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Abstract

Two Gram-stain-negative, strictly aerobic, chemoheterotrophic, short-rod-shaped and non-motile strains, forming yellow colonies and designated F47161 and F64183, were isolated from marine sediment of Xiaoshi Island, Wei Hai, PR China. Strain F47161 grew at 15–37 °C (optimally at 30 °C) and pH 6.0–9.0 (optimally at pH 7.5) and in the presence of 1–9 % (w/v) NaCl (optimally at 3 %). Strain F64183 grew at 10–37 °C (optimally at 30 °C) and pH 6.0–8.5 (optimally at pH 7.0) and in the presence of 1–8 % (w/v) NaCl (optimally at 3 %). The results of phylogenetic analysis based on 16S rRNA gene sequences indicated that F47161 and F64183 were related to members of the genus . The strains shared 97.4 % 16S rRNA gene sequence similarity to each other. F47161 and F64183 shared highest 16S rRNA gene sequence similarity to JCM 19789, and the values were 97.5 % and 98.4 %, respectively. The predominant cellular fatty acids of both F64183 and F47161 were iso-C and iso-C 3-OH, but the predominant fatty acids of F47161 also included anteiso-C. The sole respiratory quinone of F47161 and F64183 was menaquinone 6 (MK-6), consistent with that observed for all related strains. Between F47161 and F64183, the average nucleotide identity (ANI) and digital DNA–DNA hybridisation (dDDH) values were 75.8 % and 20.5 %, respectively, and between the novel isolates (F47161 and F64183) and JCM 19789 they were 76.0 % and 94.2 % and 20.6 % and 57.1 %, respectively. The genomic DNA G+C contents of F47161 and F64183 was 37.3 % and 34.5 %, respectively. The polar lipid profiles of F47161 and F64183 contained phosphatidylethanolamine, two aminolipids, one glycolipid, one phosphoglycolipid and two unidentified polar lipids. Differential phenotypic and genotypic characteristics of the two strains indicated that the two strains should be classified as representing two novel species of the genus for which the names sp. nov. and sp. nov. are proposed. The type strains are F47161 (=MCCC 1H00509=KCTC 92017) and F64183 (=MCCC 1H00507=KCTC 92016), respectively.

Funding
This study was supported by the:
  • National Natural Science Foundation of China (Award 41876166)
    • Principle Award Recipient: Da-ShuaiMu
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2023-03-24
2024-05-06
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References

  1. Bowman JP, Nichols DS. Aequorivita gen. nov., a member of the family Flavobacteriaceae isolated from terrestrial and marine Antarctic habitats. Int J Syst Evol Microbiol 2002; 52:1533–1541 [View Article]
    [Google Scholar]
  2. Wang Q, Cai SD, Liu J, Zhang DC. Aequorivita sinensis sp. nov., isolated from sediment of the East China Sea, and reclassification of Vitellibacter todarodis as Aequorivita todarodis comb. nov. and Vitellibacter aquimaris as Aequorivita aquimaris comb. nov. Int J Syst Evol Microbiol 2020; 70:3323–3327 [View Article]
    [Google Scholar]
  3. Mu DS, Ouyang Y, Chen GJ, Du ZJ. Strategies for culturing active/dormant marine microbes. Mar Life Sci Technol 2021; 3:121–131 [View Article]
    [Google Scholar]
  4. Mu D-S, Liang Q-Y, Wang X-M, Lu D-C, Shi M-J et al. Metatranscriptomic and comparative genomic insights into resuscitation mechanisms during enrichment culturing. Microbiome 2018; 6:230 [View Article]
    [Google Scholar]
  5. KleinJan H, Jeanthon C, Boyen C, Dittami SM. Exploring the cultivable Ectocarpus microbiome. Front Microbiol 2017; 8:2456 [View Article]
    [Google Scholar]
  6. Liu J-J, Zhang X-Q, Pan J, Sun C, Zhang Y et al. Aequorivita viscosa sp. nov., isolated from an intertidal zone, and emended descriptions of Aequorivita antarctica and Aequorivita capsosiphonis. Int J Syst Evol Microbiol 2013; 63:3192–3196 [View Article]
    [Google Scholar]
  7. Zhu KL, Wang XQ, Zhang TS, Shang DD, Du ZJ. Salibaculum halophilum gen. nov., sp. nov. and Salibaculum griseiflavum sp. nov., in the family Rhodobacteraceae. Int J Syst Evol Microbiol 2021; 71: [View Article]
    [Google Scholar]
  8. 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]
    [Google Scholar]
  9. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425 [View Article]
    [Google Scholar]
  10. Kannan L, Wheeler WC. Maximum parsimony on phylogenetic networks. Algorithms Mol Biol 2012; 7:9 [View Article]
    [Google Scholar]
  11. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article]
    [Google Scholar]
  12. 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]
    [Google Scholar]
  13. Hall BG. Building phylogenetic trees from molecular data with MEGA. Mol Biol Evol 2013; 30:1229–1235 [View Article]
    [Google Scholar]
  14. 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]
    [Google Scholar]
  15. Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980; 16:111–120 [View Article]
    [Google Scholar]
  16. Li R, Zhu H, Ruan J, Qian W, Fang X et al. De novo assembly of human genomes with massively parallel short read sequencing. Genome Res 2010; 20:265–272 [View Article]
    [Google Scholar]
  17. 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]
    [Google Scholar]
  18. 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]
  19. Kanehisa M, Sato Y, Morishima K. BlastKOALA and GhostKOALA: KEGG tools for functional characterization of genome and metagenome sequences. J Mol Biol 2016; 428:726–731 [View Article]
    [Google Scholar]
  20. Lombard V, Golaconda Ramulu H, Drula E, Coutinho PM, Henrissat B. The carbohydrate-active enzymes database (CAZy) in 2013. Nucleic Acids Res 2014; 42:D490–5 [View Article] [PubMed]
    [Google Scholar]
  21. Na S-I, Kim YO, Yoon S-H, Ha S, Baek I et al. UBCG: up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction. J Microbiol 2018; 56:280–285 [View Article]
    [Google Scholar]
  22. Price MN, Dehal PS, Arkin AP. FastTree 2 – approximately maximum-likelihood trees for large alignments. PLoS One 2010; 5:e9490 [View Article]
    [Google Scholar]
  23. Na S-I, Kim YO, Yoon S-H, Ha S-M, Baek I et al. UBCG: Up-to-date bacterial core gene set and pipeline for phylogenomic tree reconstruction. J Microbiol 2018; 56:280–285 [View Article]
    [Google Scholar]
  24. 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 Bacteriol 1987; 37:463–464 [View Article]
    [Google Scholar]
  25. Lee I, Chalita M, Ha SM, Na SI, Yoon SH et al. ContEst16S: an algorithm that identifies contaminated prokaryotic genomes using 16S RNA gene sequences. Int J Syst Evol Micr 2017; 67:
    [Google Scholar]
  26. Bernardet JF, Nakagawa Y, Holmes B. Subcommittee On The Taxonomy Of Flavobacterium and Cytophaga-Like Bacteria Of The International Committee On Systematics Of Prokaryotes Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int J Syst Evol Microbiol 2002; 52:1049–1070 [View Article]
    [Google Scholar]
  27. Du ZJ, Wang ZJ, Zhao JX, Chen GJ. Woeseia oceani gen. nov., sp. nov., a chemoheterotrophic member of the order Chromatiales, and proposal of Woeseiaceae fam. nov. Int J Syst Evol Microbiol 2016; 66:107–112 [View Article]
    [Google Scholar]
  28. Wang NN, Li CM, Li YX, Du ZJ. Aquimarina celericrescens sp. nov., isolated from seawater. Int J Syst Evol Microbiol 2018; 68:1683–1688 [View Article]
    [Google Scholar]
  29. Liang QY, Xu ZX, Zhang J, Chen GJ, Du ZJ. Salegentibacter sediminis sp. nov., a marine bacterium of the family Flavobacteriaceae isolated from coastal sediment. Int J Syst Evol Microbiol 2018; 68:2375–2380 [View Article]
    [Google Scholar]
  30. Athalye M, Noble WC, Minnikin DE. Analysis of cellular fatty acids by gas chromatography as a tool in the identification of medically important coryneform bacteria. J Appl Bacteriol 1985; 58:507–512 [View Article]
    [Google Scholar]
  31. 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]
  32. 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]
  33. Tindall BJ. A comparative study of the lipid composition of Halobacterium saccharovorum from various sources. Syst Appl Microbiol 1990; 13:128–130 [View Article]
    [Google Scholar]
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