Comparative genomics of Lactobacillus
Summary The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillu...
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Published in | Microbial biotechnology Vol. 4; no. 3; pp. 323 - 332 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.05.2011
John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
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Abstract | Summary
The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillus strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154 Lactobacillus species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various Lactobacillus strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The Lactobacillus pan genome was found to consist of approximately 14 000 protein‐encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the Lactobacillus core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other Lactobacillus genomes, and Group‐specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new Lactobacillus genomes. |
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AbstractList | The genus
Lactobacillus
includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several
Lactobacillus
strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154
Lactobacillus
species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various
Lactobacillus
strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The
Lactobacillus
pan genome was found to consist of approximately 14 000 protein‐encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the
Lactobacillus
core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other
Lactobacillus
genomes, and Group‐specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new
Lactobacillus
genomes. The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillus strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154 Lactobacillus species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various Lactobacillus strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The Lactobacillus pan genome was found to consist of approximately 14 000 protein-encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the Lactobacillus core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other Lactobacillus genomes, and Group-specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new Lactobacillus genomes.The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillus strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154 Lactobacillus species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various Lactobacillus strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The Lactobacillus pan genome was found to consist of approximately 14 000 protein-encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the Lactobacillus core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other Lactobacillus genomes, and Group-specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new Lactobacillus genomes. The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillus strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154 Lactobacillus species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various Lactobacillus strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The Lactobacillus pan genome was found to consist of approximately 14 000 protein-encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the Lactobacillus core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other Lactobacillus genomes, and Group-specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new Lactobacillus genomes. Summary The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In addition, various lactobacilli are natural inhabitants of the intestinal tract of humans and other animals. Finally, several Lactobacillus strains are marketed as probiotics as their consumption can confer a health benefit to host. Presently, 154 Lactobacillus species are known and a growing fraction of these are subject to draft genome sequencing. However, complete genome sequences are needed to provide a platform for detailed genomic comparisons. Therefore, we selected a total of 20 genomes of various Lactobacillus strains for which complete genomic sequences have been reported. These genomes had sizes varying from 1.8 to 3.3 Mb and other characteristic features, such as G+C content that ranged from 33% to 51%. The Lactobacillus pan genome was found to consist of approximately 14 000 protein‐encoding genes while all 20 genomes shared a total of 383 sets of orthologous genes that defined the Lactobacillus core genome (LCG). Based on advanced phylogeny of the proteins encoded by this LCG, we grouped the 20 strains into three main groups and defined core group genes present in all genomes of a single group, signature group genes shared in all genomes of one group but absent in all other Lactobacillus genomes, and Group‐specific ORFans present in core group genes of one group and absent in all other complete genomes. The latter are of specific value in defining the different groups of genomes. The study provides a platform for present individual comparisons as well as future analysis of new Lactobacillus genomes. |
Author | Blom, Jochen Palva, Airi Siezen, Roland J. de Vos, Willem M. Kant, Ravi |
AuthorAffiliation | 4 Netherlands Bioinformatics Centre, Center for Molecular and Biomolecular Informatics, Radboud University Medical Centre, Nijmegen, The Netherlands 6 Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands 2 Computational Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany 5 TI Food and Nutrition, Kluyver Centre for Genomics of Industrial Fermentation, Wageningen, The Netherlands 1 Veterinary Microbiology and Epidemiology, Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland 3 NIZO food research, Ede, The Netherlands |
AuthorAffiliation_xml | – name: 4 Netherlands Bioinformatics Centre, Center for Molecular and Biomolecular Informatics, Radboud University Medical Centre, Nijmegen, The Netherlands – name: 6 Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands – name: 3 NIZO food research, Ede, The Netherlands – name: 5 TI Food and Nutrition, Kluyver Centre for Genomics of Industrial Fermentation, Wageningen, The Netherlands – name: 1 Veterinary Microbiology and Epidemiology, Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland – name: 2 Computational Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany |
Author_xml | – sequence: 1 givenname: Ravi surname: Kant fullname: Kant, Ravi email: ravi.kant@helsinki.fi organization: Veterinary Microbiology and Epidemiology, Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland – sequence: 2 givenname: Jochen surname: Blom fullname: Blom, Jochen organization: Computational Genomics, Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany – sequence: 3 givenname: Airi surname: Palva fullname: Palva, Airi organization: Veterinary Microbiology and Epidemiology, Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland – sequence: 4 givenname: Roland J. surname: Siezen fullname: Siezen, Roland J. organization: NIZO food research, Ede, The Netherlands – sequence: 5 givenname: Willem M. surname: de Vos fullname: de Vos, Willem M. organization: Veterinary Microbiology and Epidemiology, Department of Veterinary Biosciences, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21375712$$D View this record in MEDLINE/PubMed |
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Copyright | 2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd 2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd. Copyright John Wiley & Sons, Inc. May 2011 Copyright © 2010 The Authors. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd 2010 |
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References | Kleerebezem, M., Boekhorst, J., van Kranenburg, R., Molenaar, D., Kuipers, O.P., Leer, R., et al. (2003) Complete genome sequence of Lactobacillus plantarum WCFS1. Proc Natl Acad Sci USA 100: 1990-1995. Zhang, Z.Y., Liu, C., Zhu, Y.Z., Zhong, Y., Zhu, Y.Q., Zheng, H.J., et al. (2009) Complete genome sequence of Lactobacillus plantarum JDM1. J Bacteriol 15: 5020-5021. Zhou, M., Boekhorst, J., Francke, C., and Siezen, R.J. (2008) LocateP: genome-scale subcellular-location predictor for bacterial proteins. BMC Bioinformatics 9: 173. Callanan, M., Kaleta, P., O'Callaghan, J., O'Sullivan, O., Jordan, K., McAuliffe, O., et al. (2008) Genome sequence of Lactobacillus helveticus, an organism distinguished by selective gene loss and insertion sequence element expansion. J Bacteriol 2: 727-735. De Vos, W.M. (2005) Lipotechoic acid in lactobacilli: d-alanine makes the difference. Proc Natl Acad Sci USA 102: 10763-10764. O'Sullivan, O., O'Callaghan, J., Sangrador-Vegas, A., McAuliffe, O., Slattery, L., Kaleta, P., et al. (2009) Comparative genomics of lactic acid bacteria reveals a niche-specific gene set. BMC Microbiol 9: 50. Wegmann, U., Overweg, K., Horn, N., Goesmann, A., Narbad, A., Gasson, M.J., and Shearman, C. (2009) Complete genome sequence of Lactobacillus johnsonii FI9785, a competitive exclusion agent against pathogens in poultry. J Bacteriol 22: 7142-7143. Edgar, R.C. (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792. Emanuelsson, O., Brunak, S., von Heijne, G., and Nielsen, H. (2007) Locating proteins in the cell using TargetP, SignalP, and related tools. Nat Protoc 2: 953-971. Altermann, E., Russell, W.M., Azcarate-Peril, M.A., Barrangou, R., Buck, B.L., McAuliffe, O., et al. (2005) Complete genome sequence of the probiotic lactic acid bacterium Lactobacillus acidophilus NCFM. Proc Natl Acad Sci USA 102: 3906-3912. Marco, M.L., de Vries, M.C., Wels, M., Molenaar, D., Mangell, P., Ahrne, S., et al. (2010) Convergence in probiotic Lactobacillus gut-adaptive responses in humans and mice. ISME J (in press): doi:10.1038/ismej.2010.61. Schick, J., Weber, B., Klein, J.R., and Henrich, B. (1999) PepR1, a CcpA-like transcription regulator of Lactobacillus delbrueckii subsp. lactis. Microbiology 145: 3147-3154. Chaillou, S., Champomier-Vergès, M.C., Cornet, M., Crutz-Le Coq, A.M., Dudez, A.M., Martin, V., et al. (2005) The complete genome sequence of the meat-borne lactic acid bacterium Lactobacillus sakei 23K. Nat Biotechnol 12: 1527-1533. Saxelin, M., Tynkkynen, S., Mattila-Sandholm, T., and de Vos, W.M. (2005) Probiotic and other functional microbes: from markets to mechanisms. Curr Opin Biotechnol 16: 204-211. de Vos, W.M., and Hugenholtz, J. (2004) Engineering metabolic highways in Lactococci and other lactic acid bacteria. Trends Biotechnol 22: 72-79. Fujisawa, T., Benno, Y., Yaeshima, T., and Mitsuoka, T. (1992) Taxonomic study of the Lactobacillus acidophilus group, with recognition of Lactobacillus gallinarum sp. nov. and Lactobacillus johnsonii sp. nov. and synonymy of Lactobacillus acidophilus group A3 (Johnson et al. 1980) with the type strain of Lactobacillus amylovorus (Nakamura 1981). Int J Syst Bacteriol 42: 487-491. Morel, F., Frot-Coutaz, J., Aubel, D., Portalier, R., and Atlan, D. (1990) Characterization of a prolidase from Lactobacillus delbrueckii subsp. bulgaricus CNRZ 397 with an unusual regulation of biosynthesis. Microbiology 145: 437-446. Molenaar, D., Bringel, F., Schuren, F.H., de Vos, W.M., Siezen, R.J., and Kleerebezem, M. (2005) Exploring Lactobacillus plantarum genome diversity by using microarrays. J Bacteriol 187: 6119-6127. Ojala, T., Kuparinen, V., Koskinen, J.P., Alatalo, E., Holm, L., Auvinen, P., et al. (2010) Genome sequence of Lactobacillus crispatus ST1. J Bacteriol 13: 3547-3548. Felsenstein, J. (1995) PHYLIP (Phylogeny Inference Package). Version 3.57 c. Seattle, WA, USA: Department of Genetics, University of Washington. Brooijmans, R.J., de Vos, W.M., and Hugenholtz, J. (2009) Lactobacillus plantarum WCFS1 electron transport chains. Appl Environ Microbiol 11: 3580-3585. De Keersmaecker, S.C., Verhoeven, T.L., Desair, J., Marchal, K., Vanderleyden, J., and Nagy, I. (2006) Strong antimicrobial activity of Lactobacillus rhamnosus GG against Salmonella typhimurium is due to accumulation of lactic acid. FEMS Microbiol Lett 259: 89-96. Zdobnov, E.M., and Bork, P. (2007) Quantification of insect genome divergence. Trends Genet 23: 16-20. Mazé, A., Boël, G., Zúñiga, M., Bourand, A., Loux, V., Yebra, M.J., et al. (2010) Complete genome sequence of the probiotic Lactobacillus casei strain BL23. J Bacteriol 10: 2647-2648. Pridmore, R.D., Berger, B., Desiere, F., Vilanova, D., Barretto, C., Pittet, A.C., et al. 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References_xml | – reference: Korithoski, B., Lévesque, C.M., and Cvitkovitch, D.G. (2007) Involvement of the detoxifying enzyme lactoylglutathione lyase in Streptococcus mutans aciduricity. J Bacteriol 189: 7586-7592. – reference: Brooijmans, R.J., de Vos, W.M., and Hugenholtz, J. (2009) Lactobacillus plantarum WCFS1 electron transport chains. Appl Environ Microbiol 11: 3580-3585. – reference: Canchaya, C., Claesson, M.J., Fitzgerald, G.F., van Sinderen, D., and O'Toole, P.W. (2006) Diversity of the genus Lactobacillus revealed by comparative genomics of five species. Microbiology 152: 3185-3196. – reference: de Vos, W.M., and Hugenholtz, J. (2004) Engineering metabolic highways in Lactococci and other lactic acid bacteria. Trends Biotechnol 22: 72-79. – reference: Wegmann, U., Overweg, K., Horn, N., Goesmann, A., Narbad, A., Gasson, M.J., and Shearman, C. (2009) Complete genome sequence of Lactobacillus johnsonii FI9785, a competitive exclusion agent against pathogens in poultry. J Bacteriol 22: 7142-7143. – reference: Chaillou, S., Champomier-Vergès, M.C., Cornet, M., Crutz-Le Coq, A.M., Dudez, A.M., Martin, V., et al. (2005) The complete genome sequence of the meat-borne lactic acid bacterium Lactobacillus sakei 23K. Nat Biotechnol 12: 1527-1533. – reference: Hugenholtz, P. (1998) The Genera of Lactic Acid Bacteria. London, UK: Blackie Academic & Professional. – reference: Pridmore, R.D., Berger, B., Desiere, F., Vilanova, D., Barretto, C., Pittet, A.C., et al. (2004) The genome sequence of the probiotic intestinal bacterium Lactobacillus johnsonii NCC 533. Proc Natl Acad Sci USA 101: 2512-2517. – reference: Zdobnov, E.M., and Bork, P. (2007) Quantification of insect genome divergence. Trends Genet 23: 16-20. – reference: De Keersmaecker, S.C., Verhoeven, T.L., Desair, J., Marchal, K., Vanderleyden, J., and Nagy, I. (2006) Strong antimicrobial activity of Lactobacillus rhamnosus GG against Salmonella typhimurium is due to accumulation of lactic acid. FEMS Microbiol Lett 259: 89-96. – reference: Nelson, K.E., Weinstock, G.M., Highlander, S.K., Worley, K.C., Creasy, H.H., Wortman, J.R., et al., Human Microbiome Jumpstart Reference Strains Consortium (2010) A catalog of reference genomes from the human microbiome. Science 5981: 994-999. – reference: Altermann, E., Russell, W.M., Azcarate-Peril, M.A., Barrangou, R., Buck, B.L., McAuliffe, O., et al. (2005) Complete genome sequence of the probiotic lactic acid bacterium Lactobacillus acidophilus NCFM. Proc Natl Acad Sci USA 102: 3906-3912. – reference: O'Sullivan, O., O'Callaghan, J., Sangrador-Vegas, A., McAuliffe, O., Slattery, L., Kaleta, P., et al. (2009) Comparative genomics of lactic acid bacteria reveals a niche-specific gene set. BMC Microbiol 9: 50. – reference: Claesson, M.J., van Sinderen, D., and O'Toole, P.W. (2007) The genus Lactobacillus - a genomic basis for understanding its diversity. FEMS Microbiol Lett 1: 22-28. – reference: Blom, J., Albaum, S.P., Doppmeier, D., Puhler, A., Vorholter, F.J., Zakrzewski, M., and Goesmann, A. (2009) EDGAR: a software framework for the comparative analysis of prokaryotic genomes. BMC Bioinformatics 10: 154. – reference: Edgar, R.C. (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792. – reference: Marco, M.L., de Vries, M.C., Wels, M., Molenaar, D., Mangell, P., Ahrne, S., et al. (2010) Convergence in probiotic Lactobacillus gut-adaptive responses in humans and mice. ISME J (in press): doi:10.1038/ismej.2010.61. – reference: Bron, P.A., Grangette, C., Mercenier, A., de Vos, W.M., and Kleerebezem, M. (2004) Identification of Lactobacillus plantarum genes that are induced in the gastrointestinal tract of mice. J Bacteriol 17: 5721-5729. – reference: Claesson, M.J., van Sinderen, D., and O'Toole, P.W. (2008) Lactobacillus phylogenomics -towards a reclassification of the genus. Int J Syst Evol Microbiol 58: 2945-2954. – reference: De-Vries, M.C., Vaughan, E.E., Kleerebezem, M., and de Vos, W.M. (2006) Lactobacillus plantarum - survival, functional and potential probiotic properties in the human intestinal tract. Int Dairy J 16: 1018-1028. – reference: Kleerebezem, M., Hols, P., Bernard, E., Rolain, T., Zhou, M., Siezen, R.J., and Bron, P. (2010) The extracellular biology of the lactobacilli. FEMS Microbiol Rev 34: 199-230. – reference: Mazé, A., Boël, G., Zúñiga, M., Bourand, A., Loux, V., Yebra, M.J., et al. (2010) Complete genome sequence of the probiotic Lactobacillus casei strain BL23. J Bacteriol 10: 2647-2648. – reference: Wood, B.J.B., and Warner, P.J. (2003) Genetics of Lactic Acid Bacteria. New York, USA: Kluwer Academic/Plenum Publishers. – reference: Ojala, T., Kuparinen, V., Koskinen, J.P., Alatalo, E., Holm, L., Auvinen, P., et al. (2010) Genome sequence of Lactobacillus crispatus ST1. J Bacteriol 13: 3547-3548. – reference: Talavera, G., and Castresana, J. (2007) Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst Biol 56: 564-577. – reference: Felsenstein, J. (1995) PHYLIP (Phylogeny Inference Package). Version 3.57 c. Seattle, WA, USA: Department of Genetics, University of Washington. – reference: Fujisawa, T., Benno, Y., Yaeshima, T., and Mitsuoka, T. (1992) Taxonomic study of the Lactobacillus acidophilus group, with recognition of Lactobacillus gallinarum sp. nov. and Lactobacillus johnsonii sp. nov. and synonymy of Lactobacillus acidophilus group A3 (Johnson et al. 1980) with the type strain of Lactobacillus amylovorus (Nakamura 1981). Int J Syst Bacteriol 42: 487-491. – reference: Makarova, K., Slesarev, A., Wolf, Y., Sorokin, A., Mirkin, B., Koonin, E., et al. (2006) Comparative genomics of the lactic acid bacteria. Proc Natl Acad Sci USA 103: 15611-15616. – reference: Schick, J., Weber, B., Klein, J.R., and Henrich, B. (1999) PepR1, a CcpA-like transcription regulator of Lactobacillus delbrueckii subsp. lactis. Microbiology 145: 3147-3154. – reference: Emanuelsson, O., Brunak, S., von Heijne, G., and Nielsen, H. (2007) Locating proteins in the cell using TargetP, SignalP, and related tools. Nat Protoc 2: 953-971. – reference: Boekhorst, J., de Been, M.W., Kleerebezem, M., and Siezen, R.J. (2005) Genome-wide detection and analysis of cell wall-bound proteins with LPxTG-like sorting motifs. J Bacteriol 14: 4928-4934. – reference: Morita, H., Toh, H., Fukuda, S., Horikawa, H., Oshima, K., Suzuki, T., et al. (2008) Comparative genome analysis of Lactobacillus reuteri and Lactobacillus fermentum reveal a genomic island for reuterin and cobalamin production. DNA Res 3: 151-161. – reference: Lerat, E., Daubin, V., and Moran, N.A. (2003) From gene trees to organismal phylogeny in prokaryotes: the case of the gamma-proteobacteria. PLoS Biol 1: E19. – reference: Molenaar, D., Bringel, F., Schuren, F.H., de Vos, W.M., Siezen, R.J., and Kleerebezem, M. (2005) Exploring Lactobacillus plantarum genome diversity by using microarrays. J Bacteriol 187: 6119-6127. – reference: De Vos, W.M. (2005) Lipotechoic acid in lactobacilli: d-alanine makes the difference. Proc Natl Acad Sci USA 102: 10763-10764. – reference: Zhang, Z.Y., Liu, C., Zhu, Y.Z., Zhong, Y., Zhu, Y.Q., Zheng, H.J., et al. (2009) Complete genome sequence of Lactobacillus plantarum JDM1. J Bacteriol 15: 5020-5021. – reference: Callanan, M., Kaleta, P., O'Callaghan, J., O'Sullivan, O., Jordan, K., McAuliffe, O., et al. (2008) Genome sequence of Lactobacillus helveticus, an organism distinguished by selective gene loss and insertion sequence element expansion. J Bacteriol 2: 727-735. – reference: Saxelin, M., Tynkkynen, S., Mattila-Sandholm, T., and de Vos, W.M. (2005) Probiotic and other functional microbes: from markets to mechanisms. Curr Opin Biotechnol 16: 204-211. – reference: Azcarate-Peril, M.A., Altermann, E., Goh, Y.J., Tallon, R., Sanozky-Dawes, R.B., Pfeiler, E.A., et al. (2008) Analysis of the genome sequence of Lactobacillus gasseri ATCC 33323 reveals the molecular basis of an autochthonous intestinal organism. Appl Environ Microbiol 15: 4610-4625. – reference: Altschul, S.F., Madden, T.L., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W., and Lipman, D.J. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389. – reference: van de Guchte, M., Penaud, S., Grimaldi, C., Barbe, V., Bryson, K., Nicolas, P., et al. (2006) The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution. 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The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk.... The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In... The genus Lactobacillus includes a diverse group of bacteria consisting of many species that are associated with fermentations of plants, meat or milk. In... |
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SubjectTerms | Acids Animals Bacteria Bacterial Proteins - genetics Base Composition Cattle Chickens Dairy Products - microbiology Feces - microbiology Fermentation Gene sequencing Genes Genome Size Genome, Bacterial Genomes Genomics Humans Intestine Intestines - microbiology Lactobacilli Lactobacillus Lactobacillus - classification Lactobacillus - genetics Lactobacillus - isolation & purification Meat Metabolism Milk Molecular Sequence Data Open Reading Frames Peptides Phylogenetics Phylogeny Probiotics Proteins Strains (organisms) Taxonomy Yogurt |
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Title | Comparative genomics of Lactobacillus |
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