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [112] Shankaranarayana, 1974, Volatile sulfur compounds in food flavors, Crit, Rev. Food Technol. source
- cites Table 6
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Many microorganisms are able to produce methanethiol from methionine, especially P. camemberti, G. candidum, and B. linens.
“Many microorganisms are able to produce methanethiol from methionine, especially P. camemberti, G. candidum, and B. linens (26,56,58).”
- Also stated in: § Sulfur Compound Biosynthesis · plain
“Many microorganisms are able to produce methanethiol from methionine, especially P. camemberti, G. candidum, and B. linens (26,56,58).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [26] Choisy, 1984, Les phénomènes microbiologiques et enzymatiques et la biochimie de l’affinage
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [56] Hemme, 1982, Microbial catabolism of acids during cheese ripening, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
- Also stated in: § Sulfur Compound Biosynthesis · plain
- Premisecitation
Spinnler et al. observed a correlation between styrene and oct-1-en-3-ol in the medium.
“Spinnler et al. (120) observed a correlation between styrene and oct-l-en-3-o1 in the medium.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Spinnler, 1992, Effect of culture parameters on the production of styrene (vinyl benzene) and l-octene-3-ol by Penicillium caseicolum, J. Dairy Res. source
- Premisecitation
In Brie cheeses, Karahadian et al. found sulfur compounds (dimethyldisulfide, dimethyltrisulfide, and methionol) only in aged cheese that was submitted to a second fermentation by B. linens and other coryneform bacteria.
“Nevertheless, in Brie cheeses, Karahadian et al. (63) found sulfur compounds (dimethyldisulfide, dimethyltrisulfide, and methionol) only in aged cheese that was submitted to a second fermentation by B. linens and other coryneform bacteria.”
- Also stated in: § MISCF.LLANEOUS COMPOUNDS · plain
“Nevertheless, in Brie cheeses, Karahadian et al. (63) found sulfur compounds (dimethyldisulfide, dimethyltrisulfide, and methionol) only in aged cheese that was submitted to a second fermentation by B. linens and other coryneform bacteria.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- Also stated in: § MISCF.LLANEOUS COMPOUNDS · plain
- Premisecitation
Other sulfur compounds are encountered in Camembert cheese.
“Other sulfur compounds are also encountered in Camembert cheese (Table 6).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Table 6
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Amines can be the starting point of compounds such as N-isobutylacetamide encountered in Camembert cheese, presumably by reaction with acetic acid.
“They can also be the starting point of compounds such as Nisobutylacetamide encountered in Camembert cheese, presumably by reaction with acetic acid (4).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [4] Adda, 1982, The chemistry of flavour and texture generation in cheese, Food Chem. source
- Premisecitation
Sulfur compounds essentially come from methionine degradation that results from cleavage of a bond between carbon and sulfur by a methionine demethiolase.
“Sulfur compounds essentially come from methionine degradation that results from cleavage of a bond between carbon and sulfur by a methioninedemethiolase (27,56).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] Collin, 1989, Isolement et caractérisation de la L-méthionine-γ-démethiolase de Brevibacterium linens NCDO 739, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [56] Hemme, 1982, Microbial catabolism of acids during cheese ripening, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
[13C]styrene is produced from [13C]phenylalanine.
“The [13Clstyrene is produced from [13Clphenylalanine (Spinnler et al., 1994, unpublished data).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites (Spinnler et al., 1994, unpublished data)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
These compounds have a very low detection threshold in water, from 0.02 ppb for methanethiol to 60 ppb for dimethylsulfide.
“Furthermore, these compounds have a very low detection threshold in water, from 0.02 ppb for methanethiol to 60 ppb for dimethylsulfide (112) (Table 6).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [112] Shankaranarayana, 1974, Volatile sulfur compounds in food flavors, Crit, Rev. Food Technol. source
- Premisecitation
Oct-1-en-3-ol is produced 2 to 3 d before styrene.
“Oct-l-en-3-o1 is produced 2 to 3 d before styrene.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Spinnler, 1992, Effect of culture parameters on the production of styrene (vinyl benzene) and l-octene-3-ol by Penicillium caseicolum, J. Dairy Res. source
- Premisecitation
2-Methoxy-3-isopropylpyrazine comes from L-valine degradation as found in Pseudomonas taetrolens.
“2-Methoxy-3-isopropylpyrazine comes from L-valine degradation as found in Pseudomonas taetrolens (45).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Gallois, A. 1984. Biosynthèse de la méthoxy-2-isopropyl-3 pyrazine par Pseudomonas taetrolens. Thèse de Docteur-Ingénieur, Inst. Natl. Agron., Paris-Grignon, Paris, France.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
Triethylamine, with a fishy odor, is perceived at a concentration of 0.47 ppb of free base in water.
“Triethylamine, with a fishy odor, is perceived at a concentration of 0.47 ppb of free base in water.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Amoore, 1976, Specific anosmia to trimethylamine: the fishy primary odor, J. Chem. Ecol. source
- Premisecitation
A low oxygen pressure favors amino acid decarboxylation reactions.
“A low oxygen pressure favors these reactions (52,69).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation
2-Methoxy-3-isopropylpyrazine is responsible for an aroma defect in Camembert cheese of a rotten soil, raw potato note.
“This pyrazine is responsible for an aroma defect in Camembert cheese of a rotten soil, raw potato note (89).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [89] Masuda, 1988, Olfactive properties of alkyl-pyrazines and 3-substituted 2-alkylpyrazines, J. Agnc. Food Chem. source
- Premisecitation
Johnson et al. demonstrated that some benzyl compounds came from the degradation of carotene in milk.
“Johnson et al. (57) demonstrated that some of these compounds came from the degradation of carotene in milk”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [57] Johnson, 1969, Aromatic hydrocarbons in foodstuffs and related materials, Chem. Ind.
- May combine two claims. 45
- Classified as probably not a substantial claim. 15
May combine two claims.
PremisecitationThese FFA could represent up to 10% of total FA, that is 76 mg/100 g of fresh cheese with great variations between samples.
“These FFA could represent up to 10% of total FA, that is 76 mg/100 g of fresh cheese with great variations between samples (3).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
The section on free fatty acids says that free fatty acids in Camembert can reach 10% of total fatty acids. The same section reports about 76 mg per 100 g of fresh Camembert and substantial variation between samples, but that figure is for volatile free fatty acids, not a conversion of the 10% figure for all free fatty acids. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationOf the primary alcohols, 3-methylbutan-1-ol is present in relatively large quantities in Camembert cheese and gives an alcoholic, floral note.
“Of the primary alcohols, 3-methylbutan-l-01 is present in relatively large quantities in Camembert cheese and gives an alcoholic, floral note (39, 41, 92) (Table 3).”
Quote in the paperNot a substantial claim3 of 3 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion identifies 3-methylbutan-1-ol as a major primary alcohol in the cheeses studied, and the Résumé names five washed-rind cheeses—not Camembert. The Discussion assigns floral odors to other compounds, not to 3-methylbutan-1-ol, and does not describe an alcoholic note from it. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 3) states that 3-methylbutan-1-ol, a primary alcohol, is consistently present in relatively large quantities in Camembert. The passages found do not describe it as giving an alcoholic, floral note; that sensory part of the claim is unsupported by our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
The Summary says Camembert’s volatile constituents include primary alcohols, but Table 1 does not identify 3-methylbutan-1-ol among the measured constituents. The discussion attributes aroma effects to other compounds and does not describe an alcoholic, floral note from 3-methylbutan-1-ol. Page numbers are unavailable in our copy. (LLM, conf=0.82)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationPhenylethylacetate plays an important role in raw milk Camembert cheeses, in which it is always present.
“Phenyl-2-ethanol, with a perception threshold in a cheese base of 9.1 ppm and a characteristic rose floral note (l 0 8), and its ester, phenylethylacetate, play an important role in raw milk Camembert cheeses in which they are always present (7,39,41).”
Quote in the paperNot a substantial claim2 of 3 sources checked- cites [7] Adda, 1978, Some recent advancement in the knowledge of cheese flavor source
- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion (page unavailable) identifies phenylethyl acetate as an important aromatic compound, and Table 6 lists it in all five cheeses examined. The Introduction identifies those cheeses as washed-rind varieties, not raw-milk Camembert, so the source does not establish that it is always present or important in raw-milk Camembert. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
May combine two claims.
PremisecitationMoinas et al. did not report pentan-2-ol in mature Camembert cheeses but identified it in young samples only.
“However, Moinas et al. (92) have not reported this alcohol in mature Camembert cheeses but identified this alcohol in young samples only.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
May combine two claims.
Premisecitation3-methylbutan-1-ol is present in relatively large quantities in Camembert cheese and gives an alcoholic, floral note.
“Of the primary alcohols, 3-methylbutan-l-01 is present in relatively large quantities in Camembert cheese and gives an alcoholic, floral note (39, 41, 92) (Table 3).”
Quote in the paperNot a substantial claim3 of 3 sources checked- cites [39] Dumont, 1974, Etude des composés volatils neutres présents dans les fromages à pâte molle et à croûte lavée, Lait source
The Discussion (page unavailable) identifies 3-methylbutan-1-ol as a major primary alcohol in the cheeses studied, and the Résumé names five washed-rind cheeses. Neither passage establishes its abundance in Camembert. The Discussion associates floral odors with other compounds, not with 3-methylbutan-1-ol, and does not describe an alcoholic note for it. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [41] Dumont, 1974, Etude des composés neutres volatils présents dans le Camembert, Lait source
The Discussion (p. 3) says that 3-methylbutan-1-ol, a primary alcohol, is consistently present in relatively large quantities in Camembert. It does not say that this compound gives an alcoholic, floral note; searches for that sensory description found no supporting passage. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
The Summary says Camembert contains primary and secondary alcohols, but Table 1 and the Discussion do not identify 3-methylbutan-1-ol or describe an alcoholic, floral note. Searches for the compound and its French name found no passage addressing its presence, quantity, or sensory effect. (LLM, conf=0.72)
Experimental — accuracy not yet measured
May combine two claims.
Premisecitationβ-Oxidation is a particularly important metabolic pathway because 60% of the carbonyl compounds produced by P. camemberti on a milk-based medium are methyl ketones.
“i3-0xidation is a particularly important metabolic pathway because 60% of the carbonyl compounds produced by P. camemberti on a milk-based medium are methyl ketones (99).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [99] Okumara, 1985, Methyl ketone formation by Penicillium camemberti in model systems, J. Dairy Sci. source
The Abstract and the results under “Time of Incubation” report that approximately 60% of the carbonyls produced by P. camemberti in the milk-lipid model system were methyl ketones. The paper describes oxidation of free fatty acids but does not explicitly establish that β-oxidation is the particularly important pathway responsible for that proportion. (LLM, conf=0.80)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationThese volatile compounds are not only typical of Camembert-type cheeses, but are also abundant in veined cheeses in which heptan-2-one is the compound present in the largest quantity.
“These volatile compounds are not only typical of Camembert-type cheeses, but are also abundant in veined cheeses in which heptan-2-one is the compound present in the largest quantity (3,33).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
The paper’s “2.1. Cétones” section reports methyl ketones, including 2-heptanone, in veined cheeses, while its Camembert table reports them in Camembert. In the discussion following Tables 8–10 (page unavailable), it reports that 2-heptanone was the most abundant compound in some Blue-cheese samples, but explicitly notes conflicting results; the claim overgeneralizes that finding to veined cheeses. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [33] Day, 1965, Gas chromatography and mass spectral identification of neutral components of the aroma fraction of blue cheese, J. Agric. Food Chem. source
May combine two claims.
PremisecitationIn Camembert cheese, heptan-2-ol and nonan-2-ol represent 10-20% and 5-10%, respectively, of all aromatic compounds.
“The principal secondary alcohols encountered are heptan-2-01 and nonan-2-ol, which represent, like the methyl ketones from which they are derived, 10 to 20% and 5 to 10%, respectively, of all aromatic compounds in that cheese (92).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [92] Moinas, 1973, La flaveur des fromages. 1. Une méthodologie nouvelle d’isolement de consti-tuants volatils. Application au Roquefort et au Camembert, Lait source
May combine two claims.
Premisecitation2-methylisoborneol has a very low detection threshold of 0.1 ppb, which is the reason for its major role in the flavor of soft and mold-ripened cheeses.
“Its very low detection threshold, 0.1 ppb, is the reason for its major role in the flavor of soft and mold-ripened cheeses (63,64).”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
- cites [64] Karahadian, 1985, Contribution of Penicillium sp. to the flavors of Brie and Camembert cheese, J. Dairy Sci. source
The Results and Discussion reports a 0.1 ppb detection threshold and says that even small amounts of 2-methylisoborneol can significantly affect Brie flavor. It does not establish a major role across soft and mold-ripened cheeses generally; the flavor evidence concerns Brie, while the Introduction describes it as a potential contributor to Brie and Camembert flavors. Page numbers are unavailable in our copy. (LLM, conf=0.85)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationIn mold-ripened cheeses, the proteolytic activity of P. camemberti is predominant and leads to peptide formation, which is sometimes responsible for a certain bitterness.
“In mold-ripened cheeses, the proteolytic activity of P. camemberti is predominant and leads to peptide formation, which is sometimes responsible for a certain bitterness (84,85,94).”
Quote in the paperNot a substantial claim2 of 3 sources checked- cites [84] Lemieux, 1991, Bitter flavour in dairy products. I. A review of the factors likely to influence its development, mainly in cheese manufacture, Lait source
In “Surface moulded soft cheeses (Camembert type)” (page unavailable), the review says that, when its growth is not limited, Penicillium caseicolum appears to be the principal factor responsible for bitterness in Camembert, and links reduced Penicillium growth and acid proteinase action with reduced bitterness. Its discussion of cheese proteolysis also links peptide formation to bitter taste. Our copy does not identify P. caseicolum as P. camemberti or establish that P. camemberti’s proteolytic activity is predominant across mold-ripened cheeses. (LLM, conf=0.78)
Experimental — accuracy not yet measured - cites [85] Lemieux, 1992, Bitter flavour in dairy products. II. A review of peptides from caseins: their formation, isolation and identification, structure masking and inhibition, Lait source
In the discussion of Camembert bitterness (page unavailable), the review says surface-mould proteolysis may provide peptide precursors, which starter proteinases then degrade into bitter peptides. It identifies the mould as Penicillium caseicolum; it does not establish that P. camemberti has predominant proteolytic activity or that its activity alone produces the bitter peptides. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [94] Molimard, 1994, Amertume et fractions azotées de fromages à pâte molle de type camembert: rôle de l’association de Penicillium camemberti avec Geotrichum candidum, Lait source
May combine two claims.
PremisecitationP. camemberti catabolizes valine to 2-methylpropanol and leucine to 3-methylbutanol.
“In the same way, P. camemberti catabolizes valine to 2methylpropanol and leucine to 3-methylbutanol (64).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [64] Karahadian, 1985, Contribution of Penicillium sp. to the flavors of Brie and Camembert cheese, J. Dairy Sci. source
The Results and Discussion table lists 3-methyl-1-butanol among Brie cheese volatiles, but does not link it to leucine catabolism by P. camemberti. Searches for valine, leucine, and 2-methylpropanol found no passage establishing either claimed conversion; the paper’s discussion of P. camemberti instead concerns methyl ketones and corresponding alcohols from fatty acids. (LLM, conf=0.75)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationEster appearance in fermented beverages is due to yeast activity.
“Their appearance is due to yeast activity (60,130).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [60] Kallel-Mhiri, 1993, Mechanism of ethyl acetate synthesis by Kluyveromyces fragilis, FEMS (Fed. Eur. Microbiol. Soc.) Microbiol. Lett. source
The Introduction describes ethyl acetate synthesis by several yeasts, including brewer’s yeast, and the Results examine its synthesis by Kluyveromyces fragilis. This supports yeast activity as a source of an ester, but the paper studies ethyl acetate in a whey-permeate culture, not the appearance of esters generally in fermented beverages. (LLM, conf=0.83)
Experimental — accuracy not yet measured - cites [130] Yoshioka, 1981, Ester formation by alcohol acetyltransferase from brewers’ yeast, Agric. Biol Chem. source
May combine two claims.
PremisecitationDumont et al. also identified traces of 3-methylthiopropanol (methionol) and ethyldisulfide in Camembert.
“Those researchers also identified traces of a sulfur alcohol, 3-methylthiopropanol or methionol and ethyldisulfide.”
Quote in the paperNot a substantial claim1 of 2 sources checkedMay combine two claims.
PremisecitationAdda et al. demonstrated the role played by P. camemberti in styrene production, which occurs when metabolism of linoleic and linolenic acids is higher than usual.
“Those researchers demonstrated the role played by P. camemberti in this hydrocarbon production, which occurs when metabolism of linoleic and linolenic acids is higher than usual.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [2] Adda, 1989, Production de styrène par Penicillium camemberti Thorn, Lait source
In “Origine du styrène” (page unavailable), the paper says styrene’s presence is clearly linked to Penicillium activity. The same section treats unusually intense oxidation as an inference from compounds associated with linolenic and linoleic acids; it does not demonstrate that increased metabolism of those acids causes styrene production. (LLM, conf=0.87)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationNonvolatile amines have been identified and quantified in Camembert cheese: tyramine at 0.023 to 2 ppm, histamine at 209 ppm, and tryptamine and putrescine at 92 ppm.
“Nonvolatile amines have also been identified and quantified in Camembert cheese: tyramine at 0.023 to 2 ppm, histamine at 209 ppm, and tryptamine and putrescine at 92 ppm (3,69).”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [3] Adda, 1974, Les substances responsables de l’arôme des fromages à pâte molle, Lait source
The “Amines non-volatiles” section reports Camembert histamine at 209 µg/g (equivalent to 209 ppm) and putrescine at 92 µg/g. It reports tryptamine at 20 µg/g, not 92 ppm. Table 5 gives tyramine concentrations in µg/g, but does not support the claimed 0.023–2 ppm range for Camembert. (LLM, conf=0.90)
Experimental — accuracy not yet measured - cites [69] Kinsella, 1976, Biosynthesis of flavors by Penicillium roqueforti, Biotechnol. Bioeng. source
May combine two claims.
PremisecitationShort and moderate-chain, even-numbered FA (C4 to C12) have much lower perception thresholds, and each has a characteristic note.
“Short and moderate-chain, even-numbered FA (C 4 to C12) have much lower perception thresholds, and each has a characteristic note (Table 1) (20).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] Brennand, 1989, Aroma properties and thresholds of some branched-chain and other minor volatile fatty acids occurring in milkfat and meat lipids, J. Sensory Stud. source
May combine two claims.
InterpretationreasoningAccording to their concentration and perception threshold, volatile FA can contribute to the aroma of the cheese or to a rancidity defect.
“According to their concentration and perception threshold, volatile FA can contribute to the aroma of the cheese or to a rancidity defect.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone givenP. camemberti produces a large quantity of exocellular lipase, the main agent of lipolysis in Camembert cheese.
“P. camemberti produces a large quantity of exocellular lipase, the main agent of lipolysis in Camembert cheese.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMilk fat contains 98% of glyceride neutral lipids characterized by the wide variety of FA of which they are composed.
“Milk fat contains 98% of glyceride neutral lipids characterized by the wide variety of FA of which they are composed (26).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [26] Choisy, 1984, Les phénomènes microbiologiques et enzymatiques et la biochimie de l’affinage
May combine two claims.
Premisenone givenMethyl ketones with even-numbered chains, except for butan-2-one, appear later during ripening and are never present in large amounts, except in very ripe cheeses, which is also true for unsaturated methyl ketones.
“Methyl ketones with even-numbered chains, except for butan-2-one, appear later during ripening and are never present in large amounts, except in very ripe cheeses, which is also true for unsaturated methyl ketones.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPhenyl-2-ethanol has a perception threshold in a cheese base of 9.1 ppm and a characteristic rose floral note.
“Phenyl-2-ethanol, with a perception threshold in a cheese base of 9.1 ppm and a characteristic rose floral note (l 0 8), and its ester, phenylethylacetate, play an important role in raw milk Camembert cheeses in which they are always present (7,39,41).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [108] Roger, 1988, Production of phenyl ethyl alcohol and its esters during ripening of traditional Camembert, J. Food Chem. source
May combine two claims.
PremisecitationGeotricum candidum produces methyl ketones, such as pentan-2-one, heptan-2-one, nonan-2-one, and undecan-2-one, and also pentan-3-one.
“Geotricum candidum produces methyl ketones, such as pentan-2-one, heptan-2-one, nonan-2-one, and undecan-2-one (58, 79), and also pentan-3-one, which was first identified by Jollivet et a1.(58) in the cultures of eight strains of G. candidum.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
- cites [79] Latrasse, 1987, Production d’un arôme fruité par Geotnchum candidum (Staron), Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationOct-1-en-3-one has a mushroom note in aqueous media and a metallic note in lipid media.
“Oct-1-en-3-one has a mushroom note in aqueous media and a metallic note in lipid media (90,124).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [90] Meilgaard, 1975, Flavor chemistry of beer. Part I. Flavor and threshold of 239 aroma volatiles, Tech. Q.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [124] Teranishi, 1981, Some properties of odoriferous molecules source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationDiacetyl and acetoin are well known for their buttery notes.
“Diacetyl and acetoin are well known for their buttery notes (14,78).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenAll methyl ketones in Camembert and Brie cheeses are present from the 8th d of ripening onward.
“All methyl ketones in Camembert and Brie cheeses are present from the 8th d of ripening onward.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationCamembert cheeses made of raw milk contain more even-numbered carbon methyl ketones and also contain ramified methyl ketones.
“Camembert cheeses made of raw milk contain more even-numbered carbon methyl ketones and also contain ramified methyl ketones.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe eight strains of G. candidum studied by Jollivet et al. produced 2-methylpropan-3-ol, an alcohol which had never been described before in cheese.
“The eight strains of G. candidum studied by Jollivet et al. (58) produced 2-methylpropan-3-01, an alcohol, which had never been described before in cheese.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [58] Jollivet, 1994, Production of volatile compounds in model milk and cheese media by eight strains of Geotrichum candidum Link, J. Dairy Res. source
May combine two claims.
PremisecitationAlcohols appear rapidly after methyl ketone synthesis and seem to be a detoxifying pathway to protect microorganisms.
“The alcohols appear rapidly after methyl ketone synthesis, and seem to be a detoxifying pathway to protect the microorganisms (69).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [69] Kinsella, 1976, Biosynthesis of flavors by Penicillium roqueforti, Biotechnol. Bioeng. source
May combine two claims.
InterpretationreasoningOct-1-en-3-ol only appears late in the cheese ripening process because it is produced by P. camemberti metabolism.
“Furthermore, because it is produced by P. camemberti metabolism, oct-1-en-3-o1 only appears late in the cheese ripening process.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPhenyl-2-ethanol concentration is lower than its detection threshold of 9.1 ppm but close to the detection threshold of the best judge of the panel used in the study of Roger et al.
“This concentration, which stabilizes at approxi-mately 1 ppm at the end of the ripening process, IS lower than the detection threshold, 9.1 ppm, but is close to the detection threshold of the best judge of the panel used in the study of Roger et a1.(108).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [108] Roger, 1988, Production of phenyl ethyl alcohol and its esters during ripening of traditional Camembert, J. Food Chem. source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe most commonly cited aromatic notes describing esters are pineapple, banana, apricot, pear, floral, rose, honey, and wine.
“The most commonly cited aromatic notes describing these compounds are pineapple, banana, apricot, pear, floral, rose, honey, and wine (55,90).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [55] 1978, Imitation flavorings
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [90] Meilgaard, 1975, Flavor chemistry of beer. Part I. Flavor and threshold of 239 aroma volatiles, Tech. Q.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Premisecitation2-methylpropanal, 2-methylbutanal, and 3-methylbutanal have detection thresholds in malt culture media of 0.1, 0.13 and 0.06 ppm respectively.
“With detection thresholds in malt culture media of 0.1, 0.13 and 0.06 ppm respectively, 2methylpropanal, 2-methylbutanal, and 3methylbutanal are also encountered in cheeses, especially mold-ripened cheeses (88).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [88] Margalith, 1981, Dairy products
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationIsoamyl acetate is detected in water at a concentration of 2 ppb.
“Such is the case of isoamyl acetate, which is detected in water at a concentration of 2 ppb (105).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [105] Piendl, 1980, Technological factors in the formation of esters during fermentation, Brew. Dig.
May combine two claims.
PremisecitationHexanal and (E)-hex-2-enal perception thresholds in water are 9.18 and 24.2 ppb, respectively.
“Their perception thresholds in water are 9.18 and 24.2 ppb, respectively (8).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] Ahmed, 1978, Flavor and odor thresholds in water of selected orange juice components, J. Agric. Food Chem. source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThis potential is used for biotechnological production of aromatic aldehydes.
“This potential is used for biotechnological production of aromatic aldehydes (96).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [96] Murray, 1988, Development of biotechnological processes for the production of natural flavors and fragrances
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationOn the 7th day of ripening, 2-phenylethyl acetate is the principal compound of the aromatic profile at a concentration of 4.6 ppm.
“On the 7th d of ripening, 2-phenylethyl acetate is the principal compound of the aromatic profile at a concentration of 4.6 ppm.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [108] Roger, 1988, Production of phenyl ethyl alcohol and its esters during ripening of traditional Camembert, J. Food Chem. source
May combine two claims.
PremisecitationLipases can liberate hydroxy acids, and the triglycerides are then cyclized.
“Lipases can liberate them, and the triglycerides are then cyclized.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [126] Urbach, 1972, Volatile compounds in butter oil. II. Flavour and flavour thresholds of lactones, fatty acids, phenols, indole and skatole in deodorized synthetic butter, J. Dairy Res. source
May combine two claims.
PremisecitationThis reaction is simple and can occur without enzymatic catalysis during ripening.
“This reaction is simple and can occur without enzymatic catalysis during ripening (67).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [67] Keeney, 1957, Probable role of the Strecker degradation of amino acids in development of cheese flavor, J. Dairy Sci. source
May combine two claims.
PremisecitationThresholds are relatively low for γ-octalactones, γ-decalactones, and γ-dodecalactones (7 to 11 ppb in water) and even lower for shorter chain lactones.
“These thresholds are relatively low for -y-octalactones, -y-decalactones, and -ydodecalactones (7 to 11 ppb in water) and even lower for shorter chain lactones (36).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [36] Dufossé, 1994, Importance des lactones dans les arômes alimentaires: structures, distribution, propriétés sensorielles et biosynthèse, Sci. Aliment.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationHexanal, heptanal, and nonanal detection thresholds in deodorized butter oil are 0.19, 0.75, and 1 ppm, respectively.
“Hexanal, heptanal, and nonanal detection thresholds in deodorized butter oil are 0.19,0.75, and 1 ppm, respectively ( 116).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [116] Siek, 1969, Taste thresholds of butter volatiles in deodorized butteroil medium, J. Food Sci. source
May combine two claims.
PremisecitationHydroxylated FA can come from normal catabolism of FA and can be generated from unsaturated FA by the action of lipoxygenases or hydratases.
“Nevertheless, hydroxylated FA can come from the normal catabolism of FA and can be generated from unsaturated FA by the action oflipoxygenases or hydratases (36).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [36] Dufossé, 1994, Importance des lactones dans les arômes alimentaires: structures, distribution, propriétés sensorielles et biosynthèse, Sci. Aliment.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationBenzaldehyde is described as having an aromatic note of bitter almond and a detection threshold in water of 350 ppb.
“Benzaldehyde is described as having an aromatic note of bitter almond and a detection threshold in water of 350 ppb (21).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [21] Buttery, 1988, Contribution of volatiles to rice aroma, J. Agric. Food Chem. source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationChalier and Crouzet performed the bioconversion from soy and copra oil with spores.
“Chalier and Crouzet (24) performed the bioconversion from soy and copra oil with spores.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [24] Chalier, 1992, Production of lactones by Penicillium roqueforti, Biotechnol. Lett. source
Probably not a substantial claim: may not pass S4 (based).
InterpretationreasoningThis result can be explained by their high volatility.
“This result can be explained by their high volatility.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationStyrene and oct-1-en-3-ol are produced after 15 d of culturing, when there is no more glucose in the growth medium.
“These two compounds are produced after 15 d of culturing, when there is no more glucose in the growth medium.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Spinnler, 1992, Effect of culture parameters on the production of styrene (vinyl benzene) and l-octene-3-ol by Penicillium caseicolum, J. Dairy Res. source
May combine two claims.
InterpretationreasoningStyrene and oct-1-en-3-ol are secondary metabolites.
“These are then secondary metabolites.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisecitation2,5-Dimethylpyrazine imparts a toasted hazelnut note, which could come from threonine degradation.
“2,5-Dimethylpyrazine imparts a toasted hazelnut note (89), which could come from threonine degradation.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [89] Masuda, 1988, Olfactive properties of alkyl-pyrazines and 3-substituted 2-alkylpyrazines, J. Agnc. Food Chem. source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationStyrene's perception threshold in cream is 5 ppb.
“Its perception threshold in cream is 5 ppb (91).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [91] Miltz, 1980, Sensory threshold of styrene and the monomer migration from polystyrene food packages, J. Food Process. Preserv. source
May combine two claims.
PremisecitationEthylamine and butylamine have basic perception thresholds in water from 0.83 to 3.63 and 0.24 to 13.9 ppm of free base, respectively.
“Ethylamine and butylamine have basic perception thresholds in water from 0.83 to 3.63 and 0.24 to 13.9 ppm of free base, respectively (74).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [74] Laivg, 1978, Olfactory properties of amines and n-butanol, Chem. Sens. Flavour source
May combine two claims.
PremisecitationNitrosamines have been described in Camembert cheese at a concentration of 25 nmol/10 g, but not in Blue cheeses.
“Nitrosamines have also been described in Camembert cheese at a concentration of 25 nmol/l0 g, but not in Blue cheeses (69).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [69] Kinsella, 1976, Biosynthesis of flavors by Penicillium roqueforti, Biotechnol. Bioeng. source
May combine two claims.
PremisecitationMethylamine, dimethylamine, and propylamine have perception thresholds in water of 182, 34.4, and 62.4 ppm of free base, respectively.
“Methylamine, dimethylamine, and propylamine have perception thresholds in water of 182, 34.4, and 62.4 ppm of free base, respectively (10).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Amoore, 1976, Specific anosmia to trimethylamine: the fishy primary odor, J. Chem. Ecol. source
May combine two claims.
PremisecitationMethionine is a methanethiol precursor, and methanethiol is the starting point of dimethyldisulfide and dimethyltrisulfide.
“This amino acid is a methanethiol precursor, which is itself the starting point of a few other compounds, such as dimethyldisulfide and dimethyltrisulfide (49,112).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationSeven percent of the population has a specific anosmia for triethylamine, which is a widespread pheromone in mammalia.
“Seven percent of the population has a specific anosmia for this amine, which is a widespread pheromone in mammalia (10).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Amoore, 1976, Specific anosmia to trimethylamine: the fishy primary odor, J. Chem. Ecol. source
May combine two claims.
PremisecitationMethionine is a methanethiol precursor, which is itself the starting point of a few other compounds, such as dimethyldisulfide and dimethyltrisulfide.
“This amino acid is a methanethiol precursor, which is itself the starting point of a few other compounds, such as dimethyldisulfide and dimethyltrisulfide (49,112).”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenFor chlorinated compounds in Camembert, an external origin is not excluded (e.g., pesticides, cleaning agents, pollution, or artifacts from solvent extraction).
“For those compounds, an external origin is not excluded (e.g., pesticides, cleaning agents, pollution, or artifacts from solvent extraction).”
Quote in the paperNot a substantial claimMay combine two claims.
Premisecitation2-Methoxy-3-isopropylpyrazine has a very low perception threshold (0.002 ppb in a milk medium), demonstrating its importance when present even in very low amounts.
“Its perception threshold is very low (0.002 ppb in a milk medium), demonstrating its importance when present even in very low amounts (45,46,63).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [45] Gallois, A. 1984. Biosynthèse de la méthoxy-2-isopropyl-3 pyrazine par Pseudomonas taetrolens. Thèse de Docteur-Ingénieur, Inst. Natl. Agron., Paris-Grignon, Paris, France.
- cites [46] Gallois, 1984, Les pyrazines présentes dans nos aliments. Etat actuel de nos connaissances, Sci. Aliment.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [63] Karahadian, 1985, Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors, J. Agric. Food Chem. source
The paper relies on this without support.
The enzymatic activities involved in the transformation of amino acids and fatty acids to aroma compounds are not well known, and the metabolic pathways are hypothetical.
“The enzymatic activities involved in the transformation of amino acids and fatty acids (FA) to aroma compounds are not well known, and the metabolic pathways are hypothetical.”
The paper relies on this without support.
Few thresholds in oil or butter appear in the literature.
“Few thresholds in oil or butter appear in the literature.”
The paper relies on this without support.
The concentration of odorous compounds is often low, and the sensitivity of physical detectors is not high enough to reveal them at concentrations lower than 10 ppb.
“Furthermore, on the one hand, the concentration of odorous compounds is often low, and the sensitivity of the physical detectors is not high enough to reveal them at concentrations lower than 10 ppb.”
The paper relies on this without support.
The major nonvolatile constituents of cheese are not compatible with direct chromatographic analysis.
“On the other hand, the major nonvolatile constituents of cheese are not compatible with direct chromatographic analysis.”
The paper relies on this without support.
The wide diversity of physical and chemical properties of the compounds involved in the aroma of food and the interactions between aromatic molecules and the matrix are the reasons why no ideal extraction method exists.
“The wide diversity of physical and chemical properties of the compounds involved in the aroma of food and the interactions between aromatic molecules and the matrix are the reasons why no ideal extraction method exists.”
The paper relies on this without support.
Diacetyl and acetoin come from citrate present in milk.
“Diacetyl and acetoin come from citrate present in milk.”
The paper relies on this without support.
Methyl ketones can be reduced to the corresponding secondary alcohols by reductase activity.
“Methyl ketones can be reduced to the corresponding secondary alcohols by reductase activity.”
The paper relies on this without support.
Aldehydes originate from amino acids either by transamination, leading to an imide that can be decarboxylated, or by Strecker degradation.
“Aldehydes originate from amino acids either by transamination, leading to an imide that can be decarboxylated, or by Strecker degradation.”
The paper relies on this without support.
The closing of the lactone ring occurs by the action of pH, microorganisms, or both.
“The closing of the ring occurs by the action of pH, microorganisms, or both.”
The paper relies on this without support.
Esterification reactions occur between short-to medium-chain FA and alcohols (ethanol) derived from lactose fermentation or from amino acid catabolism.
“Esterification reactions occur between short-to medium-chain FA and alcohols (ethanol) derived from lactose fermentation or from amino acid catabolism.”
The paper relies on this without support.
Disulfides are generally absent in young cheeses.
“Disulfides are generally absent in young cheeses.”
The paper relies on this without support.
In young cheeses, limited proteolysis yields only few sulfur amino acids, which are precursors of disulfides.
“In those cheeses, limited proteolysis yields only few sulfur amino acids, which are precursors of disulfides.”
The paper relies on this without support.
Ammonia, derived from amino acid deamination, is an important element of Camembert cheese aroma.
“It should be remembered that ammonia, derived from amino acid deamination, is also an important element of Camembert cheese aroma.”
The paper relies on this without support.
Amino acid decarboxylation leads to carbon dioxide and free amines.
“Amino acid decarboxylation leads to carbon dioxide and free amines.”
The paper relies on this without support.
The amino acid decarboxylation reaction needs pyridoxal-phosphate as coenzyme.
“This reaction needs the presence of pyridoxal-phosphate as coenzyme.”
The paper relies on this without support.
Leucine gives isobutylamine, phenylalanine gives phenylethylamine, and tyrosine gives tyramine.
“Leucine thus gives isobutylamine, phenylalanine gives phenylethylamine, and tyrosine gives tyramine.”
The paper relies on this without support.
Amines are not a final step.
“Amines are not a final step.”
The paper relies on this without support.
Amines can be submitted to oxidative deamination, which would give aldehydes.
“They can be submitted to oxidative deamination, which would give aldehydes.”
The paper relies on this without support.
Styrene has a very strong plastic odor.
“Styrene has a very strong plastic odor.”
The paper relies on this without support.
Benzyl compounds have been identified in Camembert: benzene, ethylbenzene, dimethylbenzene, trimethylbenzene, and toluene.
“In the same way, benzyl compounds have been identified: benzene, ethylbenzene, dimethylbenzene, trimethylbenzene, and toluene.”
The paper relies on this without support.
Most studies demonstrating the presence of traces of benzyl compounds have been conducted on extracts obtained by use of solvents.
“most studies demonstrating the presence of traces of these compounds have been conducted on extracts that were obtained by use of solvents.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Both P. roqueforti and P. camemberti produce aspartyl proteinases and metalloproteinases; P. camemberti also possesses an intracellular acid proteinase, whereas P. roqueforti produces a broad specificity carboxypeptidase, an extracellular metallo-aminopeptidase and amino- and carboxypeptidases.
“Both species produce aspartyl proteinases and metalloproteinases; P. camemberti also possesses an intracellular acid proteinase, whereas P. roqueforti produces a broad specificity carboxypeptidase, an extracellular metallo-aminopeptidase (see [57]) and amino-and carboxypeptidases [110].”
From Biochemical pathways for the production of flavour compounds in cheeses during ripening: A review (2000) · cites this paper as [110]
Split into 2 atoms — 0 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 2 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
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Effects of Diet on Short-Term Regulation of Feed Intake by Lactating Dairy Cattle
Allen, M. S. (2000) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(00)75030-2 · Cited by 1,550 · see citing works
Biochemical pathways for the production of flavour compounds in cheeses during ripening: A review
McSweeney, P. L. H., & Sousa, M. J. (2000) · Le Lait · doi:10.1051/lait:2000127 · Cited by 1,266 · see citing works
The Composition of Bovine Milk Lipids: January 1995 to December 2000
Jensen, R. G. (2002) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(02)74079-4 · Cited by 1,077 · see citing works
Biochemistry of cheese ripening
McSweeney, P. L. H. (2004) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.2004.00147.x · Cited by 1,048 · see citing works
“…early stages of β-oxidation caused by the action of spores and vegetative mycelia of P. roqueforti (Urbach 1997; Chalier and Crouzet 1998; Collins et al. 2003b, 2004) and perhaps other fungi (e.g. P. camemberti or G. candidum) (Lamberet et al. 1982; Cerning et al. 1987; Molimard and Spinnler 1996).”
BackgroundFlavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products
Smit, G., Smit, B. A., & Engels, W. J. M. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.fmrre.2005.04.002 · Cited by 949 · see citing works
Lipolysis and free fatty acid catabolism in cheese: a review of current knowledge
Collins, Y. F., McSweeney, P. L. H., & Wilkinson, M. G. (2003) · International Dairy Journal · doi:10.1016/s0958-6946(03)00109-2 · Cited by 777 · see citing works
Key odorants in various cheese types as determined by gas chromatography-olfactometry
Curioni, P. M. G., & Bosset, J. O. (2002) · International Dairy Journal · doi:10.1016/s0958-6946(02)00124-3 · Cited by 733 · see citing works
Cheese flavour formation by amino acid catabolism
Yvon, M., & Rijnen, L. (2001) · International Dairy Journal · doi:10.1016/s0958-6946(01)00049-8 · Cited by 736 · see citing works
Bacterial populations and the volatilome associated to meat spoilage
Casaburi, A., Piombino, P., Nychas, G. E., Villani, F., & Ercolini, D. (2014) · Food Microbiology · doi:10.1016/j.fm.2014.02.002 · Cited by 724 · see citing works
“Fatty acids having generally between 2 and 6 carbon atoms come from the 424 degradation of amino acids and can also arise from ketones, esters and aldehydes by oxidation 425 (Molimard and Spinnler, 1996).”
BackgroundTraditional Cheeses: Rich and Diverse Microbiota with Associated Benefits
Montel, M.-C., Buchin, S., Mallet, A., Delbes-Paus, C., Vuitton, D. A., Desmasures, N., & Berthier, F. (2014) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2014.02.019 · Cited by 665 · see citing works
“Penicillium species are decisive for the flavour and texture of whitemould-ripened cheeses owing to their lipolytic and oxidative activities, leading to high production of aromatic ketones and alcohols (Molimard and Spinnler, 1996).”
BackgroundVolatile Flavor Compounds in Yogurt: A Review
Cheng, H. (2010) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408390903044081 · Cited by 607 · see citing works
“Most esters have a fruity and floral flavor and may contribute to the aroma and flavor by minimizing the sharpness and bitterness imparted by fatty acids and amines (Guler, 2007; Molimard and Spinnler, 1996).”
BackgroundInfluentialMicrobial modulation of aromatic esters in wine: Current knowledge and future prospects
Sumby, K. M., Grbin, P. R., & Jiranek, V. (2009) · Food Chemistry · doi:10.1016/j.foodchem.2009.12.004 · Cited by 567 · see citing works
Microbes from raw milk for fermented dairy products
Wouters, J. T. M., Ayad, E. H. E., Hugenholtz, J., & Smit, G. (2002) · International Dairy Journal · doi:10.1016/s0958-6946(01)00151-0 · Cited by 561 · see citing works
Influence of Supplemental Fats on Reproductive Tissues and Performance of Lactating Cows
Staples, C. R., Burke, J. M., & Thatcher, W. W. (1998) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(98)75644-9 · Cited by 446 · see citing works
Physiology, ecology and industrial applications of aroma formation in yeast
Dzialo, M. C., Park, R., Steensels, J., Lievens, B., & Verstrepen, K. J. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux031 · Cited by 435 · see citing works
“Vicinal diketones can provide a pleasant nutty, toasty and toffeelike flavor in fermented foods and beverages, most notably beer, wine and dairy products (Molimard and Spinnler 1996; Bartowsky and Henschke 2004; Krogerus and Gibson 2013a).”
BackgroundEsters and their biosynthesis in fermented dairy products: a review
Liu, S.-Q., Holland, R., & Crow, V. L. (2004) · International Dairy Journal · doi:10.1016/j.idairyj.2004.02.010 · Cited by 421 · see citing works
Production of Aroma Compounds in Lactic Fermentations
Smid, E. J., & Kleerebezem, M. (2014) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-030713-092339 · Cited by 354 · see citing works
Role of lactic acid bacteria in flavor development in traditional Chinese fermented foods: A review
Hu, Y., Zhang, L., Wen, R., Chen, Q., & Kong, B. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1858269 · Cited by 330 · see citing works
Bacterial Role in Flavour Development
Montel, M., Masson, F., & Talòn, R. (1998) · Meat Science · doi:10.1016/s0309-1740(98)90042-0 · Cited by 326 · see citing works
Engels, W. J. M., Dekker, R., de Jong, C., Neeter, R., & Visser, S. (1997) · International Dairy Journal · doi:10.1016/s0958-6946(97)00003-4 · Cited by 266 · see citing works
The flavour of milk and dairy products: II. Cheese: contribution of volatile compounds
Urbach, G. (1997) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.1997.tb01743.x · Cited by 246 · see citing works
Molecular Gastronomy: A New Emerging Scientific Discipline
Barham, P., Skibsted, L. H., Bredie, W. L. P., Frøst, M. B., Møller, P., Risbo, J., Snitkjær, P., & Mortensen, L. M. (2010) · Chemical Reviews · doi:10.1021/cr900105w · Cited by 232 · see citing works
Frank, D. C., Owen, C. M., & Patterson, J. (2003) · LWT · doi:10.1016/s0023-6438(03)00144-0 · Cited by 218 · see citing works
van Kranenburg, R., Kleerebezem, M., Vlieg, J. V. H., Ursing, B. M., Boekhorst, J., Smit, B., Ayad, E. H. E., Smit, G., & Siezen, R. J. (2002) · International Dairy Journal · doi:10.1016/s0958-6946(01)00132-7 · Cited by 217 · see citing works
Interests in Geotrichum candidum for cheese technology
Boutrou, R., & Guéguen, M. (2005) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2004.12.028 · Cited by 218 · see citing works
Delgado, F. J., González‐Crespo, J., Cava, R., García‐Parra, J., & Ramírez, R. (2009) · Food Chemistry · doi:10.1016/j.foodchem.2009.04.081 · Cited by 199 · see citing works
Ayad, E. H. E., Verheul, A., de Jong, C., Wouters, J. T. M., & Smit, G. (1999) · International Dairy Journal · doi:10.1016/s0958-6946(99)00140-5 · Cited by 199 · see citing works
Cheese in nutrition and health
Walther, B., Schmid, A., Sieber, R., & Wehrmüller, K. (2008) · Dairy Science and Technology · doi:10.1051/dst:2008012 · Cited by 196 · see citing works
“Additionally, they differ in flavor as well as some bioactive components, which are mainly created during the different stages of ripening when the main ingredients lactose, protein and fat are broken down by fermentation, proteolysis and lipolysis [58].”
BackgroundCagno, R. D., Surico, R. F., Paradiso, A., Angelis, M. D., Salmon, J.-C., Buchin, S., Gara, L. D., & Gobbetti, M. (2008) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2008.10.017 · Cited by 191 · see citing works
“The low redox potential of TJsmight favor the reduction of aldehydes and ketones to primary and secondary alcohols (Molimard and Spinnler, 1996).”
BackgroundFilannino, P., Cardinali, G., Rizzello, C. G., Buchin, S., Angelis, M. D., Gobbetti, M., & Cagno, R. D. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.03885-13 · Cited by 179 · see citing works
“secondary alcohols (50) or, as discussed before, branched alcohols may have derived from the 393 catabolism of BCAA (Fig.”
BackgroundGroot, M. N. N., & de Bont, J. A. M. (1998) · Applied and Environmental Microbiology · doi:10.1128/aem.64.8.3009-3013.1998 · Cited by 173 · see citing works
“Benzaldehyde was found in the volatile fractions of several cheeses and may contribute to the flavor of these products (2, 19).”
BackgroundCurrent Knowledge of Soft Cheeses Flavor and Related Compounds
Sablé, S., & Cottenceau, G. (1999) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf990414f · Cited by 172 · see citing works
Venkat, H. K., Sahu, N. P., & Jain, K. K. (2004) · Aquaculture Research · doi:10.1111/j.1365-2109.2004.01045.x · Cited by 170 · see citing works
A 100-Year Review: Cheese production and quality
Johnson, M. E. (2017) · Journal of Dairy Science · doi:10.3168/jds.2017-12979 · Cited by 167 · see citing works
Influence of Lactobacillus plantarum P-8 on Fermented Milk Flavor and Storage Stability
Tong, D., Chen, H., Li, T., Tian, J., Ren, W., Zhang, H., & Sun, T. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03133 · Cited by 158 · see citing works
Formation of the aroma of a raw goat milk cheese during maturation analysed by SPME–GC–MS
Delgado, F. J., González-Crespo, J., Cava, R., & Ramírez, R. (2011) · Food Chemistry · doi:10.1016/j.foodchem.2011.05.096 · Cited by 155 · see citing works
Lactic acid fermentation: A novel approach to eliminate unpleasant aroma in pea protein isolates
Shi, Y., Singh, A., Kitts, D. D., & Singh, A. P. (2021) · LWT · doi:10.1016/j.lwt.2021.111927 · Cited by 145 · see citing works
Overview of a Surface-Ripened Cheese Community Functioning by Meta-Omics Analyses
Dugat‐Bony, É., Straub, C., Teissandier, A., Onésime, D., Loux, V., Monnet, C., Irlinger, F., Landaud, S., Leclercq-Perlat, M.-N., Bento, P., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124360 · Cited by 135 · see citing works
Lipolysis and Metabolism of Fatty Acids in Cheese
Thierry, A., Collins, Y. F., Mukdsi, M. C. A., McSweeney, P. L. H., Wilkinson, M. G., & Spinnler, H.-É. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-417012-4.00017-x · Cited by 146 · see citing works
Self-citationIzco, J. M. (2000) · Food Chemistry · doi:10.1016/s0308-8146(00)00100-x · Cited by 136 · see citing works
Hayaloğlu, A. A., Çakmakçı, S., Brechany, E. Y., Deegan, K. C., & McSweeney, P. L. H. (2007) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(07)71597-7 · Cited by 130 · see citing works
“Acetaldehyde is produced by degradation of Thr or fermentation of glucose by the action of lactic acid bacteria ( Molimard and Spinnler, 1996 ).”
BackgroundInfluentialChen, Q., Kong, B., Sun, Q., Dong, F., & Liu, Q. (2015) · Meat Science · doi:10.1016/j.meatsci.2015.07.021 · Cited by 126 · see citing works
Cagno, R. D., Banks, J., Sheehan, L., Fox, P. F., Brechany, E. Y., Corsetti, A., & Gobbetti, M. (2003) · International Dairy Journal · doi:10.1016/s0958-6946(03)00145-6 · Cited by 125 · see citing works
Tong, D., Wang, D., Wu, S., Jin, R., Ren, W., & Sun, T. (2017) · Molecules · doi:10.3390/molecules22101633 · Cited by 126 · see citing works
“3-Methylbutanol is present in relatively large quantities in dairy products and imparts an “alcoholic and floral” flavor to fermented milk [41].”
BackgroundInfluentialAndrade, M. J., Córdoba, J. J., Casado, E. M., et al. (2010) · Meat Science · doi:10.1016/j.meatsci.2010.01.009 · Cited by 121 · see citing works
Deetae, P., Bonnarme, P., Spinnler, H.-É., & Hélinck, S. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-1095-5 · Cited by 118 · see citing works
“These compounds, characterised as odour-active components in Roquefort, “Bleu des Causses” and “Bleu d’Auvergne” cheeses (Gallois and Langlois 1990), are also significant in other varieties of cheeses, such as Swiss Gruyère (Bosset and Liardon 1984) and Camembert (Dumont et al. 1976).”
BackgroundInfluentialSelf-citationProbiotic Cheese Production Using Lactobacillus casei Cells Immobilized on Fruit Pieces
Kourkoutas, Y., Bosnea, L. A., Taboukos, S., Baras, C., Lambrou, D., & Kanellaki, M. (2006) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(06)72212-3 · Cited by 117 · see citing works
“casei on pear pieces) is well known for its raw mushroom odor (Molimard and Spinnler, 1996).”
BackgroundInfluentialCollins, Y. F., McSweeney, P. L. H., & Wilkinson, M. G. (2003) · Journal of Dairy Research · doi:10.1017/s0022029902005915 · Cited by 118 · see citing works
“…cheeses has been studied in most detail and has been shown to originate from the lipolytic action of enzymes from the mould or other secondary cultures (Anderson & Day, 1966; Dartey & Kinsella, 1973; King & Clegg, 1979; Gripon, 1993; Reps, 1993; Tomasini et al. 1993; Molimard & Spinnler, 1996).”
BackgroundDiversity of l -Methionine Catabolism Pathways in Cheese-Ripening Bacteria
Bonnarme, P., Psoni, L., & Spinnler, H.-É. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.12.5514-5517.2000 · Cited by 118 · see citing works
Self-citationTanous, C., Kieronczyk, A., Hélinck, S., Chambellon, É., & Yvon, M. (2002) · Springer eBooks · doi:10.1007/978-94-017-2029-8_17 · Cited by 118 · see citing works
A study of the volatile composition of Minas cheese
Nogueira, M. C. L., Lubachevsky, G., & Rankin, S. A. (2004) · LWT · doi:10.1016/j.lwt.2004.07.019 · Cited by 114 · see citing works
Production of sulfur compounds by several yeasts of technological interest for cheese ripening
Spinnler, H.-É., Berger, C., Lapadatescu, C., & Bonnarme, P. (2001) · International Dairy Journal · doi:10.1016/s0958-6946(01)00054-1 · Cited by 113 · see citing works
Self-citationThierry, A., & Maillard, M.-B. (2002) · Le Lait · doi:10.1051/lait:2001002 · Cited by 110 · see citing works
Lessard, M.-H., Viel, C., Boyle, B., St‐Gelais, D., & Labrie, S. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-235 · Cited by 113 · see citing works
“Lipids have major roles in Camembert-type cheeses since they modulate the texture, act as the carrier for aroma compounds and are the major precursor for flavor compounds such as methylketones, lactones, esters and alcohols [2,62,82,83].”
BackgroundTanous, C., Kieronczyk, A., Hélinck, S., Chambellon, É., & Yvon, M. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020616506703 · Cited by 112 · see citing works
“The compounds derived from aromatic amino acids have a rather floral or fruity note, those derived from branched-chain amino acids have generally malty or animal note and the compounds derived from methionine have a characteristic sulphur aroma reminiscent of cabbage, cauliflower or garlic ( Molimard & Spinnler 1996;…”
BackgroundDimitrellou, D., Kandylis, P., Lević, S., Petrović, T. Ž., Ivanović, S., Nedović, V., & Kourkoutas, Y. (2019) · LWT · doi:10.1016/j.lwt.2019.108501 · Cited by 110 · see citing works
Ong, L., & Shah, N. P. (2009) · LWT · doi:10.1016/j.lwt.2009.01.011 · Cited by 108 · see citing works
Bruna, J. M., Hierro, E. M., de la Hoz, L., Mottram, D. S., Fernández, M., & Pereda, J. A. O. (2001) · Meat Science · doi:10.1016/s0309-1740(01)00058-4 · Cited by 106 · see citing works
Dahl, S., Tavaria, F. K., & Malcata, F. X. (2000) · International Dairy Journal · doi:10.1016/s0958-6946(00)00042-x · Cited by 106 · see citing works
“This observation is usually ascribed to lipolytic activity brought about by psychrotrophic bacteria and yeasts (Molimard & Spinnler, 1996).”
BackgroundAmino Acid Catabolism and Generation of Volatiles by Lactic Acid Bacteria
Tavaria, F. K., Dahl, S., Carballo, J., & Malcata, F. X. (2002) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(02)74328-2 · Cited by 104 · see citing works
“Subsequent processes encompass reduction (or oxidation) of Strecker degradation products, rearrangements, and cyclizations, as well as reactions between secondary products of FAA catabolism (Molimard and Spinnler, 1996).”
BackgroundAyad, E. H. E., Verheul, A., Engels, W. J. M., Wouters, J. T. M., & Smit, G. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01219.x · Cited by 104 · see citing works
“Despite the fact that the formation of high amounts of these aldehydes has been reported as off-¯avours in raw milk (Morgan 1976; Molimard and Spinnler 1996), these compounds are also recognized as key ¯avour compounds in a number of cheeses (Bosset and Gauch 1993; Barbieri et al. 1994; Neeter et…”
BackgroundLiu, C., Yang, P., Wang, H., et al. (2021) · LWT · doi:10.1016/j.lwt.2021.112689 · Cited by 103 · see citing works
Amárita, F., Yvon, M., Nardi, M., et al. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.12.7348-7354.2004 · Cited by 102 · see citing works
Pinho, O., Ferreira, I. M. P. L. V. O., & Ferreira, M. A. (2002) · Analytical Chemistry · doi:10.1021/ac020296m · Cited by 102 · see citing works
Production of Sulfur Flavors by Ten Strains of Geotrichum candidum
Berger, C., Khan, J. A., Molimard, P., Martin, N., & Spinnler, H.-É. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.12.5510-5514.1999 · Cited by 102 · see citing works
Self-citationWang, J., Yang, Z., Xu, L. Y., Wang, B., Zhang, J. H., Li, B., Cao, Y., & Tan, L. (2020) · Journal of Dairy Science · doi:10.3168/jds.2020-18757 · Cited by 101 · see citing works
“With the cheese ripening, the contents of short-chain fatty acids and medium long-chain fatty acids were gradually increased by the degradation of milk fat, which will increase the concentrations of esters in Cheddar cheeses during maturation as shown in Table 4 (Molimard and Spinnler, 1996).”
BackgroundTong, D., Ren, W., Yang, L., Tian, J., Chen, H., Li, T., & Liu, W. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02183 · Cited by 98 · see citing works
Monnet, C., Loux, V., Gibrat, J.-F., Spinnler, H.-É., Barbe, V., Vacherie, B., Gavory, F., Gourbeyre, E., Siguier, P., Chandler, M., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015489 · Cited by 92 · see citing works
“Volatile sulfur compounds are major flavour compounds in many types of cheeses [44].”
BackgroundSelf-citationApplication of wild starter cultures for flavour development in pilot plant cheese making
Ayad, E. H. E., Verheul, A., Wouters, J. T. M., & Smit, G. (2000) · International Dairy Journal · doi:10.1016/s0958-6946(00)00041-8 · Cited by 96 · see citing works
A study of the effects of adjunct cultures on the aroma compounds of Feta-type cheese
Bintsis, Τ., & Robinson, R. K. (2004) · Food Chemistry · doi:10.1016/j.foodchem.2004.01.057 · Cited by 97 · see citing works
Flavours and Off-Flavours in Milk and Dairy Products
Cadwallader, K. R., & Singh, T. K. (2009) · Springer eBooks · doi:10.1007/978-0-387-84865-5_14 · Cited by 104 · see citing works
Carbonell, M., Núñez, M., & Fernández-Garcı́a, E. (2002) · Le Lait · doi:10.1051/lait:2002042 · Cited by 95 · see citing works
“Several review articles summarise the present knowledge on volatile formation and significance [10, 18, 29, 33, 38, 41, 42], and on the analytical techniques used for their study [12, 27, 37].”
BackgroundMethodInfluentialAddition of buttermilk improves the flavor and volatile compound profiles of low-fat yogurt
Zhao, L., Feng, R., Ren, F., et al. (2018) · LWT · doi:10.1016/j.lwt.2018.08.029 · Cited by 94 · see citing works
Bontinis, T. G., Mallatou, H., Pappa, E. C., et al. (2012) · Small Ruminant Research · doi:10.1016/j.smallrumres.2012.01.003 · Cited by 94 · see citing works
Kaminarides, S. E., Stamou, P., & Massouras, T. (2005) · Food Chemistry · doi:10.1016/j.foodchem.2005.09.039 · Cited by 93 · see citing works
Instrumental analysis of volatile (flavour) compounds in milk and dairy products
Mariaca, R. G., & Bosset, J. O. (1997) · Le Lait · doi:10.1051/lait:199712 · Cited by 93 · see citing works
Pecorino Crotonese cheese: Study of bacterial population and flavour compounds
Randazzo, C. L., Pitino, I., Ribbera, A., & Caggia, C. (2009) · Food Microbiology · doi:10.1016/j.fm.2009.11.010 · Cited by 91 · see citing works
Bruna, J. M., Hierro, E. M., de la Hoz, L., Mottram, D. S., Fernández, M., & Pereda, J. A. O. (2002) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(02)00505-6 · Cited by 91 · see citing works
Aroma Compound Production in Cheese Curd by Coculturing with Selected Yeast and Bacteria
Martin, N., Berger, C., Du, C. L., & Spinnler, H.-É. (2001) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(01)74657-7 · Cited by 91 · see citing works
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Pasquale, I. D., Cagno, R. D., Buchin, S., Angelis, M. D., & Gobbetti, M. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.02097-14 · Cited by 89 · see citing works
Aroma characterisation of Gouda-type cheeses
Leuven, I. V., Caelenberg, T. V., & Dirinck, P. (2008) · International Dairy Journal · doi:10.1016/j.idairyj.2008.01.001 · Cited by 89 · see citing works
“Ethyl esters, originated from the enzymatic or chemical esterification of fatty acids with ethanol, possess pleasant sweet and fruity notes (Bosset & Liardon, 1984; Fernández-Garcı́a, Mariaca, & Nuñez, 1998; Moio & Addeo, 1998; Molimard & Spinnler, 1996).”
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Andrés, A. I., Cava, R., & Ruiz, J. (2002) · Journal of Chromatography A · doi:10.1016/s0021-9673(02)00139-5 · Cited by 86 · see citing works
Ortigosa, M., Torre, P., & Izco, J. M. (2001) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(01)70161-0 · Cited by 84 · see citing works
“The methylketones are afterwards reduced to their corresponding secondary alcohols by bacterial reductases as a defense mechanism of the micro-organisms against toxicity (Molimard and Spinnler, 1996).”
BackgroundHannon, J. A., Kilcawley, K. N., Wilkinson, M. G., Delahunty, C. M., & Beresford, T. P. (2006) · International Dairy Journal · doi:10.1016/j.idairyj.2006.03.001 · Cited by 84 · see citing works
Evaluation of fat‐derived aroma compounds in blue cheese by dynamic headspace GC/Olfactometry‐MS
Qian, M. C., Nelson, C., & Bloomer, S. (2002) · Journal of the American Oil Chemists Society · doi:10.1007/s11746-002-0540-4 · Cited by 84 · see citing works
“In Camembert cheese, which is also moldripened, methyl ketones are the most abundant aroma compounds, with concentrations on the order of 25 to 60 µmol/100 g of fat ( 14 ).”
BackgroundProteolytic, lipolytic and molecular characterisation of Yarrowia lipolytica isolated from cheese
Suzzi, G., Lanorte, M. T., Galgano, F., Andrighetto, C., Lombardi, A., Lanciotti, R., & Guerzoni, M. E. (2001) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(01)00574-8 · Cited by 84 · see citing works
Randazzo, C. L., Pitino, I., Luca, S. D., Scifò, G. O., & Caggia, C. (2007) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2007.12.005 · Cited by 80 · see citing works
Ziino, M., Condurso, C., Romeo, V., Giuffrida, D., & Verzera, A. (2005) · International Dairy Journal · doi:10.1016/j.idairyj.2004.07.024 · Cited by 80 · see citing works
The effect of microbial lipase on the lipolysis during the ripening of Tulum cheese
Yilmaz, G., Ayar, A., & Akın, N. (2004) · Journal of Food Engineering · doi:10.1016/j.jfoodeng.2004.08.017 · Cited by 78 · see citing works
Dissecting Yogurt: the Impact of Milk Types, Probiotics, and Selected Additives on Yogurt Quality
Farag, M. A., Saleh, H. A., Ahmady, S. E., & Elmassry, M. M. (2021) · Food Reviews International · doi:10.1080/87559129.2021.1877301 · Cited by 79 · see citing works
Secondary and Adjunct Cultures
Irlinger, F., Hélinck, S., & Jany, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-417012-4.00011-9 · Cited by 83 · see citing works
A framework for identifying characteristic odor compounds in municipal wastewater effluent
Agus, E., Zhang, L., & Sedlak, D. L. (2012) · Water Research · doi:10.1016/j.watres.2012.08.018 · Cited by 76 · see citing works
Changes in salted yoghurt during storage
Güler, Z. (2007) · International Journal of Food Science & Technology · doi:10.1111/j.1365-2621.2006.01505.x · Cited by 76 · see citing works
Coda, R., Brechany, E. Y., Angelis, M. D., de Candia, S., Cagno, R. D., & Gobbetti, M. (2006) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(06)72458-4 · Cited by 71 · see citing works
“Overall, the strong reducing conditions in cheese may favor the rapid reduction of aldehydes and ketones to primary and secondary alcohols ( Molimard and Spinnler, 1996 ).”
BackgroundLawlor, J., Delahunty, C. M., Sheehan, J. J., & Wilkinson, M. G. (2003) · International Dairy Journal · doi:10.1016/s0958-6946(03)00048-7 · Cited by 75 · see citing works
Nonstarter lactic acid bacteria volatilomes produced using cheese components
Sgarbi, E., Lazzi, C., Tabanelli, G., Gatti, M., Neviani, E., & Gardini, F. (2013) · Journal of Dairy Science · doi:10.3168/jds.2012-6472 · Cited by 77 · see citing works
Chen, C., Liu, Z., Yu, H., Xu, Z., & Tian, H. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.130736 · Cited by 75 · see citing works
Rapid Phenotypic and Metabolomic Domestication of Wild Penicillium Molds on Cheese
Bodinaku, I., Shaffer, J., Connors, A. B., Steenwyk, J. L., Biango‐Daniels, M. N., Kastman, E. K., Rokas, A., Robbat, A., & Wolfe, B. E. (2019) · mBio · doi:10.1128/mbio.02445-19 · Cited by 73 · see citing works
- Authors
- Molimard, P., & Spinnler, H. E.
- Affiliations
- Institut National de la Recherche Agronomique (FR)
- Venue
- Journal of Dairy Science
- Publisher
- American Dairy Science Association
- Published
- 1996-02
- Volume
- 79
- Issue
- 2
- Pages
- 169-184
- ISSN
- 0022-0302 (ISSN-L)
- OpenAlex
- W2001267052
- Cited by
- 611
- References
- 126
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 17 · 2023: 20 · 2022: 19 · 2021: 26 · 2020: 32 · 2019: 19 · 2018: 26 · 2017: 30 · 2016: 17 · 2015: 26 · 2014: 26 · 2013: 27 · 2012: 21
- FWCI
- 17.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Dairy Science (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Fermentation and Sensory Analysis
- Life Sciences › Agricultural and Biological Sciences › Food Science › Food Chemistry and Fat Analysis
- Life Sciences › Agricultural and Biological Sciences › Food Science › Sensory Analysis and Statistical Methods
- Keywords
- cheese flavor, volatile flavor compounds, lipid hydrolysis, free fatty acids, proteolysis, amino acids, cheese ripening
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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