TY - JOUR
T1 - Proteome and transcriptome analysis of the virulence genes regulated by the VirR/VirS system in Clostridium perfringens
AU - Shimizu, Takeshi
AU - Shima, Kensuke
AU - Yoshino, Ken Ichi
AU - Yonezawa, Kazuyoshi
AU - Shimizu, Tohru
AU - Hayashi, Hideo
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2002
Y1 - 2002
N2 - The proteins under the control of the two-component system VirR/VirS in Clostridium perfringens were analyzed by using two-dimensional gel electrophoresis of the culture supernatant from the wild type and the virR mutant. Based on matrix-assisted laser desorption ionization-time of flight/mass spectrometry, seven positively regulated proteins and eight negatively regulated proteins were identified. Transcriptome analysis confirmed that 7 of the 15 proteins were regulated by the VirR/VirS system at the transcriptional level, but the remaining proteins were modified with a VirR/VirS-directed protease at the posttranslation and secretion levels. We purified and characterized the VirR/VirS-directed protease from the culture supernatant and identified it as a kind of clostripain. Because this proteolytic activity was strongly inhibited by leupeptin and antipain, it was concluded that this protease was a member of the family of cysteine proteases of C. perfringens.
AB - The proteins under the control of the two-component system VirR/VirS in Clostridium perfringens were analyzed by using two-dimensional gel electrophoresis of the culture supernatant from the wild type and the virR mutant. Based on matrix-assisted laser desorption ionization-time of flight/mass spectrometry, seven positively regulated proteins and eight negatively regulated proteins were identified. Transcriptome analysis confirmed that 7 of the 15 proteins were regulated by the VirR/VirS system at the transcriptional level, but the remaining proteins were modified with a VirR/VirS-directed protease at the posttranslation and secretion levels. We purified and characterized the VirR/VirS-directed protease from the culture supernatant and identified it as a kind of clostripain. Because this proteolytic activity was strongly inhibited by leupeptin and antipain, it was concluded that this protease was a member of the family of cysteine proteases of C. perfringens.
UR - http://www.scopus.com/inward/record.url?scp=0036239635&partnerID=8YFLogxK
U2 - 10.1128/JB.184.10.2587-2594.2002
DO - 10.1128/JB.184.10.2587-2594.2002
M3 - Journal articles
C2 - 11976286
AN - SCOPUS:0036239635
SN - 0021-9193
VL - 184
SP - 2587
EP - 2594
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 10
ER -