OVERPRODUCTION AND CHARACTERIZATION OF THE ICLR GENE-PRODUCT OF ESCHERICHIA-COLI-K-12 AND COMPARISON WITH THAT OF SALMONELLA-TYPHIMURIUM-LT2

被引:29
作者
NEGRE, D
CORTAY, JC
OLD, IG
GALINIER, A
RICHAUD, C
SAINTGIRONS, I
COZZONE, AJ
机构
[1] UNIV LYON 1, CNRS, INST BIOL & CHIM PROT, 43 BLVD ONZE NOVEMBRE, F-69622 VILLEURBANNE, FRANCE
[2] INST PASTEUR, DEPT BACTERIOL & MYCOL, UNITE LEPTOSPIRES, F-75724 PARIS, FRANCE
关键词
RECOMBINANT DNA; ACETATE OPERON; TRANSCRIPTIONAL REPRESSOR; BACTERIAL GENE EXPRESSION; PROTEIN PHOSPHORYLATION;
D O I
10.1016/0378-1119(91)90006-W
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The iclR gene of Escherichia coli K-12, which encodes a regulatory protein (repressor) for the aceBAK operon, is located between that operon and metH in the 91-min region of the chromosome. The iclR gene was cloned and expressed in a coupled T7 RNA polymerase/promoter system and the gene product was identified by specific binding to a fragment containing the aceBAK operator region. The iclR gene product is a polypeptide of 274 amino acids (aa) with a calculated M(r) of 29741. Comparison of the deduced IclR aa sequence to that of Salmonella typhimurium revealed that the two IclR repressors exhibit 89% identity. A possible helix-turn-helix motif characteristic of DNA-binding proteins was found within the IclR sequence. A search in protein data banks revealed that IclR has a score of similarity of 43.7% with GylR, a transcriptional regulator of the glycerol operon of Streptomyces coelicolor.
引用
收藏
页码:29 / 37
页数:9
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