Sporolactobacillus vineae sp. nov., a spore-forming lactic acid bacterium isolated from vineyard soil
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- Sporolactobacillus vineae sp. nov., a spore-forming lactic acid bacterium isolated from vineyard soil
- Young Hyo Chang; Min-Yeong Jung; Insoon Park; Hee-Mock Oh
- Bibliographic Citation
- International Journal of Systematic and Evolutionary Microbiology, vol. 58, no. 10, pp. 2316-2320
- Publication Year
- Two spore-forming, facultatively anaerobic, lactic acid bacteria, strains SL153T and SL1153, were isolated from vineyard soil in Korea. Cells of both strains were slightly curved, Gram-positive, motile rods that measured between 1 and 4 μm in length and were approximately 0.5 μm in diameter. Strains SL153T and SL1153 fermented glucose, fructose, mannose and sorbitol, but were negative for nitrate reduction, catalase and oxidase. The predominant cellular fatty acids of the two isolates were iso-C15:0 anteiso-C15:0 and anteiso-C17:0. meso-Diaminopimelic acid, glucose, mannose and galactose were determined in their whole-cell hydrolysates. 16S rRNA gene sequences from the two strains were almost identical (99.9%) and they could be placed in the genus Sporolactobacillus according to phylogenetic analysis. The species most closely related to SL153T were Sporolactobacillus inulinus and Sporolactobacillus terrae with 16S rRNA gene similarities of 95.7 and 95.5%, respectively, with the type strains. Levels of DNA-DNA relatedness between strain SL153T and the type strains of S. inulinus, S. terrae and Sporolactobacillus kofuensis were 18.5, 18.0 and 17.0%, respectively. On the basis of the phylogenetic (16S rRNA gene), chemotaxonomic and phenotypic evidence given in this study, it is proposed that strains SL153T and SL1153 should be assigned to the genus Sporolactobacillus as representatives of the novel species Sporolactobacillus vineae sp. nov. The type strain is SL 153T (=KCTC 5376T=JCM 14637T).
- Microbiology Soc
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- Ochang Branch Institute > Division of Bioinfrastructure > ABS Research Support Center > 1. Journal Articles
Division of Biomaterials Research > Cell Factory Research Center > 1. Journal Articles
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