Affiliation:
1. Department of Molecular and Cell Biology, University of Texas at Dallas, Richardson, Texas, USA
Abstract
ABSTRACT
Cysteine is potentially toxic and can affect diverse functions such as oxidative stress, antibiotic resistance, and swarming motility. The contribution of cysteine catabolism in modulating responses to cysteine has not been examined, in part because the genes have not been identified and mutants lacking these genes have not been isolated or characterized. We identified the gene for a previously described cysteine desulfhydrase, which we designated
cdsH
(formerly STM0458). We also identified a divergently transcribed gene that regulates
cdsH
expression, which we designated
cutR
(formerly
ybaO
, or STM0459). CdsH appears to be the major cysteine-degrading and sulfide-producing enzyme aerobically but not anaerobically. Mutants with deletions of
cdsH
and
ybaO
exhibited increased sensitivity to cysteine toxicity and altered swarming motility but unaltered cysteine-enhanced antibiotic resistance and survival in macrophages.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
67 articles.
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