Abstract
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.
| Original language | English |
|---|---|
| Journal | Journal of Bacteriology |
| Volume | 184 |
| Issue number | 10 |
| Pages (from-to) | 2587-2594 |
| Number of pages | 8 |
| ISSN | 0021-9193 |
| DOIs | |
| Publication status | Published - 2002 |
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
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