1887

Abstract

A lactic acid bacterial strain, HBUAS57009, isolated from traditionally fermented food (Zha-Chili) in China, was characterized to clarify its taxonomic status using a polyphasic approach. Strain HBUAS57009 was phylogenetically closely related to DCY50, 218-6, 112-3, TUM BP 140423000-2250, 218-10 and THK-V8 with sequence similarities of 98.6–99.3 %. The genome-to-genome distance and average nucleotide identity values between the genomes of strain HBUAS57009 and type strains of closely related species were less than 32.0 and 86.0 %, respectively; this is below the threshold for species boundaries. The major cellular fatty acids (>10 %) were C, C ω9 and iso-C. The G+C content of the genomic DNA of strain HBUAS57009 was 47.8 mol%. Examination of the functional categories of the genome revealed that strain HBUAS57009 could perform both homolactic and heterolactic fermentation processes to produce lactic acid via complete glycolysis and the pentose phosphate pathway. The putative biosynthesis pathway of butane-2,3-diol and acetoin, two important flavour compounds in the food industry, were identified using mapper analysis. Based on its genotypic and phenotypic features, strain HBUAS57009 (=GDMCC 1.1664=KACC 21424) is designated as the type strain of a novel species, for which the name sp. nov. is proposed.

Funding
This study was supported by the:
  • Projects of Innovation and Development Pillar Program for Key Industries in Southern Xinjiang of Xinjiang Production and Construction Corps (Award 2018DB002)
    • Principle Award Recipient: Zhuang Guo
  • Xinjiang Production and Construction Corps Innovation Team Building Projects in Key Areas (Award 2017CB012)
    • Principle Award Recipient: Zhuang Guo
  • Cultivation of Teachers' Scientific Research Ability Foundation of Hubei University of Arts and Science (Award 2017kypy051)
    • Principle Award Recipient: Zhuang Guo
  • National Natural Science Foundation of China (Award 31600947)
    • Principle Award Recipient: Zhuang Guo
  • National Natural Science Foundation of China (Award 31501455)
    • Principle Award Recipient: Zhuang Guo
Loading

Article metrics loading...

/content/journal/ijsem/10.1099/ijsem.0.004072
2020-03-04
2024-04-18
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/70/4/2580.html?itemId=/content/journal/ijsem/10.1099/ijsem.0.004072&mimeType=html&fmt=ahah

References

  1. Claesson MJ, van Sinderen D, O'Toole PW. The genus Lactobacillus--a genomic basis for understanding its diversity. FEMS Microbiol Lett 2007; 269:22–28 [View Article]
    [Google Scholar]
  2. Cui S, Zhao N, Lu W, Zhao F, Zheng S et al. Effect of different Lactobacillus species on volatile and nonvolatile flavor compounds in juices fermentation. Food Sci Nutr 2019; 7:2214–2223 [View Article]
    [Google Scholar]
  3. Liu S, Chen Q, Zou H, Yu Y, Zhou Z et al. A metagenomic analysis of the relationship between microorganisms and flavor development in Shaoxing mechanized huangjiu fermentation mashes. Int J Food Microbiol 2019; 303:9–18 [View Article]
    [Google Scholar]
  4. Beijerinck MW. Sur les ferments lactiques de l’industrie. Archiv Néerlandaises des Sciences Exactes et Naturelles 1901; 6:212–243
    [Google Scholar]
  5. Parte AC. LPSN--list of prokaryotic names with standing in nomenclature. Nucleic Acids Res 2014; 42:D613–D616 [View Article]
    [Google Scholar]
  6. Salvetti E, Torriani S, Felis GE. The genus Lactobacillus: a taxonomic update. Probiotics Antimicrob Proteins 2012; 4:217–226 [View Article]
    [Google Scholar]
  7. Liu D, Tong C. Bacterial community diversity of traditional fermented vegetables in China. LWT 2017; 86:40–48 [View Article]
    [Google Scholar]
  8. Long GY, Gu CT. Lactobacillus jixianensis sp. nov., Lactobacillus baoqingensis sp. nov., Lactobacillus jiayinensis sp. nov., Lactobacillus zhaoyuanensis sp. nov., Lactobacillus lindianensis sp. nov., Lactobacillus huananensis sp. nov., Lactobacillus tangyuanensis sp. nov., Lactobacillus fuyuanensis sp. nov., Lactobacillus tongjiangensis sp. nov., Lactobacillus fujinensis sp. nov. and Lactobacillus mulengensis sp. nov., isolated from Chinese traditional pickle. Int J Syst Evol Microbiol 2019; 69:2340–2353 [View Article]
    [Google Scholar]
  9. Wei YX, Gu CT. Lactobacillus yilanensis sp. nov., Lactobacillus bayanensis sp. nov., Lactobacillus keshanensis sp. nov., Lactobacillus kedongensis sp. nov., Lactobacillus baiquanensis sp. nov., Lactobacillus jidongensis sp. nov., Lactobacillus hulinensis sp. nov., Lactobacillus mishanensis sp. nov. and Lactobacillus zhongbaensis sp. nov., isolated from Chinese traditional pickle and yogurt. Int J Syst Evol Microbiol 2019; 69:3178–3190 [View Article]
    [Google Scholar]
  10. Liu DD, Gu CT. Lactobacillus pingfangensis sp. nov., Lactobacillus daoliensis sp. nov., Lactobacillus nangangensis sp. nov., Lactobacillus daowaiensis sp. nov., Lactobacillus dongliensis sp. nov., Lactobacillus songbeiensis sp. nov. and Lactobacillus kaifaensis sp. nov., isolated from traditional Chinese pickle. Int J Syst Evol Microbiol 2019; 69:3237–3247 [View Article]
    [Google Scholar]
  11. Zhang Z, Hou Q, Wang Y, Li W, Zhao H et al. Lactobacillus zhachilii sp. nov., a lactic acid bacterium isolated from Zha-Chili. Int J Syst Evol Microbiol 2019; 69:2196–2201 [View Article]
    [Google Scholar]
  12. Sakamoto M, Takeuchi Y, Umeda M, Ishikawa I, Benno Y. Application of terminal RFLP analysis to characterize oral bacterial flora in saliva of healthy subjects and patients with periodontitis. J Med Microbiol 2003; 52:79–89 [View Article]
    [Google Scholar]
  13. 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; 67:16131617 [View Article]
    [Google Scholar]
  14. 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]
  15. Kim M, Oh H-S, Park S-C, Chun J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes. Int J Syst Evol Microbiol 2014; 64:346–351 [View Article]
    [Google Scholar]
  16. Costilow RN. Manual of methods for general bacteriology, American Society for Microbiology, Washington. DC 198169–70
    [Google Scholar]
  17. Handley PS, Carter PL, Wyatt JE, Hesketh LM. Surface structures (peritrichous fibrils and tufts of fibrils) found on Streptococcus sanguis strains may be related to their ability to coaggregate with other oral genera. Infect Immun 1985; 47:217–227 [View Article]
    [Google Scholar]
  18. Barer MR, Marsh PJ. Rapid cytochemical demonstration of cytochrome oxidase activity in pathogenic bacteria. J Clin Pathol 1992; 45:487–489 [View Article]
    [Google Scholar]
  19. Tittsler RP, Sandholzer LA. The use of semi-solid agar for the detection of bacterial motility. J Bacteriol 1936; 31:575580 [View Article]
    [Google Scholar]
  20. Da X, Jiang F, Chang X, Ren L, Qiu X et al. Pedobacter ardleyensis sp. nov., isolated from soil in Antarctica. Int J Syst Evol Microbiol 2015; 65:3841–3846 [View Article]
    [Google Scholar]
  21. Chen W, Luo L, He L-Y, Wang Q, Sheng X-F. Distinct mineral weathering behaviors of the novel mineral-weathering strains Rhizobium yantingense H66 and Rhizobium etli CFN42. Appl Environ Microbiol 2016; 82:4090–4099 [View Article]
    [Google Scholar]
  22. 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]
  23. 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]
  24. Kroppenstedt RM. Separation of bacterial menaquinones by HPLC using reverse phase (RP18) and a silver loaded ion exchanger as stationary phases. J Liq Chromatogr 1982; 5:2359–2367 [View Article]
    [Google Scholar]
  25. Kämpfer P, Kroppenstedt RM. Numerical analysis of fatty acid patterns of coryneform bacteria and related taxa. Can J Microbiol 1996; 42:989–1005 [View Article]
    [Google Scholar]
  26. Li R, Yu C, Li Y, Lam T-W, Yiu S-M et al. SOAP2: an improved ultrafast tool for short read alignment. Bioinformatics 2009; 25:1966–1967 [View Article]
    [Google Scholar]
  27. Seemann T. Prokka: rapid prokaryotic genome annotation. Bioinformatics 2014; 30:2068–2069 [View Article]
    [Google Scholar]
  28. 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]
  29. Meier-Kolthoff JP, Auch AF, Klenk H-P, Göker M. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 2013; 14:60 [View Article]
    [Google Scholar]
  30. Chaudhari NM, Gupta VK, Dutta C. BPGA- an ultra-fast pan-genome analysis pipeline. Sci Rep 2016; 6:24373 [View Article]
    [Google Scholar]
  31. Institute of Evolutionary Biology University of Edinburgh. Figtree.
  32. Kant R, Blom J, Palva A, Siezen RJ, de Vos WM. Comparative genomics of Lactobacillus . Microb Biotechnol 2011; 4:323–332 [View Article]
    [Google Scholar]
  33. 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]
  34. Darzi Y, Letunic I, Bork P, Yamada T. iPath3.0: interactive pathways explorer V3. Nucleic Acids Res 2018; 46:W510–W513 [View Article]
    [Google Scholar]
  35. Kanehisa M. Enzyme Annotation and Metabolic Reconstruction Using KEGG. In Protein Function Prediction New York, NY: Humana Press; 2017 pp 135–145
    [Google Scholar]
  36. Martinez FAC, Balciunas EM, Salgado JM, González JMD, Converti A et al. Applications and production: a review. Trends food Sci Technol 2013; 30:70–83
    [Google Scholar]
  37. Reddy G, Altaf M, Naveena BJ, Venkateshwar M, Kumar EV. Amylolytic bacterial lactic acid fermentation—a review. Biotechnol Adv 2008; 26:22–34 [View Article]
    [Google Scholar]
  38. Iskandar CF, Cailliez-Grimal C, Borges F, Revol-Junelles A-M. Review of lactose and galactose metabolism in lactic acid bacteria dedicated to expert genomic annotation. Trends in Food Science & Technology 2019; 88:121–132 [View Article]
    [Google Scholar]
  39. Meng X, Wu Q, Wang L, Wang D, Chen L et al. Improving flavor metabolism of Saccharomyces cerevisiae by mixed culture with Bacillus licheniformis for Chinese Maotai-flavor liquor making. J Ind Microbiol Biotechnol 2015; 42:1601–1608 [View Article]
    [Google Scholar]
  40. Xiao Z, Lu JR. Generation of acetoin and its derivatives in foods. J Agric Food Chem 2014; 62:6487–6497 [View Article]
    [Google Scholar]
  41. Celińska E, Grajek W. Biotechnological production of 2,3-butanediol—current state and prospects. Biotechnol Adv 2009; 27:715–725 [View Article]
    [Google Scholar]
  42. Lin S-T, Wang L-T, Wang H-M, Tamura T, Mori K et al. Lactobacillus suantsaicola sp. nov. and Lactobacillus suantsaiihabitans sp. nov., isolated from suan-tsai, a traditional fermented mustard green product of Taiwan. Int J Syst Evol Microbiol 2019in press [View Article]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/ijsem.0.004072
Loading
/content/journal/ijsem/10.1099/ijsem.0.004072
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