Transcriptional regulation of the proC gene of Salmonella typhimurium.
Identifieur interne : 000142 ( Ncbi/Merge ); précédent : 000141; suivant : 000143Transcriptional regulation of the proC gene of Salmonella typhimurium.
Auteurs : R A Brady ; L N CsonkaSource :
- Journal of Bacteriology [ 0021-9193 ] ; 1988.
Abstract
We found that the expression of beta-galactosidase in Salmonella typhimurium strains carrying proC-lacZ fusions was neither repressed by excess proline nor derepressed by proline limitation. Except for a three- to fourfold decrease in the beta-galactosidase specific activity under conditions causing a severely reduced growth rate, the expression of the proC-lacZ fusions was nearly invariant under a variety of culture conditions. Thus, the proC gene is unlike most other amino acid biosynthetic genes in that its expression is nearly constitutive.
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PubMed: 3129409
PubMed Central: 211133
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<series><title level="j">Journal of Bacteriology</title>
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<front><div type="abstract" xml:lang="en"><p>We found that the expression of beta-galactosidase in Salmonella typhimurium strains carrying proC-lacZ fusions was neither repressed by excess proline nor derepressed by proline limitation. Except for a three- to fourfold decrease in the beta-galactosidase specific activity under conditions causing a severely reduced growth rate, the expression of the proC-lacZ fusions was nearly invariant under a variety of culture conditions. Thus, the proC gene is unlike most other amino acid biosynthetic genes in that its expression is nearly constitutive.</p>
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<pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Bacteriol</journal-id>
<journal-title>Journal of Bacteriology</journal-title>
<issn pub-type="ppub">0021-9193</issn>
<issn pub-type="epub">1098-5530</issn>
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<title-group><article-title>Transcriptional regulation of the proC gene of Salmonella typhimurium.</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Brady</surname>
<given-names>R A</given-names>
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<contrib contrib-type="author"><name><surname>Csonka</surname>
<given-names>L N</given-names>
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<aff>Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.</aff>
<pub-date pub-type="ppub"><month>5</month>
<year>1988</year>
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<volume>170</volume>
<issue>5</issue>
<fpage>2379</fpage>
<lpage>2382</lpage>
<abstract><p>We found that the expression of beta-galactosidase in Salmonella typhimurium strains carrying proC-lacZ fusions was neither repressed by excess proline nor derepressed by proline limitation. Except for a three- to fourfold decrease in the beta-galactosidase specific activity under conditions causing a severely reduced growth rate, the expression of the proC-lacZ fusions was nearly invariant under a variety of culture conditions. Thus, the proC gene is unlike most other amino acid biosynthetic genes in that its expression is nearly constitutive.</p>
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