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Abstract

Two pink-pigmented bacteria, designated strains NEAU-140 and NEAU-K, were isolated from field soil collected from Linyi, Shandong Province, PR China. Both isolates were aerobic, Gram-stain-negative, rod-shaped, and facultatively methylotrophic. 16S rRNA gene sequences analysis showed that these two strains belong to the genus . Strain NEAU-140 exhibited high 16S rRNA gene sequence similarities to NBRC 15690 (97.43 %) and NBRC 105206 (97.36 %). Strain NEAU-K exhibited high 16S rRNA gene sequence similarities to NBRC 105206 (99.00 %) and DSM 23933 (98.72 %). A phylogenetic tree based on 16S rRNA gene sequences showed that strain NEAU-140 formed a clade with (95.94 %), (95.66 %) and (96.87 %), and strain NEAU-K formed a cluster with and . The predominant fatty acid in both strains was C 7. Both strains contained ubiquinone Q-10 as the only respiratory quinone. The polar lipid profiles of both strains contained diphosphatidylglycerol, phosphatidylethanolamine, and phosphatidylcholine. Whole-genome phylogeny showed that strains NEAU-140 and NEAU-K formed a phyletic line with , , , , , , and . The orthologous average nucleotide identity (ANI) and digital DNA–DNA hybridization (dDDH) values between strain NEAU-140 and its closely related strains were lower than 82.62 and 25.90  %, respectively. The ANI and dDDH values between strain NEAU-K and its closely related strains were lower than 86.29 and 31.7 %, respectively. The genomic DNA G+C contents were 71.63 mol% for strain NEAU-140 and 69.08 mol% for strain NEAU-K. On the basis of their phenotypic and phylogenetic distinctiveness and the results of dDDH and ANI hybridization, these two isolates represent two novel species within the genus , for which the names sp. nov. (type strain NEAU-140=MCCC 1K08801=DSM 110568) and sp. nov. (type strain NEAU-K=MCCC 1K08800=DSM 110567) are proposed.

Funding
This study was supported by the:
  • Postdoctoral Scientific Research Development Fund of Heilongjiang Province (Award LBH-Q21072)
    • Principle Award Recipient: JunweiZhao
  • the Outstanding Youth Project of Natural Science Foundation of Heilongjiang Province (Award YQ2021C012)
    • Principle Award Recipient: JunweiZhao
  • the Research Team Project of Natural Science Foundation of Heilongjiang Province (Award TD2022C002)
    • Principle Award Recipient: WenshengXiang
  • Key Programme (Award 32030090)
    • Principle Award Recipient: WenshengXiang
  • Key Programme (Award U22A20483)
    • Principle Award Recipient: XiangjingWang
  • the National Key Research and Development Program of China (Award 2022YFD1700205)
    • Principle Award Recipient: XiangjingWang
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2024-07-15
2025-06-19
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References

  1. Patt TE, Cole GC, Hanson RS. Methylobacterium, a new genus of facultatively methylotrophic bacteria. Int J Syst Bacteriol 1976; 26:226–229 [View Article]
    [Google Scholar]
  2. Green PN, Bousfield IJ. Emendation of Methylobacterium (Patt, Cole, and Hanson 1976); Methylobacterium rhodinum (Heumann 1962) comb. nov. corrig.; Methylobacterium radiotolerans (Ito and Iizuka 1971) comb. nov. corrig.; and Methylobacterium mesophilicum (Austin and Goodfellow 1979) comb. nov. Int J Syst Bacteriol 1983; 33:875–877 [View Article]
    [Google Scholar]
  3. Kelly DP, Mcdonald IR, Wood AP. The Family Methylobacteriaceae Berlin Heidelberg: Springer; 2014
    [Google Scholar]
  4. Green PN, Ardley JK. Review of the genus Methylobacterium and closely related organisms: a proposal that some Methylobacterium species be reclassified into a new genus, Methylorubrum gen. nov. Int J Syst Evol Microbiol 2018; 68:2727–2748 [View Article] [PubMed]
    [Google Scholar]
  5. Alessa O, Ogura Y, Fujitani Y, Takami H, Hayashi T et al. Comprehensive comparative genomics and phenotyping of Methylobacterium species. Front Microbiol 2021; 12:740610 [View Article] [PubMed]
    [Google Scholar]
  6. Leducq J-B, Sneddon D, Santos M, Condrain-Morel D, Bourret G et al. Comprehensive phylogenomics of methylobacterium reveals four evolutionary distinct groups and underappreciated phyllosphere diversity. Genome Biol Evol 2022; 14:evac123 [View Article] [PubMed]
    [Google Scholar]
  7. Kato Y, Asahara M, Goto K, Kasai H, Yokota A. Methylobacterium persicinum sp. nov., Methylobacterium komagatae sp. nov., Methylobacterium brachiatum sp. nov., Methylobacterium tardum sp. nov. and Methylobacterium gregans sp. nov., isolated from freshwater. Int J Syst Evol Microbiol 2008; 58:1134–1141 [View Article] [PubMed]
    [Google Scholar]
  8. Gallego V, García MT, Ventosa A. Methylobacterium isbiliense sp. nov., isolated from the drinking water system of Sevilla, Spain. Int J Syst Evol Microbiol 2005; 55:2333–2337 [View Article] [PubMed]
    [Google Scholar]
  9. Gallego V, García MT. Methylobacterium hispanicum sp. nov. and Methylobacterium aquaticum sp. nov., isolated from drinking water. Int J Syst Evol Microbiol 2005; 55:281–287 [View Article]
    [Google Scholar]
  10. Jia LJ, Zhang KS, Tang K, Meng JY, Zheng C et al. Methylobacterium crusticola sp. nov., isolated from biological soil crusts. Int J Syst Evol Microbiol 2020; 70:2089–2095 [View Article] [PubMed]
    [Google Scholar]
  11. Feng G-D, Chen W, Zhang X-J, Zhang J, Wang S-N et al. Methylobacterium nonmethylotrophicum sp. nov., isolated from tungsten mine tailing. Int J Syst Evol Microbiol 2020; 70:2867–2872 [View Article] [PubMed]
    [Google Scholar]
  12. Madhaiyan M, Poonguzhali S. Methylobacterium pseudosasicola sp. nov. and Methylobacterium phyllostachyos sp. nov. two novel species isolated from bamboo leaf surfaces. Int J Syst Evol Microbiol 2014; 64:2376–2384 [View Article]
    [Google Scholar]
  13. Lee Y, Jeon CO. Methylobacterium frigidaeris sp. nov., isolated from an air conditioning system. Int J Syst Evol Microbiol 2018; 68:299–304 [View Article]
    [Google Scholar]
  14. Aslam Z, Lee CS, Kim K-H, Im W-T, Ten LN et al. Methylobacterium jeotgali sp. nov., a non-pigmented, facultatively methylotrophic bacterium isolated from jeotgal, a traditional Korean fermented seafood. Int J Syst Evol Microbiol 2007; 57:566–571 [View Article] [PubMed]
    [Google Scholar]
  15. McDonald IR, Doronina NV, Trotsenko YA, McAnulla C, Murrell JC. Hyphomicrobium chloromethanicum sp. nov. and Methylobacterium chloromethanicum sp. nov., chloromethane-utilizing bacteria isolated from a polluted environment. Int J Syst Evol Microbiol 2001; 51:119–122 [View Article] [PubMed]
    [Google Scholar]
  16. Reasoner DJ, Geldreich EE. A new medium for the enumeration and subculture of bacteria from potable water. Appl Environ Microbiol 1985; 49:1–7 [View Article] [PubMed]
    [Google Scholar]
  17. Chun JS, Goodfellow M. A phylogenetic analysis of the genus Nocardia with 16S rRNA gene sequences. Int J Syst Bacteriol 1995; 45:240–245 [View Article]
    [Google Scholar]
  18. 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]
  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. 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. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  22. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791 [View Article] [PubMed]
    [Google Scholar]
  23. 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] [PubMed]
    [Google Scholar]
  24. Nikodinovic J, Barrow KD, Chuck JA. High yield preparation of genomic DNA from Streptomyces. Biotechniques 2003; 35:932–934 [View Article] [PubMed]
    [Google Scholar]
  25. Li R, Li Y, Kristiansen K, Wang J. SOAP: short oligonucleotide alignment program. Bioinformatics 2008; 24:713–714 [View Article] [PubMed]
    [Google Scholar]
  26. 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] [PubMed]
    [Google Scholar]
  27. 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]
  28. Blin K, Shaw S, Steinke K, Villebro R, Ziemert N et al. antiSMASH 5.0: updates to the secondary metabolite genome mining pipeline. Nucl Acids Res 2019; 47:W81–W87 [View Article]
    [Google Scholar]
  29. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR et al. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Bacteriol 2018; 68:461–466 [View Article]
    [Google Scholar]
  30. Riesco R, Trujillo ME. Update on the proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 2024; 74:006300 [View Article] [PubMed]
    [Google Scholar]
  31. Xu C, Su X, Wang J, Zhang F, Shen G et al. Characteristics and functional bacteria in a microbial consortium for rice straw lignin-degrading. Bioresour Technol 2021; 331:125066 [View Article] [PubMed]
    [Google Scholar]
  32. Vladimirova A, Patskovsky Y, Fedorov AA, Bonanno JB, Fedorov EV et al. Substrate distortion and the catalytic reaction mechanism of 5-carboxyvanillate decarboxylase. J Am Chem Soc 2016; 138:826–836 [View Article] [PubMed]
    [Google Scholar]
  33. Sentausa E, Fournier P-E. Advantages and limitations of genomics in prokaryotic taxonomy. Clin Microbiol Infect 2013; 19:790–795 [View Article] [PubMed]
    [Google Scholar]
  34. Dussault HP. An improved technique for staining red halophilic bacteria. J Bacteriol 1955; 70:484–485 [View Article] [PubMed]
    [Google Scholar]
  35. Kelly KL. Inter-Society Colour Council-National Bureau of Standards Colour-Name Charts Illustrated with Centroid Colours Washington, DC: US Government Printing Office; 1964
    [Google Scholar]
  36. Gordon RE, Barnett DA, Handerhan JE, Pang CH-N. Nocardia coeliaca, Nocardia autotrophica, and the nocardin strain. Int J Syst Bacteriol 1974; 24:54–63 [View Article]
    [Google Scholar]
  37. Williams ST, Goodfellow M, Alderson G. Genus Streptomyces Waksman and Henrici 1943, 339AL. In Williams ST, ME S, Holt JG. eds Bergey’s Manual of Systematic Bacteriology vol 4 Baltimore: Williams and Willkins; 1989 pp 2453–2492
    [Google Scholar]
  38. Zhang H, Wang Z, Yu X, Cao J, Bao T et al. The phylogeny and metabolic potentials of a lignocellulosic material-degrading Aliiglaciecola bacterium isolated from intertidal seawater in East China Sea. Microorganisms 2024; 12:144 [View Article] [PubMed]
    [Google Scholar]
  39. Atlas RM. Handbook of Microbiological Media. In Handbook of Microbiological Media, 4th edn Washington, DC: Taylor & Francis Group; 2010 p 95 [View Article]
    [Google Scholar]
  40. Zhao J, Han L, Yu M, Cao P, Li D et al. Characterization of Streptomyces sporangiiformans sp. nov., a novel soil actinomycete with antibacterial activity against Ralstonia solanacearum. Microorganisms 2019; 7:360 [View Article] [PubMed]
    [Google Scholar]
  41. 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]
  42. Xiang W, Liu C, Wang X, Du J, Xi L et al. Actinoalloteichus nanshanensis sp. nov., isolated from the rhizosphere of a fig tree (Ficus religiosa). Int J Syst Evol Microbiol 2011; 61:1165–1169 [View Article] [PubMed]
    [Google Scholar]
  43. Collins MD. Chemical methods in bacterial systematics. In Goodfellow M, Minnikin DE. eds Isoprenoid Quinone Analyses in Bacterial Classification and Identification Academic Press; 1985 pp 267–284
    [Google Scholar]
  44. Wu C, Lu X, Qin M, Wang Y, Ruan J. Analysis of menaquinone compound in microbial cells by HPLC. Microbiology 1989; 16:176–178
    [Google Scholar]
  45. Weon H-Y, Kim B-Y, Joa J-H, Son J-A, Song M-H et al. Methylobacterium iners sp. nov. and Methylobacterium aerolatum sp. nov., isolated from air samples in Korea. Int J Syst Evol Microbiol 2008; 58:93–96 [View Article] [PubMed]
    [Google Scholar]
  46. Madhaiyan M, Kim B-Y, Poonguzhali S, Kwon S-W, Song M-H et al. Methylobacterium oryzae sp. nov., an aerobic, pink-pigmented, facultatively methylotrophic, 1-aminocyclopropane-1-carboxylate deaminase-producing bacterium isolated from rice. Int J Syst Evol Microbiol 2007; 57:326–331 [View Article] [PubMed]
    [Google Scholar]
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