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The YjbH adaptor protein enhances proteolysis of the transcriptional regulator Spx in Staphylococcus aureus.

Engman, Jakob LU ; Rogstam, Annika LU ; Frees, Dorte ; Ingmer, Hanne and von Wachenfeldt, Claes LU (2012) In Journal of Bacteriology 194(5). p.1186-1194
Abstract
Spx is a global regulator that is widespread among the low G+C Gram-positive bacteria. Spx has been extensively studied in Bacillus subtilis, where it acts as an activator and a repressor of transcription in response to disulfide stress. Under non-stress conditions, Spx is rapidly degraded by the ClpXP protease. This degradation is enhanced by the YjbH adaptor protein. Upon disulfide stress, the amount of Spx rapidly increases due to a decrease in degradation. In the opportunistic pathogen Staphylococcus aureus, Spx is a global regulator influencing growth, biofilm formation and general stress protection, and cells lacking the spx gene exhibit poor growth also under non-stress conditions. To investigate the mechanism by which the activity... (More)
Spx is a global regulator that is widespread among the low G+C Gram-positive bacteria. Spx has been extensively studied in Bacillus subtilis, where it acts as an activator and a repressor of transcription in response to disulfide stress. Under non-stress conditions, Spx is rapidly degraded by the ClpXP protease. This degradation is enhanced by the YjbH adaptor protein. Upon disulfide stress, the amount of Spx rapidly increases due to a decrease in degradation. In the opportunistic pathogen Staphylococcus aureus, Spx is a global regulator influencing growth, biofilm formation and general stress protection, and cells lacking the spx gene exhibit poor growth also under non-stress conditions. To investigate the mechanism by which the activity of Spx is regulated we identified a homolog in S. aureus of the B. subtilis yjbH gene. The gene encodes a protein that shows approximately 30% sequence identity to YjbH of B. subtilis. Heterologous expression of S. aureus yjbH in a B. subtilis yjbH mutant restored Spx to wild type levels both under non-stress conditions and under conditions of disulfide stress. From these studies we conclude that the two YjbH homologues have a conserved physiological function. Accordingly, inactivation of yjbH in S. aureus increased the level of Spx protein and transcription of the Spx-regulated gene trxB. Notably, the yjbH mutant exhibited reduced growth and increased pigmentation, and both phenotypes were reversed by complementation of the yjbH gene. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Journal of Bacteriology
volume
194
issue
5
pages
1186 - 1194
publisher
American Society for Microbiology
external identifiers
  • wos:000300530800030
  • pmid:22194450
  • scopus:84857871745
  • pmid:22194450
ISSN
0021-9193
DOI
10.1128/JB.06414-11
language
English
LU publication?
yes
id
1c3eaed5-301d-4c04-a214-ddbb2b169239 (old id 2273590)
date added to LUP
2016-04-01 10:49:23
date last changed
2022-03-20 00:20:19
@article{1c3eaed5-301d-4c04-a214-ddbb2b169239,
  abstract     = {{Spx is a global regulator that is widespread among the low G+C Gram-positive bacteria. Spx has been extensively studied in Bacillus subtilis, where it acts as an activator and a repressor of transcription in response to disulfide stress. Under non-stress conditions, Spx is rapidly degraded by the ClpXP protease. This degradation is enhanced by the YjbH adaptor protein. Upon disulfide stress, the amount of Spx rapidly increases due to a decrease in degradation. In the opportunistic pathogen Staphylococcus aureus, Spx is a global regulator influencing growth, biofilm formation and general stress protection, and cells lacking the spx gene exhibit poor growth also under non-stress conditions. To investigate the mechanism by which the activity of Spx is regulated we identified a homolog in S. aureus of the B. subtilis yjbH gene. The gene encodes a protein that shows approximately 30% sequence identity to YjbH of B. subtilis. Heterologous expression of S. aureus yjbH in a B. subtilis yjbH mutant restored Spx to wild type levels both under non-stress conditions and under conditions of disulfide stress. From these studies we conclude that the two YjbH homologues have a conserved physiological function. Accordingly, inactivation of yjbH in S. aureus increased the level of Spx protein and transcription of the Spx-regulated gene trxB. Notably, the yjbH mutant exhibited reduced growth and increased pigmentation, and both phenotypes were reversed by complementation of the yjbH gene.}},
  author       = {{Engman, Jakob and Rogstam, Annika and Frees, Dorte and Ingmer, Hanne and von Wachenfeldt, Claes}},
  issn         = {{0021-9193}},
  language     = {{eng}},
  number       = {{5}},
  pages        = {{1186--1194}},
  publisher    = {{American Society for Microbiology}},
  series       = {{Journal of Bacteriology}},
  title        = {{The YjbH adaptor protein enhances proteolysis of the transcriptional regulator Spx in Staphylococcus aureus.}},
  url          = {{http://dx.doi.org/10.1128/JB.06414-11}},
  doi          = {{10.1128/JB.06414-11}},
  volume       = {{194}},
  year         = {{2012}},
}