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Abstract

A Gram-stain-negative, aerobic, rod-shaped, motile and flagellated novel bacterial strain, designated MAHUQ-64, was isolated from the rhizosphere of rice. The colonies were observed to be creamy white-coloured, smooth, spherical and 0.5–1.1 mm in diameter when grown on Reasoner’s 2A agar medium for 2 days. Strain MAHUQ-64 was able to grow at 10–40 °C, at pH 5.0–9.5 and in the presence of 0–2.0% NaCl (w/v). The strain was positive for both catalase and oxidase tests. The strain was positive for hydrolysis of -tyrosine. According to the 16S rRNA gene sequence comparisons, the isolate was identified as a member of the genus and is closely related to L3B39 (98.6% sequence similarity) and TTM-24 (98.2%). The novel strain MAHUQ-64 has a draft genome size of 3 827 146 bp (22 contigs), annotated with 3612 protein-coding genes, 74 tRNA and 4 rRNA genes. The average nucleotide identity (ANI) and digital DNA–DNA hybridization (dDDH) values between strain MAHUQ-64 and its closest member L3B39 were 86.5 and 33.4%, respectively. genome mining revealed several biosynthetic gene clusters in the genome of the novel strain MAHUQ-64. The genomic DNA G+C content was determined to be 63.4 mol%. The predominant isoprenoid quinone was ubiquinone-8. The major fatty acids were identified as summed feature 3 (comprising C 7 and/or C 6) and C. Based on dDDH, ANI value, genotypic analysis and chemotaxonomic and physiological data, strain MAHUQ-64 represents a novel species within the genus , for which the name sp. nov. is proposed, with MAHUQ-64 (=KACC 22245=CGMCC 1.19000) as the type strain.

  • 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.
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2025-02-26
2025-12-12

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References

  1. Grimes DJ, Woese CR, MacDonell MT, Colwell RR. Systematic study of the genus Vogesella gen. nov. and its type species, Vogesella indigofera comb. nov. Int J Syst Bacteriol 1997; 47:19–27 [View Article] [PubMed]
    [Google Scholar]
  2. Subhash Y, Tushar L, Sasikala C, Ramana CV. Vogesella alkaliphila sp. nov., isolated from an alkaline soil, and emended description of the genus Vogesella. Int J Syst Evol Microbiol 2013; 63:2338–2343 [View Article] [PubMed]
    [Google Scholar]
  3. Sheu SY, Chen JC, Young CC, Chen WM. Vogesella fluminis sp. nov., isolated from a freshwater river, and emended description of the genus Vogesella. Int J Syst Evol Microbiol 2013; 63:3043–3049 [View Article]
    [Google Scholar]
  4. Krieg NR. Genus vogesella. In Brenner DJ, Krieg NR, Staley JT, Garrity GM. eds In Bergey’s Manual of Systematic Bacteriology vol 2 New York: Springer; 2005 pp 858–859
    [Google Scholar]
  5. Rameshkumar N, Lang E, Tanaka N. Description of Vogesella oryzae sp. nov., isolated from the rhizosphere of saline tolerant pokkali rice. Syst Appl Microbiol 2016; 39:20–24 [View Article] [PubMed]
    [Google Scholar]
  6. Sheu SY, Chen YL, Young CC, Chen WM. Vogesella facilis sp. nov., isolated from a freshwater river, and emended description of the genus Vogesella. Int J Syst Evol Microbiol 2016; 66:817–823 [View Article] [PubMed]
    [Google Scholar]
  7. Akter S, Huq MA. Fluviicola chungangensis sp. nov., a bacterium isolated from rice field. Arch Microbiol 2020; 202:293–298 [View Article] [PubMed]
    [Google Scholar]
  8. Xie CH, Yokota A. Zoogloea oryzae sp. nov., a nitrogen-fixing bacterium isolated from rice paddy soil, and reclassification of the strain ATCC 19623 as Crabtreella saccharophila gen. nov., sp. nov. Int J Syst Evol Microbiol 2006; 56:619–624 [View Article] [PubMed]
    [Google Scholar]
  9. Jeon Y, Lee S-S, Chung BS, Kim JM, Bae J-W et al. Mucilaginibacter oryzae sp. nov., isolated from soil of a rice paddy. Int J Syst Evol Microbiol 2009; 59:1451–1454 [View Article]
    [Google Scholar]
  10. Huq MA, Akter S. Characterization and genome analysis of Arthrobacter bangladeshi sp. nov., applied for the green synthesis of silver nanoparticles and their antibacterial efficacy against drug-resistant human pathogens. Pharmaceutics 2021; 13:1691 [View Article] [PubMed]
    [Google Scholar]
  11. Akter S, Huq MA, Yi TH. Lysobacter humi sp. nov., a bacterium isolated from rice field. Arch Microbiol 2016; 198:1005–1012 [View Article] [PubMed]
    [Google Scholar]
  12. Alam K, Hao J, Zhang Y, Li A. Synthetic biology-inspired strategies and tools for engineering of microbial natural product biosynthetic pathways. Biotechnol Adv 2021; 49:107759 [View Article] [PubMed]
    [Google Scholar]
  13. Lane DJ. 16S/23S rRNA sequencing. In Stackebrandt E, Goodfellow M. eds Nucleic Acid Techniques in Bacterial Systematic New York: Wiley; 1991 pp 115–175
    [Google Scholar]
  14. 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]
  15. 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]
  16. Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucl Acids Symp Ser 1999; 41:95–98
    [Google Scholar]
  17. Kimura M. The Neutral Theory of Molecular Evolution Cambridge: Cambridge University Press; 1983
    [Google Scholar]
  18. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Bio Evol 1987; 4:406–425
    [Google Scholar]
  19. 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]
  20. 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]
  21. Emms DM, Kelly S. OrthoFinder: phylogenetic orthology inference for comparative genomics. Genome Biol 2019; 20:238 [View Article] [PubMed]
    [Google Scholar]
  22. Shi W, Sun Q, Fan G, Hideaki S, Moriya O et al. gcType: a high-quality type strain genome database for microbial phylogenetic and functional research. Nucleic Acids Res 2021; 49:D694–D705 [View Article] [PubMed]
    [Google Scholar]
  23. Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Nawrocki EP et al. NCBI prokaryotic genome annotation pipeline. Nucleic Acids Res 2016; 44:6614–6624 [View Article] [PubMed]
    [Google Scholar]
  24. Yoon SH, Ha SM, Lim JM, Kwon SJ, Chun J. A large-scale evaluation of algorithms to calculate average nucleotide identity. Antonie van Leeuwenhoek 2017; 110:1281–1286 [View Article] [PubMed]
    [Google Scholar]
  25. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinf 2013; 14:60 [View Article] [PubMed]
    [Google Scholar]
  26. Wayne LG, Brenner DJ, Colwell RR, Grimont PAD, Kandler O et al. International committee on systematic bacteriology. report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Int J Syst Bacteriol 1987; 37:463–464 [View Article]
    [Google Scholar]
  27. Stackebrandt E, Goebel BM. Taxonomic note: a place for DNA-DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology. Int J Syst Bacteriol 1994; 44:846–849 [View Article]
    [Google Scholar]
  28. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 2009; 106:19126–19131 [View Article]
    [Google Scholar]
  29. Meier-Kolthoff JP, Göker M. TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat Commun 2019; 10:1–10 [View Article]
    [Google Scholar]
  30. Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J et al. BLAST+: architecture and applications. BMC Bioinf 2009; 10:421 [View Article] [PubMed]
    [Google Scholar]
  31. 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]
  32. Hitch TCA, Riedel T, Oren A, Overmann J, Lawley TD et al. Automated analysis of genomic sequences facilitates high-throughput and comprehensive description of bacteria. ISME Commun 2021; 1:16 [View Article] [PubMed]
    [Google Scholar]
  33. Grant JR, Stothard P. The CGView Server: a comparative genomics tool for circular genomes. Nucleic Acids Research 2008; 36:W181–W184 [View Article]
    [Google Scholar]
  34. Qin Q-L, Xie B-B, Zhang X-Y, Chen X-L, Zhou B-C et al. A proposed genus boundary for the prokaryotes based on genomic insights. J Bacteriol 2014; 196:2210–2215 [View Article] [PubMed]
    [Google Scholar]
  35. 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]
  36. Huq MA. Chryseobacterium chungangensis sp. nov., a bacterium isolated from soil of sweet gourd garden. Arch Microbiol 2018; 200:581–587 [View Article] [PubMed]
    [Google Scholar]
  37. Cappuccino JG, Sherman N. Biochemical activities of microorganisms. In Microbiology, A Laboratory Manual; The Benjamin/Cummings Publishing Co., Inc.: Menlo Park CA, USA: 1992 pp 188–247
    [Google Scholar]
  38. Fautz E, Reichenbach H. A simple test for flexirubin-type pigments. FEMS Microbiol Lett 1980; 8:87–91 [View Article]
    [Google Scholar]
  39. Huq MA. Caenispirillum humi sp. nov., a bacterium isolated from the soil of Korean pine garden. Arch Microbiol 2018; 200:343–348 [View Article]
    [Google Scholar]
  40. Sasser M. Identification of bacteria by gas chromatography of cellular fatty acids. In MIDI Technical Note 101 vol 101 Newark, DE: MIDI Inc; 1990
    [Google Scholar]
  41. Hiraishi A, Ueda Y, Ishihara J, Mori T. Comparative lipoquinone analysis of influent sewage and activated sludge by high-performance liquid chromatography and photodiode array detection. J Gen Appl Microbiol 1996; 42:457–469 [View Article]
    [Google Scholar]
  42. Collins MD, Jones D. Distribution of isoprenoid quinone structural types in bacteria and their taxonomic implication. Microbiol Rev 1981; 45:316–354 [View Article] [PubMed]
    [Google Scholar]
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