1887

Abstract

A novel pale white-pigmented bacterial strain designated YC-7-48 was isolated from activated sludge in China. Cells of the strain, which grew at 15–37 °C (optimum at 30 °C) and pH 6.0–9.0 (optimum at 7.0), were Gram-stain-negative, rod-shaped and motile. Strain YC-7-48 had 97.4–97.1% 16S rRNA gene sequence similarity to type strains of eight species in the genera , , , and of the family . Phylogenetic analysis based on 16S rRNA gene sequencing placed the strain on a separate branch in the genus and showed that it exhibited 97.4, 97.3 and 96.6% similarity to EBR-8-1, BN9 and 17-4A, respectively. The genome size of strain YC-7-48 was 3202438 bp, with 54.3 mol% G+C content. According to the genome analysis, YC-7-48 encodes several heavy metal resistance proteins and enzymes related to the metabolism of nicotine and aromatic compounds. The results of digital DNA–DNA hybridization and average nucleotide identity analyses based on whole genome sequences between strain YC-7-48 and the closely related strains indicated that the strain represented a new species of the genus . The chemotaxonomic results identified Q-8 as the predominant respiratory quinone, phosphatidylethanolamine, phosphatidylmonomethylethanolamine, diphosphatidylglycerol and two unidentified aminolipids as the major polar lipids, and C (27.4 %), C cyclo (22.0 %), C (11.7 %) and C cyclo 8 (9.5 %) as the major fatty acids. Thus, based on morphological, chemotaxonomic and phylogenetic characterization and genomic data, we proposed that the isolate is a representative of a novel species named sp. nov., with the type strain YC-7-48 (=CGMCC 1.17466=KACC 21349).

Funding
This study was supported by the:
  • Doctoral Scientific Research Foundation of Yancheng Teachers University (Award 72071671003C)
    • Principle Award Recipient: LiYao
  • National Natural Science Foundation of China (Award 31700096)
    • Principle Award Recipient: LiYao
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2022-04-22
2024-04-19
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References

  1. Stolz A, Bürger S, Kuhm A, Kämpfer P, Busse HJ. Pusillimonas noertemannii gen. nov., sp. nov., a new member of the family Alcaligenaceae that degrades substituted salicylates. Int J Syst Evol Microbiol 2005; 55:1077–1081 [View Article] [PubMed]
    [Google Scholar]
  2. Karvelis L, Gasparavičiūtė R, Klimavičius A, Jančienė R, Stankevičiūtė J et al. Pusillimonas sp. 5HP degrading 5-hydroxypicolinic acid. Biodegradation 2014; 25:11–19 [View Article] [PubMed]
    [Google Scholar]
  3. Li P, Wang L, Feng L. Characterization of a novel Rieske-type alkane monooxygenase system in Pusillimonas sp. strain T7-7. J Bacteriol 2013; 195:1892–1901 [View Article] [PubMed]
    [Google Scholar]
  4. Ma Y, Wen RT, Qiu JG, Hong J, Liu M et al. Biodegradation of nicotine by a novel strain Pusillimonas. Res Microbiol 2015; 166:67–71 [View Article] [PubMed]
    [Google Scholar]
  5. Yuan M, Zhang YT, Zhao LL, Ma Y, He Q et al. Identification and characterisation of a new three-component nicotinic acid hydroxylase nahab1b2 from pusillimonas sp. strain T2. Lett Appl Microbiol 2018; 66:321–328
    [Google Scholar]
  6. Li JY, Qi MM, Lai QL, Dong CM, Liu XP et al. Pusillimonas maritima sp. nov., isolated from surface seawater. Int J Syst Evol Microbiol 2020; 70:3483–3490 [View Article] [PubMed]
    [Google Scholar]
  7. Jin L, Ko S-R, Cui Y, Lee CS, Oh H-M et al. Pusillimonas caeni sp. nov., isolated from a sludge sample of a biofilm reactor. Antonie van Leeuwenhoek 2017; 110:125–132 [View Article] [PubMed]
    [Google Scholar]
  8. Koh HW, Song MS, Do KT, Kim H, Park SJ. Pusillimonas thiosulfatoxidans sp. nov., a thiosulfate oxidizer isolated from activated sludge. Int J Syst Evol Microbiol 2019; 69:1041–1046 [View Article] [PubMed]
    [Google Scholar]
  9. Srinivasan S, Kim MK, Sathiyaraj G, Kim YJ, Yang DC. Pusillimonas ginsengisoli sp. nov., isolated from soil of a ginseng field. Int J Syst Evol Microbiol 2010; 60:1783–1787 [View Article] [PubMed]
    [Google Scholar]
  10. Lee M, Woo SG, Chae M, Ten LN. Pusillimonas soli sp. nov., isolated from farm soil. Int J Syst Evol Microbiol 2010; 60:2326–2330 [View Article] [PubMed]
    [Google Scholar]
  11. Park MS, Park YJ, Jung JY, Lee SH, Park W et al. Pusillimonas harenae sp. nov., isolated from a sandy beach, and emended description of the genus Pusillimonas. Int J Syst Evol Microbiol 2011; 61:2901–2906 [View Article] [PubMed]
    [Google Scholar]
  12. Lane DJ. 16S/23S rRNA sequencing. In Stackebrandt E, Goodfellow M. eds Nucleic Acid Techniques in Bacterial Systematics London John Wiley & Sons Ltd; 1991 pp 115–174
    [Google Scholar]
  13. Yoon SH, Ha SM, 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]
  14. 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]
  15. Kimura M. The Neutral Theory of Molecular Evolution Cambridge University Press Cambridge; 1983
    [Google Scholar]
  16. 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]
  17. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 14:406–425
    [Google Scholar]
  18. Rzhetsky A, Nei M. Theoretical foundation of the minimum-evolution method of phylogenetic inference. Mol Biol Evol 1993; 10:1073–1095 [View Article] [PubMed]
    [Google Scholar]
  19. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  20. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791 [View Article] [PubMed]
    [Google Scholar]
  21. Simpson JT, Wong K, Jackman SD, Schein JE, Jones SJM et al. ABySS: a parallel assembler for short read sequence data. Genome Res 2009; 19:1117–1123 [View Article] [PubMed]
    [Google Scholar]
  22. 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] [PubMed]
    [Google Scholar]
  23. Lechner M, Findeiss S, Steiner L, Marz M, Stadler PF et al. Proteinortho: detection of (co-)orthologs in large-scale analysis. BMC Bioinformatics 2011; 12:124 [View Article] [PubMed]
    [Google Scholar]
  24. Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 2004; 32:1792–1797 [View Article] [PubMed]
    [Google Scholar]
  25. Price MN, Dehal PS, Arkin AP. FastTree: computing large minimum evolution trees with profiles instead of a distance matrix. Mol Biol Evol 2009; 26:1641–1650 [View Article] [PubMed]
    [Google Scholar]
  26. Zhang C, Rabiee M, Sayyari E, Mirarab S. ASTRAL-III: polynomial time species tree reconstruction from partially resolved gene trees. BMC Bioinformatics 2018; 19:S6 [View Article] [PubMed]
    [Google Scholar]
  27. 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]
  28. Richter M, Rosselló-Móra R, Oliver Glöckner F, Peplies J. JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison. Bioinformatics 2016; 32:929–931 [View Article] [PubMed]
    [Google Scholar]
  29. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci US A 2009; 106:19126–19131 [View Article] [PubMed]
    [Google Scholar]
  30. Moore WEC, Stackebrandt E, Kandler O, Colwell RR, Krichevsky MI et al. Report of the Ad Hoc committee on reconciliation of approaches to bacterial systematics. Int J Syst Evol Microbiol 1987; 37:463–464 [View Article]
    [Google Scholar]
  31. Konstantinidis KT, Rosselló-Móra R, Amann R. Uncultivated microbes in need of their own taxonomy. ISME J 2017; 11:2399–2406 [View Article] [PubMed]
    [Google Scholar]
  32. Tarrand JJ, Gröschel DH. Rapid, modified oxidase test for oxidase-variable bacterial isolates. J Clin Microbiol 1982; 16:772–774 [View Article] [PubMed]
    [Google Scholar]
  33. 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]
  34. Sasser M. Identification of Bacteria by Gas Chromatography of Cellular Fatty Acids, MIDI Technical Note 101 Newark, DE: MIDI Inc; 1990
    [Google Scholar]
  35. Minnikin DE, Collins MD, Goodfellow M. Fatty acid and polar lipid composition in the classification of Cellulomonas, Oerskovia and related taxa. J Appl Bacteriol 1979; 47:87–95 [View Article]
    [Google Scholar]
  36. Felföldi T, Vengring A, Kéki Z, Márialigeti K, Schumann P et al. Eoetvoesia caeni gen. nov., sp. nov., isolated from an activated sludge system treating coke plant effluent. Int J Syst Evol Microbiol 2014; 64:1920–1925 [View Article]
    [Google Scholar]
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