1887

Abstract

A novel Gram-positive, aerobic, rod-shaped, non-motile, endospore-forming salt-tolerant bacterium strain (80), was isolated from woodland soil collected near Kanas lake in the Altay region of Xinjiang, PR China. The strain grew at 15−45 °C, pH6.0–9.0 and with 0–14 % (w/v) NaCl. The complete genome size of the novel strain was 4 031 766 bp including a circle chromosome and a circle plasmid. The genomic DNA G+C content was 38.99 mol %. Phylogenetic analysis based on 16S rRNA gene sequence and genome showed that strain 80 has the highest similarity to TKL69. However, the novel strain showed an average nucleotide identity value of 78.65 % (lower than 95 %) and a digital DNA–DNA hybridization value of 22.30 % with TKL69 based on the genome sequences. The major fatty acids were anteiso-C, iso-C, anteiso-C and C ω7 alcohol. The only respiratory quinone was MK-7. The cell wall peptidoglycan was -diaminopimelic acid. Diphosphatidylglycerol, phosphatidylglycerol, one unidentified phospholipid, one unidentified aminophospholipid and two unidentified glycolipids were identified as the major polar lipids. The phylogenetic, phenotypic and chemotaxonomic analyses showed that strain 80 represents a novel species of the genus and the name sp. nov. is proposed. The type strain is 80 (=GDMCC 1.2844=JCM 35077).

Keyword(s): halotolerant and Radiobacillus
Funding
This study was supported by the:
  • the Project of Renovation Capacity Building for the Young Sci-Tech Talents Sponsored by Xinjiang Academy of Agricultural Science (Award XJNKQ-2019019)
    • Principle Award Recipient: LijuanZhang
  • the Opening Project of Key Laboratory in Xinjiang (Award 2020D04032)
    • Principle Award Recipient: WeiWang
  • National Key Research and Development Program of China (Award 2020YFC1806603)
    • Principle Award Recipient: WeiWang
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/content/journal/ijsem/10.1099/ijsem.0.005718
2023-02-23
2024-05-07
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References

  1. Li J, Zhang B, Liu G, Liu Y, Yang H et al. Radiobacillus deserti gen. nov., sp. nov., a UV-resistant bacterium isolated from desert soil. Int J Syst Evol Microbiol 2020; 70:6338–6347 [View Article]
    [Google Scholar]
  2. Wang N, Sayim G, Hou M, Sun J, Ahmat M et al. Litoribacter populi sp. nov., isolated from the soil of a Populus euphratica forest. Arch Microbiol 2021; 203:5011–5016 [View Article] [PubMed]
    [Google Scholar]
  3. Jiang F, Xue X, Qiu X, Zhang K, Chang X et al. Desertibacter xinjiangensis sp. nov., isolated from the soil of a Euphrates poplar forest, and emended description of the genus Desertibacter. Int J Syst Evol Microbiol 2014; 64:3690–3694 [View Article] [PubMed]
    [Google Scholar]
  4. Wang W, Zhang Z, Tang Q, Mao J, Wei D et al. Lechevalieria xinjiangensis sp. nov., a novel actinomycete isolated from radiation-polluted soil in China. Int J Syst Evol Microbiol 2007; 57:2819–2822 [View Article] [PubMed]
    [Google Scholar]
  5. Peng F, Liu M, Zhang L, Dai J, Luo X et al. Planobacterium taklimakanense gen. nov., sp. nov., a member of the family Flavobacteriaceae that exhibits swimming motility, isolated from desert soil. Int J Syst Evol Microbiol 2009; 59:1672–1678 [View Article] [PubMed]
    [Google Scholar]
  6. Guo Q, Zhou Z, Zhang L, Zhang C, Chen M et al. Skermanella pratensis sp. nov., isolated from meadow soil, and emended description of the genus Skermanella. Int J Syst Evol Microbiol 2020; 70:1605–1609 [View Article] [PubMed]
    [Google Scholar]
  7. Guo Q, Wang B, Zhou Z, Ke X, Zhang L et al. Ornithinimicrobium pratense sp. nov., isolated from meadow soil. Int J Syst Evol Microbiol 2020; 70:6450–6457 [View Article] [PubMed]
    [Google Scholar]
  8. Mao J, Wang J, Dai H-Q, Zhang Z-D, Tang Q-Y et al. Yuhushiella deserti gen. nov., sp. nov., a new member of the suborder Pseudonocardineae. Int J Syst Evol Microbiol 2011; 61:621–630 [View Article]
    [Google Scholar]
  9. Zhu J, Li S-H, Tang Q-Y, Chu M, Wang W et al. Deinococcus malanensis sp. nov., isolated from radiation-polluted soil. Arch Microbiol 2017; 199:621–626 [View Article] [PubMed]
    [Google Scholar]
  10. Zhang W-Y, Hu J, Zhang X-Q, Zhu X-F, Wu M. Bacillus salitolerans sp. nov., a novel bacterium isolated from a salt mine in Xinjiang province, China. Antonie van Leeuwenhoek 2015; 108:443–451 [View Article] [PubMed]
    [Google Scholar]
  11. Gregory GJ, Boyd EF. Stressed out: Bacterial response to high salinity using compatible solute biosynthesis and uptake systems, lessons from Vibrionaceae. Comput Struct Biotechnol J 2021; 19:1014–1027 [View Article] [PubMed]
    [Google Scholar]
  12. Bugno A, Almodóvar AAB, Pereira TC. Enumeration of heterotrophic bacteria in water for dialysis: comparison of the efficiency of Reasoner’2 agar and plate count agar. Braz J Microbiol 2010; 41:15–18 [View Article] [PubMed]
    [Google Scholar]
  13. Datta MS, Sliwerska E, Gore J, Polz MF, Cordero OX. Microbial interactions lead to rapid micro-scale successions on model marine particles. Nat Commun 2016; 7:11965 [View Article] [PubMed]
    [Google Scholar]
  14. Saygin H, Nouioui I, Ay H, Guven K, Cetin D et al. Polyphasic classification of Nonomuraea strains isolated from the Karakum Desert and description of Nonomuraea deserti sp. nov., Nonomuraea diastatica sp. nov., Nonomuraea longispora sp. nov. and Nonomuraea mesophila sp. nov. Int J Syst Evol Microbiol 2020; 70:636–647 [View Article]
    [Google Scholar]
  15. 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]
  16. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA et al. Clustal W and Clustal X version 2.0. Bioinformatics 2007; 23:2947–2948 [View Article] [PubMed]
    [Google Scholar]
  17. 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]
  18. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  19. Fitch WM. Toward defining the course of evolution: minimum change for a specific tree topology. Syst Zool 1971; 20:406 [View Article]
    [Google Scholar]
  20. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Mol Biol Evol 2018; 35:1547–1549 [View Article] [PubMed]
    [Google Scholar]
  21. Felsenstein J. Confidence limits on phylogenies: An approach using the bootstrap. Evolution 1985; 39:783–791 [View Article] [PubMed]
    [Google Scholar]
  22. Lowe TM, Eddy SR. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res 1997; 25:955–964 [View Article] [PubMed]
    [Google Scholar]
  23. Delcher AL, Bratke KA, Powers EC, Salzberg SL. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 2007; 23:673–679 [View Article] [PubMed]
    [Google Scholar]
  24. Ashburner M, Ball CA, Blake JA, Botstein D, Butler H et al. Gene Ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 2000; 25:25–29 [View Article]
    [Google Scholar]
  25. Jones P, Binns D, Chang H-Y, Fraser M, Li W et al. InterProScan 5: genome-scale protein function classification. Bioinformatics 2014; 30:1236–1240 [View Article] [PubMed]
    [Google Scholar]
  26. Kanehisa M, Sato Y, Kawashima M, Furumichi M, Tanabe M. KEGG as a reference resource for gene and protein annotation. Nucleic Acids Res 2016; 44:D457–62 [View Article] [PubMed]
    [Google Scholar]
  27. Galperin MY, Makarova KS, Wolf YI, Koonin EV. Expanded microbial genome coverage and improved protein family annotation in the COG database. Nucleic Acids Res 2015; 43:D261–9 [View Article] [PubMed]
    [Google Scholar]
  28. Makarova KS, Wolf YI, Koonin EV. Archaeal clusters of orthologous genes (arCOGs): an update and application for analysis of shared features between Thermococcales, Methanococcales, and Methanobacteriales. Life (Basel) 2015; 5:818–840 [View Article] [PubMed]
    [Google Scholar]
  29. Huerta-Cepas J, Szklarczyk D, Forslund K, Cook H, Heller D et al. eggNOG 4.5: a hierarchical orthology framework with improved functional annotations for eukaryotic, prokaryotic and viral sequences. Nucleic Acids Res 2016; 44:D286–93 [View Article] [PubMed]
    [Google Scholar]
  30. Meier-Kolthoff JP, Carbasse JS, Peinado-Olarte RL, Göker M. TYGS and LPSN: a database tandem for fast and reliable genome-based classification and nomenclature of prokaryotes. Nucleic Acids Res 2022; 50:D801–D807 [View Article] [PubMed]
    [Google Scholar]
  31. 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]
  32. Blin K, Medema MH, Kazempour D, Fischbach MA, Breitling R et al. antiSMASH 2.0–a versatile platform for genome mining of secondary metabolite producers. Nucleic Acids Res 2013; 41:W204–12 [View Article]
    [Google Scholar]
  33. Yoon SH, Ha SM, Lim J, Kwon S, 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]
  34. Xu L, Dong Z, Fang L, Luo Y, Wei Z et al. OrthoVenn2: a web server for whole-genome comparison and annotation of orthologous clusters across multiple species. Nucleic Acids Res 2019; 47:W52–W58 [View Article] [PubMed]
    [Google Scholar]
  35. Lefort V, Desper R, Gascuel O. FastME 2.0: a comprehensive, accurate, and fast distance-based phylogeny inference program. Mol Biol Evol 2015; 32:2798–2800 [View Article] [PubMed]
    [Google Scholar]
  36. Farris JS. Estimating phylogenetic trees from distance matrices. The American Naturalist 1972; 106:645–668 [View Article]
    [Google Scholar]
  37. Kreft L, Botzki A, Coppens F, Vandepoele K, Van Bel M. PhyD3: A phylogenetic tree viewer with extended phyloXML support for functional genomics data visualization. Bioinformatics 2017; 33:2946–2947 [View Article] [PubMed]
    [Google Scholar]
  38. Hobmeier K, Oppermann M, Stasinski N, Kremling A, Pflüger-Grau K et al. Metabolic engineering of Halomonas elongata: ectoine secretion is increased by demand and supply driven approaches. Front Microbiol 2022; 13:968983 [View Article] [PubMed]
    [Google Scholar]
  39. Qu JH, Fu YH, Yue YF, Li HF. Description of Ornithinibacillus gellani sp. nov., a halophilic bacterium isolated from lake sediment, and emended description of the genus Ornithinibacillus. Int J Syst Evol Microbiol 2019; 69:2632–2637 [View Article] [PubMed]
    [Google Scholar]
  40. Logan NA, Berge O, Bishop AH, Busse H-J, De Vos P et al. Proposed minimal standards for describing new taxa of aerobic, endospore-forming bacteria. Int J Syst Evol Microbiol 2009; 59:2114–2121 [View Article] [PubMed]
    [Google Scholar]
  41. Lee JC, Whang KS. Salirhabdus salicampi sp. nov., a halotolerant bacterium isolated from a saltern. Int J Syst Evol Microbiol 2017; 67:4578–4583 [View Article] [PubMed]
    [Google Scholar]
  42. Yang N, Ren B, Liu Z-H, Dai H-Q, Wang J et al. Salinibacillus xinjiangensis sp. nov., a halophilic bacterium from a hypersaline lake. Int J Syst Evol Microbiol 2014; 64:27–32 [View Article] [PubMed]
    [Google Scholar]
  43. Safronova VI, Kuznetsova IG, Sazanova AL, Kimeklis AK, Belimov AA et al. Bosea vaviloviae sp. nov., a new species of slow-growing rhizobia isolated from nodules of the relict species Vavilovia formosa (Stev.) Fed. Antonie van Leeuwenhoek 2015; 107:911–920 [View Article] [PubMed]
    [Google Scholar]
  44. Kämpfer P, Kroppenstedt RM. Numerical analysis of fatty acid patterns of coryneform bacteria and related taxa. Can J Microbiol 1996; 42:989–1005 [View Article]
    [Google Scholar]
  45. 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]
  46. Yoon M-H, Ten LN, Im W-T, Lee S-T. Cellulomonas chitinilytica sp. nov., a chitinolytic bacterium isolated from cattle-farm compost. Int J Syst Evol Microbiol 2008; 58:1878–1884 [View Article] [PubMed]
    [Google Scholar]
  47. Komagata K, Suzuki K. Lipid and cell-wall analysis in bacterial systematics. Methods Microbiol 1987; 19:161–208
    [Google Scholar]
  48. Collins MD. Isoprenoid quinone analyses in bacterial classification and identification. In Society for Applied Bacteriology vol 20 Technical Series; 1985 pp 267–287
    [Google Scholar]
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