z-logo
open-access-imgOpen Access
Pseudomonas tructae sp. nov., novel species isolated from rainbow trout kidney
Author(s) -
Woo Taek Oh,
Jin Woo Jun,
Sib Sankar Giri,
Sukyoung Yun,
Hyoun Joong Kim,
Sang Guen Kim,
Jeong Woo Kang,
Su Jin Han,
Jun Kwon,
Ji Hyung Kim,
Theo H. M. Smits
Publication year - 2019
Publication title -
international journal of systematic and evolutionary microbiology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 173
eISSN - 1466-5034
pISSN - 1466-5026
DOI - 10.1099/ijsem.0.003696
Subject(s) - biology , rpob , 16s ribosomal rna , pseudomonas putida , strain (injury) , pseudomonas , microbiology and biotechnology , phylogenetic tree , genetics , gene , bacteria , anatomy
This study describes the biochemical and phylogenetic characteristics of a Gram-negative strain, SNU WT1 T , isolated from rainbow trout kidney. The 16S rRNA gene sequencing indicated that strain SNU WT1 T was highly similar to Pseudomonas wadenswilerensis CCOS 864 T and closely related to other Pseudomonas putida -related strains. Multilocus sequence analysis of concatenated partial gyrB, rpoB and rpoD sequences revealed that strain SNU WT1 T was distinct from P. putida -related strains and formed a separate clade. The average nucleotide identity and Genome-to-Genome Distance Calculator values were 90.19 and 41.7 %with its closest relative P. wadenswilerensis CCOS 864 T ; however, it was phenotypically distinct from CCOS 864 T with respect to arginine dihydrolase, glucose fermentation, aesculin hydrolysis and N -acetyl-glucosamine assimilation. The major polar lipid of the strain was phosphatidylethanolamine and the major quinone was Q-9. The genome of strain SNU WT1 T had 5 685 196 bp with a G+C content of 61.83 mol%. We describe a novel species of genus Pseudomonas , for which the name Pseudomonastructae has been proposed, with SNU WT1 T (=KCTC 72265=JCM 33436) as the type strain.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here