Skip to content
1887

Abstract

A Gram-positive, oval-shaped and non-motile strain, designated MMS21-DH1MA12, was isolated from riverside soil and subjected to polyphasic taxonomic characterization. Strain MMS21-DH1MA12 grew optimally in tryptic soy agar, forming yellow-coloured, convex and smooth colonies. The optimal growth conditions of the strain were 30 °C, pH 7 and absence of NaCl. Strain MMS21-DH1MA12 shared the highest 16S rRNA gene sequence similarity with NS18 (97.3%), and then with 6408 J-67 (97.1%) and CGMCC 1.11101 (96.9%), all belonging to the family . Strain MMS21-DH1MA12 had a genome size of 2.4 Mbp and G+C content of 62.6%. The digital DNA–DNA hybridization (dDDH), orthologous average nucleotide identity (orthoANI) and average amino acid identity (AAI) values between strain MMS21-DH1MA12 and related type strains of the genera within the family were no higher than 22.2%, 71.54% and 60.19%, respectively. The dDDH, orthoANI and AAI values of MMS21-DH1MA12 with related taxa were no higher than 22.2%, 71.54% and 61.96%, thus showing a distant relationship of the strain with other members of . It was also notable that the species sharing the highest similarities were different for all three indices. The major polar lipids were diphosphatidylglycerol, phosphatidylglycerol and phosphatidylinositol. The main cellular fatty acids were -C, -C and -C. The predominant menaquinones were MK-10 and MK-11. The combination of physiological and biochemical properties, as well as chemotaxonomic features, clearly separated strain MMS21-DH1MA12 from related taxa of . It is, thus, evident that MMS21-DH1MA12 represents a novel species in a novel genus, for which the name gen. nov., sp. nov. is proposed (type strain=MMS21-DH1MA12 = KCTC 49751 = LMG 32525=JCM 37009).

Funding
This study was supported by the:
  • National Institute of Biological Resources
    • Principal Award Recipient: SeungBum Kim
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.006786
2025-05-21
2026-02-07

Metrics

Loading full text...

Full text loading...

References

  1. Park YH, Suzuki K, Yim DG, Lee KC, Kim E et al. Suprageneric classification of peptidoglycan group B actinomycetes by nucleotide sequencing of 5S ribosomal RNA. Antonie van Leeuwenhoek 1993; 64:307–313 [View Article] [PubMed]
    [Google Scholar]
  2. Stackebrandt E, Rainey FA, Ward-rainey NL. Proposal for a new hierarchic classification system, actinobacteria classis nov. Int J Syst Bacteriol 1997; 47:479–491 [View Article]
    [Google Scholar]
  3. Zhi XY, Li WJ, Stackebrandt E. An update of the structure and 16S rRNA gene sequence-based definition of higher ranks of the class actinobacteria, with the proposal of two new suborders and four new families and emended descriptions of the existing higher taxa. Int J Syst Evol Microbiol 2009; 59:589–608 [View Article] [PubMed]
    [Google Scholar]
  4. Evtushenko LI, Takeuchi M. The Family Microbacteriaceae. In Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrandt E. eds The Prokaryotes, 3rd ed. vol 3 New York: Springer; 2006 pp 1020–1098
    [Google Scholar]
  5. Evtushenko LI. Family XI. Microbacteriaceae. In Goodfellow M, Kämpfer P, Busse HJ, Trujillo ME, Suzuki KI. eds Bergey’s Manual of Systematic Bacteriology, 2nd ed. vol 5 New York: Springer; 2012 pp 807–994
    [Google Scholar]
  6. 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: [View Article] [PubMed]
    [Google Scholar]
  7. Lee DH, Ra JS, Kim MJ, Kim SB. Micromonospora antibiotica sp. nov. and Micromonospora humidisoli sp. nov., two new actinobacterial species exhibiting antimicrobial potential. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  8. Lee JH, Kim YS, Kim SB. Streptomyces guryensis sp. nov. exhibiting antimicrobial activity, isolated from riverside soil. Int J Syst Evol Microbiol 2023; 73: [View Article] [PubMed]
    [Google Scholar]
  9. Ra JS, Oh ET, Han JH, Kim SB. Flavobacterium humidisoli sp. nov., isolated from riverside soil. Int J Syst Evol Microbiol 2023; 73: [View Article] [PubMed]
    [Google Scholar]
  10. Kim JH, Ham YJ, Kim SB. Nocardioides okcheonensis sp. nov., isolated from riverside soil. Int J Syst Evol Microbiol 2023; 73: [View Article] [PubMed]
    [Google Scholar]
  11. Lee JH, Shin YM, Ra JS, Kim SB. Brevibacillus humidisoli sp. nov., a moderately thermoalkaliphilic and halotolerant species isolated from riverside soil. Int J Syst Evol Microbiol 2023; 73: [View Article] [PubMed]
    [Google Scholar]
  12. Molina Ayala KM, Kim SB. Description of Microcella humidisoli sp. nov. and Microcella daejeonensis sp. nov., isolated from riverside soil, reclassification of Marinisubtilis pacificus as Microcella pacifica comb. nov., and emended description of the genus Microcella. Int J Syst Evol Microbiol 2023; 73: [View Article]
    [Google Scholar]
  13. Lee DH, Kim SB. Quorum quenching potential of Reyranella sp. isolated from riverside soil and description of Reyranella humidisoli sp. no. J Microbiol 2024; 62:449–461 [View Article] [PubMed]
    [Google Scholar]
  14. Oh ET, Jeong JW, Kim SB. Paenarthrobacter aromaticivorans sp. nov., a paraoxon-degrading bacterium isolated from red pepper cultivation soil. Int J Syst Evol Microbiol 2024; 74: [View Article] [PubMed]
    [Google Scholar]
  15. 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] [PubMed]
    [Google Scholar]
  16. 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]
  17. 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]
  18. 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]
  19. Cowan ST, Steel KJ. Manual for the Identification of Medical Bacteria Cambridge: University Press; 1965
    [Google Scholar]
  20. 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]
  21. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids. In Tech. Note #101 Newark: MIDI Inc; 1990
    [Google Scholar]
  22. 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]
  23. 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]
  24. 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]
  25. Riesco R, Trujillo ME. Update on the proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 2024; 74:006300 [View Article] [PubMed]
    [Google Scholar]
/content/journal/ijsem/10.1099/ijsem.0.006786
Loading
/content/journal/ijsem/10.1099/ijsem.0.006786
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