Impact of Aeration and Heme-Activated Respiration on Lactococcus lactis Gene Expression: Identification of a Heme-Responsive Operon

Experiments in molecular genetics

Miller, J. H. (1972) · Medical Entomology and Zoology · Cited by 27,157 · see citing works

Comparative genomics of the lactic acid bacteria.

Makarova, K., Slesarev, A., Wolf, Y., Sorokin, A., Mirkin, B., Koonin, E., Pavlov, A., Pavlova, N., Karamychev, V., Polouchine, N., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607117103 · Cited by 1,391 · see citing works

Plasmid complements of Streptococcus lactis NCDO 712 and other lactic streptococci after protoplast-induced curing

Gasson, M. J. (1983) · Journal of Bacteriology · doi:10.1128/jb.154.1.1-9.1983 · Cited by 1,326 · see citing works

The Complete Genome Sequence of the Lactic Acid Bacterium Lactococcus lactis ssp. lactis IL1403

Bolotin, A., Wincker, P., Mauger, S., Jaillon, O., Malarme, K., Weissenbach, J., Ehrlich, S. D., & Sorokin, A. (2001) · Genome Research · doi:10.1101/gr.gr-1697r · Cited by 1,139 · see citing works

The Complete Genome Sequence of the Lactic Acid Bacterium Lactococcus lactis ssp. lactis IL1403Preprint

Bolotin, A., Wincker, P., Mauger, S., Jaillon, O., Malarme, K., Weissenbach, J., Ehrlich, S. D., & Sorokin, A. (2001) · Genome Research · doi:10.1101/gr.169701 · Cited by 1,133 · see citing works

Oxidative stress

Storz, G., & Imlayt, J. A. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)80033-2 · Cited by 1,077 · see citing works

A novel DNA-binding protein with regulatory and protective roles in starved Escherichia coli.Preprint

Almirón, M. A., Link, A. J., Furlong, D., & Kolter, R. (1992) · Genes & Development · doi:10.1101/gad.6.12b.2646 · Cited by 768 · see citing works

Analysis of a Complete Library of Putative Drug Transporter Genes in Escherichia coli

Nishino, K., & Yamaguchi, A. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.20.5803-5812.2001 · Cited by 667 · see citing works

Efficient insertional mutagenesis in lactococci and other gram-positive bacteria

Maguin, E., Prévost, H., Ehrlich, S. D., & Gruss, A. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.3.931-935.1996 · Cited by 486 · see citing works

The bacterial universal stress protein: function and regulation

Kvint, K., Nachin, L., Diez, A., & Nyström, T. (2003) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(03)00025-0 · Cited by 474 · see citing works

Complete Genome Sequence of the Prototype Lactic Acid Bacterium Lactococcus lactis subsp. cremoris MG1363

Wegmann, U., Motherway, M. O., Zomer, A., Buist, G., Shearman, C. A., Canchaya, C. A., Ventura, M., Goesmann, A., Gasson, M. J., Kuipers, O. P., et al. (2007) · Journal of Bacteriology · doi:10.1128/jb.01768-06 · Cited by 418 · see citing works

Control of the shift from homolactic acid to mixed-acid fermentation in Lactococcus lactis: predominant role of the NADH/NAD+ ratio

Garrigues, C., Loubière, P., Lindley, N. D., & Cocaign‐Bousquet, M. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.17.5282-5287.1997 · Cited by 347 · see citing works

Escherichia coli peptide methionine sulfoxide reductase gene: regulation of expression and role in protecting against oxidative damage

Moskovitz, J., Rahman, M. A., Strassman, J., Yancey, S. O., Kushner, S. R., Brot, N., & Weissbach, H. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.3.502-507.1995 · Cited by 294 · see citing works

Thiol-Based Regulatory Switches

Paget, M. S. B., & Buttner, M. J. (2003) · Annual Review of Genetics · doi:10.1146/annurev.genet.37.110801.142538 · Cited by 294 · see citing works

Role of the arginine deiminase system in protecting oral bacteria and an enzymatic basis for acid tolerance

Casiano-Colón, A. E., & Marquis, R. E. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.6.1318-1324.1988 · Cited by 270 · see citing works

Bacterial defenses against oxidants: mechanistic features of cysteine-based peroxidases and their flavoprotein reductases

Poole, L. B. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.09.006 · Cited by 246 · see citing works

Respiration Capacity of the Fermenting Bacterium Lactococcus lactis and Its Positive Effects on Growth and Survival

Duwat, P., Sourice, S., Cesselin, B., Lamberet, G., Vido, K., Gaudu, P., Loir, Y. L., Violet, F., Loubière, P., & Gruss, A. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.15.4509-4516.2001 · Cited by 245 · see citing works

A Staphylococcus aureus Regulatory System that Responds to Host Heme and Modulates Virulence

Torres, V. J., Stauff, D. L., Pishchany, G., Bezbradica, J. S., Gordy, L. E., Iturregui, J., Anderson, K. L., Dunman, P. M., Joyce, S., & Skaar, E. P. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.03.001 · Cited by 241 · see citing works

Cofactor Engineering: a Novel Approach to Metabolic Engineering in Lactococcus lactis by Controlled Expression of NADH Oxidase

de Felipe, F. L., Kleerebezem, M., de Vos, W. M., & Hugenholtz, J. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.15.3804-3808.1998 · Cited by 223 · see citing works

Staphylococcus aureus Redirects Central Metabolism to Increase Iron Availability

Friedman, D. B., Stauff, D. L., Pishchany, G., Whitwell, C. W., Torres, V. J., & Skaar, E. P. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020087 · Cited by 222 · see citing works

A Bacterial Glutathione Transporter (Escherichia coli CydDC) Exports Reductant to the Periplasm

Pittman, M. S., Robinson, H. C., & Poole, R. K. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503075200 · Cited by 185 · see citing works

Single-crossover integration in the Lactobacillus sake chromosome and insertional inactivation of the ptsI and lacL genes

Leloup, L., Ehrlich, S. D., Zagorec, M., & MOREL‐DEVILLE, F. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.6.2117-2123.1997 · Cited by 153 · see citing works

Stress response in Lactococcus lactis: cloning, expression analysis, and mutation of the lactococcal superoxide dismutase gene

Sanders, J.-W., Leenhouts, K. J., Haandrikman, A. J., Venema, G., & Kok, J. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.18.5254-5260.1995 · Cited by 151 · see citing works

Characterization of the lactose-specific enzymes of the phosphotransferase system in Lactococcus lactis.

de Vos, W. M., Boerrigter, I. J., van Rooyen, R. J., Reiche, B., & Hengstenberg, W. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45741-9 · Cited by 134 · see citing works

The Escherichia coli histone‐like protein HU regulates rpoS translation

Balandina, A., Claret, L., Hengge‐Aronis, R., & Rouvière‐Yaniv, J. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02305.x · Cited by 119 · see citing works

Respiration metabolism reduces oxidative and acid stress to improve long‐term survival of Lactococcus lactis

Rezaı̈ki, L., Cesselin, B., Yamamoto, Y., Vido, K., West, E. V., Gaudu, P., & Gruss, A. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04217.x · Cited by 116 · see citing works

Structure, Regulation, and Putative Function of the Arginine Deiminase System ofStreptococcus suis

Gruening, P., Fulde, M., Valentin‐Weigand, P., & Goethe, R. (2005) · Journal of Bacteriology · doi:10.1128/jb.188.2.361-369.2006 · Cited by 116 · see citing works

Design of oligonucleotides for microarrays and perspectives for design of multi-transcriptome arrays

Nielsen, H. B. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg622 · Cited by 113 · see citing works

Anaerobic regulation of transcription initiation in the arcDABC operon of Pseudomonas aeruginosa

Gamper, M., Zimmermann, A., & Haas, D. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.15.4742-4750.1991 · Cited by 112 · see citing works

Relationships between arginine degradation, pH and survival inLactobacillus sakei

Champomier‐Vergès, M., Zuñiga, M., Morel-Deville, F., Pérez‐Martínez, G., Zagorec, M., & Ehrlich, S. D. (1999) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1999.tb08809.x · Cited by 105 · see citing works

In vivo functional characterization of the Escherichia coli ammonium channel AmtB: evidence for metabolic coupling of AmtB to glutamine synthetase

Javelle, A., Thomas, G. H., Marini, A., Krämer, R., & Merrick, M. (2005) · Biochemical Journal · doi:10.1042/bj20042094 · Cited by 101 · see citing works

Respiration capacity and consequences in Lactococcus lactis

Gaudu, P., Vido, K., Cesselin, B., Kulakauskas, S., Tremblay, J., Rezaı̈ki, L., Lamberet, G., Sourice, S., Duwat, P., & Gruss, A. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020635600343 · Cited by 100 · see citing works

Induction of cytochrome formation and stimulation of oxidative dissimilation by hemin inStreptococcus lactis andLeuconostoc mesenteroides

Sijpesteijn, A. K. (1970) · Antonie van Leeuwenhoek · doi:10.1007/bf02069035 · Cited by 98 · see citing works

The temperature-sensitive growth and survival phenotypes of Escherichia coli cydDC and cydAB strains are due to deficiencies in cytochrome bd and are corrected by exogenous catalase and reducing agents

Goldman, B. S., Gabbert, K. K., & Kranz, R. G. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.21.6348-6351.1996 · Cited by 97 · see citing works

Sequence analysis of the lactococcal bacteriophage bIL170: insights into structural proteins and HNH endonucleases in dairy phages The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are bIL170, AF009630; bIL120, AY054975; bIL15, AY054976; bIL191, AY054977; bIL77, AY054978.

Coq, A.-M. C.-L., Cesselin, B., Commissaire, J., & Anba‐Mondoloni, J. (2002) · Microbiology · doi:10.1099/00221287-148-4-985 · Cited by 96 · see citing works

The long and winding road from the research laboratory to industrial applications of lactic acid bacteria

Pedersen, M. B., Iversen, S. L., Sørensen, K. I., & Johansen, E. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.fmrre.2005.04.001 · Cited by 96 · see citing works

CcpA regulation of aerobic and respiration growth in Lactococcus lactis

Gaudu, P., Lamberet, G., Poncet, S., & Gruss, A. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03700.x · Cited by 94 · see citing works

Effect of Initial Oxygen Concentration on Diacetyl and Acetoin Production by Lactococcus lactis subsp. lactis biovar diacetylactis

Bassit, N., Boquien, C., Picque, D., & Corrieu, G. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.6.1893-1897.1993 · Cited by 89 · see citing works

Proteome Analyses of Heme-Dependent Respiration inLactococcus lactis: Involvement of the Proteolytic System

Vido, K., Bars, D. L., Mistou, M., Anglade, P., Gruss, A., & Gaudu, P. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.6.1648-1657.2004 · Cited by 85 · see citing works

Acetoin Fermentation by Citrate-Positive <i>Lactococcus lactis</i> subsp. <i>lactis</i> 3022 Grown Aerobically in the Presence of Hemin or Cu ²⁺

Kaneko, T., Takahashi, M., & Suzuki, H. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.9.2644-2649.1990 · Cited by 72 · see citing works

Generation of a Membrane Potential by Lactococcus lactis through Aerobic Electron Transport

Brooijmans, R. J. W., Poolman, B., Schuurman‐Wolters, G. K., de Vos, W. M., & Hugenholtz, J. (2007) · Journal of Bacteriology · doi:10.1128/jb.00361-07 · Cited by 72 · see citing works

Lactococcus lactis produces short‐chain quinones that cross‐feed Group B Streptococcus to activate respiration growth

Rezaı̈ki, L., Lamberet, G., Derré‐Bobillot, A., Gruss, A., & Gaudu, P. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.06083.x · Cited by 69 · see citing works

The Group B Streptococcus NADH oxidase Nox‐2 is involved in fatty acid biosynthesis during aerobic growth and contributes to virulence

Yamamoto, Y., Pargade, V., Lamberet, G., Gaudu, P., Thomas, F., Texereau, J., Gruss, A., Trieu‐Cuot, P., & Poyart, C. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05406.x · Cited by 61 · see citing works

Experimental determination of control of glycolysis in Lactococcus lactis.

Koebmann, B. J., Andersen, H. W., Solem, C., & Jensen, P. R. (2002) · PubMed · Cited by 58 · see citing works

Multiple Transcriptional Control of the Lactococcus lactis trp Operon

Raya, R. R., Bardowski, J. K., Andersen, P. S., Ehrlich, S. D., & Chopin, A. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.12.3174-3180.1998 · Cited by 55 · see citing works

Cloning of the Lactococcus lactis adhE Gene, Encoding a Multifunctional Alcohol Dehydrogenase, by Complementation of a Fermentative Mutant of Escherichia coli

Arnau, J., Jørgensen, F., Madsen, S., Vrang, A., & Israelsen, H. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.12.3049-3055.1998 · Cited by 54 · see citing works

Experimental determination of control of glycolysis in Lactococcus lactis

Koebmann, B. J., Andersen, H. W., Solem, C., & Jensen, P. R. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020643918089 · Cited by 51 · see citing works

The <i>Lactococcus lactis</i> sex‐factor aggregation gene <i>cluA</i>

Godon, J., Jury, K., Shearman, C. A., & Gasson, M. J. (1994) · Molecular Microbiology · doi:10.1111/j.1365-2958.1994.tb01053.x · Cited by 50 · see citing works

One of Two OsmC Homologs in Bacillus subtilis Is Part of the ς B -Dependent General Stress Regulon

Völker, U., Andersen, K. K., Antelmann, H., Devine, K. M., & Hecker, M. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.16.4212-4218.1998 · Cited by 49 · see citing works

Metabolic and Transcriptomic Adaptation of Lactococcus lactis subsp. lactis Biovar diacetylactis in Response to Autoacidification and Temperature Downshift in Skim Milk

Raynaud, S., Perrin, R., Cocaign‐Bousquet, M., & Loubière, P. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.12.8016-8023.2005 · Cited by 48 · see citing works

Hemin Reconstitutes Proton Extrusion in an H + -ATPase-Negative Mutant of Lactococcus lactis

Blank, L. M., Koebmann, B. J., Michelsen, O., Nielsen, L. K., & Jensen, P. R. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.22.6707-6709.2001 · Cited by 48 · see citing works

Characterisation of Bifidobacterium animalis subsp. lactis BB-12 and other probiotic bacteria using genomics, transcriptomics and proteomics

Garrigues, C., Stuer‐Lauridsen, B., & Johansen, E. (2005) · Australian Journal of Dairy Technology · Cited by 40 · see citing works

Nucleotide sequence and characterization of the cell envelope proteinase plasmid in Lactococcus lactis subsp. cremoris HP

Christensson, C., Pillidge, C. J., Ward, L. J. H., & O’Toole, P. W. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01390.x · Cited by 24 · see citing works

Repression of the pyr Operon in Lactobacillus plantarum Prevents Its Ability To Grow at Low Carbon Dioxide Levels

Nicoloff, H., Elagöz, A., Arsène‐Ploetze, F., Kammerer, B., Martinussen, J., & Bringel, F. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.6.2093-2104.2005 · Cited by 21 · see citing works

Determination of α-Acetolactic Acid and Volatile Compounds by Headspace Gas Chromatography

Richelieu, M., Houlberg, U., & Nielsen, J. C. (1997) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(97)76132-0 · Cited by 20 · see citing works

Glucose/Citrate Cometabolism in Lactococcus lactis subsp. lactis biovar diacetylactis with Impaired α-Acetolactate Decarboxylase

Curic, M., Richelieu, M., Henriksen, C. M., Jokumsen, K. V., Villadsen, J., & Nilsson, D. (1999) · Metabolic Engineering · doi:10.1006/mben.1999.0123 · Cited by 19 · see citing works

Getting high (OD) on heme

Garrigues, C., Johansen, E., Pedersen, M. B., Møllgaard, H., Sørensen, K. I., Gaudu, P., Gruss, A., & Lamberet, G. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1403-c1 · Cited by 14 · see citing works

Oxygen inhibition of nitrogenase activity in Klebsiella pneumoniae

Kavanagh, E. P., & Hill, S. (1993) · Journal of General Microbiology · doi:10.1099/00221287-139-6-1307 · Cited by 9 · see citing works

The World Market for Cheese 1995–2004

O’Connor, D. (2007) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.2007.00286.x · Cited by 7 · see citing works

Lactic metabolism revisited: metabolism of lactic acid bacteria in food fermentations and food spoilage.

Gänzle, M. G. (2015) · Current Opinion in Food Science · doi:10.1016/j.cofs.2015.03.001 · Cited by 936 · see citing works

Stress Physiology of Lactic Acid Bacteria.

Papadimitriou, K., Alegría, Á., Bron, P. A., de Angelis, M., Gobbetti, M., Kleerebezem, M., Lemos, J. A., Linares, D. M., Ross, P., Stanton, C., et al. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00076-15 · Cited by 914 · see citing works

Overcoming the Heme Paradox: Heme Toxicity and Tolerance in Bacterial Pathogens

Anzaldi, L. L., & Skaar, E. P. (2010) · Infection and Immunity · doi:10.1128/iai.00613-10 · Cited by 295 · see citing works

Aerobic metabolism in the genus<i>Lactobacillus</i>: impact on stress response and potential applications in the food industry

Zotta, T., Parente, E., & Ricciardi, A. (2017) · Journal of Applied Microbiology · doi:10.1111/jam.13399 · Cited by 202 · see citing works

Aerobic Respiration Metabolism in Lactic Acid Bacteria and Uses in Biotechnology

Pedersen, M. B., Gaudu, P., Lechardeur, D., Petit, M.-A., & Gruss, A. (2012) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-022811-101255 · Cited by 197 · see citing works

A battle for iron: host sequestration and Staphylococcus aureus acquisition

Haley, K. P., & Skaar, E. P. (2012) · Microbes and Infection · doi:10.1016/j.micinf.2011.11.001 · Cited by 157 · see citing works

Bifidobacterium asteroides PRL2011 Genome Analysis Reveals Clues for Colonization of the Insect Gut

Bottacini, F., Milani, C., Turroni, F., Sánchez, B., Foroni, E., Duranti, S., Serafini, F., Viappiani, A., Strati, F., Ferrarini, A., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044229 · Cited by 144 · see citing works

Systems Solutions by Lactic Acid Bacteria: From Paradigms to Practice

de Vos, W. M. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-s1-s2 · Cited by 134 · see citing works

Using heme as an energy boost for lactic acid bacteria

Lechardeur, D., Cesselin, B., Fernandez, A., Lamberet, G., Garrigues, C., Pedersen, M. B., Gaudu, P., & Gruss, A. (2011) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.12.001 · Cited by 127 · see citing works

Extracellular electron transfer increases fermentation in lactic acid bacteria via a hybrid metabolism

Tejedor‐Sanz, S., Stevens, E. T., Li, S., Finnegan, P., Nelson, J., Knoesen, A., Light, S. H., Ajo-Franklin, C. M., & Marco, M. L. (2021) · eLife · doi:10.7554/elife.70684 · Cited by 109 · see citing works

Menaquinone biosynthesis potentiates haem toxicity in <i><scp>S</scp>taphylococcus aureus</i>

Wakeman, C. A., Hammer, N. D., Stauff, D. L., Attia, A. S., Anzaldi, L. L., Dikalov, S. I., Calcutt, M. W., & Skaar, E. P. (2012) · Molecular Microbiology · doi:10.1111/mmi.12063 · Cited by 94 · see citing works

Functional Genomics for Food Fermentation Processes

Smid, E. J., & Hugenholtz, J. (2010) · Annual Review of Food Science and Technology · doi:10.1146/annurev.food.102308.124143 · Cited by 89 · see citing works

<i>Bacillus anthracis</i> HssRS signalling to HrtAB regulates haem resistance during infection

Stauff, D. L., & Skaar, E. P. (2009) · Molecular Microbiology · doi:10.1111/j.1365-2958.2009.06684.x · Cited by 81 · see citing works

Combined Transcriptome and Proteome Analysis ofBifidobacterium animalissubsp.lactisBB-12 Grown on Xylo-Oligosaccharides and a Model of Their Utilization

Gilad, O., Jacobsen, S., Stuer‐Lauridsen, B., Pedersen, M. B., Garrigues, C., & Svensson, B. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00738-10 · Cited by 78 · see citing works

Fine Tuning of the Lactate and Diacetyl Production through Promoter Engineering in Lactococcus lactis

Guo, T., Kong, J., Zhang, L., Zhang, C., & Hu, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036296 · Cited by 76 · see citing works

Significance of Heme-Based Respiration in Meat Spoilage Caused by Leuconostoc gasicomitatum

Jääskeläinen, E. L., Johansson, P., Kostiainen, O., Nieminen, T. T., Schmidt, G., Somervuo, P. J., Mohsina, M., Vanninen, P. S., Auvinen, P., & Björkroth, J. K. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02943-12 · Cited by 72 · see citing works

Structural Basis for the Transcriptional Regulation of Heme Homeostasis in Lactococcus lactis

Sawai, H., Yamanaka, M., Sugimoto, H., Shiro, Y., & Aono, S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.370916 · Cited by 71 · see citing works

Dynamic Analysis of the Lactococcus lactis Transcriptome in Cheeses Made from Milk Concentrated by Ultrafiltration Reveals Multiple Strategies of Adaptation to Stresses

Cretenet, M., Laroute, V., Ulvé, V., Jeanson, S., Nouaille, S., Even, S., Piot, M., Girbal, L., Loir, Y. L., Loubière, P., et al. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.01174-10 · Cited by 70 · see citing works

Adaptation to Aerobic Environment of Lactobacillus johnsonii/gasseri Strains

Maresca, D., Zotta, T., & Mauriello, G. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00157 · Cited by 66 · see citing works

Two coregulated efflux transporters modulate intracellular heme and protoporphyrin IX availability in Streptococcus agalactiae

Fernandez, A., Lechardeur, D., Derré-Bobillot, A., Couvé, E., Gaudu, P., & Gruss, A. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000860 · Cited by 65 · see citing works

Combining metabolic engineering and biocompatible chemistry for high-yield production of homo-diacetyl and homo-(S,S)-2,3-butanediol

Liu, J., Chan, S. H. J., Brock‐Nannestad, T., Chen, J., Lee, S. Y., Solem, C., & Jensen, P. R. (2016) · Metabolic Engineering · doi:10.1016/j.ymben.2016.02.008 · Cited by 65 · see citing works

Genome Sequence of a Food Spoilage Lactic Acid Bacterium, Leuconostoc gasicomitatum LMG 18811 T , in Association with Specific Spoilage Reactions

Johansson, P., Paulin, L. G., Säde, E., Salovuori, N., Alatalo, E., Björkroth, J. K., & Auvinen, P. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.00102-11 · Cited by 64 · see citing works

Understanding the industrial application potential of lactic acid bacteria through genomics

Zhu, Y., Zhang, Y., & Li, Y. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2034-4 · Cited by 63 · see citing works

Improved viability of bifidobacteria in fermented milk by cocultivation with Lactococcus lactis subspecies lactis

Odamaki, T., Xiao, J., YONEZAWA, S., Yaeshima, T., & Iwatsuki, K. (2011) · Journal of Dairy Science · doi:10.3168/jds.2010-3286 · Cited by 57 · see citing works

Long-chain vitamin K2 production in Lactococcus lactis is influenced by temperature, carbon source, aeration and mode of energy metabolism

Liu, Y., van Bennekom, E. O., Zhang, Y., Abee, T., & Smid, E. J. (2019) · Microbial Cell Factories · doi:10.1186/s12934-019-1179-9 · Cited by 56 · see citing works

Whole-genome mapping of 5′ RNA ends in bacteria by tagged sequencing: a comprehensive view in Enterococcus faecalis

Innocenti, N., Golumbeanu, M., d'Hérouël, A. F., Lacoux, C., Bonnin, R. A., Kennedy, S., Wessner, F., Serror, P., Bouloc, P., Repoila, F., et al. (2015) · RNA · doi:10.1261/rna.048470.114 · Cited by 50 · see citing works

Temperature and respiration affect the growth and stress resistance of Lactobacillus plantarum C17

Zotta, T., Guidone, A., Ianniello, R. G., Parente, E., & Ricciardi, A. (2013) · Journal of Applied Microbiology · doi:10.1111/jam.12285 · Cited by 50 · see citing works

Environmental Heme Utilization by Heme-Auxotrophic Bacteria

Gruss, A., Borezée‐Durant, E., & Lechardeur, D. (2012) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-394423-8.00003-2 · Cited by 47 · see citing works

Contribution of the NADH-oxidase (Nox) to the aerobic life of Lactobacillus sanfranciscensis DSM20451T

Jänsch, A., Freiding, S., Behr, J., & Vogel, R. F. (2010) · Food Microbiology · doi:10.1016/j.fm.2010.08.001 · Cited by 48 · see citing works

Transcriptomic Response of Lactococcus lactis in Mixed Culture with Staphylococcus aureus

Nouaille, S., Even, S., Charlier, C., Loir, Y. L., Cocaign‐Bousquet, M., & Loubière, P. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02653-08 · Cited by 48 · see citing works

Heme proteins in lactic acid bacteria

Baureder, M., & Hederstedt, L. (2013) · Advances in Microbial Physiology · doi:10.1016/b978-0-12-410515-7.00001-9 · Cited by 45 · see citing works

Differential activation of Staphylococcus aureus heme detoxification machinery by heme analogues

Wakeman, C. A., Stauff, D. L., Zhang, Y., & Skaar, E. P. (2014) · Journal of Bacteriology · doi:10.1128/jb.01067-13 · Cited by 45 · see citing works

Investigation of the adaptation of Lactococcus lactis to isoleucine starvation integrating dynamic transcriptome and proteome information

Dressaire, C., Redon, E., Gitton, C., Loubière, P., Monnet, V., & Cocaign‐Bousquet, M. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-s1-s18 · Cited by 41 · see citing works

Effect of respirative and catalase-positive Lactobacillus casei adjuncts on the production and quality of Cheddar-type cheese

Reale, A., Ianniello, R. G., Ciocia, F., Renzo, T. D., Boscaino, F., Ricciardi, A., Coppola, R., Parente, E., Zotta, T., & McSweeney, P. L. H. (2016) · International Dairy Journal · doi:10.1016/j.idairyj.2016.08.005 · Cited by 41 · see citing works

Whole genome mapping of 5' RNA ends in bacteria by tagged sequencing : A comprehensive view in Enterococcus faecalisPreprint

Innocenti, N., Golumbeanu, M., d’Hérouël, A. F., Lacoux, C., Bonnin, R. A., Kennedy, S., Wessner, F., Serror, P., Bouloc, P., Repoila, F., et al. (2014) · doi:10.3929/ethz-b-000100386 · Cited by 40 · see citing works

The impact of iron on Listeria monocytogenes; inside and outside the host

McLaughlin, H. P., Hill, C., & Gahan, C. G. M. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.10.005 · Cited by 32 · see citing works

Biochemical analysis of respiratory metabolism in the heterofermentativeLactobacillus spicheriandLactobacillus reuteri

Ianniello, R. G., Zheng, J., Zotta, T., Ricciardi, A., & Gänzle, M. G. (2015) · Journal of Applied Microbiology · doi:10.1111/jam.12853 · Cited by 33 · see citing works

Solution Structure of the PAS Domain of a Thermophilic YybT Protein Homolog Reveals a Potential Ligand-binding Site

Tan, E., Rao, F., Pasunooti, S., Pham, H. T., Soehano, I., Turner, M. S., Liew, C. W., Lescar, J., Pervushin, K. V., & Liang, Z. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.437764 · Cited by 33 · see citing works

<scp>HrtBA</scp> and menaquinones control haem homeostasis in <scp><i>L</i></scp><i>actococcus lactis</i>

Joubert, L., Derré‐Bobillot, A., Gaudu, P., Gruss, A., & Lechardeur, D. (2014) · Molecular Microbiology · doi:10.1111/mmi.12705 · Cited by 32 · see citing works

Electrochemical wiring of the Gram-positive bacterium Enterococcus faecalis with osmium redox polymer modified electrodes

Pankratova, G., Hasan, K., Leech, D., Hederstedt, L., & Gorton, L. G. O. (2016) · Electrochemistry Communications · doi:10.1016/j.elecom.2016.12.010 · Cited by 31 · see citing works

Mechanisms of Acetoin Toxicity and Adaptive Responses in an Acetoin-Producing Species, Lactococcus lactis

Cesselin, B., Henry, C., Gruss, A., Gloux, K., & Gaudu, P. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01079-21 · Cited by 29 · see citing works

Early adaptation to oxygen is key to the industrially important traits of Lactococcus lactis ssp. cremoris during milk fermentation

Cretenet, M., Gall, G. L., Wegmann, U., Even, S., Shearman, C. A., Stentz, R., & Jeanson, S. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-1054 · Cited by 28 · see citing works

Engineered Probiotic Lactococcus lactis for Lycopene Production against ROS Stress in Intestinal Epithelial Cells

Wu, J., Tian, X., Xu, X., Gu, X., Kong, J., & Guo, T. (2022) · ACS Synthetic Biology · doi:10.1021/acssynbio.1c00639 · Cited by 28 · see citing works

Redox reactions in food fermentations

Hansen, E. B. (2018) · Current Opinion in Food Science · doi:10.1016/j.cofs.2018.03.004 · Cited by 24 · see citing works

Effect of Respiratory Growth on the Metabolite Production and Stress Robustness of Lactobacillus casei N87 Cultivated in Cheese Whey Permeate Medium

Ricciardi, A., Zotta, T., Ianniello, R. G., Boscaino, F., Matera, A., & Parente, E. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00851 · Cited by 24 · see citing works

Transcriptomics of Lactobacillus paracasei: metabolism patterns and cellular responses under high-density culture conditions

Li, L., Zhang, H., Meng, D., & Yin, H. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1274020 · Cited by 23 · see citing works

The CydDC family of transporters

Poole, R. K., Cozens, A. G., & Shepherd, M. (2019) · Research in Microbiology · doi:10.1016/j.resmic.2019.06.003 · Cited by 23 · see citing works

Respiratory Physiology of Lactococcus lactis in Chemostat Cultures and Its Effect on Cellular Robustness in Frozen and Freeze-Dried Starter Cultures

Johanson, A., Goel, A., Lisbeth Olsson, A., & Franzén, C. J. (2020) · Applied and Environmental Microbiology · doi:10.1128/aem.02785-19 · Cited by 23 · see citing works

Increasing the Heme-Dependent Respiratory Efficiency of Lactococcus lactis by Inhibition of Lactate Dehydrogenase

Arioli, S., Zambelli, D., Guglielmetti, S., Noni, I. D., Pedersen, M. B., Pedersen, P. D., Bello, F. D., & Mora, D. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02734-12 · Cited by 23 · see citing works

Updates on Metabolism in Lactic Acid Bacteria in Light of “Omic” Technologies

Kowalczyk, M., Mayo, B., Fernández, M., & Aleksandrzak‐Piekarczyk, T. (2015) · Wiley eBooks · doi:10.1002/9781118868386.ch1 · Cited by 25 · see citing works

Efficient Production of Nisin A from Low-Value Dairy Side Streams Using a Nonengineered Dairy Lactococcus lactis Strain with Low Lactate Dehydrogenase Activity

Zhao, G., Liu, J., Zhao, J., Dorau, R., Jensen, P. R., & Solem, C. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c07816 · Cited by 22 · see citing works

Probiotic Effects and Metabolic Products of Enterococcus faecalis LD33 with Respiration Capacity

Jiao, Y., Yang, H. M., Shigwedha, N., Zhang, S., Liu, F., & Zhang, L. (2022) · Foods · doi:10.3390/foods11040606 · Cited by 21 · see citing works

Transcriptome analysis of Lactococcus lactis subsp. lactis during milk acidification as affected by dissolved oxygen and the redox potential

Larsen, N., Moslehi‐Jenabian, S., Werner, B. B., Jensen, M. L., Garrigues, C., Vogensen, F. K., & Jespersen, L. (2016) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2016.03.002 · Cited by 21 · see citing works

Task Distribution between Acetate and Acetoin Pathways To Prolong Growth in Lactococcus lactis under Respiration Conditions

Cesselin, B., Garrigues, C., Pedersen, M. B., Roussel, C., Gruss, A., & Gaudu, P. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.01005-18 · Cited by 21 · see citing works

Electron transport chains of lactic acid bacteria - walking on crutches is part of their lifestyle

Brooijmans, R. J. W., de Vos, W. M., & Hugenholtz, J. (2009) · F1000 Biology Reports · doi:10.3410/b1-34 · Cited by 22 · see citing works

NAD‐dependent lactate dehydrogenase catalyses the first step in respiratory utilization of lactate by Lactococcus lactis

Zhao, R. X., Zheng, S., Duan, C., Liu, F., Yang, L., & Huo, G. (2013) · FEBS Open Bio · doi:10.1016/j.fob.2013.08.005 · Cited by 20 · see citing works

Aerobic condition increases carotenoid production associated with oxidative stress tolerance inEnterococcus gilvus

Hagi, T., Kobayashi, M., & Nomura, M. (2013) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12341 · Cited by 20 · see citing works

Identification of a Conserved Sequence in Flavoproteins Essential for the Correct Conformation and Activity of the NADH Oxidase NoxE of Lactococcus lactis

Tachon, S., Chambellon, É., & Yvon, M. (2011) · Journal of Bacteriology · doi:10.1128/jb.01466-10 · Cited by 20 · see citing works

Responses of Lactic Acid Bacteria to Oxidative Stress

Cesselin, B., Derré‐Bobillot, A., Fernandez, A., Lamberet, G., Lechardeur, D., Yamamoto, Y., Pedersen, M. B., Garrigues, C., Gruss, A., & Gaudu, P. (2011) · Springer eBooks · doi:10.1007/978-0-387-92771-8_6 · Cited by 20 · see citing works

A genomic view on lactic metabolism

Qiao, N., & Gänzle, M. G. (2025) · Food Microbiology · doi:10.1016/j.fm.2025.104945 · Cited by 18 · see citing works

Impact of aerobic and respirative life-style on Lactobacillus casei N87 proteome

Siciliano, R. A., Pannella, G., Lippolis, R., Ricciardi, A., Mazzeo, M. F., & Zotta, T. (2019) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2019.03.006 · Cited by 18 · see citing works

Characterization of D-lactic acid, spore-forming bacteria and Terrilactibacillus laevilacticus SK5-6 as potential industrial strains

Prasirtsak, B., Thitiprasert, S., Tolieng, V., Assabumrungrat, S., Tanasupawat, S., & Thongchul, N. (2017) · Annals of Microbiology · doi:10.1007/s13213-017-1306-y · Cited by 18 · see citing works

Listeria monocytogenes Relies on the Heme-Regulated Transporter hrtAB to Resist Heme Toxicity and Uses Heme as a Signal to Induce Transcription of lmo1634, Encoding Listeria Adhesion Protein

dos Santos, P. T., Larsen, P. T., Menendez-Gil, P., Lillebæk, E. M. S., & Kallipolitis, B. H. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03090 · Cited by 17 · see citing works

The crimson conundrum: heme toxicity and tolerance in GAS

Sachla, A. J., Breton, Y. S. L., Akhter, F., McIver, K. S., & Eichenbaum, Z. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00159 · Cited by 16 · see citing works

Adaptation of Lacticaseibacillus rhamnosus CM MSU 529 to Aerobic Growth: A Proteomic Approach

Dinarieva, T. Y., Klimko, A. I., Kahnt, J., Cherdyntseva, T. A., & Netrusov, A. I. (2023) · Microorganisms · doi:10.3390/microorganisms11020313 · Cited by 15 · see citing works

Aerobic conditions increase isoprenoid biosynthesis pathway gene expression levels for carotenoid production in Enterococcus gilvus

Hagi, T., Kobayashi, M., & Nomura, M. (2015) · FEMS Microbiology Letters · doi:10.1093/femsle/fnv075 · Cited by 15 · see citing works

Molecular Mechanisms of Stress Resistance in Lactococcus lactis

Smith, W. M., Dykes, G. A., Soomro, A. H., & Turner, M. S. (2010) · Cited by 15 · see citing works

Transcriptional responses in Lactococcus lactis subsp. cremoris to the changes in oxygen and redox potential during milk acidification

Larsen, N., Werner, B. B., & Jespersen, L. (2016) · Letters in Applied Microbiology · doi:10.1111/lam.12596 · Cited by 14 · see citing works

Tween 80 and respiratory growth affect metabolite production and membrane fatty acids inLactobacillus caseiN87

Zotta, T., Tabanelli, G., Montanari, C., Ianniello, R. G., Parente, E., Gardini, F., & Ricciardi, A. (2016) · Journal of Applied Microbiology · doi:10.1111/jam.13373 · Cited by 13 · see citing works

Hyaluronic acid production is enhanced by harnessing the heme-induced respiration in recombinant Lactococcus lactis cultures

Jeeva, P., Jayaprakash, S. R., & Jayaraman, G. (2022) · Biochemical Engineering Journal · doi:10.1016/j.bej.2022.108428 · Cited by 12 · see citing works

Effects of agitation speed, temperature, carbon and nitrogen sources on the growth of recombinant Lactococcus lactis NZ9000 carrying domain 1 of aerolysin gene.

Ibrahim, S. B., Rahman, N. A., Mohamad, R., & Rahim, R. A. (2010) · Universiti Putra Malaysia Institutional Repository (Universiti Putra Malaysia) · Cited by 11 · see citing works

Presence of galactose in precultures induces lacS and leads to short lag phase in lactose-grown Lactococcus lactis cultures

Lorántfy, B., Johanson, A., Faria‐Oliveira, F., Franzén, C. J., Mapelli, V., & Lisbeth Olsson, A. (2018) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-018-2099-0 · Cited by 11 · see citing works

Genetics of Lactococci

Gaudu, P., Yamamoto, Y., Jensen, P. R., Hammer, K., Lechardeur, D., & Gruss, A. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0035-2018 · Cited by 10 · see citing works

Detection ofhssS,hssR,hrtA, andhrtBgenes and their expression by hemin inStaphylococcus epidermidis

Juárez-Verdayes, M. A., González-Uribe, P. M., Peralta, H., Rodríguez–Martínez, S., Jan‐Roblero, J., Escamilla, R., Cancino-Diaz, M. E., & Cancino‐Díaz, J. C. (2012) · Canadian Journal of Microbiology · doi:10.1139/w2012-086 · Cited by 10 · see citing works

New Insights into the Anti-pathogenic Potential of Lactococcus garvieae against Staphylococcus aureus Based on RNA Sequencing Profiling

Delpech, P., Rifa, É., Ball, G., Nidelet, S., Dubois, E., Gagné, G., Montel, M., Delbès, C., & Bornes, S. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00359 · Cited by 10 · see citing works

Respiration, a strategy to avoid oxidative stress in Lactococcus lactis, is regulated by the heme status

Cesselin, B., Derré‐Bobillot, A., Fernandez, A., Lamberet, G., Lechardeur, D., Yamamoto, Y., Pedersen, M. B., Garrigues, C., & Gaudu, P. (2010) · Japanese Journal of Lactic Acid Bacteria · doi:10.4109/jslab.21.10 · Cited by 9 · see citing works

Heme sensing inBacillus thuringiensis: a supplementary HssRS-regulated heme resistance system

Schmidt, R. M., Carter, M. M., Chu, M. L., Latario, C. J., Stadler, S. K., & Stauff, D. L. (2016) · FEMS Microbiology Letters · doi:10.1093/femsle/fnw076 · Cited by 8 · see citing works

Heme Dependent Catalase Conditionally Contributes to Oxygen Tolerance of Tetragenococcus halophilus Strains Isolated from Soy Sauce Moromi

Li, J., Wang, B., Chen, J., Du, G., & Fang, F. (2022) · Applied Sciences · doi:10.3390/app12168039 · Cited by 6 · see citing works

Improvement of L‐lactic acid production with a two‐step OUR control strategy

Tian, X., Wang, Y., Chu, J., Zhuang, Y., & Zhang, S. (2015) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.4844 · Cited by 6 · see citing works

A new biological function of heme as a signaling molecule

Muraki, N., Kitatsuji, C., & Aono, S. (2015) · Journal of Porphyrins and Phthalocyanines · doi:10.1142/s1088424614501090 · Cited by 6 · see citing works

Metabolite profiling coupled with metabolic flux analysis reveals physiological and metabolic impacts on Lactobacillus paracasei oxygen metabolism

Tian, X., Wang, Y., Chu, J., Zhuang, Y., & Zhang, S. (2017) · Process Biochemistry · doi:10.1016/j.procbio.2017.11.017 · Cited by 6 · see citing works

Higher nisin yield is reached with glutathione and pyruvate compared with heme in Lactococcus lactis N8

Ersoy, Z. G., Kayıhan, C., & Tunca, S. (2020) · Brazilian Journal of Microbiology · doi:10.1007/s42770-019-00216-w · Cited by 4 · see citing works

Respirative metabolism improves the growth performance and stress response properties of Lactiplantibacillus plantarum SXC48

Tian, J., Wu, J., Huang, L., & Zhang, J.-G. (2024) · LWT · doi:10.1016/j.lwt.2024.116012 · Cited by 4 · see citing works

Improvement of the respiration efficiency of Lactococcus lactis by decreasing the culture pH

Shi, W., Li, Y., Gao, X., & Fu, R. (2015) · Biotechnology Letters · doi:10.1007/s10529-015-1999-6 · Cited by 3 · see citing works

Metabolic Profiling and Cold-Starvation Stress Response of Oxygen-Tolerant Lactobacillus gasseri Strains Cultured in Batch Bioreactor

Maresca, D., Filippis, F. D., Robertiello, A., & Mauriello, G. (2019) · Microorganisms · doi:10.3390/microorganisms7070200 · Cited by 2 · see citing works

Identification of a Lactic Acid Bacteria Strain from Traditional Dairy Products

Jiao, Y. H., Zhang, L., & Liu, F. (2013) · Advanced materials research · doi:10.4028/www.scientific.net/amr.781-784.1599 · Cited by 2 · see citing works

Biological traits of lactic acid bacteria: industrial relevance and new perspectives in dairy applications

Mora, D., Bello, F. D., & Arioli, S. (2017) · doi:10.1002/9781119115007.ch12 · Cited by 2 · see citing works

Stress survival of probiotics

Pal, A. D. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-27622-4.00025-0 · Cited by 1 · see citing works

Core strategies of lactic acid biosynthesis in key Lactobacillaceae species: Phylogenetic patterns, metabolic pathways, and genetic regulation

Беленко, А. А., Путилов, В. Э., Непомнящий, А. П., Prichepa, A. O., Semenova, A. A., Sitnov, V. Y., & Sorokina, N. P. (2026) · Food systems · doi:10.21323/2618-9771-2025-8-4-541-554 · Cited by 1 · see citing works

The Lactococcus lactis Thioredoxin System

Efler, P., Hägglund, P., & Svensson, B. (2013) · Cited by 1 · see citing works

Compréhension des mécanismes physiologiques et génétiques impliqués dans l'activité réductrice de Lactococcus lactis

Roussel, C. (2015) · doi:10.70675/186dfbabzaae7z4ea5zbb1az44370124a892 · Cited by 1 · see citing works

Comprendre l’adaptation de Lactococcus lactis par uneapproche de biologie intégrative à l’échelle du génome

Dressaire, C. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Characterization of two Lactococcus lactis zinc membrane proteins, Llmg_0524 and Llmg_0526, and role of Llmg_0524 in cell wall integrity

Roussel, C., Cesselin, B., Cachon, R., & Gaudu, P. (2015) · BMC Microbiology · doi:10.1186/s12866-015-0587-1

Molecular probes for studying heme toxicity and tolerance in gram positive pathogens

Mike, L. A. (2013)

Aerobic Respiration in Lactic Acid Bacteria

Pophaly, S. D., Chauhan, M., Tarak, J., Bashetty, S. B., Singh, T. P., & Tomar, S. K. (2018) · Advances in medical technologies and clinical practice book series · doi:10.4018/978-1-5225-5363-2.ch005

Genetics of Lactococci

Gaudu, P., Yamamoto, Y., Jensen, P. R., Hammer, K., Lechardeur, D., & Gruss, A. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch29

Enhanced production of thermostable catalase for efficient gluconic acid biocatalysis

Huang, J., Wang, J., He, J., Wu, Y., Chen, L., Zhou, S., Bian, Y., & Li, Y. (2024) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2024.1465445

Biomanufacturing of Biobased Material Monomers

Tian, X., Luo, Y., Lu, J., Jiang, J., Chen, Y., Zhao, L., & Wu, H. (2025) · Springer eBooks · doi:10.1007/978-981-95-1188-4_2

Métabolisme du fer et de l'hème chez Lactobacillus sakei

Duhutrel, P. (2011) · theses.fr (ABES) · doi:10.70675/bfd9ff84z3925z4f76z96deza9085c27340b

Diversité génétique, génomique et fonctionnelle de Lactococcus lactis

Passerini, D. (2011) · doi:10.70675/49ff70d4z12fcz4bc0z964azd18b0a27a3d1

Respiration, a strategy to avoid oxidative stress in Lactococcus lactis, is regulated by the heme status

Cesselin, B., Derré‐Bobillot, A., Fernandez, A., Lamberet, G., Lechardeur, D., Yamamoto, Y., Pedersen, M. B., Garrigues, C., & Gaudu, P. (2010) · Japanese Journal of Lactic Acid Bacteria · doi:10.4109/jslab.21.10 · Cited by 9 · see citing works

Respiration capacity and consequences in Lactococcus lactis

Gaudu, P., Vido, K., Cesselin, B., Kulakauskas, S., Tremblay, J., Rezaı̈ki, L., Lamberet, G., Sourice, S., Duwat, P., & Gruss, A. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020635600343 · Cited by 100 · see citing works

Respiration Capacity of the Fermenting Bacterium Lactococcus lactis and Its Positive Effects on Growth and Survival

Duwat, P., Sourice, S., Cesselin, B., Lamberet, G., Vido, K., Gaudu, P., Loir, Y. L., Violet, F., Loubière, P., & Gruss, A. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.15.4509-4516.2001 · Cited by 245 · see citing works

Getting high (OD) on heme

Garrigues, C., Johansen, E., Pedersen, M. B., Møllgaard, H., Sørensen, K. I., Gaudu, P., Gruss, A., & Lamberet, G. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1403-c1 · Cited by 14 · see citing works

Research Progress in Aerobic Respiration Metabolism of Lactic Acid Bacteria

Jiang, N. (2009) · Food Science