Affiliation:
1. Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School, Schleswig-Holstein, Campus Kiel, Kiel, Germany
Abstract
ABSTRACT
3α-Hydroxysteroid dehydrogenase/carbonyl reductase (3α-HSD/CR) from
Comamonas testosteroni
is a key enzyme in steroid degradation in soil and water. 3α-HSD/CR gene (
hsdA
) expression can be induced by steroids like testosterone and progesterone. Previously, we have shown that the induction of
hsdA
expression by steroids is a derepression where steroidal inducers bind to two repressors, RepA and RepB, thereby preventing the blocking of
hsdA
transcription and translation, respectively (G. Xiong and E. Maser, J. Biol. Chem.
276:
9961-9970, 2001; G. Xiong, H. J. Martin, and E. Maser, J. Biol. Chem.
278
:47400–47407, 2003). In the present study, a new LysR-type transcriptional factor, HsdR, for 3α-HSD/CR expression in
C. testosteroni
has been identified. The
hsdR
gene is located 2.58 kb downstream from
hsdA
on the
C. testosteroni
ATCC 11996 chromosome with an orientation opposite that of
hsdA
. The
hsdR
gene was cloned and recombinant HsdR protein was produced, as was anti-HsdR polyclonal antibodies. While heterologous transformation systems revealed that HsdR activates the expression of the
hsdA
gene, electrophoresis mobility shift assays showed that HsdR specifically binds to the
hsdA
promoter region. Interestingly, the activity of HsdR is dependent on decreased repression by RepA. Furthermore,
in vitro
binding assays indicated that HsdR can come into contact with RNA polymerase. As expected, an
hsdR
knockout mutant expressed low levels of 3α-HSD/CR compared to that of wild-type
C. testosteroni
after testosterone induction. In conclusion, HsdR is a positive transcription factor for the
hsdA
gene and promotes the induction of 3α-HSD/CR expression in
C. testosteroni
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
15 articles.
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