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DNA binding properties of the Escherichia coli nitric oxide sensor NorR : towards an understanding of the regulation of flavorubredoxin expression

Tucker, N and D'autréaux, B and Spiro, S and Dixon, R (2005) DNA binding properties of the Escherichia coli nitric oxide sensor NorR : towards an understanding of the regulation of flavorubredoxin expression. Biochemical Society Transactions, 33 (Part 1). pp. 181-183. ISSN 0300-5127

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Abstract

Nitric oxide is an intermediate of denitrification, and is one of the radical species deployed by macrophages against invading pathogens, therefore bacterial responses to NO are of considerable importance. The Escherichia coli flavorubredoxin and its associated oxidoreductase reduce NO to nitrous oxide under anaerobic conditions, and are encoded by the norVW transcription unit. Expression of norVW requires the NO sensing regulatory protein NorR and is dependent on RNA polymerase containing the alternative sigma factor, sigma(54). We have purified NorR and shown that it binds to three sites in the norVW promoter region, located 75-140 bp upstream of the experimentally verified transcription start site. We have also identified two binding sites for the integration host factor, one between the NorR sites and the sigma(54)-RNA polymerase binding site, and a second downstream of the norVW transcription start site. Comparison of the norVW promoters of enteric bacteria along with known and putative NorR-regulated promoters from Vibrio, Ralstonia and Pseudomonas species suggests that NorR binding sites contain an invariant GT(N7)AC motif flanking an AT-rich central region. The identification of a consensus for NorR binding sites will help to elucidate additional members of the NorR regulon.

Item type: Article
ID code: 31499
Keywords: base sequence, binding sites, DNA, escherichia coli, escherichia coli proteins, gene expression regulation, molecular sequence data, promoter regions, sequence homology, transcription factors, bacterial, nucleic acid, Pharmacy and materia medica, Biochemistry
Subjects: Medicine > Pharmacy and materia medica
Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Related URLs:
    Depositing user: Pure Administrator
    Date Deposited: 01 Jul 2011 15:10
    Last modified: 05 Sep 2014 09:20
    URI: http://strathprints.strath.ac.uk/id/eprint/31499

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