Limosilactobacillus, 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.4728728 |
persistent identifier |
https://treatment.plazi.org/id/03A8D903-D23F-0270-FC95-FA0F50C330C5 |
treatment provided by |
Valdenar (2021-04-29 20:05:09, last updated by Guilherme 2025-02-06 14:43:30) |
scientific name |
Limosilactobacillus |
status |
gen. nov. |
DESCRIPTIONOF LIMOSILACTOBACILLUS GEN. NOV.
Limosilactobacillus (Li.mo.si.lac.to.ba.cil'lus. L. masc. adj. limosus, slimy, referring to the property of most strains in the genus to produce exopolysaccharides from sucrose; N.L. masc. n. Lactobacillus a bacterial genus name; N.L. masc. n. Limosilactobacillus , a slimy lactobacillus.
Gram-positive, rod- or coccoid-shaped, catalase-negative, heterofermentative, and anaerobic or aerotolerant. Growth is observed at 37 °C and, for most species, at 45 °C but not at 15 °C. Strains in the genus have very small genomes ranging from 1.6 Mbp for L. equigenerosi to 2.25 Mbp for L. mucosae ; the mol % G+C content as calculated from whole genome shotgun sequences ranges from 38.6.1 to 53.4. In comparison to other heterofermentative lactobacilli, Limosilactobacillus speciesferment a relativelybroad spectrumof carbohydrates, however, several species do not ferment glucose. Acid resistance is typically mediated by expression of urease, glutaminase, glutamate decarboxylase and / or arginine deiminase activities [ 252]. With the exception of L. fermentum and L. secaliphilus , strains in the genus were isolated from intestinal habitats, or were shown experimentally to have adapted to theintestine of vertebrate animals. Limosilactobacillus reuteri and other strains in the genus produce exopolysaccharides from sucrose to support biofilm formation on non-secretory epithelia in the upper intestinal tract [ 14, 253]. In their natural habitat, Limosilactobacillus species generally form stable associations with Lactobacillus spp. ; the same association is observed in food fermentations with Limosilactobacillus . Limosilactobacillus species. , particularly L. reuteri , are produced commercially for use as starter culture and as probiotic culture.
Aphylogenetic tree on the basis of 16S rRNA genes of all species in the genus Limosilactobacillus is provided in Figure S6N View Fig .
The type species of the genusis Limosilactobacillus fermentum comb. nov.; Limosilactobacillus was previously referred to as the Lactobacillus reuteri group.
252. Teixeira JS, Seeras A, Sanchez-Maldonado AF, Zhang C, Su MS- W et al. Glutamine, glutamate, and arginine-based acid resistance in Lactobacillus reuteri. Food Microbiol 2014; 42: 172 - 180.
253. Tieking M, Kaditzky S, Valcheva R, Korakli M, Vogel RF et al. Extracellular homopolysaccharides and oligosaccharides from intestinal lactobacilli. J Appl Microbiol 2005; 99: 692 - 702.
14. Zheng J, Ruan L, Sun M, Ganzle M. A genomic view of lactobacilli and pediococci demonstrates that phylogeny matches ecology and physiology. Appl Environ Microbiol 2015; 81: 7233 - 7243.
Fig. 6. Gene family presence/absence patterns in Lactobacillaceae and Leuconostocaceae. Each column represents a gene family presence/absence pattern in species of Lactobacillaceae and Leuconostoaceae, where presence is indicated with a dot. The absolute number of gene families that conform to each pattern is visualized in the marginal bar plot at the top. Separations between phylogroups are indicated with horizontal black lines. We defined genes that were present in all genomes of a clade and in none of the genomes outside of that clade as ‘signature genes’ (dark blue); other genes are shown in light blue. Only presence/absence patterns followed by four or more gene families are shown. Patterns of presence in a single species or all species are not shown. Unassigned species are clusters of closely related genomes which could not be assigned to a known species due to low whole-genome similarity to a type strain and/or low 16S rRNA similarity to a type strain.
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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