The binding site of the IclR repressor protein overlaps the promoter of aceBAK

Bin Pan; Indira Unnikrishnan; David C. LaPorte

doi:10.1128/jb.178.13.3982-3984.1996

The binding site of the IclR repressor protein overlaps the promoter of aceBAK

Bin Pan, Indira Unnikrishnan, David C. LaPorte

Molecular Biology (TMED)

Research output: Contribution to journal › Article › peer-review

26 Scopus citations

Abstract

In Escherichia coli, repression of the aceBAK operon is mediated by the IclR protein. We used an in vitro oligonucleotide selection technique to determine the consensus recognition sequence for IclR. Mutational analysis confirmed the contribution of this sequence to repression in vivo and identified the -35 element of the promoter.

Original language	English (US)
Pages (from-to)	3982-3984
Number of pages	3
Journal	Journal of bacteriology
Volume	178
Issue number	13
DOIs	https://doi.org/10.1128/jb.178.13.3982-3984.1996
State	Published - 1996

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title = "The binding site of the IclR repressor protein overlaps the promoter of aceBAK",

abstract = "In Escherichia coli, repression of the aceBAK operon is mediated by the IclR protein. We used an in vitro oligonucleotide selection technique to determine the consensus recognition sequence for IclR. Mutational analysis confirmed the contribution of this sequence to repression in vivo and identified the -35 element of the promoter.",

author = "Bin Pan and Indira Unnikrishnan and LaPorte, {David C.}",

year = "1996",

doi = "10.1128/jb.178.13.3982-3984.1996",

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AU - Unnikrishnan, Indira

AU - LaPorte, David C.

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N2 - In Escherichia coli, repression of the aceBAK operon is mediated by the IclR protein. We used an in vitro oligonucleotide selection technique to determine the consensus recognition sequence for IclR. Mutational analysis confirmed the contribution of this sequence to repression in vivo and identified the -35 element of the promoter.

AB - In Escherichia coli, repression of the aceBAK operon is mediated by the IclR protein. We used an in vitro oligonucleotide selection technique to determine the consensus recognition sequence for IclR. Mutational analysis confirmed the contribution of this sequence to repression in vivo and identified the -35 element of the promoter.

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JO - Journal of Bacteriology

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