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Characterization of the sigma 38-dependent expression of a core Escherichia coli starvation gene, pexB.

Abstract
A reverse genetics approach was used to clone a pex starvation gene that codes for an 18-kDa polypeptide, designated PexB. Single-copy pexB-lacZ operon fusions were constructed to study transcriptional regulation and the promoter region of this gene. The induction by carbon starvation or osmotic stress was transcriptional and controlled by sigma 38 but was independent of this sigma factor by the oxidative stress; presumably, it was sigma 70 mediated under the latter stress. During nitrogen starvation, the induction was controlled at the posttranscriptional level. The pexB upstream region contained 245 nucleotides within which sequences approximating the consensus for cyclic AMP receptor protein and integration host factor binding sites were discernible. Deletion of 164 bp of the upstream region, which included these consensus sequences, did not affect starvation-or osmotic stress-mediated induction of pexB but abolished its induction by oxidative stress. The same start site was used in transcription during carbon starvation, osmotic stress, or oxidative stress, suggesting that the pexB promoter can be recognized in vivo by both sigma 38 and sigma 70, depending, presumably, on the presence of appropriate transcriptional factors. The -10 and -35 regions of pexB resembled those of some but not all genes known to be controlled by sigma 38.
AuthorsO L Lomovskaya, J P Kidwell, A Matin
JournalJournal of bacteriology (J Bacteriol) Vol. 176 Issue 13 Pg. 3928-35 (Jul 1994) ISSN: 0021-9193 [Print] United States
PMID8021175 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bacterial Outer Membrane Proteins
  • Bacterial Proteins
  • Escherichia coli Proteins
  • Recombinant Fusion Proteins
  • Sigma Factor
  • dps protein, E coli
  • sigma factor KatF protein, Bacteria
Topics
  • Adaptation, Physiological (genetics)
  • Bacterial Outer Membrane Proteins (genetics)
  • Bacterial Proteins (metabolism)
  • Base Sequence
  • Cloning, Molecular
  • Escherichia coli (genetics, metabolism)
  • Escherichia coli Proteins
  • Gene Expression Regulation, Bacterial
  • Genes, Bacterial (genetics)
  • Molecular Sequence Data
  • Osmotic Pressure
  • Oxidation-Reduction
  • Protein Biosynthesis
  • Recombinant Fusion Proteins (biosynthesis)
  • Sigma Factor (metabolism)
  • Transcription, Genetic

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