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Journal of Bacteriology, May 1999, p. 2889-2894, Vol. 181, No. 9
Department of Biochemistry and Molecular
Biology, University of Oklahoma Health Sciences Center, Oklahoma
City, Oklahoma 73190
Received 30 November 1998/Accepted 6 February 1999
BkdR is the transcriptional activator of the bkd
operon, which encodes the four proteins of the branched-chain keto acid
dehydrogenase multienzyme complex of Pseudomonas putida. In
this study, hydroxyl radical footprinting revealed that BkdR
bound to only one face of DNA over the same region identified in
DNase I protection assays. Deletions of even a few
bases in the 5' region of the BkdR-binding site greatly
reduced transcription, confirming that the entire protected region is necessary for transcription. In vitro transcription of the bkd operon was obtained by using a vector
containing the bkdR-bkdA1 intergenic region plus the
putative
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
In Vitro Transcriptional Studies of the
bkd Operon of Pseudomonas putida:
L-Branched-Chain Amino Acids and D-Leucine
Are the Inducers
-independent terminator of the bkd
operon. Substrate DNA, BkdR, and any of the
L-branched-chain amino acids or D-leucine was
required for transcription. Branched-chain keto acids,
D-valine, and D-isoleucine did not promote
transcription. Therefore, the L-branched-chain amino acids
and D-leucine are the inducers of the bkd
operon. The concentration of L-valine required for
half-maximal transcription was 2.8 mM, which is similar to that needed
to cause half-maximal proteolysis due to a conformational change in
BkdR. A model for transcriptional activation of the bkd
operon by BkdR during enzyme induction which incorporates these
results is presented.
*
Corresponding author. Mailing address: Department of
Biochemistry and Molecular Biology, University of Oklahoma Health
Sciences Center, P.O. Box 26901, Oklahoma City, OK 73190. Phone:
(405) 271-2227. Fax: (405) 271-3092. E-mail:
john-sokatch{at}ouhsc.edu.
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