Abstract
A site has been found that is required for repression of the Escherichia coli araBAD operon. This site was detected by the in vivo properties of deletion mutants. In vitro protection studies with DNase I and dimethylsulfate showed that araC protein can specifically bind in this area to nucleotides lying at position -265 to -294 with respect to the araBAD operon promoter (PBAD) transcription start point. The previously known sites of protein binding in the ara operon lie between +20 and -160. Since the properties of deletion strains show that all the sites required for araBAD induction lie between +20 and -110, the new site at -280 exerts its repressive action over an unusually large distance along the DNA. Insertions of -16, -8, 0, 5, 11, 15, 24, and 31 base pairs of DNA between the new site and PBAD were constructed. Repression was impaired in those cases in which half-integral turns of the DNA helix were introduced, but repression was nearly normal for the insertions of 0, +11, and +31 base pairs.
MeSH Terms
AraC Transcription Factor
Bacterial Proteins
Chromosome Deletion
DNA Restriction Enzymes
Escherichia coli/genetics
Escherichia coli Proteins
Galactokinase/genetics
Genes
Genes, Bacterial
Genes, Regulator
Operon
Plasmids
Protein Binding
Repressor Proteins/genetics
Transcription Factors/genetics
Chemicals
AraC Transcription Factor
AraC protein, E coli
Bacterial Proteins
Escherichia coli Proteins
Repressor Proteins
Transcription Factors
Galactokinase
DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dunn T M
Hahn S
Ogden S
Schleif R F
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