DOI QR코드

DOI QR Code

Ramlibacter terrae sp. nov. and Ramlibacter montanisoli sp. nov., Isolated from Soil

  • Received : 2021.05.18
  • Accepted : 2021.07.19
  • Published : 2021.09.28

Abstract

Two gram-negative, catalase-positive, strictly aerobic, and white colony-forming bacteria, strains H242T and B156T, were isolated from soil in South Korea. Cells of strain H242T were oxidase-positive and non-motile short rods, while those of strain B156T were oxidase-negative and long non-motile rods. Ubiquinone-8 was identified as the sole isoprenoid quinone in both strains. C16:0, cyclo-C17:0, andsummed feature 3 (C16:1 ω7c and/or C16:1 ω6c) and phosphatidylethanolamine, phosphatidylglycerol, and diphosphatidylglycerol were identified in both strains as the major cellular fatty acids and polar lipids, respectively. The DNA G+C contents of strains H242T and B156T were 69.4 mol% and 69.3 mol%, respectively. Phylogenetic analyses based on 16S rRNA and 92 concatenated core gene sequences revealed that strains H242T and B156T formed distinct phylogenic lineages from other Ramlibacter type strains. The DNA-DNA hybridization (DDH) value between strains H242T and B156T was 24.6%. Strains H242T and B156T were most closely related to Ramlibacter ginsenosidimutans BXN5-27T and Ramlibacter monticola G-3-2T with 98.4% and 98.6% 16S rRNA gene sequence similarities, respectively. Digital DDH values between strain H242T and R. ginsenosidimutans and between strain B156T and R. monticola were 23.5% and 26.1%, respectively. Phenotypic, chemotaxonomic, and molecular analyses indicated that strains H242T and B156T represent two novel species of the genus Ramlibacter, for which the names Ramlibacter terrae sp. nov. and Ramlibacter montanisoli sp. nov., respectively, are proposed. The type strains of R. terrae and R. montanisoli are H242T (=KACC 21667T=JCM 33922T) and B156T (=KACC 21665T=JCM 33920T), respectively.

Keywords

Acknowledgement

We thank Prof. Aharon Oren for his expert suggestion for correct species epithet and Latin etymology. This work was supported by the Program for Collection of Domestic Biological Resources from the National Institute of Biological Resources (NIBR No. 2020-02-001) of the Ministry of Environment (MOE) and the National Research Foundation (2017M3C1B5019250) of the Ministry of Science and ICT, Republic of Korea.

References

  1. Heulin T, Barakat M, Christen R, Lesourd M, Sutra L, De Luca G, et al. 2003. Ramlibacter tataouinensis gen. nov., sp. nov., and Ramlibacter henchirensis sp. nov., cyst-producing bacteria isolated from subdesert soil in Tunisia. Int. J. Syst. Evol. Microbiol. 53: 589-594. https://doi.org/10.1099/ijs.0.02482-0
  2. Lee DH, Cha CJ. 2017. Ramlibacter alkalitolerans sp. nov., alkali-tolerant bacterium isolated from soil of ginseng. Int. J. Syst. Evol. Microbiol. 67: 4619-4623. https://doi.org/10.1099/ijsem.0.002342
  3. Wang L, An DS, Kim SG, Jin FX, Kim SC, Lee ST, et al. 2012. Ramlibacter ginsenosidimutans sp. nov., with ginsenoside-converting activity. J. Microbiol. Biotechnol. 22: 311-315. https://doi.org/10.4014/jmb.1106.06041
  4. Lee HJ, Lee SH, Lee SS, Lee JS, Kim Y, Kim SC, et al. 2014. Ramlibacter solisilvae sp. nov., isolated from forest soil, and emended description of the genus Ramlibacter. Int. J. Syst. Evol. Microbiol. 64: 1317-1322. https://doi.org/10.1099/ijs.0.058396-0
  5. Chaudhary DK, Kim J. 2017. Ramlibacter monticola sp. nov., isolated from forest soil. Int. J. Syst. Evol. Microbiol. 67: 4468-4474. https://doi.org/10.1099/ijsem.0.002314
  6. Zhang XJ, Feng GD, Yao Q, Wang YH, Yang SZ, Zhu HH. 2019. Ramlibacter humi sp. nov., isolated from tropical forest soil. Int. J. Syst. Evol. Microbiol. 69: 3460-3464. https://doi.org/10.1099/ijsem.0.003641
  7. Yan ZF, Trinh H, Moya G, Lin P, Li CT, Kook M, et al. 2017. Ramlibacter rhizophilus sp. nov., isolated from rhizosphere soil of national flower Mugunghwa from South Korea. Int. J. Syst. Evol. Microbiol. 67: 3773-3777. https://doi.org/10.1099/ijsem.0.002191
  8. Akter S, Nam K, Lee SY, Moon SK, Choi C, Balusamy SR, et al. 2020. Ramlibacter pinisoli sp. nov., a novel bacterial species isolated from pine garden soil. Int. J. Syst. Evol. Microbiol. 70: 5841-5847. https://doi.org/10.1099/ijsem.0.004486
  9. Props R, Monsieurs P, Vandamme P, Leys N, Denef VJ, Boon N. 2019. Gene expansion and positive selection as bacterial adaptations to oligotrophic conditions. mSphere 4: e00011-19.
  10. Khan SA, Jung HS, Park HY, Jeon CO. 2021. Maritimibacter harenae sp. nov. and Sneathiella litorea sp. nov.: members of Alphaproteobacteria isolated from sea sand. Antonie Van Leeuwenhoek. 114: 799-811. https://doi.org/10.1007/s10482-021-01559-x
  11. Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, et al. 2017. Introducing EzBioCloud: A taxonomically united database of 16S rRNA and whole genome assemblies. Int. J. Syst. Evol. Microbiol. 67: 1613-1617. https://doi.org/10.1099/ijsem.0.001755
  12. Wang Q, Garrity GM, Tiedje JM, Cole JR. 2007. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl. Environ. Microbiol. 73: 5261-5267. https://doi.org/10.1128/AEM.00062-07
  13. Kumar S, Stecher G, Tamura K, Dudley J. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33: 1870-1874. https://doi.org/10.1093/molbev/msw054
  14. Sambrook J, Fritsch EF, Maniatis T. 1989. Molecular cloning: a laboratory manual, 2nd, Ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory.
  15. Wick RR, Judd LM, Gorrie CL, Holt KE. 2017. Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads. PLoS Comput. Biol. 13: e1005595. https://doi.org/10.1371/journal.pcbi.1005595
  16. Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. 2019. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 25: 1043-1055. https://doi.org/10.1101/gr.186072.114
  17. Lee I, Ouk Kim Y, Park SC, Chun J. 2016. OrthoANI: an improved algorithm and software for calculating average nucleotide identity. Int. J. Syst. Evol. Microbiol. 66: 1100-1103. https://doi.org/10.1099/ijsem.0.000760
  18. Meier-Kolthoff JP, Auch AF, Klenk H-P, Goker M. 2013. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 14: 60. https://doi.org/10.1186/1471-2105-14-60
  19. Kim J, Na SI, Kim D, Chun J. 2021. UBCG2: up-to-date bacterial core gene and pipeline for phylogenomic analysis. J. Microbiol. 59: 609-615. https://doi.org/10.1007/s12275-021-1231-4
  20. Gomori G. 1955. Preparation of buffers for use in enzyme studies. Methods Enzymol. 1: 138-146. https://doi.org/10.1016/0076-6879(55)01020-3
  21. Bernardet JF, Nakagawa Y, Holmes B. 2002. Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int. J. Syst. Evol. Microbiol. 52: 1049-1070. https://doi.org/10.1099/ijs.0.02136-0
  22. Tindall BJ, Sikorski J, Smibert RA, Krieg NR. 2007. Phenotypic characterization and the principles of comparative systematics. In Methods for General and Molecular Microbiology, pp. 330-393. Edited by Reddy CA, Beveridge TJ, Breznak JA, Marzluf G, Schmidt TM, Snyder LR. Washington DC: American Society for Microbiology.
  23. Lanyi B. 1987. Classical and rapid identification methods for medically important bacteria. Methods Microbiol. 19: 1-67.
  24. Minnikin DE, O'Donnell A, Goodfellow M, Alderson G, Athalye M, Schaal A, et al. 1984. An integrated procedure for the extraction of bacterial isoprenoid quinones and polar lipids. J. Microbiol. Methods 2: 233-241. https://doi.org/10.1016/0167-7012(84)90018-6
  25. Sasser M. 1990. Identification of bacteria by gas chromatography of cellular fatty acids, MIDI Technical Note 101.MIDI Inc, Newark.
  26. Minnikin DE, Patel PV, Alshamaony L, Goodfellow M. 1977. Polar lipid composition in the classification of Nocardia and related bacteria. Int. J. Syst. Evol. Microbiol. 27: 104-117.
  27. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR, da Costa MS, et al. 2018. Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int. J. Syst. Evol. Microbiol. 68: 461-466. https://doi.org/10.1099/ijsem.0.002516