1887

Abstract

An aerobic, Gram-staining-positive, endospore-forming bacterium, isolated from the rhizosphere of roots of maize (), was taxonomically studied. On the basis of 16S rRNA gene sequence similarity comparisons, strain JJ-125 clustered together with species of the genus and showed the highest similarities with (98.7 %). The 16S rRNA gene sequence similarities to the sequences of the type strains of other species of the genus were <98.4 %. The genome sequence of JJ-125 was 4 516 360 bp long and had a DNA G+C content of 37.3 %. A DNA–DNA hybridization with the type strain of DSM 23010 resulted in values of 42.3 and 43.9 % (reciprocal). The average nucleotide identity, average amino acid identity and digital DNA–DNA hybridization values between the JJ-125 genome assembly and those of the other type strains of species of the genus were <75%, <80 % and <21 %, respectively. Chemotaxonomic features supported the grouping of the strain with the genus e.g. the major fatty acids included iso-C iso-C ω10 and iso-C, the polar lipid profile contained the major components diphosphatidylglycerol, phosphatidylglycerol and phosphatidylethanolamine, the only quinone was menaquinone MK-7 and the characteristic diamino acid was -diaminopimelic acid. Physiological and biochemical test results were also different from those of the most closely related species. As a consequence, JJ-125 represents a novel species of the genus , for which we propose the name sp. nov., with JJ-125 (= CIP 111883 = LMG 32156 = CCM 9046) as the type strain.

Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.005590
2022-10-11
2024-04-25
Loading full text...

Full text loading...

References

  1. Gupta RS, Patel S, Saini N, Chen S. Robust demarcation of 17 distinct Bacillus species clades, proposed as novel Bacillaceae genera, by phylogenomics and comparative genomic analyses: description of Robertmurraya kyonggiensis sp. nov. and proposal for an emended genus Bacillus limiting it only to the members of the Subtilis and Cereus clades of species. Int J Syst Evol Microbiol 2020; 70:5753–5798 [View Article]
    [Google Scholar]
  2. Sultanpuram VR, Mothe T, Chintalapati S, Chintalapati VR. Bacillus catenulatus sp. nov., an alkalitolerant bacterium isolated from a soda lake. Arch Microbiol 2017; 199:1391–1397 [View Article]
    [Google Scholar]
  3. Spanka R, Fritze D. Bacillus cohnii sp. nov., a new, obligately alkaliphilic, oval-spore-forming Bacillus species with ornithine and aspartic acid instead of diaminopimelic acid in the cell wall. Int J Syst Bacteriol 1993; 43:150–156 [View Article]
    [Google Scholar]
  4. Nielsen P, Fritze D, Priest FG. Phenetic diversity of alkaliphilic Bacillus strains: proposal for nine new species. Microbiology 1995; 141:1745–1761 [View Article]
    [Google Scholar]
  5. Bae P, Zhang S, Chen Y, Ping W, Pang H et al. Sutcliffiella deserti sp. nov., isolated from desert soil. Int J Syst Evol Microbiol 2022; 72005259:
    [Google Scholar]
  6. Chen Y-G, Hu S-P, Tang S-K, He J-W, Xiao J-Q et al. Bacillus zhanjiangensis sp. nov., isolated from an oyster in South China Sea. Antonie Van Leeuwenhoek 2011; 99:473–480 [View Article]
    [Google Scholar]
  7. Lane DJ. 16S/23S rRNA sequencing. In Stackebrandt E, Goodfellow M. eds Nucleic Acid Techniques in Bacterial Systematics London: Wiley; 1990 pp 115–175
    [Google Scholar]
  8. Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A 1977; 74:5463–5467 [View Article]
    [Google Scholar]
  9. Coloqhoun JA. Discovery of deep-sea actinomycetes. PhD dissertation Canterbury, UK: Research school of biosciences, university of Kent; 1997
    [Google Scholar]
  10. Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article]
    [Google Scholar]
  11. Brosius J, Palmer ML, Kennedy PJ, Noller HF. Complete nucleotide sequence of a 16S ribosomal RNA gene from Escherichia coli. Proc Natl Acad Sci U S A 1978; 75:4801–4805 [View Article]
    [Google Scholar]
  12. Yoon S-H, Ha S-M, Kwon S, Lim J, Kim Y et al. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 2017; 67:1613–1617 [View Article]
    [Google Scholar]
  13. Ludwig W, Viver T, Westram R, Francisco Gago J, Bustos-Caparros E et al. Release LTP_12_2020, featuring a new ARB alignment and improved 16S rRNA tree for prokaryotic type strains. Syst Appl Microbiol 2021; 44:126218 [View Article] [PubMed]
    [Google Scholar]
  14. Yarza P, Richter M, Peplies J, Euzeby J, Amann R et al. The all-species living tree project: a 16S rRNA-based phylogenetic tree of all sequenced type strains. Syst Appl Microbiol 2008; 31:241–250 [View Article]
    [Google Scholar]
  15. Ludwig W, Strunk O, Westram R, Richter L, Meier H et al. ARB: a software environment for sequence data. Nucleic Acids Res 2004; 32:1363–1371 [View Article]
    [Google Scholar]
  16. Stamatakis A. RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 2006; 22:2688–2690 [View Article] [PubMed]
    [Google Scholar]
  17. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791 [View Article]
    [Google Scholar]
  18. Cherif-Silini H, Thissera B, Bouket AC, Saadaoui N, Silini A et al. Durum wheat stress tolerance induced by endophyte Pantoea agglomerans with genes contributing to plant functions and secondary metabolite arsenal. Int J Mol Sci 2019; 20:3989 [View Article]
    [Google Scholar]
  19. Blin K, Shaw S, Kloosterman AM, Charlop-Powers Z, van Wezel GP et al. antiSMASH 6.0: improving cluster detection and comparison capabilities. Nucleic Acids Res 2021; 49:W29–W35 [View Article] [PubMed]
    [Google Scholar]
  20. Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol 2013; 30:772–780 [View Article] [PubMed]
    [Google Scholar]
  21. Katoh K, Standley DM. A simple method to control over-alignment in the MAFFT multiple sequence alignment program. Bioinformatics 2016; 32:1933–1942 [View Article]
    [Google Scholar]
  22. Criscuolo A, Gribaldo S. BMGE (block mapping and gathering with entropy): a new software for selection of phylogenetic informative regions from multiple sequence alignments. BMC Evol Biol 2010; 10:210 [View Article]
    [Google Scholar]
  23. Minh BQ, Schmidt HA, Chernomor O, Schrempf D, Woodhams MD et al. IQ-TREE 2: new models and efficient methods for phylogenetic inference in the genomic era. Mol Biol Evol 2020; 37:1530–1534 [View Article]
    [Google Scholar]
  24. Ziemke F, Höfle MG, Lalucat J, Rosselló-Mora R. Reclassification of Shewanella putrefaciens Owen’s genomic group II as Shewanella baltica sp. nov. Int J Syst Bacteriol 1998; 48 Pt 1:179–186 [View Article]
    [Google Scholar]
  25. Gerhardt P, Murray RGE, Wood WA, Krieg NR. Methods for general and molecular bacteriology Washington, DC: American society for microbiology; 1994
    [Google Scholar]
  26. Kämpfer P, Steiof M, Dott W. Microbiological characterization of a fuel-oil contaminated site including numerical identification of heterotrophic water and soil bacteria. Microb Ecol 1991; 21:227–251 [View Article]
    [Google Scholar]
  27. Kämpfer P. Evaluation of the titertek-enterobac-automated system (TTE-AS) for identification of members of the family Enterobacteriaceae. Zentralbl Bakteriol 1990; 273:164–172 [View Article]
    [Google Scholar]
  28. Smibert RM, Krieg NR. Phenotypic characterization. In Gerhardt P, Murray RGE, Wood WA, Krieg NR. eds In Methods for General and Molecular Bacteriology Washington, DC: American Society for Microbiology; 1994 pp 607–654
    [Google Scholar]
  29. Kämpfer P, Kroppenstedt RM. Numerical analysis of fatty acid patterns of coryneform bacteria and related taxa. Can J Microbiol 1990; 42:989–1005 [View Article]
    [Google Scholar]
  30. 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]
  31. Wiertz R, Schulz SC, Müller U, Kämpfer P, Lipski A. Corynebacterium frankenforstense sp. nov. and Corynebacterium lactis sp. nov., isolated from raw cow milk. Int J Syst Evol Microbiol 2013; 63:4495–4501 [View Article]
    [Google Scholar]
  32. Schumann P. Peptidoglycan structure. In Rainey F, Oren A. eds In Taxonomy of Prokaryotes, Methods in Microbiology vol 38 London: Academic Press; 2011 pp 101–129
    [Google Scholar]
  33. Jiang Z, Zhang D-F, Khieu T-N, Son CK, Zhang X-M et al. Bacillus tianshenii sp. nov., isolated from a marine sediment sample. Int J Syst Evol Microbiol 2014; 64:1998–2002 [View Article]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.005590
Loading
/content/journal/ijsem/10.1099/ijsem.0.005590
Loading

Data & Media loading...

Supplements

Supplementary material 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error