Liquorilactobacillus vini, Zheng & Wittouck & Salvetti & Franz & Harris & Mattarelli & O’Toole & Pot & Vandamme & Walter & Watanabe & Wuyts & Felis & Gänzle & Lebeer, 2020
publication ID |
https://doi.org/ 10.1099/ijsem.0.004107 |
DOI |
https://doi.org/10.5281/zenodo.4728620 |
persistent identifier |
https://treatment.plazi.org/id/03A8D903-D228-0266-FFD0-FB79535F3446 |
treatment provided by |
Valdenar |
scientific name |
Liquorilactobacillus vini |
status |
comb. nov. |
DESCRIPTIONOF LIQUORILACTOBACILLUS VINI COMB. NOV.
Liquorilactobacillus vini (vi’ni. L. gen. n. vini of wine).
Basonym: Lactobacillus vini Rodas et al. 2006 , 516 VP
The cells are motile rods, they do not produce exopolysaccharide from sucrose, but they utilize citric and malic acids [ 208]. L. vini was the first organism for which metabolism of pentoses via the pentose phosphate pathway to lactate as sole end product was described [ 18]. The metabolism for homofermentative metabolism of pentoses was initially described for strains later classified as L. vini [ 18, 209]. Thegenome size of the type strain is 2.24 Mbp. The mol% G+C content of DNAis 37.5.
Isolated from fermenting Spanish grape must and from bioethanol industrial processes in different distilleries of Brazil.
Thetypestrainis Mont 4 T = CECT 5924 T = DSM 20605 T =JCM 14280 T.
Genome sequence accession number: AYYX00000000.
16S rRNA gene accession number: AJ576009 View Materials .
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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