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Abstract

An actinobacterial strain designated MMS20-HV4-12, displaying a high hydrolytic potential for various substrates, was isolated from a riverside soil sample and characterized by polyphasic taxonomic analysis. Growth occurred at 10–37 °C (optimum, 30°C), with NaCl concentrations of 0–4 % (optimum, 0 %) and at pH 7–9 (optimum, pH 8). MMS20-HV4-12 was catalase-positive, oxidase-negative, rod-shaped and formed creamy white-coloured colonies. Based on the results of 16S rRNA gene sequence analysis, MMS20-HV4-12 was found to be mostly related to the type strains of (98.3 % sequence similarity), (98.1 %) and (98.0 %). MMS20-HV4-12 showed optimal growth on Reaoner's 2A agar, forming white-coloured colonies. The diagnostic polar lipid profile consisted of diphosphatidylglycerol, phosphatidylglycerol and phosphatidylinositol, the major fatty acids were iso-C, C ω8 and 10-methyl-C, the major isoprenoid quinone was MK-8(H), the diagnostic cell-wall sugar was galactose, and the cell-wall diamino acid was -diaminopimelic acid. The genome of MMS20-HV4-12 was 4.47 Mbp in size with a G+C content of 72.9 mol%. The genome based analysis indicated low relatedness between MMS20-HV4-12 and all compared species of , as the highest digital DNA–DNA hybridization and the orthologous average nucleotide identity values were 26.8 and 83.8% respectively. Based on genotypic, phenotypic and phylogenomic characterization, MMS20-HV4-12 evidently represents a novel species of genus , for which the name sp. nov. (type strain=MMS20-HV4-12=KCTC 49651=LMG 32360) is proposed.

Funding
This study was supported by the:
  • National Research Foundation of Korea (Award 2020R1F1A1076440)
    • Principle Award Recipient: SeungBum Kim
  • National Institute of Biological Resources
    • Principle Award Recipient: SeungBum Kim
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2023-03-20
2024-04-28
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References

  1. Anandan R, Dharumadurai D, Manogaran GP. An Introduction to Actinobacteria. In Dhanasekaran D. eds Actinobacteria - Basics and Biotechnological Applications Intechopen; 2016 pp 3–37
    [Google Scholar]
  2. Ikunaga Y, Sato I, Grond S, Numaziri N, Yoshida S et al. Nocardioides sp. strain WSN05-2, isolated from a wheat field, degrades deoxynivalenol, producing the novel intermediate 3-epi-deoxynivalenol. Appl Microbiol Biotechnol 2011; 89:419–427 [View Article]
    [Google Scholar]
  3. Yoon JH, Park YH. The genus Nocardioides. In Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrandt E. eds The Prokaryotes vol 3 Archaea. Bacteria: Firmicutes, Actinomycetes; 2006 pp 1099–1113
    [Google Scholar]
  4. Evtushenko LI, Krausova VI, Yoon JH et al. Genus I. Nocardioides. In Goodfellow M, Kämpfer P, Busse HJ, Trujillo ME, Suzuki KI. eds Bergey’s Manual of Systematic Bacteriology, 2nd. edn vol 5, Part A New York: Springer; 2012 pp 1197–1250
    [Google Scholar]
  5. Sun B, Xia Z, Yuan L, Wan C, Zhang L. Streptomyces tailanensis sp. nov., an actinomycete isolated from riverside silt. Int J Syst Evol Microbiol 2020; 70:2760–2765 [View Article] [PubMed]
    [Google Scholar]
  6. Kim CM, Jeong JW, Lee DH, Kim SB. Pseudomonas guryensis sp. nov. and Pseudomonas ullengensis sp. nov., isolated from soil. Int J Syst Evol Microbiol 2021; 71:11 [View Article]
    [Google Scholar]
  7. Ra JS, Kim MJ, Lee DH, Jeong JW, Kim SB. Micromonospora humida sp. nov., exhibiting antimicrobial potential, isolated from riverside soil. Int J Syst Evol Microbiol 2021; 71:12 [View Article] [PubMed]
    [Google Scholar]
  8. Hayakawa M, Nonomura H. Humic acid-vitamin agar, a new medium for the selective isolation of soil actinomycetes. J Ferment Technol 1987; 65:501–509 [View Article]
    [Google Scholar]
  9. Kim MJ, Roh SG, Kim MK, Park C, Kim S et al. Kitasatospora acidiphila sp. nov., isolated from pine grove soil, exhibiting antimicrobial potential. Int J Syst Evol Microbiol 2020; 70:5567–5575 [View Article] [PubMed]
    [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. 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]
  12. Jeon Y-S, Lee K, Park S-C, Kim B-S, Cho Y-J et al. EzEditor: a versatile sequence alignment editor for both rRNA- and protein-coding genes. Int J Syst Evol Microbiol 2014; 64:689–691 [View Article] [PubMed]
    [Google Scholar]
  13. Jukes TH, Cantor CR. Evolution of Protein Molecules. In Mammalian Protein Metabolism New York: Academic Press; 1969 pp 21–132
    [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. Williams ST, Goodfellow M, Alderson G, Wellington EM, Sneath PH et al. Numerical classification of Streptomyces and related genera. J Gen Microbiol 1983; 129:1743–1813 [View Article] [PubMed]
    [Google Scholar]
  16. Vancanneyti M, Witt S, Abraham W-R, Kersters K, Fredrickson HL. Fatty acid content in whole-cell hydrolysates and phospholipid and phospholipid fractions of Pseudomonads: a taxonomic evaluation. Syst Appl Microbiol 1996; 19:528–540 [View Article]
    [Google Scholar]
  17. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids. USFCC Newsl 1990; 20:1–7
    [Google Scholar]
  18. 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]
  19. Cummins CS, Harris H. The chemical composition of the cell wall in some gram-positive bacteria and its possible value as a taxonomic character. J Gen Microbiol 1956; 14:583–600 [View Article]
    [Google Scholar]
  20. Partridge SM. Aniline hydrogen phthalate as a spraying reagent for chromatography of sugars. Nature 1949; 164:443 [View Article]
    [Google Scholar]
  21. SALTON MR. Studies of the bacterial cell wall. IV. The composition of the cell walls of some Gram-positive and Gram-negative bacteria. Biochim Biophys Acta 1953; 10:512–523 [View Article]
    [Google Scholar]
  22. Zhang D-C, Schumann P, Redzic M, Zhou Y-G, Liu H-C et al. Nocardioides alpinus sp. nov., a psychrophilic actinomycete isolated from alpine glacier cryoconite. Int J Syst Evol Microbiol 2012; 62:445–450 [View Article]
    [Google Scholar]
  23. Lee I, Ouk Kim Y, Park SC, Chun J. OrthoANI: An improved algorithm and software for calculating average nucleotide identity. Int J Syst Evol Microbiol 2016; 66:1100–1103 [View Article] [PubMed]
    [Google Scholar]
  24. Meier-Kolthoff JP, Göker M. TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat Commun 2019; 10:2182 [View Article] [PubMed]
    [Google Scholar]
  25. Lee SD. Nocardioides furvisabuli sp. nov., isolated from black sand. Int J Syst Evol Microbiol 2007; 57:35–39 [View Article]
    [Google Scholar]
  26. Kämpfer P, Glaeser SP, McInroy JA, Busse HJ. Nocardioides zeicaulis sp. nov., an endophyte actinobacterium of maize. Int J Syst Evol Microbiol 2016; 66:1869–1874 [View Article]
    [Google Scholar]
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