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Abstract

A Gram-stain-positive, facultatively anaerobic and endospore-forming rod-shaped bacterium, designed strain CPB3-1, was isolated from tree bark. This homofermentative strain produced -lactic acid from glucose. It grew at 20–45 °C, pH 4.0–9.5 and in 0-3.0 % (w/v) NaCl. It contained -diaminopimelic acid in cell-wall peptidoglycan and had menaquinone with seven isoprene units (MK-7) as the predominant component. The major fatty acid was anteiso-C. The polar lipids were phosphatidylglycerol, diphosphatidylglycerol, an unknown phospholipid and an unknown lipid. Based on the results of 16S rRNA gene sequence analysis, strain CPB3-1 belonged to the genus and was closely related to DSM 11701 and BK117-1 (both 96.7 % similarity), NRIC 1133 and DSM 11697 (both 96.6 % similarity), and MK21-7, DSM 442, BK92 and GD201205 (all 95.8–96.5 % similarity). The draft genome of strain CPB3-1 contained 2 930 919 bps with 3117 coding genes. The DNA G+C content was 45.1 mol%. The digital DNA–DNA hybridization values between strain CPB3-1 and closely related type strains were 19.2–24.0 %. The average nucleotide identity (84.0–87.6 %) and average amino acid identity (66.5–76.3 %) values were lower than the cut-off values for species delineation. Strain CPB3-1 was clearly distinguished from related species based on its phenotypic and chemotaxonomic characteristics, 16S rRNA gene sequence similarity and the results of draft genome analysis. Therefore, the strain represents a novel species of the genus , for which the name sp. nov. is proposed. The type strain is CPB3-1 (=JCM 35082=TISTR 10004).

Funding
This study was supported by the:
  • the Grant of Faculty of Pharmaceutical Sciences, Chulalongkorn University (Award Phar2565-RG002)
    • Principle Award Recipient: SomboonTanasupawat
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2023-07-26
2025-03-23
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References

  1. Kitahara K, Suzuki J. Sporolactobacillus nov. subgen. J Gen Appl Microbiol 1963; 9:59–71 [View Article]
    [Google Scholar]
  2. Kitahara K, Lai C-L. On the spore formation of Sporolactobacillus inulinus. J Gen Appl Microbiol 1967; 13:197–203 [View Article]
    [Google Scholar]
  3. Chang YH, Stackebrandt E. The Family Sporolactobacillaceae. In DeLong EF, Lory S, Stackebrandt E, Thompson F. eds The Prokaryotes: Firmicutes and Tenericutes Heidelberg: Springer; 2014 pp 353–362 [View Article]
    [Google Scholar]
  4. De Vos P, Garrity GM, Jones D, Krieg NR, Ludwig W et al. Sporolactobacillus. In Ludwig W, Schleifer KH, Whitman WB. eds Bergey’s Manual of Systematic Bacteriology: The Firmicutes, 2nd ed. vol 3 New York: Springer; 2009 pp 386–391
    [Google Scholar]
  5. Yanagida F, Suzuki K-I, Kozaki M, Komagata K. Proposal of Sporolactobacillus nakayamae subsp. nakayamae sp. nov., subsp. nov., Sporolactobacillus nakayamae subsp. racemicus subsp. nov., Sporolactobacillus terrae sp. nov., Sporolactobacillus kofuensis sp. nov., and Sporolactobacillus lactosus sp. nov. Int J Syst Bacteriol 1997; 47:499–504 [View Article]
    [Google Scholar]
  6. Nakayama O, Yanoshi M. Spore-bearing lactic acid bacteria isolated from rhizosphere I. Taxonomic studies on Bacillus laevolacticus nov. sp. and Bacillus racemilacticus nov. sp. J Gen Appl Microbiol 1967; 13:139–153 [View Article]
    [Google Scholar]
  7. Andersch I, Pianka S, Fritze D, Claus D. Description of Bacillus laevolacticus (ex Nakayama and Yanoshi 1967) sp. nov., nom. rev. Int J Syst Bacteriol 1994; 44:659–664 [View Article]
    [Google Scholar]
  8. Hatayama K, Shoun H, Ueda Y, Nakamura A. Tuberibacillus calidus gen. nov., sp. nov., isolated from a compost pile and reclassification of Bacillus naganoensis Tomimura et al. 1990 as Pullulanibacillus naganoensis gen. nov., comb. nov. and Bacillus laevolacticus Andersch et al. 1994 as Sporolactobacillus laevolacticus comb. Nov. Int J Syst Evol Microbiol 2006; 56:2545–2551
    [Google Scholar]
  9. Chang Y-H, Jung MY, Park I-S, Oh H-M. Sporolactobacillus vineae sp. nov., a spore-forming lactic acid bacterium isolated from vineyard soil. Int J Syst Evol Microbiol 2008; 58:2316–2320 [View Article] [PubMed]
    [Google Scholar]
  10. Fujita R, Mochida K, Kato Y, Goto K. Sporolactobacillus putidus sp. nov., an endospore-forming lactic acid bacterium isolated from spoiled orange juice. Int J Syst Evol Microbiol 2010; 60:1499–1503 [View Article] [PubMed]
    [Google Scholar]
  11. Thamacharoensuk T, Kitahara M, Ohkuma M, Thongchul N, Tanasupawat S. Sporolactobacillus shoreae sp. nov. and Sporolactobacillus spathodeae sp. nov., two spore-forming lactic acid bacteria isolated from tree barks in Thailand. Int J Syst Evol Microbiol 2015; 65:1220–1226 [View Article] [PubMed]
    [Google Scholar]
  12. Lan QX, Chen J, Lin L, Ye XL, Yan QY et al. Sporolactobacillus pectinivorans sp. nov., an anaerobic bacterium isolated from spoiled jelly. Int J Syst Evol Microbiol 2016; 66:4323–4328 [View Article] [PubMed]
    [Google Scholar]
  13. Tolieng V, Prasirtsak B, Miyashita M, Shibata C, Tanaka N et al. Sporolactobacillus shoreicorticis sp. nov., a lactic acid-producing bacterium isolated from tree bark. Int J Syst Evol Microbiol 2017; 67:2363–2369 [View Article] [PubMed]
    [Google Scholar]
  14. Parte AC. LPSN - List of Prokaryotic names with Standing in Nomenclature (bacterio.net), 20 years on. Int J Syst Evol Microbiol 2018; 68:1825–1829 [View Article] [PubMed]
    [Google Scholar]
  15. Prasirtsak B, Tanasupawat S, Boonsombat R, Kodama K, Thongchul N. Characterization of lactic acid producing bacteria from Thai sources. J App Pharm Sci 2013; 3:33–38
    [Google Scholar]
  16. Lane D. 16S/23S rRNA sequencing. In Nucleic Acid Techniques in Bacterial Systematics Chichester: Wiley; 1991 pp 115–148
    [Google Scholar]
  17. Hall T. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. In Paper presented at the Nucleic Acids Symposium Series 1999
    [Google Scholar]
  18. Kim O-S, Cho Y-J, Lee K, Yoon S-H, Kim M et al. Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 2012; 62:716–721 [View Article] [PubMed]
    [Google Scholar]
  19. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T et al. The RAST server: rapid annotations using subsystems technology. BMC Genom 2008; 9:75 [View Article] [PubMed]
    [Google Scholar]
  20. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25:4876–4882 [View Article] [PubMed]
    [Google Scholar]
  21. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425 [View Article] [PubMed]
    [Google Scholar]
  22. Felsenstein J. Evolutionary trees from gene frequencies and quantitative characters: finding maximum likelihood estimates. Evolution 1981; 35:1229–1242 [View Article] [PubMed]
    [Google Scholar]
  23. Kluge AG, Farris JS. Quantitative phyletics and the evolution of anurans. Syst Biol 1969; 18:1–32 [View Article]
    [Google Scholar]
  24. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791 [View Article] [PubMed]
    [Google Scholar]
  25. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol Biol Evol 2018; 35:1547–1549 [View Article] [PubMed]
    [Google Scholar]
  26. Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980; 16:111–120 [View Article] [PubMed]
    [Google Scholar]
  27. Jones DT, Taylor WR, Thornton JM. The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci 1992; 8:275–282 [View Article] [PubMed]
    [Google Scholar]
  28. Alanjary M, Steinke K, Ziemert N. AutoMLST: an automated web server for generating multi-locus species trees highlighting natural product potential. Nucleic Acids Res 2019; 47:W276–W282 [View Article] [PubMed]
    [Google Scholar]
  29. Saito H, Miura KI. Preparation of transforming deoxyribonucleic acid by phenol treatment. Biochim Biophys Acta 1963; 72:619–629 [PubMed]
    [Google Scholar]
  30. Chen SF, Zhou YQ, Chen YR, Gu J. fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinform 2018; 34:i884–i890 [View Article] [PubMed]
    [Google Scholar]
  31. Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 2012; 19:455–477 [View Article] [PubMed]
    [Google Scholar]
  32. Richter M, Rosselló-Móra R, Oliver Glöckner F, Peplies J. JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinform 2016; 32:929–931 [View Article] [PubMed]
    [Google Scholar]
  33. Rodriguez-R LM, Konstantinidis KT. The enveomics collection: a toolbox for specialized analyses of microbial genomes and metagenomes. PeerJ Preprints 2016; 4:e1900v1 [View Article]
    [Google Scholar]
  34. Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinform 2013; 14:60 [View Article] [PubMed]
    [Google Scholar]
  35. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci 2009; 106:19126–19131 [View Article] [PubMed]
    [Google Scholar]
  36. Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P et al. DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 2007; 57:81–91 [View Article] [PubMed]
    [Google Scholar]
  37. Slepecky R, Foster JW. Alterations in metal content of spores of Bacillus megaterium and the effect on some spore properties. J Bacteriol 1959; 78:117–123 [View Article] [PubMed]
    [Google Scholar]
  38. Tanasupawat S, Okada S, Komagata K. Lactic acid bacteria found in fermented fish in Thailand. J Gen Appl Microbiol 1998; 44:193–200 [View Article] [PubMed]
    [Google Scholar]
  39. Tanasupawat S, Thongsanit J, Okada S, Komagata K. Lactic acid bacteria isolated from soy sauce mash in Thailand. J Gen Appl Microbiol 2002; 48:201–209 [View Article] [PubMed]
    [Google Scholar]
  40. Forbes L. Rapid flagella stain. J Clin Microbiol 1981; 13:807–809 [View Article] [PubMed]
    [Google Scholar]
  41. Sorokin DY. Is there a limit for high-pH life?. Int J Syst Evol Microbiol 2005; 55:1405–1406 [View Article] [PubMed]
    [Google Scholar]
  42. Hucker GC. Methods of Gram staining. N Y state Agric Exp Stn Tech Bull 1923; 93:
    [Google Scholar]
  43. Staneck JL, Roberts GD. Simplified approach to identification of aerobic actinomycetes by thin-layer chromatography. Appl Microbiol 1974; 28:226–231 [View Article] [PubMed]
    [Google Scholar]
  44. Collins MD, Pirouz T, Goodfellow M, Minnikin DE. Distribution of menaquinones in actinomycetes and corynebacteria. J Gen Microbiol 1977; 100:221–230 [View Article] [PubMed]
    [Google Scholar]
  45. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids. USFCC Newsl 1990; 20:1–6
    [Google Scholar]
  46. Minnikin DE, O’Donnell AG, Goodfellow M, Alderson G, Athalye M et al. An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J Microbiol Methods 1984; 2:233–241 [View Article]
    [Google Scholar]
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