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An FNR-Type Regulator Controls the Anaerobic Expression of Hyn Hydrogenase in Thiocapsa roseopersicina
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ABSTRACT
The purple sulfur photosynthetic bacterium
Thiocapsa roseopersicina
BBS contains a heat-stable membrane-associated hydrogenase encoded by the
hyn
operon. Expression from the
hyn
operon regulatory region is up-regulated under anaerobic conditions.
cis
elements were mapped between positions −602 and −514 upstream from the
hynS
gene. Within this region two sequences that resemble DNA sites for FNR were recognized. The gene of an FNR homologue, FnrT, was identified in the genome of
T. roseopersicina
, and an
fnrT
knockout mutant was constructed. Anaerobic induction of
hynS
expression was abolished in the
fnrT
mutant, suggesting that FnrT is an activator of the
hynS
promoter. The
T. roseopersicina hynS
promoter could be activated in
Escherichia coli
, and this regulation was dependent on
E. coli
FNR. In vitro experiments with purified
E. coli
Ala154 FNR protein and purified
E. coli
RNA polymerase showed that FNR bound to two sites in the
hyn
regulatory region, that FNR could activate transcription initiation at the
hynS
promoter, and that FNR bound at the two target sites activated to different extents.
American Society for Microbiology
Title: An FNR-Type Regulator Controls the Anaerobic Expression of Hyn Hydrogenase in
Thiocapsa roseopersicina
Description:
ABSTRACT
The purple sulfur photosynthetic bacterium
Thiocapsa roseopersicina
BBS contains a heat-stable membrane-associated hydrogenase encoded by the
hyn
operon.
Expression from the
hyn
operon regulatory region is up-regulated under anaerobic conditions.
cis
elements were mapped between positions −602 and −514 upstream from the
hynS
gene.
Within this region two sequences that resemble DNA sites for FNR were recognized.
The gene of an FNR homologue, FnrT, was identified in the genome of
T.
roseopersicina
, and an
fnrT
knockout mutant was constructed.
Anaerobic induction of
hynS
expression was abolished in the
fnrT
mutant, suggesting that FnrT is an activator of the
hynS
promoter.
The
T.
roseopersicina hynS
promoter could be activated in
Escherichia coli
, and this regulation was dependent on
E.
coli
FNR.
In vitro experiments with purified
E.
coli
Ala154 FNR protein and purified
E.
coli
RNA polymerase showed that FNR bound to two sites in the
hyn
regulatory region, that FNR could activate transcription initiation at the
hynS
promoter, and that FNR bound at the two target sites activated to different extents.
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