1887

Abstract

Five aerobic, Gram-stain-negative, non-motile, non-spore-forming, short rod bacteria strains, designated as C3-1-R+6, C3-2-M9, B3-2-R-7, B3-2-R-21 and C3-2-M2, were isolated from shore soil of LungmuCo Lake in Tibet of China. The 16S rRNA gene sequence comparisons confirmed their affiliation to the genus of the family , and showed that they were most closely related to KACC 18788 with 94.26 % similarities. The average nucleotide identity (ANI), average amino acid identity (AAI) and digital DNA–DNA hybridization (dDDH) values between them and the validly published species were all below the thresholds for delineating species, supporting that they were novel species of genus . The ANI, AAI and dDDH values between strains C3-1-R+6 and KACC 18788 were 72, 75, and 18% respectively. Meanwhile, the ANI/AAI and dDDH values between these five isolates were higher than the threshold values, showing that they belonged to the same species of . According to genome comparison, the novel isolates have some special biosynthetic gene clusters of secondary metabolites including bacteriton, aryl-polyene, lantipeptide and t1pks, which were absent from their most related phylogenetic neighbours KACC 18788 and CGMCC 1.12195. The main polar lipids contained phosphatidylethanolamine, one unidentified phospholipid, one unidentified aminolipid, one unidentified glycolipid and five unidentified lipids. The predominant respiratory quinone was MK-7. The major cellular fatty acids were iso-C, summed feature 3 (C 7 and/or C 6) and iso-C 3-OH. The genome size of strain C3-1-R+6 was 5 984 948 bp, and its genomic DNA G+C content was 46.21 mol%. To sum up, the five strains were identified as a novel species of the genus , for which the name sp. nov. was proposed. The type strain was C3-1-R+6 (=CGMCC 1.19194=KCTC 92150).

Funding
This study was supported by the:
  • the Strategic Biological Resources Capacity Building Project of Chinese Academy of Sciences (Award KFJ-BRP-017-73)
    • Principle Award Recipient: Ai-HuaLi
  • the National Natural Science Foundation of China (Award 31970004)
    • Principle Award Recipient: Ai-HuaLi
  • This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.005784
2023-03-31
2024-04-28
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/73/3/ijsem005784.html?itemId=/content/journal/ijsem/10.1099/ijsem.0.005784&mimeType=html&fmt=ahah

References

  1. Kim MK, Na J-R, Cho DH, Soung N-K, Yang D-C. Parapedobacter koreensis gen. nov., sp. nov. Int J Syst Evol Microbiol 2007; 57:1336–1341 [View Article]
    [Google Scholar]
  2. Yang L, Wang Y-H, Zhu H-Z, Muhadesi J-B, Wang B-J et al. Parapedobacter defluvii sp. nov., isolated from the sewage treatment packing of a coking chemical plant. Int J Syst Evol Microbiol 2017; 67:4698–4703 [View Article] [PubMed]
    [Google Scholar]
  3. Liu L, Li L, Song Z, Wang S, Zhang J et al. Parapedobacter deserti sp. nov., an endophytic bacterium isolated from Haloxylon ammodendron stems. Int J Syst Evol Microbiol 2017; 67:2148–2152 [View Article] [PubMed]
    [Google Scholar]
  4. Kumar R, Dwivedi V, Nayyar N, Verma H, Singh AK et al. Parapedobacter indicus sp. nov., isolated from hexachlorocyclohexane-contaminated soil. Int J Syst Evol Microbiol 2015; 65:129–134 [View Article] [PubMed]
    [Google Scholar]
  5. Kim S-J, Weon H-Y, Kim Y-S, Yoo S-H, Kim B-Y et al. Parapedobacter luteus sp. nov. and Parapedobacter composti sp. nov., isolated from cotton waste compost. Int J Syst Evol Microbiol 2010; 60:1849–1853 [View Article] [PubMed]
    [Google Scholar]
  6. Kim JM, Lee SA, Cho H, Kim S-J, Joa J-H et al. Parapedobacter lycopersici sp. nov., isolated from the rhizosphere soil of tomato plants (Solanum lycopersicum L.). Int J Syst Evol Microbiol 2017; 67:3728–3732 [View Article] [PubMed]
    [Google Scholar]
  7. Zhao J-K, Li X-M, Zhang M-J, Jin J-H, Jiang C-Y et al. Parapedobacter pyrenivorans sp. nov., isolated from a pyrene-degrading microbial enrichment, and emended description of the genus Parapedobacter. Int J Syst Evol Microbiol 2013; 63:3994–3999 [View Article] [PubMed]
    [Google Scholar]
  8. Kim MK, Kim Y-A, Kim Y-J, Soung N-K, Yi T-H et al. Parapedobacter soli sp. nov., isolated from soil of a ginseng field. Int J Syst Evol Microbiol 2008; 58:337–340 [View Article] [PubMed]
    [Google Scholar]
  9. Karlson U, Dwyer DF, Hooper SW, Moore ER, Timmis KN et al. Two independently regulated cytochromes P-450 in a Rhodococcus rhodochrous strain that degrades 2-ethoxyphenol and 4-methoxybenzoate. J Bacteriol 1993; 175:1467–1474 [View Article] [PubMed]
    [Google Scholar]
  10. Lane DJ, Goodfellow M. 16S/23S rRNA sequencing. In Stack ebrandt E. eds Nucleic Acid Techniques in Bacterial Systematics Chichester:Wiley; 1991 pp 115–175
    [Google Scholar]
  11. 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] [PubMed]
    [Google Scholar]
  12. Hall TA. Bioedit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/nt. Nucleic Acids Res 1999; 41:95–98
    [Google Scholar]
  13. 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]
  14. 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]
  15. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  16. Fitch WM. Toward defining the course of evolution: minimum change for a specific tree topology. Systematic Zoology 1971; 20:406 [View Article]
    [Google Scholar]
  17. 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]
  18. Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 2015; 25:1043–1055 [View Article]
    [Google Scholar]
  19. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR et al. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 2018; 68:461–466 [View Article] [PubMed]
    [Google Scholar]
  20. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article] [PubMed]
    [Google Scholar]
  21. Overbeek R, Olson R, Pusch GD, Olsen GJ, Davis JJ et al. The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST). Nucleic Acids Res 2014; 42:D206–14 [View Article] [PubMed]
    [Google Scholar]
  22. Gerhardt P, Murray RGE, Wood WA, Krieg NR. Methods for General and Molecular Bacteriology Washington, DC, 791: ASM Press; 1994
    [Google Scholar]
  23. Cowan ST, Steel KJ. Manual for the Identifification of Medical Bacteria London: Cambridge University Press; 1965
    [Google Scholar]
  24. Miller LT. Single derivatization method for routine analysis of bacterial whole-cell fatty acid methyl esters, including hydroxy acids. J Clin Microbiol 1982; 16:584–586 [View Article] [PubMed]
    [Google Scholar]
  25. Sasser M. Identification of Bacteria by Gas Chromatographyof Cellular Fatty Acids, MIDI Technical Note 101 Newyork: DE: MIDI Inc; 1990
    [Google Scholar]
  26. 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]
  27. Kim M, Oh HS, Park SC, Chun J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes. Int J Syst Evol Microbiol 2014; 64:346–351 [View Article] [PubMed]
    [Google Scholar]
  28. Wayne LG. International committee on systematic bacteriology: announcement of the report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Zentralbl Bakteriol Mikrobiol Hyg A 1988; 268:433–434 [View Article]
    [Google Scholar]
  29. Schöner TA, Gassel S, Osawa A, Tobias NJ, Okuno Y et al. Aryl polyenes, a highly abundant class of bacterial natural products, are functionally related to antioxidative carotenoids. Chembiochem 2016; 17:247–253 [View Article]
    [Google Scholar]
  30. Johnston I, Osborn LJ, Markley RL, McManus EA, Kadam A et al. Identification of essential genes for Escherichia coli aryl polyene biosynthesis and function in biofilm formation. NPJ Biofilms Microbiomes 2021; 7:56 [View Article] [PubMed]
    [Google Scholar]
  31. Wang H, van der Donk WA. Biosynthesis of the class III lantipeptide catenulipeptin. ACS Chem Biol 2012; 7:1529–1535 [View Article] [PubMed]
    [Google Scholar]
  32. Chen J, van Heel AJ, Kuipers OP. Visualization and analysis of the dynamic assembly of a heterologous lantibiotic biosynthesis complex in Bacillus subtilis. mBio 2021; 12:e0121921 [View Article]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.005784
Loading
/content/journal/ijsem/10.1099/ijsem.0.005784
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