Abstract
The interaction between the core form of bacterial RNA polymerases and sigma factors is essential for specific promoter recognition, and for coordinating the expression of different sets of genes in response to varying cellular needs. The interaction between Escherichia coli core RNA polymerase and sigma 70 has been investigated by surface plasmon resonance. The His-tagged form of sigma 70 factor was immobilised on a Ni2+-NTA chip for monitoring its interaction with core polymerase. The binding constant for the interaction was found to be 1.9x10(-7) M, and the dissociation rate constant for release of sigma from core, in the absence of DNA or transcription, was 4x10(-3) s(-1), corresponding to a half-life of about 200 s.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacterial Proteins / chemistry
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Bacterial Proteins / metabolism*
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Binding, Competitive
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DNA-Directed RNA Polymerases / chemistry
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DNA-Directed RNA Polymerases / metabolism*
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Enzyme Stability
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Escherichia coli / enzymology*
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Half-Life
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Histidine / chemistry
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Holoenzymes / chemistry
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Holoenzymes / metabolism
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Kinetics
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Nickel / chemistry
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Nitrilotriacetic Acid / analogs & derivatives*
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Nitrilotriacetic Acid / chemistry
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Organometallic Compounds / chemistry
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Protein Binding
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Sigma Factor / chemistry
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Sigma Factor / metabolism*
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Surface Plasmon Resonance* / methods
Substances
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Bacterial Proteins
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Holoenzymes
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Organometallic Compounds
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Sigma Factor
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nickel nitrilotriacetic acid
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Histidine
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Nickel
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RNA polymerase sigma 70
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DNA-Directed RNA Polymerases
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Nitrilotriacetic Acid