Affiliation:
1. Laboratoire de Chimie Bactérienne, Institut de Biologie Structurale et Microbiologie, Centre National de la Recherche Scientifique, 13402 Marseille Cedex 20, France
Abstract
ABSTRACT
Several bacteria can grow by using small organic compounds such as trimethylamine oxide (TMAO) as electron acceptors. In
Shewanella
species, the TMAO reductase respiratory system is encoded by the
torECAD
operon. We showed that production of the TMAO reductase of
S. oneidensis
was induced by TMAO and repressed by oxygen, and we noticed that a three-gene cluster (
torSTR
) encoding a complex two-component regulatory system was present downstream of the
torECAD
operon. We introduced the
torSTR
gene cluster into
Escherichia coli
and showed that this regulatory gene cluster is involved in TMAO induction of the
torE
promoter but plays no role in the oxygen control. The TorR response regulator was purified, and gel shift and footprinting experiments revealed that TorR binds to a single region located about 70 bases upstream of the transcription start site of the
tor
structural operon. By deletion analysis, we confirmed that the TorR operator site is required for induction of the
tor
structural promoter. As the TMAO regulatory system of
S. oneidensis
is homologous to that of
E. coli
, we investigated a possible complementation between the TMAO regulatory components of the two bacteria. Interestingly, TorS
ec
, the TMAO sensor of
E. coli
, was able to transphosphorylate TorR
so
, the TMAO response regulator of
S. oneidensis
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
33 articles.
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