Structure and transcriptional regulation of the Escherichia coli adaptive response gene aidB
Landini, Paolo ; Hajec, Laurel I. ; Volkert, Michael R.
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Keywords
Alkylation
Amino Acid Sequence
Bacterial Proteins
Base Sequence
Cloning, Molecular
DNA Damage
Escherichia coli
*Escherichia coli Proteins
Fatty Acid Desaturases
*Gene Expression Regulation, Bacterial
Isovaleryl-CoA Dehydrogenase
Methylnitronitrosoguanidine
Molecular Sequence Data
Mutagenesis
O(6)-Methylguanine-DNA Methyltransferase
Oxidoreductases
*Oxidoreductases Acting on CH-CH Group Donors
Promoter Regions (Genetics)
Protein Binding
Recombinant Fusion Proteins
Sequence Analysis, DNA
Sequence Homology, Amino Acid
Transcription Factors
*Transcription, Genetic
Life Sciences
Medicine and Health Sciences
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Abstract
Expression of the Escherichia coli aidB gene is induced in vivo by alkylation damage in an ada-dependent pathway and by anaerobiosis or by acetate at pH 6.5 in an ada-independent fashion. In this report, we present data on aidB gene structure, function, and regulation. The aidB gene encodes a protein of ca. 60 kDa that is homologous to several mammalian acyl coenzyme A dehydrogenases. Accordingly, crude extracts from an aidB-overexpressing strain showed isovaleryl coenzyme A dehydrogenase activity. aidB overexpression also reduced N-methyl-N'-nitro-N-nitrosoguanidine-induced mutagenesis. Both ada- and acetate/pH-dependent induction of aidB are regulated at the transcriptional level, and the same transcriptional start point is used for both kinds of induction. Ada protein plays a direct role in aidB regulation: methylated Ada is able to bind to the aidB promoter region and to activate transcription from aidB in an in vitro transcription-translation system using crude E. coli extracts.
Source
J Bacteriol. 1994 Nov;176(21):6583-9.