Next-generation sequencing as an approach to dairy starter selection

DNA sequencing with chain-terminating inhibitors

Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572 · see citing works

Initial sequencing and analysis of the human genome

International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216 · see citing works

The sequence of the human genome

Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909 · see citing works

DNA polymorphisms amplified by arbitrary primers are useful as genetic markers

Williams, J. G., Kubelik, A. R., Livak, K. J., Rafalski, J. A., & Tingey, S. V. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.22.6531 · Cited by 13,077 · see citing works

AFLP: a new technique for DNA fingerprinting

Vos, P., Hogers, R. C. J., Bleeker, M., Reijans, M., van de Lee, T., Hornes, M., Frijters, A., Pot, J., Paleman, J., Kuiper, M. T. R., et al. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.21.4407 · Cited by 12,433 · see citing works

Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia

Saiki, R. K., Scharf, S., Faloona, F., Mullis, K. B., Horn, G. T., Erlich, H. A., & Arnheim, N. (1985) · Science · doi:10.1126/science.2999980 · Cited by 8,956 · see citing works

Sequencing technologies – the next generation

Metzker, M. L. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2626 · Cited by 7,066 · see citing works

The Sequence of the Human Genome

Venter, J., Adams, M., Myers, E., Li, P. W., Mural, R., Sutton, G., Smith, H., Yandell, M., Evans, C., Holt, R., et al. (2001) · Science · doi:10.1373/clinchem.2014.237016 · Cited by 6,779 · see citing works

Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data

Chin, C., Alexander, D., Marks, P., Klammer, A., Drake, J., Heiner, C., Clum, A., Copeland, A., Huddleston, J., Eichler, E., et al. (2013) · Nature Methods · doi:10.1038/nmeth.2474 · Cited by 4,008 · see citing works

Multilocus sequence typing: A portable approach to the identification of clones within populations of pathogenic microorganisms

Maiden, M. C. J., Bygraves, J. A., Feil, E. J., Morelli, G., Russell, J. E., Urwin, R., Zhang, Q., Zhou, J., Zurth, K., Caugant, D. A., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3140 · Cited by 3,838 · see citing works

Distribution of repetitive DNA sequences in eubacteria and application to finerpriting of bacterial enomes

Versalovic, J. A., Koeuth, T., & Lupski, R. L. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.24.6823 · Cited by 3,249 · see citing works

Evolution and classification of the CRISPR–Cas systems

Makarova, K. S., Haft, D. H., Barrangou, R., Brouns, S. J. J., Charpentier, E., Horvath, P., Moineau, S., Mojica, F. J. M., Wolf, Y. I., Yakunin, A. F., et al. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2577 · Cited by 2,512 · see citing works

CRISPR/Cas, the Immune System of Bacteria and Archaea

Horvath, P., & Barrangou, R. (2010) · Science · doi:10.1126/science.1179555 · Cited by 2,471 · see citing works

A tale of three next generation sequencing platforms: comparison of Ion torrent, pacific biosciences and illumina MiSeq sequencers

Quail, M., Smith, M. E., Coupland, P., Otto, T. D., Harris, S. R., Connor, T. R., Bertoni, A., Swerdlow, H. P., & Gu, Y. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-341 · Cited by 2,031 · see citing works

Lactic acid bacteria as functional starter cultures for the food fermentation industry

Leroy, F., & De Vuyst, L. (2004) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2003.09.004 · Cited by 1,852 · see citing works

Continuous base identification for single-molecule nanopore DNA sequencing

Clarke, J., Wu, H., Jayasinghe, L., Patel, A., Reid, S., & Bayley, H. (2009) · Nature Nanotechnology · doi:10.1038/nnano.2009.12 · Cited by 1,813 · see citing works

Direct detection of DNA methylation during single-molecule, real-time sequencing

Flusberg, B. A., Webster, D. R., Lee, J. H., Travers, K. J., Olivares, E. C., Clark, T. A., Korlach, J., & Turner, S. W. (2010) · Nature Methods · doi:10.1038/nmeth.1459 · Cited by 1,460 · 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

Performance comparison of benchtop high-throughput sequencing platforms

Loman, N. J., Misra, R., Dallman, T. J., Constantinidou, C., Gharbia, S. E., Wain, J. R., & Pallen, M. J. (2012) · Nature Biotechnology · doi:10.1038/nbt.2198 · Cited by 1,334 · see citing works

Biochemical pathways for the production of flavour compounds in cheeses during ripening: A review

McSweeney, P. L. H., & Sousa, M. J. (2000) · Le Lait · doi:10.1051/lait:2000127 · Cited by 1,266 · cited 5× · see citing works

Phage Response to CRISPR-Encoded Resistance in Streptococcus thermophilus

Deveau, H., Barrangou, R., Garneau, J. E., Labonté, J., Fremaux, C., Boyaval, P., Romero, D. A., Horvath, P., & Moineau, S. (2007) · Journal of Bacteriology · doi:10.1128/jb.01412-07 · Cited by 1,196 · 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

Biochemistry of cheese ripening

McSweeney, P. L. H. (2004) · International Journal of Dairy Technology · doi:10.1111/j.1471-0307.2004.00147.x · Cited by 1,048 · see citing works

Principles and Applications of Methods for DNA-Based Typing of Microbial Organisms

Olive, D. M., & Bean, P. (1999) · Journal of Clinical Microbiology · doi:10.1128/jcm.37.6.1661-1669.1999 · Cited by 924 · see citing works

‘Interfacial activation’ of lipases: facts and artifacts

Verger, R. (1997) · Trends in biotechnology · doi:10.1016/s0167-7799(96)10064-0 · Cited by 884 · see citing works

Recent advances in cheese microbiology

Beresford, T. P., Fitzsimons, N. A., Brennan, N. L., & Cogan, T. M. (2001) · International Dairy Journal · doi:10.1016/s0958-6946(01)00056-5 · Cited by 823 · see citing works

Diversity, Activity, and Evolution of CRISPR Loci in Streptococcus thermophilus

Horvath, P., Romero, D. A., Coûté-Monvoisin, A.-C., Richards, M., Deveau, H., Moineau, S., Boyaval, P., Fremaux, C., & Barrangou, R. (2007) · Journal of Bacteriology · doi:10.1128/jb.01415-07 · Cited by 775 · see citing works

A nomenclature for restriction enzymes, DNA methyltransferases, homing endonucleases and their genes

Roberts, R. J. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg274 · Cited by 755 · see citing works

Laboratory Methods in Food Microbiology

Harrigan, W. F. (1998) · Medical Entomology and Zoology · Cited by 746 · see citing works

Bacteriocin Production: a Probiotic Trait?

Dobson, A., Cotter, P. D., Ross, R. P., & Hill, C. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.05576-11 · Cited by 690 · see citing works

Detection and activity of lactacin B, a bacteriocin produced by Lactobacillus acidophilus

Barefoot, S. F., & Klaenhammer, T. R. (1983) · Applied and Environmental Microbiology · doi:10.1128/aem.45.6.1808-1815.1983 · Cited by 638 · see citing works

CRISPR/Cas System and Its Role in Phage-Bacteria Interactions

Deveau, H., Garneau, J. E., & Moineau, S. (2010) · Annual Review of Microbiology · doi:10.1146/annurev.micro.112408.134123 · Cited by 624 · see citing works

Repetitive extragenic palindromic sequences: A major component of the bacterial genome

Stern, M., Ames, G. F., Smith, N. H., et al. (1984) · Cell · doi:10.1016/0092-8674(84)90436-7 · Cited by 576 · see citing works

Novel method to extract large amounts of bacteriocins from lactic acid bacteria

Yang, R., Johnson, M. C., & Ray, B. (1992) · Applied and Environmental Microbiology · doi:10.1128/aem.58.10.3355-3359.1992 · Cited by 535 · see citing works

CRISPR-based adaptive and heritable immunity in prokaryotes

John van der, O. O. S. T., Jore, M. M., Westra, E. R., Lundgren, M., & Brouns, S. J. J. (2009) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2009.05.002 · Cited by 524 · see citing works

Variation in Biofilm Formation among Strains of <i>Listeriamonocytogenes</i>

Borucki, M. K., Peppin, J. D., White, D., Loge, F., & Call, D. R. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.12.7336-7342.2003 · Cited by 519 · see citing works

Complete sequence and comparative genome analysis of the dairy bacterium Streptococcus thermophilus

Bolotin, A., Quinquis, B., Renault, P., Sorokin, A., Ehrlich, S. D., Kulakauskas, S., Lapidus, A. L., Goltsman, E., Mazur, M., Pusch, G. D., et al. (2004) · Nature Biotechnology · doi:10.1038/nbt1034 · Cited by 496 · see citing works

Transfer of Streptococcus lactis and Related Streptococci to the Genus Lactococcus gen. nov.

SCHLEIFER, K. H., Kraus, J., Dvorak, C., Kilpper-Bälz, R., Collins, M. D., & Fischer, W. (1985) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(85)80052-7 · Cited by 479 · see citing works

High-throughput bacterial genome sequencing: an embarrassment of choice, a world of opportunity

Loman, N. J., Constantinidou, C., Chan, J. Z.-M., Halachev, M. R., Sergeant, M. J., Penn, C. W., Robinson, E., & Pallen, M. J. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2850 · Cited by 426 · 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

Generations of sequencing technologies

Pettersson, E., Lundeberg, J., & Ahmadian, A. (2008) · Genomics · doi:10.1016/j.ygeno.2008.10.003 · Cited by 392 · see citing works

The CRISPR System: Small RNA-Guided Defense in Bacteria and Archaea

Karginov, F. V., & Hannon, G. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2009.12.033 · Cited by 384 · see citing works

The proteolytic system of lactic acid bacteria revisited: a genomic comparison

Liu, M., Bayjanov, J. R., Renckens, B., Nauta, A., & Siezen, R. J. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-36 · Cited by 384 · see citing works

Accuracy and quality assessment of 454 GS-FLX Titanium pyrosequencing

Gilles, A., Meglécz, E., Pech, N., Ferreira, S., Malausa, T., & Martin, J. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-245 · Cited by 377 · see citing works

Phage abortive infection in lactococci: variations on a theme

Chopin, M., Chopin, A., & Bidnenko, E. (2005) · Current Opinion in Microbiology · doi:10.1016/j.mib.2005.06.006 · Cited by 368 · see citing works

Phage_Finder: Automated identification and classification of prophage regions in complete bacterial genome sequences

Fouts, D. E. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl732 · Cited by 333 · see citing works

Characterization of DNA methyltransferase specificities using single-molecule, real-time DNA sequencing

Clark, T. A., Murray, I. A., Morgan, R., Kislyuk, A. O., Spittle, K. E., Boitano, M., Fomenkov, A. I., Roberts, R. J., & Korlach, J. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1146 · Cited by 315 · see citing works

Molecular and Chemotaxonomic Approaches to the Classification of Streptococci, Enterococci and Lactococci: A Review

SCHLEIFER, K. H., & Kilpper-Bälz, R. (1987) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(87)80002-4 · Cited by 308 · see citing works

Differential subsequence conservation of interspersed repetitive Streptococcus pneumoniae BOX elements in diverse bacteria.Preprint

Koeuth, T., Versalovic, J. A., & Lupski, J. R. (1995) · Genome Research · doi:10.1101/gr.5.4.408 · Cited by 280 · see citing works

De novo fragment assembly with short mate-paired reads: Does the read length matter?

Chaisson, M. J., Brinza, D., & Pevzner, P. A. (2009) · Genome Research · doi:10.1101/gr.079053.108 · Cited by 279 · see citing works

Type II restriction endonucleases—a historical perspective and more

Pingoud, A. M., Wilson, G. G., & Wende, W. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku447 · Cited by 274 · see citing works

Microstructure and Rheology of Yogurt Made with Cultures Differing Only in Their Ability to Produce Exopolysaccharides

Hassan, A. N., Ipsen, R., Janzen, T., & Qvist, K. B. (2003) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(03)73748-5 · Cited by 267 · see citing works

The methylomes of six bacteria

Murray, I. A., Clark, T. A., Morgan, R., Boitano, M., Anton, B. P., Luong, K., Fomenkov, A. I., Turner, S. W., Korlach, J., & Roberts, R. J. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks891 · Cited by 253 · see citing works

Type I restriction enzymes and their relatives

Loenen, W. A., Dryden, D., Raleigh, E., & Wilson, G. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt847 · Cited by 250 · see citing works

Molecular cloning and nucleotide sequence of the gene encoding the major peptidoglycan hydrolase of Lactococcus lactis, a muramidase needed for cell separation

Buist, G., Kok, J., Leenhouts, K. J., Dabrowska, M., Venema, G., & Haandrikman, A. J. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.6.1554-1563.1995 · Cited by 247 · see citing works

Sequencing 16S rRNA gene fragments using the PacBio SMRT DNA sequencing system.

Schloss, P. D., Jenior, M. L., Koumpouras, C. C., Westcott, S. L., & Highlander, S. K. (2016) · PeerJ · doi:10.7717/peerj.1869 · Cited by 226 · see citing works

Autolysis and proteolysis in different strains of starter bacteria during Cheddar cheese ripening

Wilkinson, M. G., Guinee, T. P., O'Callaghan, D. M., & Fox, P. F. (1994) · Journal of Dairy Research · doi:10.1017/s0022029900028260 · Cited by 208 · see citing works

Rapid identification of dairy lactic acid bacteria by M13-generated, RAPD-PCR fingerprint databases

Rossetti, L., & Giraffa, G. (2005) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2005.03.001 · Cited by 196 · see citing works

Pulsed-Field Gel Electrophoresis of Very Large DNA Molecules

Cantor, C. R., Smith, C. L., & Mathew, M. K. (1988) · Annual Review of Biophysics and Biophysical Chemistry · doi:10.1146/annurev.bb.17.060188.001443 · Cited by 196 · see citing works

Archaeology: The milk revolution

Curry, A. (2013) · Nature · doi:10.1038/500020a · Cited by 185 · see citing works

Loss of Lactose Metabolism in Lactic Streptococci

McKay, L. L., Baldwin, K. A., & Zottola, E. A. (1972) · Applied Microbiology · doi:10.1128/am.23.6.1090-1096.1972 · Cited by 184 · see citing works

Analysis of six prophages in Lactococcus lactis IL1403: different genetic structure of temperate and virulent phage populations

Chopin, A. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.3.644 · Cited by 183 · see citing works

Enterobacterial Repetitive Intergenic Consensus (ERIC) Sequences in Escherichia coli: Evolution and Implications for ERIC-PCR

Wilson, L. A. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msj125 · Cited by 155 · see citing works

ADSA Foundation Scholar Award: Possibilities and Challenges of Exopolysaccharide-Producing Lactic Cultures in Dairy Foods

Hassan, A. N. (2008) · Journal of Dairy Science · doi:10.3168/jds.2007-0558 · Cited by 151 · see citing works

Cooperation between Lactococcus lactis and Nonstarter Lactobacilli in the Formation of Cheese Aroma from Amino Acids

Kieronczyk, A., Skeie, S. B., Langsrud, T., & Yvon, M. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.2.734-739.2003 · Cited by 151 · see citing works

Type III restriction-modification enzymes: a historical perspective

Rao, D. N., Dryden, D. T. F., & Bheemanaik, S. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt616 · Cited by 149 · see citing works

Next-Generation Sequencing: A Review of Technologies and Tools for Wound Microbiome Research

Hodkinson, B. P., & Grice, E. A. (2014) · Advances in Wound Care · doi:10.1089/wound.2014.0542 · Cited by 149 · see citing works

Complete Sequences of Four Plasmids of Lactococcus lactis subsp. cremoris SK11 Reveal Extensive Adaptation to the Dairy Environment

Siezen, R. J., Renckens, B., van Swam, I. I., Peters, S., van Kranenburg, R., Kleerebezem, M., & de Vos, W. M. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.12.8371-8382.2005 · Cited by 145 · see citing works

Perspectives on the contribution of lactic acid bacteria to cheese flavor development

Steele, J. L., Broadbent, J. R., & Kok, J. (2012) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.12.001 · Cited by 143 · see citing works

Cloning and DNA sequence analysis of two abortive infection phage resistance determinants from the lactococcal plasmid pNP40

Garvey, P., Fitzgerald, G. F., & Hill, C. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.12.4321-4328.1995 · Cited by 142 · see citing works

Beginner’s guide to comparative bacterial genome analysis using next-generation sequence data

Edwards, D., & Holt, K. E. (2013) · Microbial Informatics and Experimentation · doi:10.1186/2042-5783-3-2 · Cited by 139 · see citing works

New Method for Detecting Bacteriocin Production

Kékessy, D. A., & Piguet, J. D. (1970) · Applied Microbiology · doi:10.1128/am.20.2.282-283.1970 · Cited by 138 · see citing works

Transcriptional Pattern of Genes Coding for the Proteolytic System of Lactococcus lactis and Evidence for Coordinated Regulation of Key Enzymes by Peptide Supply

Guédon, É., Renault, P., Ehrlich, S. D., & Delorme, C. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.12.3614-3622.2001 · Cited by 137 · see citing works

Identification and characterization of phage‐resistance genes in temperate lactococcal bacteriophages

McGrath, S., Fitzgerald, G. F., & van Sinderen, D. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.02763.x · Cited by 133 · see citing works

Characterization of the Lactococcus lactis lactose operon promoter: contribution of flanking sequences and LacR repressor to promoter activity

van Rooijen, R. J., Gasson, M. J., & de Vos, W. M. (1992) · Journal of Bacteriology · doi:10.1128/jb.174.7.2273-2280.1992 · Cited by 132 · see citing works

Phage Resistance Mechanisms in Lactic Acid Bacteria

Allison, G. E., & Klaenhammer, T. R. (1998) · International Dairy Journal · doi:10.1016/s0958-6946(98)00043-0 · Cited by 131 · see citing works

Genes but Not Genomes Reveal Bacterial Domestication of Lactococcus Lactis

Passerini, D., Beltramo, C., Coddeville, M., Quentin, Y., Ritzenthaler, P., Daveran‐Mingot, M., & Bourgeois, P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015306 · Cited by 131 · see citing works

Genome Sequences of Lactococcus lactis MG1363 (Revised) and NZ9000 and Comparative Physiological Studies

Linares, D. M., Kok, J., & Poolman, B. (2010) · Journal of Bacteriology · doi:10.1128/jb.00533-10 · Cited by 131 · see citing works

Chromosomal diversity in Lactococcus lactis and the origin of dairy starter cultures

Kelly, W. J., Ward, L. J. H., & Leahy, S. C. (2010) · Genome Biology and Evolution · doi:10.1093/gbe/evq056 · Cited by 130 · see citing works

Molecular cloning, transcriptional analysis, and nucleotide sequence of lacR, a gene encoding the repressor of the lactose phosphotransferase system of Lactococcus lactis.

van Rooijen, R. J., & de Vos, W. M. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)44779-x · Cited by 129 · see citing works

Specialized adaptation of a lactic acid bacterium to the milk environment: the comparative genomics of Streptococcus thermophilus LMD-9

Goh, Y. J., Goin, C., O’Flaherty, S., Altermann, E., & Hutkins, R. W. (2011) · Microbial Cell Factories · doi:10.1186/1475-2859-10-s1-s22 · Cited by 123 · see citing works

Pulsed-Field Gel Electrophoresis of Sma I Digests of Lactococcal Genomic DNA, a Novel Method of Strain Identification

Tanskanen, E. I., Tulloch, D. L., Hillier, A. J., et al. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.10.3105-3111.1990 · Cited by 121 · see citing works

Lactose and d -Galactose Metabolism in Group N Streptococci: Presence of Enzymes for Both the d -Galactose 1-Phosphate and d -Tagatose 6-Phosphate Pathways 1

Bissett, D. L., & Anderson, R. L. (1974) · Journal of Bacteriology · doi:10.1128/jb.117.1.318-320.1974 · Cited by 119 · see citing works

Glutamate dehydrogenase activity: a major criterion for the selection of flavour-producing lactic acid bacteria strains

Tanous, C., Kieronczyk, A., Hélinck, S., Chambellon, É., & Yvon, M. (2002) · Springer eBooks · doi:10.1007/978-94-017-2029-8_17 · Cited by 118 · see citing works

Purification and Properties of a Fructose-1,6-Diphosphate-Activated Lactate Dehydrogenase from Streptococcus faecalis

Wittenberger, C. L., & Angelo, N. (1970) · Journal of Bacteriology · doi:10.1128/jb.101.3.717-724.1970 · Cited by 118 · see citing works

Efficacy of a 3rd generation high-throughput sequencing platform for analyses of 16S rRNA genes from environmental samples

Mosher, J. J., Bernberg, E. L., Shevchenko, O., Kan, J., & Kaplan, L. A. (2013) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2013.08.009 · Cited by 117 · see citing works

Functional implications of the microbial community structure of undefined mesophilic starter cultures

Smid, E. J., Erkus, O., Spus, M., Wolkers-Rooijackers, J. C., Alexeeva, S., & Kleerebezem, M. (2014) · Microbial Cell Factories · doi:10.1186/1475-2859-13-s1-s2 · Cited by 117 · see citing works

Detection and characterization of a bacteriocin, garviecin L1-5, produced by Lactococcus garvieae isolated from raw cow’s milk

Villani, F., Aponte, M., Blaiotta, G., Mauriello, G., Pepe, O., & Moschetti, G. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01261.x · Cited by 115 · see citing works

Formation of Yogurt Microstructure and Three-Dimensional Visualization as Determined by Confocal Scanning Laser Microscopy

Hassan, A. N., Frank, J. F., Farmer, M. A., Schmidt, K. A., & Shalabi, S. I. (1995) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(95)76892-8 · Cited by 114 · see citing works

Investigation of the Relationship between Lactococcal Host Cell Wall Polysaccharide Genotype and 936 Phage Receptor Binding Protein Phylogeny

Mahony, J., Kot, W., Murphy, J., Ainsworth, S., Neve, H., Hansen, L. H., Heller, K. J., S�rensen, S. J., Hammer, K., Cambillau, C., et al. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.00653-13 · Cited by 114 · see citing works

Differences in Lactococcal Cell Wall Polysaccharide Structure Are Major Determining Factors in Bacteriophage Sensitivity

Ainsworth, S., Sadovskaya, I., Vinogradov, E., Courtin, P., Guérardel, Y., Mahony, J., Grard, T., Cambillau, C., Chapot, M.-P., & van Sinderen, D. (2014) · mBio · doi:10.1128/mbio.00880-14 · Cited by 112 · see citing works

Complete Genome Sequence of Lactococcus lactis subsp. lactis KF147, a Plant-Associated Lactic Acid Bacterium

Siezen, R. J., Bayjanov, J. R., Renckens, B., Wels, M., van Hijum, S. A. F. T., Douwe Molenaar, B., & Vlieg, J. E. T. V. H. (2010) · Journal of Bacteriology · doi:10.1128/jb.00276-10 · Cited by 112 · see citing works

Identification and Characterization of Lactococcal-Prophage-Carried Superinfection Exclusion Genes

Mahony, J., McGrath, S., Fitzgerald, G. F., & van Sinderen, D. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.01053-08 · Cited by 111 · see citing works

Diversity Analysis of Dairy and Nondairy Lactococcus lactis Isolates, Using a Novel Multilocus Sequence Analysis Scheme and (GTG) 5 -PCR Fingerprinting

Rademaker, J. L. W., Herbet, H., Starrenburg, M. J. C., Naser, S. M., Gevers, D., Kelly, W. J., Hugenholtz, J., Swings, J., & Vlieg, J. E. T. V. H. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01017-07 · Cited by 111 · see citing works

Emergence of a Cell Wall Protease in the Streptococcus thermophilus Population

Delorme, C., Bartholini, C., Bolotine, A., Ehrlich, S. D., & Renault, P. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01018-09 · Cited by 105 · see citing works

Diacetyl: Occurrence, Analysis, and Toxicity

Shibamoto, T. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf500615u · Cited by 104 · see citing works

Genomic insights into high exopolysaccharide-producing dairy starter bacterium Streptococcus thermophilus ASCC 1275

Wu, Q., Tun, H. M., Leung, F. C.-C., & Shah, N. P. (2014) · Scientific Reports · doi:10.1038/srep04974 · Cited by 101 · see citing works

The conjugative plasmid pTR2030 encodes two bacteriophage defense mechanisms in lactococci, restriction modification (R+/M+) and abortive infection (Hsp+)

Hill, C., Pierce, K. A., & Klaenhammer, T. R. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.9.2416-2419.1989 · Cited by 98 · see citing works

Fluorescence assay of X-prolyl dipeptidyl-aminopeptidase activity with a new fluorogenic substrate

Kato, T., Nagatsu, T., Kimura, T., & Sakakibara, S. (1978) · Biochemical Medicine · doi:10.1016/0006-2944(78)90035-2 · Cited by 93 · see citing works

Mobile CRISPR/Cas-Mediated Bacteriophage Resistance in Lactococcus lactis

Millen, A. M., Horvath, P., Boyaval, P., & Romero, D. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051663 · Cited by 92 · see citing works

Contribution of Lactococcus lactis Cell Envelope Proteinase Specificity to Peptide Accumulation and Bitterness in Reduced-Fat Cheddar Cheese

Broadbent, J. R., Barnes, M., Brennand, C., Strickland, M., Houck, K., Johnson, M. E., & Steele, J. L. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.4.1778-1785.2002 · Cited by 91 · see citing works

Amplified Fragment Length Polymorphism: An Invaluable Fingerprinting Technique for Genomic, Transcriptomic, and Epigenetic Studies

Paun, O., & Schönswetter, P. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-609-8_7 · Cited by 90 · see citing works

Comparative Phenotypic and Molecular Genetic Profiling of Wild Lactococcus lactis subsp. lactis Strains of the L. lactis subsp. lactis and L. lactis subsp. cremoris Genotypes, Isolated from Starter-Free Cheeses Made of Raw Milk

Fernández, E., Alegría, Á., Delgado, S., Martín, M. C., & Mayo, B. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02991-10 · Cited by 90 · see citing works

Loss of Lactose Metabolism in Lactic Streptococci1

McKay, L. L., Baldwin, K. A., & Zottola, E. A. (1972) · Applied Microbiology · doi:10.1128/aem.23.6.1090-1096.1972 · Cited by 90 · see citing works

Analysis of the lacZ sequences from two Streptococcus thermophilus strains: comparison with the Escherichia coli and Lactobacillus bulgaricus β-galactosidase sequences

Schroeder, C. J., Robert, C., Lenzen, G., et al. (1991) · Microbiology · doi:10.1099/00221287-137-2-369 · Cited by 87 · see citing works

AFLP technology for DNA fingerprinting

Vuylsteke, M., Peleman, J. D., & van Eijk, M. J. (2007) · Nature Protocols · doi:10.1038/nprot.2007.175 · Cited by 85 · see citing works

S-Adenosyl-L-methionine–Dependent Restriction Enzymes

Sistla, S., & Rao, D. N. (2004) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230490440532 · Cited by 85 · see citing works

High-resolution separation and accurate size determination in pulsed-field gel electrophoresis of DNA. 1. DNA size standards and the effect of agarose and temperature

Mathew, M. K., Smith, C. L., & Cantor, C. R. (1988) · Biochemistry · doi:10.1021/bi00426a019 · Cited by 80 · see citing works

A Polyphasic Approach towards the Identification of Strains Belonging to Lactobacillus acidophilus and Related Species

Gancheva, A., Pot, B., Vanhonacker, K., et al. (1999) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(99)80011-3 · Cited by 80 · see citing works

ScrFI: a new sequence–specific endonuclease fromStreptococcus cremoris

Fitzgerlad, G. F., Daly, C., Brown, L. R., et al. (1982) · Nucleic Acids Research · doi:10.1093/nar/10.24.8171 · Cited by 79 · see citing works

Complete Genome Sequence of Lactococcus lactis subsp. lactis CV56, a Probiotic Strain Isolated from the Vaginas of Healthy Women

Gao, Y., Lu, Y. C., Teng, K., et al. (2011) · Journal of Bacteriology · doi:10.1128/jb.00358-11 · Cited by 76 · see citing works

Rapid Identification of Streptococcus thermophilus by Primer-specific PCR Amplification Based on its lacZ Gene

Lick, S., Keller, M., Bockelmann, W., & Heller, J. (1996) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(96)80012-9 · Cited by 73 · see citing works

Molecular Diversity and Relationship within Lactococcus lactis, as revealed by Randomly Amplified Polymorphic DNA (RAPD)

Tailliez, P., Tremblay, J., Ehrlich, S. D., & Chopin, A. (1998) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(98)80065-9 · Cited by 72 · see citing works

Extent of Horizontal Gene Transfer in Evolution of Streptococci of the Salivarius Group

Delorme, C., Poyart, C., Ehrlich, S. D., & Renault, P. (2007) · Journal of Bacteriology · doi:10.1128/jb.01058-06 · Cited by 72 · see citing works

Comparative and functional genomics of lactococci

Kok, J., Buist, G., Zomer, A., van Hijum, S. A. F. T., & Kuipers, O. P. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.fmrre.2005.04.004 · Cited by 70 · see citing works

TheLactococcus lactisplasmidome: much learnt, yet still lots to discover

Ainsworth, S., Stockdale, S. R., Bottacini, F., Mahony, J., & van Sinderen, D. (2014) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12074 · Cited by 69 · see citing works

DNA fingerprinting of pathogenic bacteria by fluorophore-enhanced repetitive sequence-based polymerase chain reaction.

Versalovic, J. A., Kapur, V., Koeuth, T., et al. (1995) · PubMed · Cited by 66 · see citing works

A Natural Large Chromosomal Inversion in Lactococcus lactis Is Mediated by Homologous Recombination between Two Insertion Sequences

Daveran‐Mingot, M., Campo, N., Ritzenthaler, P., & Bourgeois, P. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.18.4834-4842.1998 · Cited by 66 · see citing works

Lactococcal Plasmid pNP40 Encodes a Novel, Temperature-Sensitive Restriction-Modification System

O’Driscoll, J., Glynn, F., Cahalane, O., Motherway, M. O., Fitzgerald, G. F., & van Sinderen, D. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.9.5546-5556.2004 · Cited by 66 · see citing works

Observation of Encapsulated Lactic Acid Bacteria Using Confocal Scanning Laser Microscopy

Hassan, A. N., Frank, J. F., Farmer, M. A., Schmidt, K. A., & Shalabi, S. I. (1995) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(95)76891-6 · Cited by 65 · see citing works

Thermoinducible Lysis of Temperature-Sensitive Streptococcus cremoris Strains

Feirtag, J. M., & McKay, L. L. (1987) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(87)80214-x · Cited by 64 · see citing works

Palindromic sequence impedes sequencing-by-ligation mechanism

Huang, Y., Chen, S.-C., Chiang, Y., Chen, T.-H., & Chiu, K. (2012) · BMC Systems Biology · doi:10.1186/1752-0509-6-s2-s10 · Cited by 64 · see citing works

Conjugal Transfer of Bacteriophage Resistance Determinants on pTR2030 into Streptococcus cremoris Strains

Sing, W. D., & Klaenhammer, T. R. (1986) · Applied and Environmental Microbiology · doi:10.1128/aem.51.6.1264-1271.1986 · Cited by 63 · see citing works

Plasmid-Determined Systems for Restriction and Modification Activity and Abortive Infection in Streptococcus cremoris

Gautier, M., & Chopin, M. (1987) · Applied and Environmental Microbiology · doi:10.1128/aem.53.5.923-927.1987 · Cited by 63 · see citing works

CRISPR analysis of bacteriophage‐insensitive mutants (BIMs) of industrial Streptococcus thermophilus – implications for starter design

Mills, S., Griffin, C., Coffey, A., Meijer, W. C., Hafkamp, B., & Ross, R. P. (2009) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2009.04486.x · Cited by 63 · see citing works

Two methods for the genetic differentiation of Lactococcus lactis ssp. lactis and cremoris based on differences in the 16S rRNA gene sequence

Ward, L. J. H., Brown, J. C. S., & Davey, G. P. (1998) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1998.tb13177.x · Cited by 63 · see citing works

New Method for Detecting Bacteriocin Production

Kékessy, D. A., & Jd, P. (1970) · Applied Microbiology · doi:10.1128/aem.20.2.282-283.1970 · Cited by 63 · see citing works

Characterization of a Novel Type II Restriction-Modification System, <i>Sth</i> 368I, Encoded by the Integrative Element ICE <i>St1</i> of <i>Streptococcus thermophilus</i> CNRZ368

Burrus, V., Bontemps, C., Decaris, B., & Guédon, G. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.4.1522-1528.2001 · Cited by 62 · see citing works

Complete Genome Sequence of Streptococcus thermophilus Strain ND03

Sun, Z., Chen, X., Wang, J., Zhao, W., Shao, Y., Wu, L., Zhou, Z., Sun, T., Wang, L., Meng, H., et al. (2010) · Journal of Bacteriology · doi:10.1128/jb.01374-10 · Cited by 62 · see citing works

The EstA esterase is responsible for the main capacity of Lactococcus lactis to synthesize short chain fatty acid esters in vitro

Nardi, M., Fiez-Vandal, C., Tailliez, P., & Monnet, V. (2002) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2002.01793.x · Cited by 61 · see citing works

Interactions of the cell-wall glycopolymers of lactic acid bacteria with their bacteriophages

Chapot, M.-P. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00236 · Cited by 60 · see citing works

REP code: defining bacterial identity in extragenic space

Tobes, R., & Ramos, J. L. (2004) · Environmental Microbiology · doi:10.1111/j.1462-2920.2004.00704.x · Cited by 59 · see citing works

Complete Genome Sequence of Lactococcus lactis IO-1, a Lactic Acid Bacterium That Utilizes Xylose and Produces High Levels of l -Lactic Acid

Kato, H., Shiwa, Y., Oshima, K., et al. (2012) · Journal of Bacteriology · doi:10.1128/jb.00074-12 · Cited by 56 · see citing works

The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages

Sozhamannan, S., Chute, M. D., McAfee, F. D., et al. (2006) · BMC Microbiology · doi:10.1186/1471-2180-6-34 · Cited by 55 · see citing works

Rapid PCR-Based Method Which Can Determine Both Phenotype and Genotype of Lactococcus lactis Subspecies

Nomura, M., Kobayashi, M., & Okamoto, T. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.5.2209-2213.2002 · Cited by 53 · see citing works

The Streptococcus thermophilus Autolytic Phenotype Results from a Leaky Prophage

Husson-Kao, C., Mengaud, J., Cesselin, B., van Sinderen, D., Benbadis, L., & Chapot, M.-P. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.2.558-565.2000 · Cited by 50 · see citing works

Genetic organization and expression of citrate permease in lactic acid bacteria.

Drider, D., Békal, S., & Prévost, H. (2004) · PubMed · Cited by 49 · see citing works

Biodiversity of lactococcal bacteriophages isolated from 3 Gouda-type cheese-producing plants

Murphy, J., Royer, B., Mahony, J., et al. (2013) · Journal of Dairy Science · doi:10.3168/jds.2013-6748 · Cited by 47 · see citing works

Interaction between the genomes of Lactococcus lactis and phages of the P335 species

Kelly, W. J., Altermann, E., Lambie, S. C., & Leahy, S. C. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00257 · Cited by 45 · see citing works

Prophage-Cured Derivatives of Streptococcus lactis and Streptococcus cremoris

Gasson, M. J., & Davies, F. L. (1980) · Applied and Environmental Microbiology · doi:10.1128/aem.40.5.964-966.1980 · Cited by 43 · see citing works

Application of AFLP fingerprint analysis for studying the biodiversity of Streptococcus thermophilus

Lazzi, C., Bove, C. G., Sgarbi, E., Gatti, M., Gioia, F. L., Torriani, S., & Neviani, E. (2009) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2009.07.021 · Cited by 42 · see citing works

Isolation and Characterization of a Streptococcus thermophilus Plasmid Closely Related to the pMV158 Family

Turgeon, N., & Moineau, S. (2001) · Plasmid · doi:10.1006/plas.2001.1517 · Cited by 41 · see citing works

Complete Genome Sequence of the Pigmented Streptococcus thermophilus Strain JIM8232

Delorme, C., Bartholini, C., Luraschi, M., et al. (2011) · Journal of Bacteriology · doi:10.1128/jb.05404-11 · Cited by 41 · see citing works

Complete Genome of Lactococcus lactis subsp. cremoris UC509.9, Host for a Model Lactococcal P335 Bacteriophage

Ainsworth, S., Zomer, A., de Jager, V., Bottacini, F., van Hijum, S. A. F. T., Mahony, J., & van Sinderen, D. (2013) · Genome Announcements · doi:10.1128/genomea.00119-12 · Cited by 41 · see citing works

Loss of Plasmid-Mediated Oligopeptide Transport System in Lactococci: Another Reason for Slow Milk Coagulation

Yu, W., Gillies, K., Kondo, J. K., et al. (1996) · Plasmid · doi:10.1006/plas.1996.0017 · Cited by 39 · see citing works

A Specific Mutation in the Promoter Region of the Silent cel Cluster Accounts for the Appearance of Lactose-Utilizing Lactococcus lactis MG1363

Solopova, A., Bachmann, H., Teusink, B., Kok, J., Neves, A. R., & Kuipers, O. P. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.00455-12 · Cited by 39 · see citing works

Characterization of Streptococcus thermophilus lytic bacteriophages from mozzarella cheese plants

Zinno, P., Janzen, T., Bennedsen, M., et al. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.12.008 · Cited by 38 · see citing works

Fluorescent-BOX-PCR for resolving bacterial genetic diversity, endemism and biogeography

Brusetti, L., Malkhazova, I., Gtari, M., Tamagnini, I., Borin, S., Merabishvili, M., Чанішвілі, Н., Mora, D., Cappitelli, F., & Daffonchio, D. G. (2008) · BMC Microbiology · doi:10.1186/1471-2180-8-220 · Cited by 38 · see citing works

Methyltransferases acquired by lactococcal 936-type phage provide protection against restriction endonuclease activity

Murphy, J., Klumpp, J., Mahony, J., Motherway, M. O., Nauta, A., & van Sinderen, D. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-831 · Cited by 37 · see citing works

Identification of Restriction-Modification Systems of Bifidobacterium animalis subsp. lactis CNCM I-2494 by SMRT Sequencing and Associated Methylome Analysis

Motherway, M. O., Watson, D., Bottacini, F., Clark, T. A., Roberts, R. J., Korlach, J., Garault, P., Chervaux, C., Vlieg, J. E. T. V. H., Smokvina, T., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094875 · Cited by 36 · see citing works

Advances in the genetics of thermophilic lactic acid bacteria

Delcour, J., Ferain, T., & Hols, P. (2000) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(00)00134-8 · Cited by 36 · see citing works

Complete Genome Sequence of Streptococcus thermophilus Strain MN-ZLW-002

Kang, X., Ling, N., Sun, G., Zhou, Q., Zhang, L., & Sheng, Q. (2012) · Journal of Bacteriology · doi:10.1128/jb.00740-12 · Cited by 35 · see citing works

The ldh phylogeny for environmental isolates of Lactococcus lactis is consistent with rRNA genotypes but not with phenotypes

Urbach, E., Daniels, B., Salama, M. S., et al. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.2.694-702.1997 · Cited by 33 · see citing works

Transcriptional Regulation and Evolution of Lactose Genes in the Galactose-Lactose Operon of Lactococcus lactis NCDO2054

Vaughan, E. E., Pridmore, R. D., & Mollet, B. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.18.4893-4902.1998 · Cited by 33 · see citing works

LlaAI and LlaBI, two type-II restriction endonucleases from Lactococcus lactis subsp. cremoris W9 and W56 recognizing, respectively, 5'-/GATC-3' and 5'-C/TRYAG-3'

Nyengaard, N. R., Vogensen, F. K., & Josephsen, J. (1993) · Gene · doi:10.1016/0378-1119(93)90499-s · Cited by 32 · see citing works

Genetic investigation within Lactococcus garvieae revealed two genomic lineages

Ferrario, C., Ricci, G., Borgo, F., Rollando, A., & Fortina, M. G. (2012) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2012.02591.x · Cited by 31 · see citing works

Restriction/modification in Streptococcus thermophilus: isolation and characterization of a type II restriction endonuclease Sth455I

Guimont, C., Henry, P., & Linden, G. (1993) · Applied Microbiology and Biotechnology · doi:10.1007/bf00228609 · Cited by 30 · see citing works

Genome Sequence of Lactococcus lactis subsp. lactis NCDO 2118, a GABA-Producing Strain

Oliveira, L. D. C., Saraiva, T. D. L., Soares, S. D. C., Ramos, R. T. J., de Sá, P. H. C. G., Carneiro, A. R., Miranda, F. M., Freire, M., Renan, W., Oliveira, A., et al. (2014) · Genome Announcements · doi:10.1128/genomea.00980-14 · Cited by 29 · see citing works

Biology of the temperate Streptococcus thermophilus bacteriophage TP-J34 and physical characterization of the phage genome

Neve, H., Freudenberg, W., Diestel-Feddersen, F., et al. (2003) · Virology · doi:10.1016/s0042-6822(03)00516-6 · Cited by 27 · see citing works

Complete Genome Sequence of Lactococcus lactis subsp. cremoris A76

Bolotin, A., Quinquis, B., Ehrlich, S. D., & Sorokin, A. (2012) · Journal of Bacteriology · doi:10.1128/jb.06629-11 · Cited by 27 · see citing works

Complete Sequence of the New Lactococcal Abortive Phage Resistance Gene abiO

Prévots, F., & Ritzenthaler, P. (1998) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(98)75713-3 · Cited by 25 · see citing works

Complete Genome Sequence of Lactococcus lactis subsp. lactis KLDS4.0325

Yang, X., Wang, Y., & Huo, G. (2013) · Genome Announcements · doi:10.1128/genomea.00962-13 · Cited by 24 · see citing works

Sensitivity of capsular-producing Streptococcus thermophilus strains to bacteriophage adsorption

Rodríguez, M. C., der Meulen, R. V., Vaningelgem, F., de Valdez, G. F., Raya, R. R., Vuyst, L. D., & Mozzi, F. (2008) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2008.02341.x · Cited by 24 · see citing works

The Plasmid Complement of Lactococcus lactis UC509.9 Encodes Multiple Bacteriophage Resistance Systems

Ainsworth, S., Mahony, J., & van Sinderen, D. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.01070-14 · Cited by 23 · see citing works

Characterization of the LlaCI methyltransferase from Lactococcus lactis subsp. cremoris W15 provides new insights into the biology of type II restriction–modification systems

Mruk, I., Cichowicz-Cieślak, M., & Kaczorowski, T. (2003) · Microbiology · doi:10.1099/mic.0.26562-0 · Cited by 22 · see citing works

Application of RAPD analysis for identification of Lactococcus lactis subsp. cremoris strains isolated from artisanal cultures

Samaržija, D., Sikora, S., Redžepović, S., et al. (2002) · Microbiological Research · doi:10.1078/0944-5013-00126 · Cited by 21 · see citing works

Sequencing 16S rRNA gene fragments using the PacBio SMRT DNA sequencing systemPreprint

Schloss, P. D., Westcott, S. L., Jenior, M. L., & Highlander, S. K. (2015) · doi:10.7287/peerj.preprints.778v1 · Cited by 21 · see citing works

Application of PCR, rep-PCR and RAPD techniques for typing ofLactococcus lactis strains

Prodělalová, J., Španová, A., & Rittich, B. (2005) · Folia Microbiologica · doi:10.1007/bf02931464 · Cited by 20 · see citing works

Bioprospecting of strains of Streptococcus thermophilus from Indian fermented milk products for folate production

Iyer, R., Tomar, S. K., Mohanty, A. K., et al. (2011) · Dairy Science and Technology · doi:10.1007/s13594-011-0011-z · Cited by 15 · see citing works

Complete Genome Sequence of Lactococcus lactis Strain AI06, an Endophyte of the Amazonian Açaí Palm

McCulloch, J. A., de Oliveira, V. M., Pina, A. V. D. A., et al. (2014) · Genome Announcements · doi:10.1128/genomea.01225-14 · Cited by 15 · see citing works

Identification and characterization of Streptococcus thermophilus strains by pulsed‐field gel electrophoresis

Boutrou, R., Thuault, D., & Bourgeois, C. M. (1995) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1995.tb03161.x · Cited by 15 · see citing works

Characterization of closely related lactococcal starter strains which show differing patterns of bacteriophage sensitivity

Ward, L. J. H., Heap, H. A., & Kelly, W. J. (2003) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2003.02134.x · Cited by 15 · see citing works

A PCR fingerprinting technique to distinguish isolates ofLactococcus lactis

Urbach, E., Schindler, C. K., & Giovannoni, S. J. (1998) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1998.tb12986.x · Cited by 12 · see citing works

Highly efficient production of the staphylococcal nuclease reporter inLactobacillus bulgaricusgoverned by the promoter of thehlbAgene

Chouayekh, H., Serror, P., Boudebbouze, S., et al. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01522.x · Cited by 12 · see citing works

LldI, a Plasmid-Encoded Type I Restriction and Modification System inLactococcus Lactis

Deng, Y., Liu, C.-Q., & Dunn, N. W. (2000) · DNA sequence · doi:10.3109/10425170009033237 · Cited by 11 · see citing works

Development of a PCR-RFLP assay for the identification of Lactococcus lactis ssp. lactis and cremoris

Khemariya, P., Singh, S. K., Nath, G., & Gulati, A. K. (2012) · Annals of Microbiology · doi:10.1007/s13213-012-0451-6 · Cited by 3 · see citing works

Lactic Acid Bacteria in Raw-Milk Cheeses: From Starter Cultures to Probiotic Functions

Coelho, M. C., Malcata, F. X., & Silva, C. C. G. (2022) · Foods · doi:10.3390/foods11152276 · Cited by 276 · see citing works

Symposium review: interaction of starter cultures and nonstarter lactic acid bacteria in the cheese environment

Blaya, J., Barzideh, Z., & LaPointe, G. (2018) · Journal of Dairy Science · doi:10.3168/jds.2017-13345 · Cited by 200 · see citing works

Sequencing of the cheese microbiome and its relevance to industry

Yeluri Jonnala, B. R., McSweeney, P. L. H., Sheehan, J. J., & Cotter, P. D. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01020 · Cited by 160 · see citing works

Metagenomic analysis of the bacterial microbiome, resistome and virulome distinguishes Portuguese Serra da Estrela PDO cheeses from similar non-PDO cheeses: An exploratory approach

Salamandane, A., Leech, J., Almeida, R., Silva, C., Crispie, F., Cotter, P. D., Malfeito-Ferreira, M., & Brito, L. (2024) · Food Research International · doi:10.1016/j.foodres.2024.114556 · Cited by 20 · see citing works

Starter-making Experiment of Monascus Esterifying Strain 21-3

Yu-chong, Z. (2005) · Liquor-making Science & Technology

Development of the Formula for Natural Bread-making Starter

이종열, 이시경, 조남지, et al. (2003) · Journal of the Korean Society of Food Science and Nutrition · doi:10.3746/jkfn.2003.32.8.1245 · Cited by 11 · see citing works

천연제빵 발효 Starter의 개발

이종열, 이시경, 조남지, et al. (2003) · Journal of the Korean Society of Food Science and Nutrition · Cited by 11 · see citing works

Research on the Quality of Starter of Zhijiang Daqu Produced by Different Techniques

Xu, J. (2009) · Liquor-making Science & Technology

PRODUKSI BIOGAS PADA FERMENTASI EKSRETA AYAM BROILER MENGGUNAKAN STARTER BAKTERI FIBROLITIK KOLON DOMBA

Prasetyo, D. E. (2009)