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 language | English |
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Pages (from-to) | 61-68 |
Number of pages | 8 |
Journal | Biochemical Journal |
Volume | 430 |
Issue number | 1 |
DOIs | |
Publication status | Published - 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