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Journal of Bacteriology, October 2000, p. 5596-5599, Vol. 182, No. 19
Research Center for Biomedicinal Resources
(Bio-Med RRC), Paichai University, Taejon 302-735, Korea1; Department of Molecular
Microbiology, Research Institute for Microbial Diseases, Osaka
University, 3-1 Yamadaoka, Suita, Osaka
565-0871,2 and Department of Marine
Biotechnology, Faculty of Technology, Fukuyama University,
Fukuyama, Hiroshima 729-0292,3 Japan; and
Department of Biological Sciences, Purdue University, West
Lafayette, Indiana 479074
Received 10 March 2000/Accepted 7 July 2000
We have shown that the Escherichia coli
phosphate-starvation-inducible psiE gene is regulated by
both phosphate and the carbon source by using both lacZ and
chloramphenicol acetyltransferase gene (cat) fusions. Yet,
under all conditions tested, a single transcriptional start site lying
7 bp downstream of a predicted
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Dual Transcriptional Regulation of the
Escherichia coli Phosphate-Starvation-Inducible
psiE Gene of the Phosphate Regulon by PhoB and the Cyclic
AMP (cAMP)-cAMP Receptor Protein Complex
10 region was revealed by primer
extension analysis. DNase I footprinting showed that the PhoB
transcriptional-activator protein protects two predicted
pho boxes lying upstream of and near the
35 promoter
region. Similar analysis showed that the cyclic AMP (cAMP)-cAMP
receptor protein (cAMP-CRP) complex binds a region that overlaps with
the downstream pho box. These results, together with
measurements of the in vivo psiE promoter activity under various conditions, show that expression of the psiE gene
is under direct positive and negative control by PhoB and cAMP-CRP, respectively.
*
Corresponding author. Mailing address: Department of
Molecular Microbiology, Research Institute for Microbial Diseases,
Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan. Phone: 81-6-6879-8318. Fax: 81-6-6879-8320. E-mail:
makino{at}bkns01.biken.osaka-u.ac.jp.
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