Identification and characterization of a transcriptional regulator, SucR, that influences sucCD transcription in Corynebacterium glutamicum

被引:11
作者
Cho, Hyun-Young [1 ]
Lee, Seong Gyu [1 ]
Hyeon, Jeong Eun [1 ]
Han, Sung Ok [1 ]
机构
[1] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
关键词
Transcriptional regulator; Succinyl-CoA synthetase; sucCD expression; Acetate metabolism; Corynebacterium glutamicum; TRICARBOXYLIC-ACID CYCLE; ACETATE METABOLISM; REPRESSES EXPRESSION; ESCHERICHIA-COLI; GENES; DEHYDROGENASE; RAMA;
D O I
10.1016/j.bbrc.2010.09.057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have identified and characterized a novel transcriptional regulator that binds to the promoter region of succinyl-CoA synthetase (sucCD) in Corynebacterium glutamicum. Using biotin-labeled DNA affinity beads, we identified a DeoR-type transcriptional regulator, SucR (Cg0146), which is a protein consisting of 282 amino acids with a mass of 31 kDa and RamB (Cg0444). The results of electrophoretic mobility shift assays verified that these regulators specifically bind to the sucCD promoter region. The putative SucR binding region extends from position -155 to -146 (a 10 bp sequence, ACTCTAGGGG) relative to the transcriptional start point of the sucCD operon. The expression level of sucCD in a sucR deletion mutant was seven times higher than that in wild-type cells grown on acetate. The increase in succinyl-CoA synthetase levels caused by inactivation of sucR. These assays revealed that SucR acts as a repressor of sucCD expression during acetate metabolism. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:300 / 305
页数:6
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