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Abstract

A novel yellow-pigmented catalase- and oxidase-positive bacterial strain (designated NA20) was isolated from wetland soil and characterized. Results of 16S rRNA and draft genome sequence analysis placed strain NA20 within the genus of the family . Strain NA20 showed ≤97.1 % sequence similarity to members of the genus and the highest sequence similarity was found to DY (97.1%). The draft genome of strain NA20 had a total length of 7 144 125 base pairs. A total of 5659 genes were identified, of which 5613 were CDS and 46 RNA genes were assigned a putative function. Mining the genomes revealed the presence of 225 carbohydrate genes out of 1334 genes. Strain NA20 contained iso-C, iso-C G, iso-C 3-OH and summed feature 3 (C 7 and/or C 6) as major fatty acids. The predominant quinone was MK-7. The major polar lipids were phosphatidylethanolamine, one unknown polar lipid and one unknown aminophospholipid. Additionally, the functional analysis of NA20 showed the conversion of protopanaxatriol-mix type major ginsenosides (Rb1, Rc and Rd) to minor ginsenosides F2 and weak conversion of Rh2 and C-K within 24 h. As a result, the genotypic, phenotypic and taxonomic analyses support the affiliation of NA20 within the genus , for which the name sp. nov. is proposed. The type strain is NA20 (=KACC 22218=LMG 32198).

Funding
This study was supported by the:
  • This work was supported by the project on survey and excavation of Korean indigenous species of the National Institute of Biological Resources (NIBR) under the Ministry of Environment and by and by Brainpool (BP) Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (project no. 2019H1D3A1A02070958).
    • Principle Award Recipient: MuhammadZubair Siddiqi
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2023-06-08
2024-12-01
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References

  1. Akter S, Wang X, Lee S-Y, Rahman MM, Park J-H et al. Paenibacillus roseus sp. nov., a ginsenoside-transforming bacterium isolated from forest soil. Arch Microbiol 2021; 203:3997–4004 [View Article] [PubMed]
    [Google Scholar]
  2. Siddiqi MZ, Ximenes HA, Song B-K, Park HY, Lee WH et al. Enhanced production of ginsenoside Rh2(S) from PPD-type major ginsenosides using BglSk cloned from Saccharibacillus kuerlensis together with two glycosidase in series. Saudi J Biol Sci 2021; 28:4668–4676 [View Article] [PubMed]
    [Google Scholar]
  3. Siddiqi MZ, Park HY, Kim G-R, Cui C-H, Jo YJ et al. Production of the minor ginsenoside F2 from the PPD-mix-type major ginsenosides using a novel recombinant glycoside hydrolase from Novosphingobium aromaticivorans. Biotechnol Bioproc E 2021; 26:956–967 [View Article]
    [Google Scholar]
  4. Tawab MA, Bahr U, Karas M, Wurglics M, Schubert-Zsilavecz M. Degradation of ginsenosides in humans after oral administration. Drug Metab Dispos 2003; 31:1065–1071 [View Article] [PubMed]
    [Google Scholar]
  5. Siddiqi MZ, Siddiqi MH, Kim Y-J, Jin Y, Huq MA et al. Effect of fermented red ginseng extract enriched in ginsenoside Rg3 on the differentiation and mineralization of preosteoblastic MC3T3-E1 cells. J Med Food 2015; 18:542–548 [View Article]
    [Google Scholar]
  6. Bae EA, Han MJ, Kim EJ, Kim DH. Transformation of ginseng saponins to ginsenoside Rh2 by acids and human intestinal bacteria and biological activities of their transformants. Arch Pharm Res 2004; 27:61–67 [View Article] [PubMed]
    [Google Scholar]
  7. Siddiqi MZ, Cui C-H, Park S-K, Han NS, Kim S-C et al. Comparative analysis of the expression level of recombinant ginsenoside-transforming β-glucosidase in GRAS hosts and mass production of the ginsenoside Rh2-Mix. PLoS One 2017; 12:e0176098 [View Article]
    [Google Scholar]
  8. Yun TK, Lee YS, Lee YH, Yun HY. Cancer chemopreventive compounds of red ginseng produced from panax ginseng CA Meyer. J Ginseng Res 2001; 25:107–111
    [Google Scholar]
  9. Siddiqi MZ, Shafi SM, Im WT. Complete genome sequencing of Arachidicoccus ginsenosidimutans sp. nov., and its application for production of minor ginsenosides by finding a novel ginsenoside-transforming β-glucosidase. RSC Adv 2017; 7:46745–46759 [View Article]
    [Google Scholar]
  10. Siddiqi MZ, Hashmi MS, Oh JM, Chun S, Im WT. Identification of novel glycoside hydrolases via whole genome sequencing of Niabella ginsenosidivorans for production of various minor ginsenosides. 3 Biotech 2019; 9:258 [View Article]
    [Google Scholar]
  11. Siddiqi MZ, Srinivasan S, Park HY, Im W-T. Exploration and characterization of novel glycoside hydrolases from the whole genome of Lactobacillus ginsenosidimutans and enriched production of minor ginsenoside Rg3(S) by a recombinant enzymatic process. Biomolecules 2020; 10:288 [View Article]
    [Google Scholar]
  12. Xie CH, Yokota A. Reclassification of [Flavobacterium] ferrugineum as Terrimonas ferruginea gen. nov., comb. nov., and description of Terrimonas lutea sp. nov., isolated from soil. Int J Syst Evol Microbiol 2006; 56:1117–1121 [View Article]
    [Google Scholar]
  13. Han SI, Lee YR, Kim JO, Whang KS. Terrimonas rhizosphaerae sp. nov., isolated from ginseng rhizosphere soil. Int J Syst Evol Microbiol 2017; 67:391–395 [View Article] [PubMed]
    [Google Scholar]
  14. Chen Q, Zang X-X, Hang X, Chen J, Wang H-M et al. Terrimonas suqianensis sp. nov., isolated from a tetrabromobisphenol A-contaminated soil. Antonie Van Leeuwenhoek 2017; 110:1061–1068 [View Article]
    [Google Scholar]
  15. Jiang W-K, Lu M-Y, Cui M-D, Wang X, Wang H et al. Terrimonas soli sp. nov., isolated from farmland soil. Int J Syst Evol Microbiol 2018; 68:819–823 [View Article] [PubMed]
    [Google Scholar]
  16. Zhang J, Gu T, Zhou Y, He J, Zheng L-Q et al. Terrimonas rubra sp. nov., isolated from a polluted farmland soil and emended description of the genus Terrimonas. Int J Syst Evol Microbiol 2012; 62:2593–2597 [View Article] [PubMed]
    [Google Scholar]
  17. Sheu SY, Cho NT, Arun AB, Chen WM. Terrimonas aquatica sp. nov., isolated from a freshwater spring. Int J Syst Evol Microbiol 2010; 60:2705–2709 [View Article]
    [Google Scholar]
  18. Jiang F, Qiu X, Chang X, Qu Z, Ren L et al. Terrimonas arctica sp. nov., isolated from Arctic tundra soil. Int J Syst Evol Microbiol 2014; 64:3798–3803 [View Article] [PubMed]
    [Google Scholar]
  19. Jin D, Wang P, Bai Z, Jin B, Yu Z et al. Terrimonas pekingensis sp. nov., isolated from bulking sludge, and emended descriptions of the genus Terrimonas, Terrimonas ferruginea, Terrimonas lutea and Terrimonas aquatica. Int J Syst Evol Microbiol 2013; 63:1658–1664 [View Article] [PubMed]
    [Google Scholar]
  20. Kim MC, Kang OC, Kim CM, Zhang Y, Liu Z et al. Terrimonas crocea sp. nov., isolated from the till of a high Arctic glacier. Int J Syst Evol Microbiol 2017; 67:868–874 [View Article] [PubMed]
    [Google Scholar]
  21. Kim S-J, Cho H, Ahn J-H, Weon H-Y, Joa J-H et al. Terrimonas terrae sp. nov., isolated from the rhizosphere of a tomato plant. Int J Syst Evol Microbiol 2017; 67:3105–3110 [View Article] [PubMed]
    [Google Scholar]
  22. Kim J-K, Kang M-S, Park SC, Kim K-M, Choi K et al. Sphingosinicella ginsenosidimutans sp. nov., with ginsenoside converting activity. J Microbiol 2015; 53:435–441 [View Article] [PubMed]
    [Google Scholar]
  23. 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]
  24. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25:4876–4882 [View Article] [PubMed]
    [Google Scholar]
  25. Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucleic Acids Symp Ser 1999; 41:95–98
    [Google Scholar]
  26. 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]
  27. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 1981; 17:368–376 [View Article] [PubMed]
    [Google Scholar]
  28. Fitch WM. Toward defining the course of evolution: minimum change for a specific tree topology. Syst Zool 1971; 20:406 [View Article]
    [Google Scholar]
  29. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol 2013; 30:2725–2729 [View Article]
    [Google Scholar]
  30. Kimura M. The Neutral Theory of Molecular Evolution Cambridge: Cambridge University Press.1983; 1983 [View Article]
    [Google Scholar]
  31. Felsenstein J. Confidence limit on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791 [View Article]
    [Google Scholar]
  32. Brettin T, Davis JJ, Disz T, Edwards RA, Gerdes S et al. RASTtk: a modular and extensible implementation of the RAST algorithm for building custom annotation pipelines and annotating batches of genomes. Sci Rep 2015; 5:8365 [View Article] [PubMed]
    [Google Scholar]
  33. Smibert RM, Krieg NR. Phenotypic characterization. In Gerhardt P, Murray RGE, Wood WA, Krieg NR. eds Methods for General and Molecular Bacteriology Washington, DC: American Society for Microbiology; 1944 pp 607–655
    [Google Scholar]
  34. Jain A, Jain R, Jain S. Motility testing – hanging drop method and stab. In Basic Techniques in Biochemistry, Microbiology and Molecular Biology New York, NY: Springer Protocols Handbooks. Humana; 2020 https://doi.org/10.1007/978-1-4939-9861-6_34
    [Google Scholar]
  35. Fautz E, Reichenbach H. A simple test for flexirubin-type pigments. FEMS Microbiology Letters 1980; 8:87–91 [View Article]
    [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. 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]
  38. Sasser M. Identification of bacteria through fatty acid analysis. In Klement Z, Rudolph K, Sands DC. eds Methods in Phytobacteriology Budapest: Akademiai Kaido; 1990 pp 199–204
    [Google Scholar]
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