Proteomics

Dataset Information

0

Shotgun proteomic profiling of Yersinia ruckeri strains


ABSTRACT: Project goal is to identify proteomic profiles of Yersinia ruckeri, the causative agent of enteric redmouth disease in fish. Four strains (SP-05, CSF007-82, 7959-11 and YRNC-10) of Y. ruckeri were isolated from disease rainbow trout, Oncorhynchus mykiss. Strains, SP-05 and CSF007-82, belong to serotype 1 and biotype 1 (motile and lipase positive), while strains 7959-11 and YRNC-10 belong to serotype 1 and biotype 2 (non-motile and lipase negative) and belong to serotype 1. A single colony of each strain was inoculated into tryptic soy broth (Casein peptone, dipotassium hydrogen phosphate, glucose, sodium chloride, soya peptone, Sigma) and grown at 22 °C with shaking (150 rpm). These starter cultures were then diluted with fresh sterile tryptic soy broth to an optical density (OD 600) of 0.10 ± 0.05. Five hundred microlitres of the diluted starter cultures were inoculated in duplicates, into 25 ml of tryptic soy broth. Cultures were grown overnight at 22 °C with shaking (150 rpm) until the late log phase. Cells were harvested by centrifugation, then washed three times with PBS.

INSTRUMENT(S): TripleTOF 5600

ORGANISM(S): Yersinia Ruckeri

SUBMITTER: Gokhlesh Kumar  

LAB HEAD: Dr. Gokhlesh Kumar

PROVIDER: PXD005439 | Pride | 2017-09-22

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
7959_11_A.mgf Mgf
7959_11_A.wiff Wiff
7959_11_A.xml Xml
7959_11_B.mgf Mgf
7959_11_B.wiff Wiff
Items per page:
1 - 5 of 24
altmetric image

Publications

Global proteomic profiling of Yersinia ruckeri strains.

Kumar Gokhlesh G   Hummel Karin K   Welch Timothy J TJ   Razzazi-Fazeli Ebrahim E   El-Matbouli Mansour M  

Veterinary research 20170920 1


Yersinia ruckeri is the causative agent of enteric redmouth disease (ERM) of salmonids. There is little information regarding the proteomics of Y. ruckeri. Herein, we perform whole protein identification and quantification of biotype 1 and biotype 2 strains of Y. ruckeri grown under standard culture conditions using a shotgun proteomic approach. Proteins were extracted, digested and peptides were separated by a nano liquid chromatography system and analyzed with a high-resolution hybrid triple q  ...[more]

Similar Datasets

2022-03-12 | GSE198051 | GEO
2016-03-29 | GSE74197 | GEO
2010-09-15 | E-GEOD-18289 | biostudies-arrayexpress
2016-03-29 | E-GEOD-74197 | biostudies-arrayexpress
2010-07-09 | GSE21111 | GEO
2018-09-07 | E-MTAB-7160 | biostudies-arrayexpress
2023-08-28 | GSE241582 | GEO
2010-07-08 | E-GEOD-21111 | biostudies-arrayexpress
| PRJEB23676 | ENA
2008-02-27 | GSE8526 | GEO