Fucoidans from brown seaweeds: an update on structures, extraction techniques and use of enzymes as tools for structural elucidation
Open accessAbstract
Fucoidan or fucoidans cover a family of sulfated fucose-rich polysaccharides, built of a backbone of L-fucose units, and characteristically found in brown seaweeds. Fucoidans have potential therapeutic properties, including anti-inflammatory and anti-coagulant activities, as well as anti-proliferative effects on cancer cells. Recent work has revealed distinct structural features of fucoidans obtained from different brown seaweed sources. Fucoidans are classically obtained from brown seaweeds by multi-step, hot acid extraction, but the structural and compositional traits, and possibly the bioactivity, of the fucoidan polysaccharides are significantly influenced by the extraction parameters. This review discusses the structural features of fucoidans, the significance of different extraction technologies, and reviews enzymatic degradation of fucoidans and the use of fucoidan-modifying enzymes for elucidating structural details of fucoidans. Mild extraction techniques coupled with the use of new tools such as enzymes can provide the much needed knowledge about structural characteristics of different fucoidan molecules and thus pave the way for a better understanding of the structural chemistry and bioactivities of fucoidans.
AI snapshot
Written from the paper’s full text.
TL;DR
This review synthesizes the structural diversity of fucoidans (fucose-containing sulfated polysaccharides, FCSPs) from brown seaweeds, arguing that extraction conditions strongly shape yield and composition and that no consistent "fucoidan" backbone exists. It also reviews fucoidan-modifying enzymes (fucoidanases, fucosidases) as tools for structural elucidation and discusses bioactivity and commercial prospects.
Key findings
- Fucoidan structures vary by species and cannot be predicted by algal order; the prevalent core backbones are (1→3)-linked α-L-fucopyranose and alternating (1→3)/(1→4)-linked α-L-fucopyranosyls, with variable sulfate, acetate, and branch substitutions (Table 1).
- Extraction parameters significantly affect yield and composition: in the authors' own single-step study on *Sargassum henslowianum*, temperature and time had positive effects and acid concentration a negative effect, with a maximal fucoidan yield of ~7% at 0.03 M HCl, 90 °C, 4 h; 0.2 M HCl broke polysaccharide integrity, lowering fucose at elevated time/temperature.
- Historical extraction data: a single acid hydrolysis recovered ~50% (w/w) of theoretical maximum fucoidan, while three rounds recovered >80% of fucose; the triple-step protocol (0.1 M HCl, pH 2.0–2.5, 70 °C, 1 h ×3) gave crude fucoidans with 30–36% fucose, and *F. vesiculosus* product contained 44% fucose, 26% total sulfate, and 31% ash. Yields as % fucose of total seaweed fucose were *Pelvetia canaliculata* 76%, *F. vesiculosus* 62%, *Ascophyllum nodosum* 54%, *L. cloustoni* 20%.
- Fucoidanases show specificity: an endo-1,3-α-fucoidanase from *Fucanobacter lyticus* degraded Laminariales fucoidans but not Fucales or Chordariales; enzymatic treatment of *Fucus distichus* fucoidan confirmed repeating disaccharide units [→3)-α-L-Fucp-(2,4-di-SO₃²⁻)-(1→4)-α-L-Fucp-(2-SO₃²⁻)-(1→].
Methods
- Narrative review covering fucoidan structural chemistry, extraction technology history (1913–1950s onward), extraction-parameter effects, and fucoidan-modifying enzymes.
- Includes the authors' own single-step extraction experiment using *Sargassum henslowianum* as a model brown seaweed, with HPAEC-PAD analysis of TFA hydrolysates; extraction parameters tested were acid concentration, time, and temperature.
- Enzyme data are compiled from published studies (Table 4) and classified by cleavage pattern: type 1 (1→4)-α-L-fucoidan endohydrolase, type 2 (1→3)-α-L-fucoidan endohydrolase, and type 3 exo-acting α-L-fucosidase.
Limitations
- Stated: no standardized purification procedure exists for fucoidans; the use of many different extraction techniques has exacerbated structural elucidation; the exact structural elements responsible for bioactivity remain unidentified; no pharmaceutical, dermatological, or nutraceutical applications have been officially approved.
- Stated: heterogeneity within the same seaweed species can lead to pronounced differences in extracted products.
- Evident from the text: as a narrative review it does not describe a systematic literature search or inclusion criteria, and the extraction-parameter findings derive largely from a single model species (*S. henslowianum*), limiting generalizability.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 73 cited sources checked · 0 supported · 0 flagged
- Findingreasoning§ 3.1 Influence of extraction parameters on fucoidan yield and composition
Structural integrity of the polysaccharide was best conserved at low acid treatment.
“Structural integrity of the polysaccharide was best conserved at low acid treatment.”
Quote in the paperSubstantial claim - Findingown data§ 3.1 Influence of extraction parameters on fucoidan yield and composition
A maximal fucoidan yield of about 7% was achieved by the optimal extraction procedure of 0.03 M HCl, 90°C, 4 h.
“A maximal fucoidan yield of y7% was achieved by the optimal extraction procedure of: 0.03 M HCl, 90 uC, 4 h.”
Quote in the paperNot a substantial claim - Findingcitation§ 3.1 Influence of extraction parameters on fucoidan yield and composition
HPAEC-PAD analysis of the TFA hydrolysate of S. henslowianum confirmed that fucose, galactose, and glucuronic acid were the major constituents of the extracted polysaccharides obtained by the optimized method.
“The HPAEC-PAD analysis of the TFA hydrolysate of S. henslowianum confirmed that fucose, galactose, and glucuronic acid were the major constituents of the extracted polysaccharides obtained by the optimized method.3”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] source
Not checked in the free run.
- Findingcitation§ 3.1 Influence of extraction parameters on fucoidan yield and composition
Use of 0.2 M HCl broke the integrity of the polysaccharide molecules, resulting in a decline of fucose at elevated time and temperature.
“The use of 0.2 M HCl apparently broke the integrity of the polysaccharide molecules resulting in a decline of fucose at elevated time and temperature.3”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
Not checked in the free run.
- Interpretationcitation§ Abstract
The structural and compositional traits, and possibly the bioactivity, of fucoidan polysaccharides are significantly influenced by extraction parameters.
“the structural and compositional traits, and possibly the bioactivity, of the fucoidan polysaccharides are significantly influenced by the extraction parameters.”
- Also stated in: § 3.1 Influence of extraction parameters on fucoidan yield and composition · boosted
“The data demonstrate the vulnerability of fucoidan structures to harsh extraction conditions and confirm that the extraction method significantly influences the yields and not least the composition of the extracted polysaccharides.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
Not checked in the free run.
- Also stated in: § 3.1 Influence of extraction parameters on fucoidan yield and composition · boosted
- Premisecitation§ 2 Structures and chemical nature of fucoidans
Several fucoidan structures reported in the literature have contained small amounts of various other monosaccharides, e.g. glucose, galactose, xylose, and/or mannose.
“Several of the fucoidan structures reported in the literature have also contained small amounts of various other monosaccharides e.g.glucose, galactose, xylose, and/or mannose. 1”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1] source
Not checked in the free run.
- Interpretationreasoning§ 3.1 Influence of extraction parameters on fucoidan yield and composition
Differences caused by differences in extraction methodologies may have major bearings on the results when fucoidan polysaccharide products are evaluated for biological activity.
“The differences caused by differences in extraction methodologies obviously may have major bearings on the results when the fucoidan polysaccharide products are being evaluated for biological activity.”
Quote in the paperSubstantial claim - Premisecitation§ 4.1 Fucoidan modifying enzymes
The main fucoidan structural unit from Fucus spp. consists of repeating di-saccharide units of [A3)-a-L-Fucp-(2,4di-SO3^2)-(1A4)-a-L-Fucp-(2SO3^2)-(1A].
“Likewise, the enzymatic treatment confirmed that the main fucoidan structural unit from this brown seaweed Fucus spp.consists of repeating di-saccharide units of [A3)-a-L-Fucp-(2,4di-SO 3 2 )-(1A4)-a-L-Fucp-(2SO 3 2 )-(1A].35”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [35] source
Not checked in the free run.
- Interpretationreasoning§ 2 Structures and chemical nature of fucoidans
Variations in reported structural properties of fucoidans from different brown seaweed species confirm the natural biodiversity of fucoidans across taxonomical orders, notably Fucales, Laminariales and Chordariales.
“The variations in the reported structural properties of fucoidans from different brown seaweed species clearly confirm the natural biodiversity of fucoidans as exemplified by the structures found in different seaweed taxonomical orders, notably Fucales, Laminariales and Chordariales (Table 1).”
Quote in the paperNot a substantial claim - Premisecitation§ 1 Introduction
The bioactivities of fucoidans are related to their structural make-up, monosaccharide composition, sulfate content, position of sulfate ester groups, and molecular weight.
“The bioactivities of fucoidans are related to their structural make-up, monosaccharide composition, sulfate content, position of sulfate ester groups, and molecular weight.2”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [2] source
Not checked in the free run.
- Rests on an assumption: Fucoidan polysaccharides have potential therapeutic properties, including anti-inflammatory, anti-coagulant, and anti-proliferative effects on cancer cells.
- Premisecitation§ 4.1 Fucoidan modifying enzymes
α-L-fucosidase only catalyses cleavage of α-L-fucosyl linkages at the nonreducing termini, releasing fucose from the fucose-backbone structure in fucoidans.
“a-L-fucosidase only catalyses the cleavage the a-L-fucosyl linkages at the nonreducing termini, releasing fucose from the fucose-backbone structure in fucoidans (Enzyme type 3, Fig. 1).”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation§ 4.1 Fucoidan modifying enzymes
Only various crude, commercial enzyme mixtures designed for plant material processing have been used as hydrolysis aids for extraction of brown seaweed biofunctional polysaccharide fractions, compared with the advanced stage of designed enzyme mixtures for complex plant materials or heterogeneous plant cell wall polysaccharides.
“However, as compared to the quite advanced stage of development of designed enzyme mixtures for hydrolysis of complex plant materials or heterogenous plant cell wall polysaccharides, 39,40 only various crude, commercial enzyme mixtures, designed for plant material processing, have been used as hydrolysis aids for extraction of brown seaweed biofunctional polysaccharide fractions.5,41”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationreasoning§ 2 Structures and chemical nature of fucoidans
Published structural data for algal fucoidans confirm that there is no consistent basic structure of fucoidan.
“Hence, the published structural data for algal fucoidans confirm that there is no consistent basic structure of ''fucoidan''.”
Quote in the paperSubstantial claim - Premisecitation§ 2 Structures and chemical nature of fucoidans
Sulfated pseudo-fucoidan polysaccharides extracted from Sargassum stenophyllum are built mainly of β(1→6)-D-galactose and/or β(1→2)-D-mannose units in the backbone with branching points formed by α(1→3) and/or α(1→4)-L-fucose, α(1→4)-D-glucuronic acid, terminal β-D-xylose, and sometimes α(1→4)-D-glucose.
“In contrast, the sulfated ''pseudo''-fucoidan polysaccharides extracted from some other species in the order Fucales, such as e.g.Sargassum stenophyllum, are built mainly of b(1A6)-D-galactose and/or b(1A2)-D-mannose units in the polysaccharide backbone with branching points formed by a(1A3) and/or a(1A4)-L-fucose, a(1A4)-D-glucuronic acid, terminal b-D-xylose, and sometimes a(1A4)-D-glucose.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [11] source
Not checked in the free run.
- Premisecitation§ 1 Introduction
Distinct fucoidan structures can be isolated by different extraction conditions.
“Distinct structures can be isolated by different extraction conditions.2,5”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation§ 4.1 Fucoidan modifying enzymes
Native fucoidan polysaccharides from Fucus distichus contain blocks of acetylated and partially sulfated repeating units.
“A study of the fucosidase action on fucoidan polysaccharides from Fucus distichus has thus established that the native fucoidan polysaccharides contain blocks of acetylated and partially sulfated repeating units.35”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [35] source
Not checked in the free run.
- Premisecitation§ 4.1 Fucoidan modifying enzymes
Enzyme-assisted extraction of fucoidan polysaccharides has recently been proposed, using enzymes that do not catalyze the hydrolysis of the target fucoidan polysaccharides.
“Enzyme-assisted extraction of fucoidan polysaccharides has recently been proposed, 5 using enzymes that do not catalyze the hydrolysis of the target fucoidan polysaccharides.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [5] source
Not checked in the free run.
- Premisecitation§ 2 Structures and chemical nature of fucoidans
Glucuronic acid has been detected and found to be an integral part of non-sulfated fucooligosaccharides in F. evanescens.
“Glucuronic acid (GlcA) has also been detected and found to be an integral part of the non-sulfated fucooligosaccharides: Fuc-(1A3)-GlcA, Fuc-(1A4)-Fuc-(1A3)-GlcA, Fuc-(1A3)-Fuc-(1A3)-GlcA respectively.13”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [13] source
Not checked in the free run.
- Premisecitation§ 1 Introduction
Classical extraction of fucoidans from brown seaweeds involves multi-step extended aqueous extractions, usually with hot acid (hydrochloric acid).
“Classical extraction of fucoidans from brown seaweeds involves multi-step extended aqueous extractions, usually with hot acid (hydrochloric acid), 3”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
Not checked in the free run.
- Premisecitation§ 2 Structures and chemical nature of fucoidans
The initial suggestion that fucoidan obtained from F. vesiculosus was built of α(1→2)-linked L-fucopyranosyl has been revised.
“Therefore the initial suggestion that fucoidan obtained from F. vesiculosus (Fucales) was built of a(1A2) linked L-fucopyranosyl has been revised.16”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [16] source
Not checked in the free run.
- Interpretationcitation§ Laminaria religiosa
Based on analysis of extraction methods employed in different studies, the use of different acids or no acid and differences in extraction time and temperature during extraction and purification have generated very diverse compositional results and structural suggestions for fucoidan polysaccharides.
“Based on an analysis of the extraction methods employed in different studies, it has become clear that the use of different acids-or no acid at all-and differences in extraction time and temperature during the extraction and purification treatments of fucoidans, have generated very diverse compositional results and structural suggestions for fucoidan polysaccharides 1 (Tables 2 and 3).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] source
Not checked in the free run.
- Interpretationreasoning§ 1 Introduction
The problem of elucidating the structural details of fucoidans has been exacerbated by the use of many different extraction techniques.
“The problem of elucidating the structural details of fucoidans has been exacerbated by the use of many different extraction techniques.”
Quote in the paperSubstantial claim - Interpretationreasoning§ 3.1 Influence of extraction parameters on fucoidan yield and composition
Higher acid levels might have caused a loosening of the cell wall matrix, allowing local penetration of the acid into the fucoidan.
“This indicated that the higher acid levels might have caused a loosening of the cell wall matrix allowing local penetration of the acid into the fucoidan.”
Quote in the paperNot a substantial claim - Premisecitation§ 2 Structures and chemical nature of fucoidans
More detailed analysis of F. evanescens by MALDI-TOF and tandem ESI mass spectrometry revealed minor components such as mixed mono-sulfated fucooligosaccharides containing both 2-O- and 4-O-sulfated (1→4)-bonded xylose and galactose residues.
“More detailed analysis of F. evanescens by MALDI-TOF and tandem ESI mass spectrometry has also revealed the presence of minor components such as mixed mono-sulfated fucooligosaccharides containing both 2-O-and 4-O-sulfated (1A4) bonded xylose and galactose residues: Xyl-(1A4)-Fuc, Gal-(1A4)-Fuc, Gal-(1A4)-Gal-(1A4)-Fuc, Gal-(1A4)-Gal.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [13] source
Not checked in the free run.
- Interpretationreasoning§ 5.1 Fucoidan bioactivity and potential applications
Stimulation with IL-2 and IL-12 may promote secretion of IFN-γ by NK cells, probably via enhanced NK cell activity by fucoidan.
“Hence, stimulation with IL-2 and IL-12 may promote the secretion of IFN-c by NK cells, probably via enhanced NK cell activity by fucoidan.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [50] source
Not checked in the free run.
- Interpretationnone given§ 5.1 Fucoidan bioactivity and potential applications
As a pharmaceutical or nutraceutical ingredient, fucoidans offer distinctive possibilities for immuno-modulation and anti-cancer effects.
“As a pharmaceutical or nutraceutical ingredient, fucoidans clearly offer distinctive possibilities for immuno-modulation and anti-cancer effects.”
Quote in the paperNot a substantial claim - Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Bacteria of the genera Cytophaga and Alteromonas/Pseudoalteromonas exhibited the highest fucoidanase activities.
“Bacteria of the genera Cytophaga and Alteromonas/Pseudoalteromonas exhibited the highest fucoidanase activities.36”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [36] source
Not checked in the free run.
- Premisenone given§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
The L-fucopyranose backbone of fucoidan extracted from A. nodosum and F. vesiculosus is connected by alternating α(1→3) and α(1→4) linkages with sulfate substituted at the 2- and 3-position of the fucose residues.
“The L-fucopyranose backbone of the fucoidan extracted from A. nodosum and F. vesiculosus is connected by alternating a(1A3) and a(1A4) linkages with sulfate substituted at the 2-and 3-position of the fucose residues”
Quote in the paperNot a substantial claim - Premisecitation§ 4.1 Fucoidan modifying enzymes
Another type of fucoidanase catalyses glycosidic bonds (both α(1→3)- and α(1→4)-bonds) in the fucose-backbone via random endo-type hydrolysis.
“the other type of fucoidanase catalyses the glycosidic bonds (both a(1A3)-, a(1A4)-bonds) in the fucose-back bone via random endo-type hydrolysis”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Direct anti-proliferative effects of fucoidan polysaccharides against certain cancer cells have been shown in vitro using cell viability analysis.
“The direct anti-proliferative effects of fucoidan polysaccharides against certain cancer cells have been shown in vitro using cell viability analysis.”
Quote in the paperSubstantial claim - Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Fucoidan structures of brown seaweeds from the orders Fucales and Chordariales differ from those of Laminariales.
“Fucoidan structures of brown seaweeds from the orders Fucales and Chordariales are known to differ from those of Laminariales. 1”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [1] source
Not checked in the free run.
- Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Enzymes able to catalyse modification of fucoidans from brown seaweeds may have a broad spectrum of biological roles and potential applications.
“From the information available about enzymes able to catalyse modification of fucoidans from brown seaweeds, it appears that these enzymes may have a broad spectrum of biological roles and potential applications.”
Quote in the paperSubstantial claim - Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Histochemical staining showed morphological changes of melanoma cells after exposure to fucoidans indicative of crude fucoidan induced apoptosis.
“Histochemical staining showed morphological changes of melanoma cells after exposure to the fucoidans and were indicative of crude fucoidan induced apoptosis.45”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] source
Not checked in the free run.
- Premisecitation§ 4.1 Fucoidan modifying enzymes
One type of fucoidanase catalyses cleavage of small, low molecular weight oligosaccharides from the end of fucoidan backbone chains.
“one type of fucoidanase catalyses the cleavage of small, low molecular weight oligosaccharides from the end of the fucoidan backbone chains”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Fucoidans protect the elastic fiber network in human skin culture.
“protect the elastic fiber network in human skin culture; 53”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [53]
Not checked in the free run.
- Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Fucoidan polysaccharides have potential beneficial bioactive functions, including anti-proliferative effects on certain types of cancer cells.
“Fucoidan polysaccharides have been reported to have potential beneficial bioactive functions, including anti-proliferative effects on certain types of cancer cells.45”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] source
Not checked in the free run.
- Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Both FCSPs from Sargassum sp. and fucoidan polysaccharides from Fucus vesiculosus significantly decreased the viable number of lung carcinoma and melanoma cells in vitro in a dose-response fashion.
“Both FCSPs from Sargassum sp. and more classic fucoidan polysaccahrides from Fucus vesiculosus significantly decreased the viable number of lung carcinoma and melanoma cells in vitro in a doseresponse fashion.45”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] source
Not checked in the free run.
- Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
A consistent extraction process is a prerequisite for elucidating the structure-function relationship that promotes these biological properties.
“A consistent extraction process is also a prerequisite for elucidating the structurefunction relationship that promotes these biological properties.”
Quote in the paperSubstantial claim - Premisenone given§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Fucoidan of Chorda filum and Laminaria saccharina consists of a poly-α-(1→3)-fucopyranoside backbone with sulfate mainly at C-4 and sometimes at the C-2 position.
“while fucoidan of Chorda filum and Laminaria saccharina consist of a poly-a-(1A3)-fucopyranoside backbone with sulfate mainly at C-4 and sometimes at the C-2 position (Table 1).”
Quote in the paperNot a substantial claim - Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
Fucoidanase from marine bacterium Fucanobacter lyticus exhibits extracellular endo-fucoidanase degrading activity on fucoidan polysaccharides from brown seaweed in the order Laminariales but not Fucales and Chordariales, indicating specificity of an endo-1,3-α-fucoidanase.
“Fucoidanase from the marine bacterium Fucanobacter lyticus has shown to exhibit extracellular endo-fucoidanase degrading activity on fucoidan polysaccharides obtained from brown seaweed in the order of Laminariales but not Fucales and Chordariales indicating specificity of an endo-1,3-a-fucoidanase. 44”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [44] source
Not checked in the free run.
- Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Fucoidans have potential for inclusion in lotion as a natural whitening agent.
“and to have potential for inclusion in lotion as a natural whitening agent.54”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [54]
Not checked in the free run.
- Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Anti-cancer activity of fucoidans is not a function of a single specific structural trait but a combination of many factors such as amount of sulfate groups, monosaccharide composition, and types of linkages of sugar residues.
“Nevertheless, it appears that the anti-cancer activity of fucoidans is not a function of a single specific structural trait but a combination of many factors such as the amount of sulfate groups, the monosaccharide composition, and the types of linkages of the sugar residues.1,30”
Quote in the paperNot a substantial claim0 of 2 sources checked - Premisecitation§ 4.1 Fucoidan modifying enzymes
Fucoidanase activities were first detected in several different marine microorganisms, including marine bacteria such as Vibrio sp., Alteromonas sp., Pseudoalteromonas sp., and bacteria of the family Flavobacteriaceae.
“Fucoidanase activities were first detected in several different marine microorganisms, including marine bacteria such as Vibrio sp., Alteromonas sp., Pseudoalteromonas sp., and bacteria of the family Flavobacteriaceae.32,36,37,43”
Quote in the paperNot a substantial claim0 of 4 sources checked - Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
No pharmaceutical, dermatological, nutraceutical or other applications have as yet been officially approved for fucoidan polysaccharides or their lower molar mass oligosaccharide derivatives.
“As a consequence, no pharmaceutical, dermatological, nutraceutical or other applications have as yet been officially approved for these polysaccharides or their lower molar mass oligosaccharide derivatives.”
Quote in the paperNot a substantial claim - Premisenone given§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
The exact structural element(s) in fucoidan molecules responsible for these potentially protective activities are still unidentified.
“However, the exact structural element(s) in the fucoidan molecules being responsible for these potentially protective activities are still unidentified.”
Quote in the paperSubstantial claim - Premisecitation§ 5.1 Fucoidan bioactivity and potential applications
Antitumor activity of fucoidan may be a result of an indirect effect associated with enhancement of cytolytic activity of NK cells augmented by increased production of macrophage-mediated immune response signaling molecules IL-2, IFN-γ and IL-12.
“Some findings indicate that the antitumor activity of fucoidan is a result of an indirect effect which may be associated with a significant enhancement of the cytolytic activity of natural killer (NK) cells augmented by increased production of macrophage-mediated immune response signaling molecules, 50,51 namely interleukins (IL)-2, IFN-c and IL-12.50”
Quote in the paperNot a substantial claim0 of 2 sources checked - Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single units
The extraction process employed for fucoidans is crucially important for maintaining structural integrity and relevant structural features required for specific biological activity.
“Thus the extraction process employed for the fucoidans is crucially important for maintaining the structural integrity and the relevant structural features required for specific biological activity.”
Quote in the paperSubstantial claim - Premisenone given§ 6 Conclusions and outlook
Acid treatment used as the major step/steps in extraction of fucoidans causes degradation and affects integrity of overall fucoidan makeup.
“It is also clear that acid treatment used as the major step/steps in the extraction of fucoidans causes degradation and affects the integrity of overall fucoidan makeup.”
Quote in the paperSubstantial claim - Premisenone given§ 6 Conclusions and outlook
Extraction treatment employed affects composition and thus structural features of fucoidan substances.
“It has been convincingly shown that the extraction treatment employed affects the composition and thus the structural features of the fucoidan substances.”
Quote in the paperSubstantial claim - Interpretationreasoning§ 6 Conclusions and outlook
Preservation of structural integrity of fucoidan molecules appears crucial for maintaining their biological properties.
“Preservation of the structural integrity of the fucoidan molecules appears crucial for maintaining their biological properties.”
Quote in the paperSubstantial claim - Interpretationreasoning§ 6 Conclusions and outlook
Extraction methodology employed may significantly affect results obtained when fucoidan products are evaluated for biological activity.
“The extraction methodology employed may thus significantly affect the results obtained when the fucoidan products are being evaluated for biological activity.”
Quote in the paperSubstantial claim
- May combine two claims. 33
- Classified as probably not a substantial claim. 14
May combine two claims.
Findingown data§ 3.1 Influence of extraction parameters on fucoidan yield and compositionAll extraction parameters had significant effects on the fucose-containing sulfated polysaccharide yield, with temperature and time exerting positive effects and acid concentration having a negative effect.
“All extraction parameters had significant effects on the yields, i.e. the fucose-containing sulfated polysaccharide yield, with the temperature and time exerting positive effects, and the acid concentration having a negative effect.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data§ 3.1 Influence of extraction parameters on fucoidan yield and compositionLower polysaccharide yield but relatively higher fucose content was obtained with shorter extraction time.
“Lower polysaccharide yield, but relatively higher fucose content was obtained with shorter extraction time.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Premisecitation§ AbstractFucoidans are a family of sulfated fucose-rich polysaccharides built of a backbone of L-fucose units and characteristically found in brown seaweeds.
“Fucoidan or fucoidans cover a family of sulfated fucose-rich polysaccharides, built of a backbone of Lfucose units, and characteristically found in brown seaweeds.”
- Also stated in: § 1 Introduction · plain
“Fucoidans in fact designate a group of fucose-rich, sulfated polysaccharides, usually built of a backbone of a-linked L- fucose residues having various substitutions.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] source
Not checked in the free run.
- Also stated in: § 1 Introduction · plain
May combine two claims.
Premisenone given§ 4.1 Fucoidan modifying enzymesEnzymes catalyzing modifications of fucoidan polysaccharides, i.e. fucoidanases, include Fucoidanases EC 3.2.1.44, which catalyze endo-hydrolysis of (1→2)-α-L-fucoside linkages in fucoidans without release of sulfate, and α-L-Fucosidases EC 3.2.1.51, which catalyze hydrolytic release of L-fucose via cleavage of α(1→3)-, α(1→4)- and possibly also α(1→2)-O-fucosyl bonds in fucoidan oligosaccharides.
“Enzymes catalyzing modifications of fucoidan polysaccharides, i.e. ''fucoidanases'', include: i) Fucoidanases, EC 3.2.1.44,which catalyze the endo-hydrolysis of (1A2)-a-L-fucoside linkages in fucoidans without release of sulfate, and ii) a-L-Fucosidases, EC 3.2.1.51which catalyze the hydrolytic release of L-fucose, via cleavage of a(1A3)-, a(1A4)and possibly also of a(1A2)-O-fucosyl bonds in fuc”
Quote in the paperNot a substantial claimMay combine two claims.
Premisecitation§ 3.1 Influence of extraction parameters on fucoidan yield and compositionLonger extraction time at higher temperatures led to higher polysaccharide yield with lower amounts of sulfate and a higher proportion of glucuronic acid.
“It has also been shown by others that longer extraction time at higher temperatures led to higher polysaccharide yield with lower amounts of sulfate and a higher proportion of glucuronic acid.11,17”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Interpretationown data§ 3.1 Influence of extraction parameters on fucoidan yield and compositionThe data demonstrate the vulnerability of fucoidan structures to harsh extraction conditions and confirm that the extraction method significantly influences the yields and composition of the extracted polysaccharides.
“The data demonstrate the vulnerability of fucoidan structures to harsh extraction conditions and confirm that the extraction method significantly influences the yields and not least the composition of the extracted polysaccharides.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Premisenone given§ 1 IntroductionFucoidan polysaccharides are mainly found in brown seaweeds, but fucoidans differ in structure among brown seaweed species.
“Fucoidan polysaccharides are mainly found in brown seaweeds, but fucoidans differ in structure among brown seaweed species.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone given§ 2 Structures and chemical nature of fucoidansFucoidans isolated from L. saccharina are mainly composed of α(1→3)-linked L-fucopyranose units, with sulfate at both C-2 and C-4, or at C-4 alone.
“Fucoidans isolated from L. saccharina (Laminariales) are thus mainly composed of a(1A3)-linked L- fucopyranose units, but with sulfate at both C-2 and C-4, or at C-4 alone, however (Table 1).”
Quote in the paperNot a substantial claimMay combine two claims.
Premisenone given§ 2 Structures and chemical nature of fucoidansFucoidans isolated from Ascophyllum nodosum have a backbone consisting of a repeating structure of α(1→3)-linked L-fucopyranose residues with sulfate at C-2, with α(1→3)-linked L-fucopyranose residues linked to α(1→4)-L-fucopyranose residues with disulfate at C-2 and C-3.
“These fucoidan molecules have a backbone consisting of a repeating structure of a(1A3)-linked L-fucopyranose residues with sulfate at the C-2 position, with the a(1A3)-linked L- fucopyranose residues linked to a(1A4)-L-fucopyranose residues with disulfate at C-2 and C-3 (Table 1).”
Quote in the paperNot a substantial claimMay combine two claims.
Premisecitation§ 2 Structures and chemical nature of fucoidansSulfate groups on the fucans are typically located at C-4 of an α(1→3)-linked unit or on C-2 of an α(1→4)-linked residue.
“The sulfate groups on the fucans are typically located at C-4 of a (1A3)-linked unit or on C-2 of a (1A4)-linked residue.11”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [11] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisecitation§ 1 IntroductionClassical extraction of fucoidans may include calcium addition to promote alginate precipitation during purification.
“and may include calcium addition to promote alginate precipitation during purification, 3,4”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Premisecitation§ 1 IntroductionFucoidans are vulnerable to harsh extraction conditions, and the extraction method significantly influences the yields and polysaccharide composition of extracted fucose-containing sulfated polysaccharides.
“It has recently been demonstrated that fucoidans are vulnerable to harsh extraction conditions and that the extraction method significantly influences the yields and not least the polysaccharide composition of the extracted fucose-containing sulfated polysaccharides.3”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [3] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone given§ 4.1 Fucoidan modifying enzymesFucoidanases have been intensely studied in relation to bacterial degradation of fucoidans and molecular structure elucidation of fucoidan.
“On the other hand, fucoidanases have been intensely studied in relation to bacterial degradation of fucoidans and molecular structure elucidation of fucoidan”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Interpretationreasoning§ AbstractMild extraction techniques coupled with new tools such as enzymes can provide knowledge about structural characteristics of different fucoidan molecules and pave the way for better understanding of the structural chemistry and bioactivities of fucoidans.
“Mild extraction techniques coupled with the use of new tools such as enzymes can provide the much needed knowledge about structural characteristics of different fucoidan molecules and thus pave the way for a better understanding of the structural chemistry and bioactivities of fucoidans.”
Quote in the paperSubstantial claimMay combine two claims.
Premisecitation§ 2 Structures and chemical nature of fucoidansFucoidans from Cladosiphon okamuranus are basically made up of linear backbones of α(1→3)-linked L-fucopyranose residues with a portion of the fucose residues being O-acetylated and with some sulfate substitution at C-4.
“Similarly, the fucoidans from Cladosiphon okamuranus (Chordariales) are basically made up of linear backbones of a(1A3)-linked L- fucopyranose residues (Table 1) with a portion of the fucose residues being O-acetylated and with some sulfate substitution at the C-4 position.8”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] source
Not checked in the free run.
May combine two claims.
Premisecitation§ 4.1 Fucoidan modifying enzymesFucoidanases have been intensely studied in relation to bacterial degradation of fucoidans and molecular structure elucidation of fucoidan polysaccharides.
“hand, fucoidanases have been intensely studied in relation to bacterial degradation of fucoidans and molecular structure elucidation of fucoidan polysaccharides.35,36,42”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
Premisecitation§ 2 Structures and chemical nature of fucoidansFucoidans from Chorda filum consist of a core backbone structure of poly-α(1→3)-linked L-fucopyranoses sulfated mainly at C-4, sometimes at C-2, with some α(1→3)-linked fucose residues being 2-O-acetylated.
“These structural units are similar to those found in the fucoidans from Chorda filum (Laminariales) which consist of a core backbone structure of poly-a(1A3)-linked L-fucopyranoses sulfated mainly at C-4, sometimes at the C-2 position, and with some of the a(1A3)linked fucose residues being 2-O-acetylated.4,14”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [4] source
Not checked in the free run.
- cites [14]
Not checked in the free run.
May combine two claims.
Premisecitation§ 2 Structures and chemical nature of fucoidansSulfated β-D-galactan has been isolated in trace amounts from Laminaria angustata and classified as fucoidans, even though β-D-galactose appears to be the major sugar, and L-fucose and D-glucuronic acid are present only as trace components.
“Sulfated b-D-galactan has been isolated in trace amounts from Laminaria angustata and these polysaccharides have also been classified as fucoidans, eventhough b-D-galactose appear to be the major sugar, and L-fucose and D-glucuronic acid are present only as trace components.15”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [15] source
Not checked in the free run.
May combine two claims.
Premisecitation§ 2 Structures and chemical nature of fucoidansFucoidans in the order Fucales, e.g. Fucus evanescens and Fucus serratus, possess a large proportion of both α(1→3)- and α(1→4)-linked L-fucopyranose residues, which may be substituted with sulfate on C-2 and C-4.
“The fucoidans in brown seaweeds in the order of Fucales, e.g.Fucus evanescens and Fucus serratus, represent the typical structures: They possess a large proportion of both a(1A3)and a(1A4)-linked L-fucopyranose residues, which may be substituted with sulfate (SO 3 2 ) on C-2 and C-4 (Table 1).6,7,10”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
Interpretationreasoning§ 2 Structures and chemical nature of fucoidansFucoidans extracted from brown seaweeds under the same seaweed classification (i.e. order) have different composition, and structural traits cannot be categorized or predicted according to algal order.
“It also seems clear that fucoidans extracted from brown seaweeds under the same seaweed classification (i.e.order) have different composition, and in turn that the structural traits cannot be categorized or predicted according to algal order as also indicated in Table 2.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone given§ 1 IntroductionMild extraction technology is essential for maintaining the structural integrity of fucoidan polysaccharides and for preserving their biological properties.
“Mild extraction technology is essential for maintaining the structural integrity of the fucoidan polysaccharides and for preserving their biological properties.”
Quote in the paperNot a substantial claim- Rests on an assumption: Fucoidan polysaccharides have potential therapeutic properties, including anti-inflammatory, anti-coagulant, and anti-proliferative effects on cancer cells.
May combine two claims.
Interpretationown data§ 3.1 Influence of extraction parameters on fucoidan yield and compositionAvailable published data, including the paper's own findings, generally show that the term fucoidan has been used for several chemical structures, and that fucoidans is a term covering a family of fucose-containing sulfated polysaccharides.
“The available published data, including our own findings, thus generally show that the term ''fucoidan'' has been used for several chemical structures, and vice versa, that fucoidans is a term that covers a family of fucose-containing sulfated polysaccharides.”
Quote in the paperSubstantial claimMay combine two claims.
Premisecitation§ 3.1 Influence of extraction parameters on fucoidan yield and compositionLonger extraction time led to poorer fucose content, whereas glucuronic acid increased while sulfate decreased with time; sulfate content was highest when glucuronic acid was lowest.
“Ponce et al. (2003) 17 thus reported that longer extraction time led to poorer fucose content, whereas glucuronic acid increased while sulfate decreased with time, i.e., the sulfate content was highest when glucuronic acid was lowest.17”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [17] source
Not checked in the free run.
May combine two claims.
Premisenone given§ 2 Structures and chemical nature of fucoidansFucoidans from brown seaweed algae generally consist of a backbone of α(1→3)-L-fucopyranose residues or of alternating α(1→3) and α(1→4)-linked L-fucopyranosyls, which may be substituted with sulfate or acetate and/or have side branches containing fucopyranoses or other glycosyl units, e.g. glucuronic acid.
“Fucoidans from brown seaweed algae generally consist of a backbone of a(1A3)-L-fucopyranose residues or of alternating a(1A3) and a(1A4)-linked L-fucopyranosyls, which in either case may be substituted with sulfate or acetate and/or have side branches containing fucopyranoses or other glycosyl units, e.g.glucuronic acid.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisereasoning§ 5.1 Fucoidan bioactivity and potential applicationsFucoidans are water soluble and can easily be incorporated into lotions, creams and other beauty products.
“Since fucoidans are water soluble, they can easily be incorporated into lotions, creams and other beauty products.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsMarine bacteria such as Fucophilus fucoidanolyticus are to a certain extent able to consume fucoidans of various structures and apparently synthesize a number of fucoidan-degrading enzymes.
“Marine bacteria such as Fucophilus fucoidanolyticus are to a certain extent able to consume fucoidans of various structures and apparently”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [44] source
Not checked in the free run.
Classified as probably not a substantial claim.
Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsTargeted use of fucoidanases might assist in determining the precise molecular structures accountable for preventive bioactivity effects.
“In this connection, the targeted use of fucoidanases might assist in determining the precise molecular structures accountable for preventive bioactivity effects.”
Quote in the paperSubstantial claimMay combine two claims.
Premisecitation§ 5.1 Fucoidan bioactivity and potential applicationsFucoidans may enhance dermal fibroblast proliferation and deposition of collagen.
“Fucoidans may enhance dermal fibroblast proliferation and deposition of collagen; 52”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [52] source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisenone given§ 5.1 Fucoidan bioactivity and potential applicationsProduction of pure fucoidan products is challenging because of the presence of other polysaccharides, such as alginate.
“Production of pure fucoidan products is challenging because of the presence of other polysaccharides, such as alginate.”
Quote in the paperNot a substantial claimMay combine two claims.
Premisecitation§ 5.1 Fucoidan bioactivity and potential applicationsAlgal fucoidans have diverse biological functions and possible therapeutic properties including antitumor, immunomodulatory, anti-inflammatory, antithrombotic, and anticoagulant effects.
“Algal fucoidans have been the subject of numerous scientific studies due to their diverse biological functions and possible therapeutic properties including antitumor, immunomodulatory, 45 anti-inflammatory, 6 antithrombotic, and anticoagulant effects.46”
Quote in the paperNot a substantial claim0 of 3 sources checkedMay combine two claims.
Interpretationreasoning§ 6 Conclusions and outlookFucoidans exert potentially significant pharmaceutical effects but are a family of differently structured polysaccharides comprising structural units having distinct traits.
“Among the polysaccharides from brown seaweeds, fucoidans have turned out to exert potentially significant pharmaceutical effects, but at the same time to be a family of differently structured polysaccharides comprising structural units having distinct traits.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based).
Premisenone given§ 6 Conclusions and outlookFine structural details of fucoidans vary depending on seaweed type and species.
“It is known now that the fine structural details of fucoidans vary depending on seaweed type and species.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationreasoning§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsLack of standardized extraction methodology prevents detailed comparison and obstructs understanding of the correlation between fucoidan polysaccharide structures and biological functions.
“The lack of a standardized extraction methodology prevents detailed comparison and most importantly obstructs the understanding of the correlation between fucoidan 4.”
Quote in the paperSubstantial claimMay combine two claims.
Premisecitation§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsAt least one intracellular fucoidanase from Fucophilus fucoidanolyticus seems able to catalyse splitting of 1,3α-glycosidic bonds and has been demonstrated to express deacetylase activity effective on acetylated fucoidans from Cladosiphon okamuranus.
“At least one of them (intracellular fucoidanase) seems to have the ability to catalyse the splitting of 1,3a-glycosidic bonds and has also been demonstrated to express deacetylase activity being effective on acetylated fucoidans from Cladosiphon okamuranus.33”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [33] source
Not checked in the free run.
May combine two claims.
Premisenone given§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsThe biological activity of fucoidans depends on seaweed source, compositional and structural traits, content (charge density), distribution, and bonding of sulfate substitutions, and purity of the fucoidan product.
“The biological activity of fucoidans depend on the seaweed source, the compositional and structural traits, the content (charge density), distribution, and bonding of the sulfate substitutions, and the purity of the fucoidan product.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Premisecitation§ 5.1 Fucoidan bioactivity and potential applicationsBioactive properties of fucoidans are defined by their structural make-up, notably related to fucose sulfated chains.
“It has been suggested that the bioactive properties of fucoidans are defined by their structural make-up, and notably related to the fucose sulfated chains.15”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [15] source
Not checked in the free run.
Classified as probably not a substantial claim.
Premisenone given§ 6 Conclusions and outlookExact correlations between various bioactivities and molecular and structural features of fucoidans still have to be clarified.
“Despite intensive research, the exact correlations between the various bioactivities and the molecular and structural features of fucoidans still have to be clarified.”
Quote in the paperSubstantial claimMay combine two claims.
Premisecitation§ 5.1 Fucoidan bioactivity and potential applicationsFucoidan induces apoptosis in HT-29 colon cancer cells, MCF-7 human breast cancer cells, and HS-Sultan human lymphoma cells.
“Fucoidan was also reported to induce apoptosis in HT-29 colon cancer cells, 47 MCF-7 human breast cancer cells, 48 and HS-Sultan human lymphoma cells.49”
Quote in the paperNot a substantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone given§ Kjellmaniella crassifolia [A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A3)-a-L-Fucp-(1A]; branching mainly of (1A2)-a-L-Fucp single unitsFucoidan polysaccharides and other FCSPs exhibit significant biological properties in vitro such as anti-proliferative activity on cancer cells.
“As mentioned earlier, fucoidan polysaccharides and other FCSPs exhibit significant biological properties in vitro such as anti-prolif-erative activity on cancer cells.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Premisenone given§ 6 Conclusions and outlookHarsh chemicals are environmentally burdensome and have detrimental effects on yield and compositions of end product polysaccharides.
“Harsh chemicals are environmentally burdensome and have detrimental effects on the yield and compositions of the end product polysaccharides.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S4 (based).
Interpretationreasoning§ 6 Conclusions and outlookFucoidanases may provide new tools for elucidation of detailed fucoidan structures from various sources.
“Fucoidanases may provide new tools for elucidation of detailed fucoidan structures from various sources.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Fucoidan polysaccharides have potential therapeutic properties, including anti-inflammatory, anti-coagulant, and anti-proliferative effects on cancer cells.
“Fucoidans have potential therapeutic properties, including anti-inflammatory and anti-coagulant activities, as well as anti-proliferative effects on cancer cells.”
“Fucoidan polysaccharides exhibit a number of pharmaceutically interesting biological activities, including immuno-modulatory, anti-tumor, anti-inflammatory and anti-coagulant effects (to be discussed in more detail later).”
The paper relies on this without support.
No standardized purification procedure is available for fucoidans at present.
“but no standardized purification procedure is available for fucoidans at present.”
The paper relies on this without support.
The heterogeneity of the structural make-up of seaweeds within the same species may lead to pronounced differences in the products extracted.
“In addition, the heterogeneity of the structural make-up of seaweeds within the same species may lead to pronounced differences in the products extracted.”
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?
The absence of standardized extraction methodologies has blocked official approval of polysaccharides or their fractions for pharmaceutical, dermatological, nutraceutical or other commercial uses.
“The lack of standardized extraction methodologies has prevented the approval of polysaccharides or their derived fractions to be officially approved for pharmaceutical, dermatological, nutraceutical or other commercial applications to date”
From Polysaccharides from macroalgae: Recent advances, innovative technologies and challenges in extraction and purification (2017) · cites this paper as Ale & Meyer, 2013
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Example fucose content falls outside the stated range
MinorThe passage says samples obtained by the procedure contained 30-36% fucose, then gives a product from the same protocol as an example containing 44% fucose.
“By this procedure, samples of crude fucoidans containing 30-36% fucose were obtained; for example, the fucoidan polysaccharides recovered from F. vesiculosus using this optimal extraction protocol was analyzed to contain (by weight) 44% fucose;”
“samples of crude fucoidans containing 30-36% fucose were obtained”
Cites
Fucoidan: Structure and bioactivity
Li, B., Lu, F., Wei, X., & Zhao, R. (2008) · Molecules · doi:10.3390/molecules13081671 · Cited by 1,383 · see citing works
Cumashi, A., Ushakova, N. A., Preobrazhenskaya, M. E., D'Incecco, A., Piccoli, A., Totani, L., Tinari, N., Morozevich, G. E., Berman, A. E., Bilan, M. I., et al. (2007) · Glycobiology · doi:10.1093/glycob/cwm014 · Cited by 1,026 · see citing works
Ale, M. T., Mikkelsen, J. D., & Meyer, A. S. (2011) · Marine Drugs · doi:10.3390/md9102106 · Cited by 779 · see citing works
Self-citationJournal of Biomolecular Structure and Dynamics
Sarma, R. H. (1997) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.1997.10508975 · Cited by 779 · see citing works
Berteau, O. (2003) · Glycobiology · doi:10.1093/glycob/cwg058 · Cited by 769 · see citing works
Antioxidant activities of enzymatic extracts from brown seaweeds
HEO, S., Park, E., LEE, K., & Jeon, Y. (2005) · Bioresource Technology · doi:10.1016/j.biortech.2004.07.013 · Cited by 653 · see citing works
THE JOURNAL OF BIOLOGICAL CHEMISTRY.
Hanukoglu, I., & Jefcoate, C. R. (1905) · JAMA · doi:10.1001/jama.1905.02510220045008 · Cited by 612 · see citing works
A revised structure for fucoidan may explain some of its biological activities.
Patankar, M. S., Oehninger, S., Barnett, T., Williams, R. L., & Clark, G. F. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)80609-7 · Cited by 531 · see citing works
Ponce, N. M. A., Pujol, C. A., Damonte, E. B., Flores, M. L., & Stortz, C. A. (2003) · Carbohydrate Research · doi:10.1016/s0008-6215(02)00403-2 · Cited by 484 · see citing works
Wang, J., Zhang, Q., Zhang, Z., Song, H., & Li, P. (2010) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2009.10.015 · Cited by 456 · see citing works
Structure of a fucoidan from the brown seaweed Fucus evanescens C.Ag.
Bilan, M. I., Grachev, A. A., Ustuzhanina, N. E., Shashkov, A. S., Nifantiev, N. E., & Usov, A. I. (2002) · Carbohydrate Research · doi:10.1016/s0008-6215(02)00053-8 · Cited by 412 · see citing works
Further data on the structure of brown seaweed fucans: relationships with anticoagulant activity
Chevolot, L., Foucault, A., Chaubet, F., Kervarec, N., Sinquin, C., Fisher, A.-M., & Boisson-Vidal, C. (1999) · Carbohydrate Research · doi:10.1016/s0008-6215(99)00127-5 · Cited by 330 · see citing works
A study of fucoidan from the brown seaweed Chorda filum
Chizhov, A. O., Dell, A., Morris, H. R., Haslam, S. M., McDowell, R. A., Shashkov, A. S., Nifant’ev, N. E., Khatuntseva, E. A., & Usov, A. I. (1999) · Carbohydrate Research · doi:10.1016/s0008-6215(99)00148-2 · Cited by 326 · see citing works
Structural studies on fucoidans from the brown seaweed Sargassum stenophyllum
Duarte, M. E. R., Cardoso, M. A., Noseda, M. D., & Cerezo, A. S. (2001) · Carbohydrate Research · doi:10.1016/s0008-6215(01)00149-5 · Cited by 319 · see citing works
Aisa, Y., Miyakawa, Y., Nakazato, T., Shibata, H., Saito, K., Ikeda, Y., & Kizaki, M. (2005) · American Journal of Hematology · doi:10.1002/ajh.20182 · Cited by 307 · see citing works
Novel procedures for the extraction of fucoidan from brown algae
Hahn, T., Lang, S., Ulber, R., & Muffler, K. (2012) · Process Biochemistry · doi:10.1016/j.procbio.2012.06.016 · Cited by 297 · see citing works
Fucoidan present in brown algae induces apoptosis of human colon cancer cells
Kim, E. J., Park, S. Y., Lee, J.-Y., & Park, J. H. Y. (2010) · BMC Gastroenterology · doi:10.1186/1471-230x-10-96 · Cited by 275 · see citing works
Ale, M. T., Maruyama, H., Tamauchi, H., Mikkelsen, J. D., & Meyer, A. S. (2011) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2011.05.009 · Cited by 267 · see citing works
Self-citationStructure of a fucoidan from the brown seaweed Fucus serratus L.
Bilan, M. I., Grachev, A. A., Shashkov, A. S., Nifantiev, N. E., & Usov, A. I. (2006) · Carbohydrate Research · doi:10.1016/j.carres.2005.11.009 · Cited by 263 · see citing works
Ermakova, S., Sokolova, R., Kim, S.-M., Um, B.-H., Isakov, V., & Zvyagintseva, T. (2011) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-011-9178-2 · Cited by 229 · see citing works
Fucoidan Induces Apoptosis through Activation of Caspase-8 on Human Breast Cancer MCF-7 Cells
Yamasaki-Miyamoto, Y., Yamasaki, M., Tachibana, H., & Yamada, K. (2009) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf9010406 · Cited by 181 · see citing works
Holtkamp, A. D., Kelly, S., Ulber, R., & Lang, S. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-008-1790-x · Cited by 175 · see citing works
Structural study of fucoidan from Cladosiphon okamuranus tokida
Nagaoka, M., Shibata, H., Kimura-Takagi, I., Hashimoto, S., Kimura, K., Makino, T., Aiyama, R., Ueyama, S., & Yokokura, T. (1999) · Glycoconjugate Journal · doi:10.1023/a:1006945618657 · Cited by 173 · see citing works
Hemmingson, J. A., Falshaw, R., Furneaux, R. H., & Thompson, K. (2006) · Journal of Applied Phycology · doi:10.1007/s10811-006-9096-9 · Cited by 171 · see citing works
Senni, K., Gueniche, F., Foucault-Bertaud, A., Igondjo-Tchen, S., Fioretti, F., Colliec-Jouault, S., Durand, P., Guezennec, J., Godeau, G., & Letourneur, D. (2006) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2005.11.001 · Cited by 163 · see citing works
Teruya, T., Konishi, T., Uechi, S., Tamaki, H., & Tako, M. (2007) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2007.02.010 · Cited by 156 · see citing works
Rocha, H. A. O., Moraes, F. A., Trindade, E. D. S., Franco, C. R. C., Torquato, R. J. S., Veiga, S. S., Valente, A. P., Mourão, P. A. S., Leite, E. L., Nader, H. B., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501124200 · Cited by 156 · see citing works
Maruyama, H., Tamauchi, H., Iizuka, M., & Nakano, T. (2006) · Planta Medica · doi:10.1055/s-2006-951703 · Cited by 151 · see citing works
The minimal enzyme cocktail concept for biomass processing
Meyer, A. S., Rosgaard, L., & Sørensen, H. R. (2009) · Journal of Cereal Science · doi:10.1016/j.jcs.2009.01.010 · Cited by 115 · see citing works
Self-citationAle, M. T., Mikkelsen, J. D., & Meyer, A. S. (2012) · Journal of Applied Phycology · doi:10.1007/s10811-011-9690-3 · Cited by 113 · see citing works
Self-citationSørensen, H. R., Pedersen, S., Jørgensen, C. T., & Meyer, A. S. (2007) · Biotechnology Progress · doi:10.1021/bp0601701 · Cited by 113 · see citing works
Self-citationIsolation and Culture of a Marine Bacterium Degrading the Sulfated Fucans from Marine Brown Algae
Descamps, V., Colin, S., Lahaye, M., Jam, M., Richard, C., Potin, P., Barbeyron, T., Yvin, J.-C., & Kloareg, B. (2006) · Marine Biotechnology · doi:10.1007/s10126-005-5107-0 · Cited by 108 · see citing works
Anastyuk, S. D., Shevchenko, N. M., Nazarenko, E. L., Dmitrenok, P. S., & Zvyagintseva, T. N. (2009) · Carbohydrate Research · doi:10.1016/j.carres.2009.01.023 · Cited by 96 · see citing works
145. Fucoidin. Part I. The isolation and purification of fucoidin from brown seaweeds
Percival, E. G. V., & Ross, A. G. (1950) · Journal of the Chemical Society (Resumed) · doi:10.1039/jr9500000717 · Cited by 88 · see citing works
Berteau, O., McCort‐Tranchepain, I., Goasdoué, N., Tissot, B., & Daniel, R. (2002) · Glycobiology · doi:10.1093/glycob/12.4.273 · Cited by 84 · see citing works
Shimanaka, K., Ikai, K., Kato, I., Sakai, T., & Ishizuka, K. (2003) · Marine Biotechnology · doi:10.1007/s10126-002-0107-9 · Cited by 83 · see citing works
Zhu, W., Ooi, V. E. C., Chan, P. K. S., & Ang Jr., P. O. (2003) · Biochemistry and Cell Biology · doi:10.1139/o02-169 · Cited by 79 · see citing works
A Marine Strain of Flavobacteriaceae Utilizes Brown Seaweed Fucoidan
Sakai, T., Kimura, H., & Kato, I. (2002) · Marine Biotechnology · doi:10.1007/s10126-002-0032-y · Cited by 75 · see citing works
Manufacture of algal chemicals. IV—Laboratory-scale isolation of fucoidin from brown marine algae
Black, W. A. P., Dewar, E. T., & Woodward, F. N. (1952) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.2740030305 · Cited by 75 · see citing works
Degradation of Fucoidan by the Marine Proteobacterium Pseudoalteromonas citrea
Bakunina, I. Y., Nedashkovskaya, O. I., Alekseeva, S. A., Ivanova, E. P., Romanenko, L. A., Gorshkova, N. M., Isakov, V. V., Zvyagintseva, T. N., & Mikhailov, V. V. (2002) · Microbiology · doi:10.1023/a:1017994131769 · Cited by 70 · see citing works
Isolation and Characterization of a Fucoidan-Degrading Marine Bacterial Strain and Its Fucoidanase
Sakai, T., Kawai, T., & Kato, I. (2004) · Marine Biotechnology · doi:10.1007/s10126-003-0033-5 · Cited by 69 · see citing works
Purification and Some Properties of Exo-type Fucoidanases from<i>Vibrio</i>sp. N-5
Furukawa, S.-I., Fujikawa, T., Koga, D., & Ide, A. (1992) · Bioscience, Biotechnology, and Biochemistry · doi:10.1271/bbb.56.1829 · Cited by 54 · see citing works
Abdel-Fattah, A. F., Hussein, M. M.-D., & Salem, H. M. (1974) · Carbohydrate Research · doi:10.1016/s0008-6215(00)82935-3 · Cited by 48 · see citing works
On the nature of the cell wall constituents of Laminaria spp. Mannuronic acid
Bird, G. M., & Haas, P. (1931) · Biochemical Journal · doi:10.1042/bj0250403 · Cited by 47 · see citing works
THE COMPLEX CARBOHYDRATES AND FORMS OF SULPHUR IN MARINE ALGAE OF THE PACIFIC COAST
Hoagland, D. R., & Lieb, L. L. (1915) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)87617-7 · Cited by 34 · see citing works
Nishino, T., Takabe, Y., & Nagumo, T. (1994) · Carbohydrate Polymers · doi:10.1016/0144-8617(94)90099-x · Cited by 31 · see citing works
Bilan, M. I., Kusaykin, M. I., Grachev, A. A., Tsvetkova, E. A., Zvyagintseva, T. N., Nifantiev, N. E., & Usov, A. I. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0264-3 · Cited by 30 · see citing works
Fujimura, T., TAKAHARA, K., Moriwaki, S., Kitahara, T., & Takema, Y. (2000) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.23.291 · Cited by 21 · see citing works
An antitumor fucoidan fraction from an edible brown seaweed, Laminaria religiosa
Maruyama, H., & Yamamoto, I. (1984) · Hydrobiologia · doi:10.1007/bf00027740 · Cited by 18 · see citing works
THE CARBOHYDRATE ACID SULFATE OF MACROCYSTIS PYRIFERA
Nelson, W. L., & Cretcher, L. H. (1931) · Journal of Biological Chemistry · Cited by 11 · see citing works
Flagged first, then by citations
Research works printed but not linked: 4
- H. Kylin in Hoppe-Seyleŕs Zeitschrift für physiologische Chemie, 1913, vol. 83, p. 171
- H. Kylin in Hoppe-Seyleŕs Zeitschrift für physiologische Chemie, 1915, vol. 94, p. 337
- G. Lunde , E.Heen and E.Öy in Hoppe-Seyleŕs Zeitschrift für physiologische Chemie, 1937, vol. 247, p. 189
- Shin-ichi, 1992, Biosci., Biotechnol., Biochem., 56, 1829, 10.1271/bbb.56.1829 · DOI · Paper page
Cited by
Sorted by citations
Structures, Properties and Applications of Alginates
Abka-khajouei, R., Tounsi, L., Shahabi, N., Patel, A. K., Abdelkafi, S., & Michaud, P. (2022) · Marine Drugs · doi:10.3390/md20060364 · Cited by 769 · see citing works
Antimicrobial Action of Compounds from Marine Seaweed
Pérez, M. J., Falqué, E., & Domı́nguez, H. (2016) · Marine Drugs · doi:10.3390/md14030052 · Cited by 663 · see citing works
Kumar, M., Sun, Y., Rathour, R., Pandey, A., Thakur, I. S., & Tsang, D. C. W. (2020) · Science of The Total Environment · doi:10.1016/j.scitotenv.2020.137116 · Cited by 472 · see citing works
Rhein‐Knudsen, N., Ale, M. T., & Meyer, A. S. (2015) · Marine Drugs · doi:10.3390/md13063340 · Cited by 379 · see citing works
Self-citationGarcia-Vaquero, M., Rajauria, G., O'Doherty, J. V., & Sweeney, T. (2017) · Food Research International · doi:10.1016/j.foodres.2016.11.016 · Cited by 364 · see citing works
Immunomodulatory and Anti-Inflammatory Effects of Fucoidan: A Review
Apostolova, E., Lukova, P., Baldzhieva, A., Katsarov, P., Nikolova, M., Iliev, I. N., Peychev, L. P., Trică, B., Oancea, F., Delattre, C., et al. (2020) · Polymers · doi:10.3390/polym12102338 · Cited by 350 · see citing works
Fucoidan Structure and Activity in Relation to Anti-Cancer Mechanisms
van Weelden, G. H., Bobiński, M. S., Okła, K., van Weelden, W. J., Romano, A., & Pijnenborg, J. M. A. (2019) · Marine Drugs · doi:10.3390/md17010032 · Cited by 336 · see citing works
Deniaud-Bouët, E., Hardouin, K., Potin, P., Kloareg, B., & Hervé, C. (2017) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2017.07.082 · Cited by 320 · see citing works
Salehi, B., Sharifi‐Rad, J., Seca, A. M. L., Pinto, D. C. G. A., Michalak, I., Trincone, A., Mishra, A. P., Nigam, M., Zam, W., & Martins, N. A. (2019) · Molecules · doi:10.3390/molecules24224182 · Cited by 315 · see citing works
Jönsson, M., Allahgholi, L., Sardari, R. R. R., Hreggviðsson, G. Ó., & Karlsson, E. N. (2020) · Molecules · doi:10.3390/molecules25040930 · Cited by 297 · see citing works
The Potential of Seaweeds as a Source of Functional Ingredients of Prebiotic and Antioxidant Value
Gomez-Zavaglia, A., Prieto Lage, M. A., Jimenez-Lopez, C., Mejuto, J. C., & Simal-Gandara, J. (2019) · Antioxidants · doi:10.3390/antiox8090406 · Cited by 280 · see citing works
Fucoidan Characterization: Determination of Purity and Physicochemical and Chemical Properties
Zayed, A., El‐Aasr, M., Ibrahim, A.-R. S., & Ulber, R. (2020) · Marine Drugs · doi:10.3390/md18110571 · Cited by 245 · see citing works
Sun, Y., Hou, S., Song, S., Zhang, B., Ai, C., Chen, X., & Liu, N. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.02.066 · Cited by 235 · see citing works
Brown Algae Carbohydrates: Structures, Pharmaceutical Properties, and Research Challenges
Li, Y., Zheng, Y., Zhang, Y., Yang, Y., Wang, P., Imre, B., Wong, A. C. Y., Hsieh, Y. S. Y., & Wang, D. (2021) · Marine Drugs · doi:10.3390/md19110620 · Cited by 232 · see citing works
A review of extractions of seaweed hydrocolloids: Properties and applications
Khalil, H. P. S. A., Lai, T. K., Tye, Y. Y., Rizal, S., Chong, E. W. N., Yap, S. W., Hamzah, A. A., Rawi, N. F. M., & Paridah, M. T. (2018) · eXPRESS Polymer Letters · doi:10.3144/expresspolymlett.2018.27 · Cited by 236 · see citing works
Rodrigues, D., Sousa, S., Silva, A., Amorim, M., Pereira, L., Rocha-Santos, T. A. P., Gomes, A. M. P., Duarte, A. C., & Freitas, A. C. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf504220e · Cited by 201 · see citing works
Saravana, P. S., Cho, Y.-J., Park, Y.-B., Woo, H.-C., & Chun, B.-S. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2016.08.014 · Cited by 197 · see citing works
Pozharitskaya, O. N., Obluchinskaya, E. D., & Shikov, A. N. (2020) · Marine Drugs · doi:10.3390/md18050275 · Cited by 201 · see citing works
Overview on the antiviral activities and mechanisms of marine polysaccharides from seaweeds
Qi-Min, S. H. I., Wang, A., Lu, Z., Qin, C., Jing Hua, H. U., & Yin, J. (2017) · Carbohydrate Research · doi:10.1016/j.carres.2017.10.020 · Cited by 196 · see citing works
Sanjeewa, K. K. A., Lee, J.-S., Kim, W.-S., & Jeon, Y. (2017) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2017.09.005 · Cited by 192 · see citing works
Fernando, I. P. S., Kim, D., Nah, J., & Jeon, Y. (2018) · Chemical Engineering Journal · doi:10.1016/j.cej.2018.08.115 · Cited by 183 · see citing works
Marine algal carbohydrates as carbon sources for the production of biochemicals and biomaterials
Cesário, M. T., da Fonseca, M. M. R., Marques, M. M., & de Almeida, M. C. M. D. (2018) · Biotechnology Advances · doi:10.1016/j.biotechadv.2018.02.006 · Cited by 182 · see citing works
Rioux, L., & Turgeon, S. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-418697-2.00007-6 · Cited by 162 · see citing works
Kostas, E. T., Adams, J. M. M., Ruíz, H. A., Durán-Jiménez, G., & Lye, G. J. (2021) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2021.111553 · Cited by 158 · see citing works
Brown Macroalgae as Valuable Food Ingredients
Afonso, N., Catarino, M. D., Silva, A. M. S., & Cardoso, S. M. (2019) · Antioxidants · doi:10.3390/antiox8090365 · Cited by 158 · see citing works
Oliveira, C., Neves, N. M., Reis, R. L., Martins, A. M., & Silva, T. H. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.116131 · Cited by 152 · see citing works
Nguyen, T. T., Mikkelsen, M. D., Tran, V. H. N., Trang, V. T. D., Rhein‐Knudsen, N., Holck, J., Rasin, A. B., Cao, H. T. T., Van, T. T. T., & Meyer, A. S. (2020) · Marine Drugs · doi:10.3390/md18060296 · Cited by 150 · see citing works
Self-citationCell Wall Polysaccharides of Marine Algae
Synytsya, A., Čopı́ková, J., Kim, W. J., & Park, Y. I. (2015) · Springer eBooks · doi:10.1007/978-3-642-53971-8_22 · Cited by 142 · see citing works
García-García, J. D., Sánchez‐Thomas, R., & Moreno‐Sánchez, R. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.05.003 · Cited by 139 · see citing works
Current application of algae derivatives for bioplastic production: A review
Dang, B., Bui, X., Tran, D. P.-H., Ngo, H. H., Nghiem, L. D., Hoang, T.-K.-D., Nguyen, P.-T., Nguyen, H. H., Vo, T., Lin, C., et al. (2022) · Bioresource Technology · doi:10.1016/j.biortech.2022.126698 · Cited by 141 · see citing works
Manns, D., Deutschle, A. L., Saake, B., & Meyer, A. S. (2014) · RSC Advances · doi:10.1039/c4ra03537b · Cited by 136 · see citing works
Self-citationSeaweed Bioethanol Production: A Process Selection Review on Hydrolysis and Fermentation
Offei, F., Mensah, M. Y., Thygesen, A., & Kemausuor, F. (2018) · Fermentation · doi:10.3390/fermentation4040099 · Cited by 129 · see citing works
Chollet, L., Saboural, P., Chauvierre, C., Villemin, J.-N., Letourneur, D., & Chaubet, F. (2016) · Marine Drugs · doi:10.3390/md14080145 · Cited by 122 · see citing works
Anisha, G. S., Padmakumari, S., Patel, A. K., Pandey, A., & Singhania, R. R. (2022) · Bioengineering · doi:10.3390/bioengineering9090472 · Cited by 121 · see citing works
Abdel‐Latif, H. M. R., Dawood, M. A. O., Alagawany, M. M., Faggio, C., Nowosad, J., & Kucharczyk, D. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.01.039 · Cited by 118 · see citing works
Algal Polysaccharides, Novel Application, and Outlook
Usman, A., Khalid, S., Usman, A., Hussain, Z., & Wang, Y. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812360-7.00005-7 · Cited by 116 · see citing works
“Fucoidan, a natural biopolymer in cancer combating: From edible algae to nanocarrier tailoring”
Etman, S. M., Elnaggar, Y. S. R., & Abdallah, O. Y. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.11.191 · Cited by 115 · see citing works
Fucoidan production: Approval key challenges and opportunities
Zayed, A., & Ulber, R. (2019) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2019.01.105 · Cited by 110 · see citing works
Amador-Castro, F., García‐Cayuela, T., Alper, H. S., Rodríguez‐Martínez, V., & Carrillo-Nieves, D. (2021) · Journal of Environmental Management · doi:10.1016/j.jenvman.2021.112013 · Cited by 111 · see citing works
Potential of intensification techniques for the extraction and depolymerization of fucoidan
Flórez-Fernández, N., Torres, M. D., González‐Muñoz, M. J., & Domı́nguez, H. (2018) · Algal Research · doi:10.1016/j.algal.2018.01.002 · Cited by 107 · see citing works
Manns, D., Nielsen, M. M., Bruhn, A., Saake, B., & Meyer, A. S. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-017-1056-z · Cited by 107 · see citing works
Self-citationBruhn, A., Janicek, T., Manns, D., Nielsen, M. M., Balsby, T. J. S., Meyer, A. S., Rasmussen, M. B., Hou, X., Saake, B., Göke, C., et al. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-017-1204-5 · Cited by 103 · see citing works
Self-citationIn vitro anticancer activity of fucoidan extracted from Sargassum cinereum against Caco-2 cells
Narayani, S. S., Saravanan, S., Jaganathan, R., Ramasamy, M. S., & Chitra, J. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.07.127 · Cited by 105 · see citing works
Antibacterial Properties of Fucoidans from the Brown Algae Fucus vesiculosus L. of the Barents Sea
Ayrapetyan, O. N., Obluchinskaya, E. D., Zhurishkina, E. V., Skorik, Y. А., Лебедев, Д. В., Kulminskaya, A. A., & Lapina, I. M. (2021) · Biology · doi:10.3390/biology10010067 · Cited by 103 · see citing works
The Enzymatic Conversion of Major Algal and Cyanobacterial Carbohydrates to Bioethanol
Al Abdallah, Q., Nixon, B. T., & Fortwendel, J. R. (2016) · Frontiers in Energy Research · doi:10.3389/fenrg.2016.00036 · Cited by 102 · see citing works
Sargassum contamination and consequences for downstream uses: a review
Devault, D. A., Pierre, R., Marfaing, H., Dolique, F., & Lopez, P. J. (2020) · Journal of Applied Phycology · doi:10.1007/s10811-020-02250-w · Cited by 109 · see citing works
Zayed, A., Muffler, K., Hahn, T., Rupp, S., Finkelmeier, D., Burger‐Kentischer, A., & Ulber, R. (2016) · Marine Drugs · doi:10.3390/md14040079 · Cited by 98 · see citing works
Wang, M., Veeraperumal, S., Zhong, S., & Cheong, K. (2023) · Foods · doi:10.3390/foods12040878 · Cited by 98 · see citing works
Enzyme-assisted extraction of bioactive compounds from brown seaweeds and characterization
Farvin, K. H. S., Alagarsamy, S., Sattari, Z., Al‐Haddad, S., Fakhraldeen, S. A., Al‐Ghunaim, A., & Al‐Yamani, F. (2019) · Journal of Applied Phycology · doi:10.1007/s10811-019-01906-6 · Cited by 93 · see citing works
García‐Vaquero, M., Rajauria, G., Tiwari, B. K., Sweeney, T., & O’Doherty, J. V. (2018) · Marine Drugs · doi:10.3390/md16080257 · Cited by 93 · see citing works
Vilela, C., Silva, A. C. Q., Domingues, E. M., Gonçalves, G., Martins, M. A., Figueiredo, F. M., Santos, S. A. O., & Freire, C. S. R. (2019) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2019.115604 · Cited by 92 · see citing works
Mabate, B., Daub, C. D., Malgas, S., Edkins, A. L., & Pletschke, B. I. (2021) · Marine Drugs · doi:10.3390/md19010030 · Cited by 92 · see citing works
Fucoidans: Downstream Processes and Recent Applications
Zayed, A., & Ulber, R. (2020) · Marine Drugs · doi:10.3390/md18030170 · Cited by 91 · see citing works
García‐Vaquero, M., O’Doherty, J. V., Tiwari, B. K., Sweeney, T., & Rajauria, G. (2019) · Marine Drugs · doi:10.3390/md17080457 · Cited by 88 · see citing works
Aleissa, M. S., Alkahtani, S., Abd Eldaim, M. A., Ahmed, A. M., Bungău, S. G., Almutairi, B., Bin-Jumah, M., AlKahtane, A. A., Alyousif, M. S., & Abdel-Daim, M. M. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/9316751 · Cited by 88 · see citing works
Fu, Y., Jiao, H., Sun, J., Okoye, C. O., Zhang, H., Li, Y., Lu, X., Wang, Q., & Liu, J. (2023) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2023.121533 · Cited by 87 · see citing works
Charoensiddhi, S., Lorbeer, A. J., Lahnstein, J., Bulone, V., Franco, C. M. M., & Zhang, W. Y. (2016) · Process Biochemistry · doi:10.1016/j.procbio.2016.07.014 · Cited by 84 · see citing works
Significance of fucose in intestinal health and disease
Garber, J. M., Hennet, T., & Szymanski, C. M. (2021) · Molecular Microbiology · doi:10.1111/mmi.14681 · Cited by 85 · see citing works
Systematic synthesis of low-molecular weight fucoidan derivatives and their effect on cancer cells
Kasai, A., Arafuka, S., Koshiba, N., Takahashi, D., & Toshima, K. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob01634g · Cited by 83 · see citing works
Souza, P. R., de Oliveira, A. C., Vilsinski, B. H., Kipper, M. J., & Martins, A. F. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13050621 · Cited by 84 · see citing works
Assessing methodologies for fucoidan extraction from South African brown algae
January, G. G., Naidoo, R., Kirby, B. M., & Bauer, R. (2019) · Algal Research · doi:10.1016/j.algal.2019.101517 · Cited by 81 · see citing works
Lu, J., Shi, K., Chen, S., Wang, J., Hassouna, A., White, L. N., Mérien, F., Xie, M., Kong, Q., Li, J., et al. (2018) · Marine Drugs · doi:10.3390/md16120461 · Cited by 79 · see citing works
Seaweeds in the Oncology Arena: Anti-Cancer Potential of Fucoidan as a Drug—A Review
Jin, J., Yadav, D., Madhwani, K., Puranik, N., Chavda, V. K., & Song, M. (2022) · Molecules · doi:10.3390/molecules27186032 · Cited by 78 · see citing works
Fucoidan for cardiovascular application and the factors mediating its activities
Yao, Y., & Yim, E. K. F. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2021.118347 · Cited by 80 · see citing works
Antiviral Activities of Algal-Based Sulfated Polysaccharides
Panggabean, J. A., Adiguna, S. P., Rahmawati, S. I., Ahmadi, P., Zainuddin, E. N., Bayu, A., & Putra, M. Y. (2022) · Molecules · doi:10.3390/molecules27041178 · Cited by 76 · see citing works
Biological activities and biomedical potential of sea cucumber (Stichopus japonicus): a review
Oh, G., Ko, S., Lee, D. H., Heo, S., & Jung, W. (2017) · Fisheries and aquatic sciences · doi:10.1186/s41240-017-0071-y · Cited by 77 · see citing works
Extraction of high purity fucoidans from brown seaweeds using cellulases and alginate lyases
Rhein‐Knudsen, N., Reyes-Weiss, D. S., & Horn, S. J. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.12.261 · Cited by 73 · see citing works
Hmelkov, A. B., Николаевна, З. Т., Шевченко, Н. М., Rasin, A. B., & Ermakova, S. P. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-017-1342-9 · Cited by 74 · see citing works
Therapeutic activity of fucoidan and carrageenan as marine algal polysaccharides against viruses
Oliyaei, N., Moosavi‐Nasab, M., & Mazloomi, S. M. (2022) · 3 Biotech · doi:10.1007/s13205-022-03210-6 · Cited by 72 · see citing works
Purification of a Low Molecular Weight Fucoidan for SPECT Molecular Imaging of Myocardial Infarction
Saboural, P., Chaubet, F., Rouzet, F., Al-Shoukr, F., Azzouna, R. B., Bouchemal, N., Picton, L., Louedec, L., Maire, M., Rolland, L., et al. (2014) · Marine Drugs · doi:10.3390/md12094851 · Cited by 72 · see citing works
Vickers, C. J., Liu, F., Abe, K. T., Salama-Alber, O., Jenkins, M. L., Springate, C. M. K., Burke, J. E., Withers, S. G., & Boraston, A. B. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005134 · Cited by 72 · see citing works
Lorbeer, A. J., Charoensiddhi, S., Lahnstein, J., Lars, C., Franco, C. M. M., Bulone, V., & Zhang, W. Y. (2016) · Journal of Applied Phycology · doi:10.1007/s10811-016-0990-5 · Cited by 71 · see citing works
Qi, Y., Wang, L., You, Y., Sun, X., Wen, C., Fu, Y., & Song, S. (2022) · Foods · doi:10.3390/foods11060822 · Cited by 71 · see citing works
Birgersson, P. S., Oftebro, M., Strand, W. I., Aarstad, O. A., Sætrom, G. I., Sletta, H., Arlov, Ø., & Aachmann, F. L. (2022) · Algal Research · doi:10.1016/j.algal.2022.102928 · Cited by 71 · see citing works
Hanjabam, M. D., Kumar, A., Tejpal, C. S., Krishnamoorthy, E., Kishore, P., & Ashok Kumar, K. (2019) · Bioactive Carbohydrates and Dietary Fibre · doi:10.1016/j.bcdf.2019.100200 · Cited by 69 · see citing works
Infant, S. S., Jayakumar, K., Mukherjee, A., & Chandrasekaran, N. (2018) · RSC Advances · doi:10.1039/c8ra02616e · Cited by 68 · see citing works
van Vliet, D. M., Ayudthaya, S. P. N., Diop, S., Villanueva, L., Stams, A. J. M., & Sánchez‐Andrea, I. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00253 · Cited by 69 · see citing works
Initial evaluation of six different brown algae species as source for crude bioactive fucoidans
Bittkau, K. S., Neupane, S., & Alban, S. (2019) · Algal Research · doi:10.1016/j.algal.2019.101759 · Cited by 69 · see citing works
Usov, A. I., Bilan, M. I., Ustyuzhanina, N. E., & Nifantiev, N. E. (2022) · Marine Drugs · doi:10.3390/md20100638 · Cited by 68 · see citing works
Chen, S., Sathuvan, M., Xiao, Z., Zhang, W., Tang, S., Liu, Y., & Cheong, K. (2021) · BMC Chemistry · doi:10.1186/s13065-020-00727-w · Cited by 67 · see citing works
Ashayerizadeh, O., Dastar, B., & Pourashouri, P. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.10.172 · Cited by 64 · see citing works
Structural diversity of fucoidans and their radioprotective effect
Николаевна, З. Т., Usoltseva, R. V., Шевченко, Н. М., Surits, V. V., Imbs, T. I., Malyarenko, O. S., Besednova, N. N., Ivanushko, L. A., & Ermakova, S. P. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2021.118551 · Cited by 63 · see citing works
Hepatoprotective effect of the fucoidan from the brown seaweed Turbinaria tricostata
Chalé-Dzul, J. B., Moo-Puc, R. E., Robledo, D., & Freile‐Pelegrín, Y. (2014) · Journal of Applied Phycology · doi:10.1007/s10811-014-0429-9 · Cited by 63 · see citing works
Saied, E. M., El‐Maradny, Y. A., Osman, A. A., Darwish, A. M. G., Nahas, H. H. A., Niedbała, G., Piekutowska, M., Abdel-Rahman, M. A., Balbool, B. A., & Abdel-Azeem, A. M. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13111759 · Cited by 62 · see citing works
Iliou, K., Kikionis, S., Ioannou, E., & Roussis, V. (2022) · Marine Drugs · doi:10.3390/md20050314 · Cited by 62 · see citing works
Marine Carbohydrate-Based Compounds with Medicinal Properties
Vasconcelos, A. A., & Pomin, V. H. (2018) · Marine Drugs · doi:10.3390/md16070233 · Cited by 65 · see citing works
Iqbal, M. W., Riaz, T., Mahmood, S., Bilal, M., Manzoor, M. F., Qamar, S. A., & Qi, X. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2106182 · Cited by 61 · see citing works
Hamouda, H. I., Li, T., Shabana, S., Hashem, A. H., & Yin, H. (2025) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2025.123559 · Cited by 61 · see citing works
In vitro and in vivo immunomodulatory effects of fucoidan compound agents
Peng, Y., Song, Y., Wang, Q., Hu, Y., He, Y., Ren, D., Wu, L., Liu, S., Cong, H., & Zhou, H. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.12.197 · Cited by 58 · see citing works
Balakrishnan, V., Kunjiappan, S., Aanandhalakshmi, R., Usha, S. K., & Arumugam, M. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.02.332 · Cited by 59 · see citing works
Ikeda‐Ohtsubo, W., Nadal, A. L., Zaccaria, E., Iha, M., Kitazawa, H., Kleerebezem, M., & Brugman, S. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.00067 · Cited by 58 · see citing works
Fucoidans of brown algae: Biosynthesis, localization, and physiological role in thallus
Skriptsova, A. V. (2015) · Russian Journal of Marine Biology · doi:10.1134/s1063074015030098 · Cited by 58 · see citing works
A Comparative Review of Alternative Fucoidan Extraction Techniques from Seaweed
Chadwick, M., Carvalho, L. G., Vanegas, C., & Dimartino, S. (2025) · Marine Drugs · doi:10.3390/md23010027 · Cited by 61 · see citing works
Hu, Y., Li, S., Li, J., Ye, X., Ding, T., Liu, D., Chen, J., Ge, Z., & Chen, S. (2015) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2015.06.088 · Cited by 57 · see citing works
Sichert, A., Gall, S. L., Klau, L. J., Laillet, B., Rogniaux, H., Aachmann, F. L., & Hehemann, J. (2020) · Glycobiology · doi:10.1093/glycob/cwaa064 · Cited by 60 · see citing works
Baghel, R. S., Choudhary, B., Pandey, S., Pathak, P. K., Patel, M. K., & Mishra, A. (2023) · Foods · doi:10.3390/foods12193642 · Cited by 60 · see citing works
Li, S., Li, J., Mao, G., Yan, L., Hu, Y., Ye, X., Ding, T., Linhardt, R. J., & Chen, S. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.02.001 · Cited by 56 · see citing works
The antiviral potential of algal-derived macromolecules
Liu, J., Obaidi, I., Nagar, S., Scalabrino, G., & Sheridan, H. (2021) · Current Research in Biotechnology · doi:10.1016/j.crbiot.2021.04.003 · Cited by 53 · see citing works
Advances in oligosaccharides production from algal sources and potential applications
Perumal, P. K., Dong, C., Chauhan, A. S., Anisha, G. S., Kadri, M. S., Chen, C., Singhania, R. R., & Patel, A. K. (2023) · Biotechnology Advances · doi:10.1016/j.biotechadv.2023.108195 · Cited by 52 · see citing works
- Authors
- Ale, M. T., & Meyer, A. S.
- Affiliations
- Technical University of Denmark (DK)
- Corresponding author
- Meyer, Anne S.
- Venue
- RSC Adv.
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2013
- Volume
- 3
- Issue
- 22
- Pages
- 8131-8141
- ISSN
- 2046-2069 (ISSN-L)
- OpenAlex
- W2165865189
- Semantic Scholar
- 9ec7156ada540774a377f33054ce052291b5f9dc
- Cited by
- 381
- References
- 50
- Citations by year
- 2026: 38 · 2025: 33 · 2024: 32 · 2023: 33 · 2022: 36 · 2021: 39 · 2020: 50 · 2019: 43 · 2018: 28 · 2017: 17 · 2016: 13 · 2015: 9 · 2014: 9
- FWCI
- 15.78
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- RSC Advances (publishedVersion, cc-by)
- Technical University of Denmark, DTU Orbit (Technical University of Denmark, DTU) (submittedVersion, cc-by)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Seaweed-derived Bioactive Compounds
- Life Sciences › Agricultural and Biological Sciences › Food Science › Polysaccharides Composition and Applications
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Polysaccharides and Plant Cell Walls
- Keywords
- fucoidan, brown algae, polysaccharide structure, enzymatic degradation, structure elucidation, anti-inflammatory activity, anticoagulant activity, antiproliferative activity
About these checks
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.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-07.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-07.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review