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Journal of Bacteriology, April 1999, p. 2102-2109, Vol. 181, No. 7
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
BadR, a New MarR Family Member, Regulates Anaerobic
Benzoate Degradation by Rhodopseudomonas palustris in
Concert with AadR, an Fnr Family Member
Paul G.
Egland and
Caroline S.
Harwood*
Department of Microbiology, University of
Iowa, Iowa City, Iowa 52242
Received 2 September 1998/Accepted 19 January 1999
A cluster of genes for the anaerobic degradation of benzoate has
been described for the phototrophic bacterium Rhodopseudomonas palustris. Here we provide an initial analysis of the regulation of anaerobic benzoate degradation by examining the contributions of two
regulators: a new regulator, BadR, encoded by the benzoate degradation
gene cluster, and a previously described regulator, AadR, whose gene
lies outside the cluster. Strains with single mutations in either
badR or aadR grew slowly on benzoate but were relatively unimpaired in growth on succinate and several intermediates of benzoate degradation. A badR aadR double mutant was
completely defective in anaerobic growth on benzoate. Effects of the
regulators on transcriptional activation were monitored with an
R. palustris strain carrying a chromosomal fusion of
'lacZ to the badE gene of the
badDEFG operon. This operon encodes benzoyl-coenzyme A (benzoyl-CoA) reductase, an unusual oxygen-sensitive enzyme that catalyzes the benzene ring reduction reaction that is the rate-limiting step in anaerobic benzoate degradation. Expression of
badE::'lacZ was induced 100-fold when
cells grown aerobically on succinate were shifted to anaerobic growth
on succinate plus benzoate. The aadR gene was required for
a 20-fold increase in expression that occurred in response to
anaerobiosis, and badR was responsible for a further 5-fold
increase in expression that occurred in response to benzoate. Further
studies with the badE::'lacZ fusion
strain grown with various kinds of aromatic acids indicated that BadR probably responds to benzoyl-CoA acting as an effector molecule. Sequence information indicates that BadR is a member of the MarR family
of transcriptional regulators. These studies expand the range of
functions regulated by MarR family members to include anaerobic
aromatic acid degradation and provide an example of a MarR-type protein
that acts as a positive regulator rather than as a negative regulator,
as do most MarR family members. AadR resembles the Escherichia
coli Fnr regulator in sequence and contains cysteine residues
that are spaced appropriately to serve in the capacity of a
redox-sensing protein.
*
Corresponding author. Mailing address: Department of
Microbiology, University of Iowa, Iowa City, IA 52242. Phone: (319)
335-7783. Fax: (319) 335-7679. E-mail:
caroline-harwood{at}uiowa.edu.
Journal of Bacteriology, April 1999, p. 2102-2109, Vol. 181, No. 7
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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