Synergism between the Trp repressor and Tyr repressor in repression of the aroL promoter of Escherichia coli K-12
- 1 January 1992
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 174 (1) , 331-335
- https://doi.org/10.1128/jb.174.1.331-335.1992
Abstract
Computer analysis identified a potential Trp repressor operator 56 nucleotides downstream of the transcriptional start point of aroL, the gene that encodes shikimate kinase II. Tryptophan-dependent interaction of Trp repressor with this operator was demonstrated in vitro by means of a restriction endonuclease protection assay. Regulation of expression from the aroL promoter was evaluated with several genetically marked Escherichia coli strains by using a single-copy aroL-lacZ transcriptional-translational reporter system. The expression of aroL was repressed 6.9-fold by the Tyr repressor alone and 29-fold when both Tyr and Trp repressors were present. The Trp repressor had no effect on expression from the aroL promoter in the absence of the Tyr repressor. Possible mechanisms for Trp repressor-mediated repression, including cooperative interactions with the Tyr repressor, are discussed.Keywords
This publication has 27 references indexed in Scilit:
- TyrR protein of Escherichia coli and its role as repressor and activatorMolecular Microbiology, 1991
- Position and density effects on repression by stationary and mobile DNA-binding proteins.Genes & Development, 1989
- Promoters largely determine the efficiency of repressor action.Proceedings of the National Academy of Sciences, 1988
- Mutant Trp Repressors with New DNA-Binding SpecificitiesScience, 1988
- Novel regulatory mutants of the phosphate regulon in Escherichia coli K-12Journal of Molecular Biology, 1986
- The cloning and expression of the aroL gene from Escherichia coli K12. Purification and complete amino acid sequence of shikimate kinase II, the aroL-gene productBiochemical Journal, 1986
- A comprehensive set of sequence analysis programs for the VAXNucleic Acids Research, 1984
- Deletion analysis of the CAP-cAMP binding site of theEscherichia coillactose promoterNucleic Acids Research, 1984
- Rapid and efficient cosmid cloningNucleic Acids Research, 1981
- Pedigrees of some mutant strains of Escherichia coli K-12.1972