1887

Abstract

A Gram-stain-positive, rod-shaped, strictly aerobic bacterial strain (Y6) was isolated from a sewage sludge sample collected from a fisheries processing factory in Zhoushan, Zhejiang Province, PR China. The growth range of NaCl concentration was 0–6.0 % (w/v), with an optimum at 3.0 % (w/v). The temperature range for growth was 10–42 °C, with an optimum at 37 °C. The pH range for growth was pH 7.0–10.0, with an optimum at pH 9.0. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strain Y6 belonged to the genus and showed the highest sequence similarity of 97.8 % to dk3136. The average nucleotide identity and DNA–DNA hybridization values between strain Y6 and the reference strains were 76.9–81.2 % and 20.6–23.6 %, respectively. Chemotaxonomic analysis indicated that the sole respiratory quinone was MK-8(H) and the predominant cellular fatty acids were iso-C, 10-methyl-C and C 9. The polar lipid profile was composed of diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylcholine, four unidentified phospholipids, three unidentified aminolipids and five unidentified lipids. The peptidoglycan was -2,6-diaminopimelic acid. On the basis of the phenotypic, genotypic, phylogenetic and chemotaxonomic features, strain Y6 is considered to represent a novel species, for which the name sp. nov. is proposed. The type strain is Y6 (=KCTC 49504=MCCC 1K04765).

Funding
This study was supported by the:
  • Science and Technology Project of Zhoushan city (Award 2017C12032)
    • Principle Award Recipient: GangZheng
  • Zhejiang Provincial Key R & D Program (Award 2021C02024)
    • Principle Award Recipient: GangZheng
  • China Postdoctoral Science Foundation (Award 2018M642382)
    • Principle Award Recipient: CongSun
  • Scientific Research Fund of Oceanography (Award SOA (JB1805))
    • Principle Award Recipient: CongSun
  • Sea Mountain Environmental Management Plan and APEI Construction Project Research (Award DY135-E2-2-05)
    • Principle Award Recipient: MinWu
  • Science and Technology Basic Resources Investigation Program of China (Award 2017FY100300)
    • Principle Award Recipient: MinWu
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2021-07-09
2024-04-19
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References

  1. Prauser H. Nocardioides, a new genus of the order Actinomycetales. Int J Syst Bacteriol 1976; 26:58–65 [View Article]
    [Google Scholar]
  2. Parte AC. LPSN - list of prokaryotic names with standing in nomenclature. Nucleic Acids Res 2014; 42:D613–D616 [View Article] [PubMed]
    [Google Scholar]
  3. Yoon J-H, Kim I-G, Lee M-H, Lee C-H, Oh T-K et al. Nocardioides alkalitolerans sp. nov., isolated from an alkaline serpentinite soil in Korea. Int J Syst Evol Microbiol 2005; 55:809–814 [View Article] [PubMed]
    [Google Scholar]
  4. Tuo L, Dong YP, Habden X, Liu JM, Guo L et al. Nocardioides deserti sp. nov., an actinobacterium isolated from desert soil. Int J Syst Evol Microbiol 2015; 65:1604–1610 [View Article] [PubMed]
    [Google Scholar]
  5. Sultanpuram VR, Mothe T, Mohammed F. Nocardioides solisilvae sp. nov. isolated from a forest soil. Antonie van Leeuwenhoek 2015; 107:1599–1606 [View Article] [PubMed]
    [Google Scholar]
  6. Lee DW, Hyun CG, Lee SD. Nocardioides marinisabuli sp. nov., a novel actinobacterium isolated from beach sand. Int J Syst Evol Microbiol 2007; 57:2960–2963 [View Article] [PubMed]
    [Google Scholar]
  7. Cho Y, Jang GI, Cho BC. Nocardioides marinquilinus sp. nov., isolated from coastal seawater. Int J Syst Evol Microbiol 2013; 63:2594–2599 [View Article] [PubMed]
    [Google Scholar]
  8. Lin SY, Wen CZ, Hameed A, Liu YC, Hsu YH et al. Nocardioides echinoideorum sp. nov., isolated from sea urchins (Tripneustes gratilla. Int J Syst Evol Microbiol 2015; 65:1953–1958 [View Article] [PubMed]
    [Google Scholar]
  9. Toth EM, Keki Z, Homonnay ZG, Borsodi AK, Marialigeti K et al. Nocardioides daphniae sp. nov., isolated from Daphnia cucullata (Crustacea: Cladocera. Int J Syst Evol Microbiol 2008; 58:78–83 [View Article] [PubMed]
    [Google Scholar]
  10. Yoon J-H, Kang S-J, Park S, Kim W, Oh T-K. Nocardioides caeni sp. nov., isolated from wastewater. Int J Syst Evol Microbiol 2009; 59:2794–2797 [View Article] [PubMed]
    [Google Scholar]
  11. Woo SG, Srinivasan S, Yang J, Jung YA, Kim MK et al. Nocardioides daejeonensis sp. nov., a denitrifying bacterium isolated from sludge in a sewage-disposal plant. Int J Syst Evol Microbiol 2012; 62:1199–1203 [View Article] [PubMed]
    [Google Scholar]
  12. Huang Y, Wang X, Yang J, Lu S, Lai XH et al. Nocardioides yefusunii sp. nov., isolated from Equus kiang (Tibetan wild ass) faeces. Int J Syst Evol Microbiol 2019; 69:3629–3635 [View Article] [PubMed]
    [Google Scholar]
  13. Dong K, Lu S, Yang J et al. Nocardioides jishulii sp. nov. isolated from faeces of Tibetan gazelle (Procapra picticaudata. Int J Syst Evol Microbiol 2020; 70:3665–3672 [View Article] [PubMed]
    [Google Scholar]
  14. Embley TM. The linear PCR reaction: a simple and robust method for sequencing amplified rRNA genes. Lett Appl Microbiol 1991; 13:171–174 [View Article] [PubMed]
    [Google Scholar]
  15. Kim OS, Cho YJ, Lee K, Yoon SH, 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. Sudhir K, Glen S, Koichiro T. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874
    [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. Fitch WM. Toward defining the course of evolution: minimum change for a specific tree topology. Syst Biol 1971; 20:406–416 [View Article]
    [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. Ren Y, Chen C, Ye Y, Wang R, Han S et al. Meridianimarinicoccus roseus gen. nov., sp. nov., a novel genus of the family Rhodobacteraceae isolated from seawater. Int J Syst Evol Microbiol 2019; 69:504–510 [View Article] [PubMed]
    [Google Scholar]
  21. Bernardet JF, Nakagawa Y, Holmes B. Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int J Syst Evol Microbiol 2020; 52:1049–1070
    [Google Scholar]
  22. Zhang W, Zhu S, Cheng Y, Ding L, Li S et al. Rheinheimera mangrovi sp. nov., a bacterium isolated from mangrove sediment. Int J Syst Evol Microbiol 2020; 70:6188–6194 [View Article] [PubMed]
    [Google Scholar]
  23. Lanyi B. Classical and rapid identification methods for medically important bacteria. Method Microbiol 1987; 19:1–67
    [Google Scholar]
  24. Sun C, Wang R-J, Su Y, Fu G-Y, Zhao Z et al. Hyphobacterium vulgare gen. nov., sp. nov., a novel alphaproteobacterium isolated from seawater. Int J Syst Evol Microbiol 2017; 67:1169–1176 [View Article] [PubMed]
    [Google Scholar]
  25. Chen C, Su Y, Tao T, Fu G, Zhang C et al. Maripseudobacter aurantiacus gen. nov., sp. nov., a novel member of the family Flavobacteriaceae isolated from a sedimentation basin. Int J Syst Evol Microbiol 2017; 67:778–783 [View Article] [PubMed]
    [Google Scholar]
  26. Sasser M. Identification of Bacteria by Gas Chromatography of Cellular Fatty Acids, MIDI Technical Note. 1990 pp 1–7
    [Google Scholar]
  27. Kuykendall LD, Roy MA, O’Neill JJ, Devine TE. Fatty acids, antibiotic resistance, and deoxyribonucleic acid homology groups of Bradyrhizobium japonicum. Int J Syst Bacteriol 1988; 38:358–361 [View Article]
    [Google Scholar]
  28. 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]
  29. Tindall BJ. Lipid composition of Halobacterium lacusprofundi. FEMS Microbiol Lett 1990; 66:199–202 [View Article]
    [Google Scholar]
  30. Schleifer KH, Kandler O. Peptidoglycan types of bacterial cell walls and their taxonomic implications. Bacteriol Rev 1972; 36:407 [View Article] [PubMed]
    [Google Scholar]
  31. Simpson JT, Wong K, Jackman SD, Schein JE, Jones SJ et al. ABySS: a parallel assembler for short read sequence data. Genome Res 2009; 19:1117–1123 [View Article] [PubMed]
    [Google Scholar]
  32. Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. Check M: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 2015; 25:1043–1055 [View Article] [PubMed]
    [Google Scholar]
  33. 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–D214 [View Article]
    [Google Scholar]
  34. Gerlich M, Neumann S. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res 2000; 28:27–30
    [Google Scholar]
  35. Tatusov RL et al. The COG database: new developments in phylogenetic classification of proteins from complete genomes. Nucleic Acids Res 2001; 29:22–28 [View Article]
    [Google Scholar]
  36. Kai B, Simon S, Katharina S, Rasmus V. antiSMASH 5.0: updates to the secondary metabolite genome mining pipeline; 2019; 47W81–W87
  37. 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]
  38. 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]
  39. 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 [View Article] [PubMed]
    [Google Scholar]
  40. Goris J, Klappenbach JA, Vandamme P, Coenye T, Konstantinidis KT et al. DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 2007; 57:81–91 [View Article] [PubMed]
    [Google Scholar]
  41. Richter M, Rosselló-Móra R. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 2009; 106:19126–19131 [View Article] [PubMed]
    [Google Scholar]
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