Affiliation:
1. Department of Microbiology & Immunology
2. Department of Physiology, Dartmouth Medical School, Hanover, New Hampshire
Abstract
ABSTRACT
We previously reported that the novel
Pseudomonas aeruginosa
toxin Cif is capable of decreasing apical membrane expression of the
c
ystic
f
ibrosis
t
ransmembrane conductance
r
egulator (CFTR). We further demonstrated that Cif is capable of degrading the synthetic epoxide hydrolase (EH) substrate
S
-NEPC [(2S,3S)-
trans
-3-phenyl-2-oxiranylmethyl 4-nitrophenol carbonate], suggesting that Cif may be reducing apical membrane expression of CFTR via its EH activity. Here we report that Cif is capable of degrading the xenobiotic epoxide epibromohydrin (EBH) to its vicinal diol 3-bromo-1,2-propanediol. We also demonstrate that this epoxide is a potent inducer of
cif
gene expression. We show that the predicted TetR family transcriptional repressor encoded by the PA2931 gene, which is immediately adjacent to and divergently transcribed from the
cif
-containing, three-gene operon, negatively regulates
cif
gene expression by binding to the promoter region immediately upstream of the
cif
-containing operon. Furthermore, this protein-DNA interaction is disrupted by the epoxide EBH in vitro, suggesting that the binding of EBH by the PA2931 protein product drives the disassociation from its DNA-binding site. Given its role as a repressor of
cif
gene expression, we have renamed PA2931 as CifR. Finally, we demonstrate that
P. aeruginosa
strains isolated from cystic fibrosis patient sputum with increased
cif
gene expression are impaired for the expression of the
cifR
gene.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
34 articles.
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