Unusual organization, complexity and redundancy at the Escherichia coli hcp-hcr operon promoter

David L Chismon, Douglas F Browning, Gregory K Farrant, Stephen J W Busby

Research output: Contribution to journalArticlepeer-review

Abstract

Expression from the Escherichia coli hcp-hcr operon promoter is optimally induced during anaerobic conditions in the presence of nitrite. This expression depends on transcription activation by FNR (fumarate and nitrate reduction regulator), which binds to a target centred at position -72.5 upstream of the transcript start site. Mutational analysis was exploited to identify the corresponding -10 and -35 hexamer elements. A DNA site for NarL and NarP, located at position -104.5, plays only a minor role, whereas NsrR binding to a DNA target centred at position +6 plays a major role in induction of the hcp-hcr operon promoter. Electrophoretic mobility-shift assays show that NsrR binds to this target. The consequences of this for the kinetics of induction of the hcp-hcr operon are discussed.

Original languageEnglish
Pages (from-to)61-68
Number of pages8
JournalBiochemical Journal
Volume430
Issue number1
DOIs
Publication statusPublished - 15 Aug 2010

Keywords

  • DNA-Binding Proteins/genetics
  • Electrophoretic Mobility Shift Assay
  • Escherichia coli K12/genetics
  • Escherichia coli Proteins/genetics
  • Mutation
  • Nitrates/metabolism
  • Nitrites/metabolism
  • Operon
  • Promoter Regions, Genetic
  • Transcription Factors/genetics

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