Skip to content
1887

Abstract

A novel bacterium, designated 1RM2, was isolated from Xinjiang Province, north-west PR China. This strain could grow under conditions of 20–45 °C, pH 5.0–10.0 and 0–10% (w/v) NaCl. The species with the highest similarity of 16S rRNA gene sequences to strain 1RM2 were strain Chryseobacterium bernardetii NCTC 13530 (97.1%) and DSM 15235 (96.9%). The draft genome sequence G+C content of strain 1RM2 was 39.5 mol%. The average nucleotide identity and DNA–DNA hybridization values between strain 1RM2 and the two closest neighbours were 78.6%, 77.6% and 21.8%, 21.2%, respectively. The main fatty acids of strain 1RM2 were iso-C, iso-C 3-OH, summed feature 3 (C 6 and/or C 7) and summed feature 9 (C 10-methyl and/or iso-C 9). The main isoprenoid quinone was menaquinone-6 and polar lipids were phosphatidylethanolamine, unidentified amino phospholipids and unidentified lipids. Based on phenotypic characteristics and genotype analysis, strain 1RM2 is a new species of the genus and is proposed to be named sp. nov. (=GDMCC 1.4437=KCTC 102275).

Funding
This study was supported by the:
  • Graduate Student Innovation Fund of Xinjiang Normal University (Award XSY202401039)
    • Principal Award Recipient: LiliChai
  • National Natural Science Foundation of China (Award 32160002)
    • Principal Award Recipient: WeiZhang
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.006817
2025-06-20
2026-03-13

Metrics

Loading full text...

Full text loading...

References

  1. Vandamme P, Bernardet J-F, Segers P, Kersters K, Holmes B. NOTES: new perspectives in the classification of the Flavobacteria: description of Chryseobacterium gen. nov., Bergeyella gen. nov., and Empedobacter nom. rev. Int J Syst Bacteriol 1994; 44:827–831 [View Article]
    [Google Scholar]
  2. Shen F-T, Kämpfer P, Young C-C, Lai W-A, Arun AB. Chryseobacterium taichungense sp. nov., isolated from contaminated soil. Int J Syst Evol Microbiol 2005; 55:1301–1304 [View Article] [PubMed]
    [Google Scholar]
  3. Weon H-Y, Kim B-Y, Yoo S-H, Kwon S-W, Stackebrandt E et al. Chryseobacterium soli sp. nov. and Chryseobacterium jejuense sp. nov., isolated from soil samples from Jeju, Korea. Int J Syst Evol Microbiol 2008; 58:470–473 [View Article]
    [Google Scholar]
  4. Kämpfer P, Dreyer U, Neef A, Dott W, Busse H-J. Chryseobacterium defluvii sp. nov., isolated from wastewater. Int J Syst Evol Microbiol 2003; 53:93–97 [View Article]
    [Google Scholar]
  5. Kämpfer P, Arun AB, Young C-C, Chen W-M, Sridhar KR et al. Chryseobacterium arthrosphaerae sp. nov., isolated from the faeces of the pill millipede Arthrosphaera magna attems. Int J Syst Evol Microbiol 2010; 60:1765–1769 [View Article]
    [Google Scholar]
  6. Park MS, Jung SR, Lee KH, Lee M-S, Do JO et al. Chryseobacterium soldanellicola sp. nov. and Chryseobacterium taeanense sp. nov., isolated from roots of sand-dune plants. Int J Syst Evol Microbiol 2006; 56:433–438 [View Article]
    [Google Scholar]
  7. Bernardet JF, Vancanneyt M, Matte-Tailliez O, Grisez L, Tailliez P et al. Polyphasic study of Chryseobacterium strains isolated from diseased aquatic animals. Syst Appl Microbiol 2005; 28:640–660 [View Article] [PubMed]
    [Google Scholar]
  8. Ilardi P, Fernández J, Avendaño-Herrera R. Chryseobacterium piscicola sp. nov., isolated from diseased salmonid fish. Int J Syst Evol Microbiol 2009; 59:3001–3005 [View Article] [PubMed]
    [Google Scholar]
  9. Vaneechoutte M, Kämpfer P, De Baere T, Avesani V, Janssens M et al. Chryseobacterium hominis sp. nov., to accommodate clinical isolates biochemically similar to CDC groups II-h and II-c. Int J Syst Evol Microbiol 2007; 57:2623–2628 [View Article] [PubMed]
    [Google Scholar]
  10. Nde AL, Charimba G, Hitzeroth A, Oosthuizen L, Steyn L et al. Chryseobacterium pennae sp. nov., isolated from poultry feather waste. Int J Syst Evol Microbiol 2021; 71:004912 [View Article] [PubMed]
    [Google Scholar]
  11. Son Y, Min J, Park W. Chryseobacterium faecale sp. nov., isolated from camel feces. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  12. Kong D, Wang Y, Li Q, Zhou Y, Jiang X et al. Chryseobacterium subflavum sp. nov., isolated from soil. Int J Syst Evol Microbiol 2022; 72: [View Article] [PubMed]
    [Google Scholar]
  13. Richmond ME. Glyphosate: a review of its global use, environmental impact, and potential health effects on humans and other species. J Environ Stud Sci 2018; 8:416–434 [View Article]
    [Google Scholar]
  14. Balthazor TM, Hallas LE. Glyphosate-degrading microorganisms from industrial activated sludge. Appl Environ Microbiol 1986; 51:432–434 [View Article] [PubMed]
    [Google Scholar]
  15. Pandey KK, Mayilraj S, Chakrabarti T. Pseudomonas indica sp. nov., a novel butane-utilizing species. Int J Syst Evol Microbiol 2002; 52:1559–1567 [View Article] [PubMed]
    [Google Scholar]
  16. Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 1997; 25:3389–3402 [View Article] [PubMed]
    [Google Scholar]
  17. 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]
  18. Kang M, Chhetri G, Kim J, Kim I, So Y et al. Tumebacillus amylolyticus sp. nov., isolated from garden soil in Korea. Int J Syst Evol Microbiol 2022; 72: [View Article]
    [Google Scholar]
  19. 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]
  20. 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]
  21. Guindon S, Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 2003; 52:696–704 [View Article] [PubMed]
    [Google Scholar]
  22. 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]
    [Google Scholar]
  23. 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]
  24. Sun C, Fu G-Y, Zhang C-Y, Hu J, Xu L et al. Isolation and complete genome sequence of Algibacter alginolytica sp. nov., a novel seaweed-degrading bacteroidetes bacterium with diverse putative polysaccharide utilization loci. Appl Environ Microbiol 2016; 82:2975–2987 [View Article] [PubMed]
    [Google Scholar]
  25. Lee I, Chalita M, Ha S-M, Na S-I, Yoon S-H et al. ContEst16S: an algorithm that identifies contaminated prokaryotic genomes using 16S RNA gene sequences. Int J Syst Evol Microbiol 2017; 67:2053–2057 [View Article] [PubMed]
    [Google Scholar]
  26. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T et al. The RAST server: rapid annotations using subsystems technology. BMC Genom 2008; 9:75 [View Article] [PubMed]
    [Google Scholar]
  27. Blin K, Shaw S, Steinke K, Villebro R, Ziemert N et al. antiSMASH 5.0: updates to the secondary metabolite genome mining pipeline. Nucleic Acids Res 2019; 47:W81–W87 [View Article] [PubMed]
    [Google Scholar]
  28. Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinform 2013; 14:60 [View Article] [PubMed]
    [Google Scholar]
  29. 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]
  30. Meier-Kolthoff JP, Göker M. TYGS is an automated high-throughput platform for state-of-the-art genome-based taxonomy. Nat Commun 2019; 10:2182 [View Article] [PubMed]
    [Google Scholar]
  31. 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]
  32. Sun Y-C, Li Y, Zhang H, Yan H-Q, Dowling DN et al. Reconstitution of the enzyme AroA and its glyphosate tolerance by fragment complementation. FEBS Lett 2006; 580:1521–1527 [View Article] [PubMed]
    [Google Scholar]
  33. Zhang Z, Zhao C, Wu T, Xu Y, Wang L et al. Physiological response and molecular mechanism of glyphosate degradation by Pseudomonas alcaligenes Z1–1. Biochem Eng J 2024; 209:109405 [View Article]
    [Google Scholar]
  34. Kamlage B. eds Methods for General and Molecular Bacteriology Washington, D.C: American Society for Microbiology; 1994 [View Article]
    [Google Scholar]
  35. Sakamoto M, Suzuki M, Umeda M, Ishikawa I, Benno Y. Reclassification of Bacteroides forsythus (Tanner et al. 1986) as Tannerella forsythensis corrig., gen. nov., comb. nov. Int J Syst Evol Microbiol 2002; 52:841–849 [View Article] [PubMed]
    [Google Scholar]
  36. 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]
  37. Xu X-W, Huo Y-Y, Wang C-S, Oren A, Cui H-L et al. Pelagibacterium halotolerans gen. nov., sp. nov. and Pelagibacterium luteolum sp. nov., novel members of the family Hyphomicrobiaceae. Int J Syst Evol Microbiol 2011; 61:1817–1822 [View Article] [PubMed]
    [Google Scholar]
  38. Kates M. Techniques of lipidology. In Isolation, Analysis and Identification of Lipids, 2. Rev. Edn. Netherlands: Elsevier,Amsterdam; 1986 p 484
    [Google Scholar]
  39. Kim KK, Bae H-S, Schumann P, Lee S-T. Chryseobacterium daecheongense sp. nov., isolated from freshwater lake sediment. Int J Syst Evol Microbiol 2005; 55:133–138 [View Article]
    [Google Scholar]
  40. Herzog P, Winkler I, Wolking D, Kämpfer P, Lipski A. Chryseobacterium ureilyticum sp. nov., Chryseobacterium gambrini sp. nov., Chryseobacterium pallidum sp. nov. and Chryseobacterium molle sp. nov., isolated from beer-bottling plants. Int J Syst Evol Microbiol 2008; 58:26–33 [View Article] [PubMed]
    [Google Scholar]
/content/journal/ijsem/10.1099/ijsem.0.006817
Loading
/content/journal/ijsem/10.1099/ijsem.0.006817
Loading

Data & Media loading...

Supplements

Supplementary material 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An error occurred
Approval was partially successful, following selected items could not be processed due to error