@article{89931,
  keywords = {Base Sequence, Bacterial Proteins, signal transduction, Escherichia coli, Molecular Sequence Data, Transcription, Genetic, Protein Kinases, Transcription Factors, Gene Expression Regulation, Bacterial, Membrane Proteins, Regulon, Selection, Genetic, Amino Acid Sequence, Escherichia coli Proteins, Sequence Homology, Amino Acid, Sigma Factor, Hydrogen-Ion Concentration, Lipoproteins, Bacterial Outer Membrane Proteins, Periplasm, Organophosphates, Alkalies},
  author = {Danese and Silhavy},
  title = {CpxP, a stress-combative member of the Cpx regulon},
  abstract = {<p>The CpxA/R two-component signal transduction system of Escherichia coli can combat a variety of extracytoplasmic protein-mediated toxicities. The Cpx system performs this function, in part, by increasing the synthesis of the periplasmic protease, DegP. However, other factors are also employed by the Cpx system for this stress-combative function. In an effort to identify these remaining factors, we screened a collection of random lacZ operon fusions for those fusions whose transcription is regulated by CpxA/R. Through this approach, we have identified a new locus, cpxP, whose transcription is stimulated by activation of the Cpx pathway. cpxP specifies a periplasmic protein that can combat the lethal phenotype associated with the synthesis of a toxic envelope protein. In addition, we show that cpxP transcription is strongly induced by alkaline pH in a CpxA-dependent manner and that cpxP and cpx mutant strains display hypersensitivity to growth in alkaline conditions.</p>
},
  year = {1998},
  journal = {J Bacteriol},
  volume = {180},
  pages = {831-9},
  month = {02/1998},
  issn = {0021-9193},
  doi = {10.1128/JB.180.4.831-839.1998},
  language = {eng},
}