Lactobacillus suantsaicola sp. nov. and Lactobacillus suantsaiihabitans sp. nov., isolated from suan-tsai, a traditional fermented mustard green product of Taiwan
Four Gram-stain-positive strains, R7 , R11, R19 and R27, were isolated from suan-tsai, a traditional fermented mustard green product of Taiwan. Cells were rod-shaped, non-motile, non-haemolytic, asporogenous, facultatively anaerobic, heterofermentative, and did not exhibit catalase and oxidase activ...
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Veröffentlicht in: | International journal of systematic and evolutionary microbiology 2020-05, Vol.70 (5), p.2972-2980 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Four Gram-stain-positive strains, R7
, R11, R19
and R27, were isolated from suan-tsai, a traditional fermented mustard green product of Taiwan. Cells were rod-shaped, non-motile, non-haemolytic, asporogenous, facultatively anaerobic, heterofermentative, and did not exhibit catalase and oxidase activities. Comparative analyses of 16S rRNA,
and
gene sequences demonstrated that these novel strains were members of the genus
. 16S rRNA and the concatenated
and
gene sequence similarities between strains R7
and R11, and strains R19
and R27 were very high (>99.8 % similarity), respectively. On the basis of 16S rRNA gene sequence similarities, the type strains of
(98.5 %),
(98.5 %),
(98.1 %) and
(98.1 %) were the closest neighbours to strains R7
and R11, and the type strains of
(98.9 %),
(98.4 %),
(98.4 %),
(98.4 %) and
(98.0 %) were the closest neighbours to strains R19
and R27, respectively. The average nucleotide identity values of R7
and R19
with the closely related type strains were 78.9-80.1% and 75.7-80.5 %, respectively. The digital DNA-DNA hybridization values were 22.8-23.6% and 21.0-23.1 %, respectively. Phenotypic and genotypic test results demonstrated that these strains represent two novel species of the genus
, for which the name
sp. nov. (R7
=BCRC 81127
=NBRC 113530
) and
sp. nov. (R19
=BCRC 81129
=NBRC 113532
) are proposed. |
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ISSN: | 1466-5026 1466-5034 |
DOI: | 10.1099/ijsem.0.003522 |