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醋酸钙不动杆菌KCCM 40902的丙二酸脱羧酶操纵子受丙二酸和转录阻遏物MdcY调控。

The malonate decarboxylase operon of Acinetobacter calcoaceticus KCCM 40902 is regulated by malonate and the transcriptional repressor MdcY.

作者信息

Koo J H, Cho I H, Kim Y S

机构信息

Department of Biochemistry, College of Science, Protein Network Research Center, Institute of Bioscience and Biotechnology, Yonsei University, Seoul 120-749, Korea.

出版信息

J Bacteriol. 2000 Nov;182(22):6382-90. doi: 10.1128/JB.182.22.6382-6390.2000.

Abstract

A regulatory gene-like open reading frame oriented oppositely to mdcL, coined mdcY, was found upstream from the structural genes of the mdcLMACDEGBH operon in Acinetobacter calcoaceticus KCCM 40902. To elucidate the function of this gene, mdcY was expressed in Escherichia coli, and the MdcY protein was purified to homogeneity. Its DNA binding activity and binding site were examined by gel retardation and footprinting assays in vitro and by site-directed mutagenesis of the binding sites in vivo. The regulator bound target DNA regardless of the presence of malonate, and the binding site was found centered at -65 relative to the mdcL transcriptional start site and contains a 12-bp palindromic structure (5'-ATTGTA/TACAAT-3'). Using a promoter fusion to the reporter gene luc, we found that the promoter P(mdcY) is negatively regulated by MdcY independent of malonate. However, the promoter P(mdcL) recovered its activity in the presence of malonate. When mdcY was introduced into A. calcoaceticus KCCM 40902 in which the gene is inactivated by an IS3 family element, malonate decarboxylase was significantly repressed in cultures growing in acetate, succinate, or Luria-Bertani medium. However, in cells growing in malonate, malonate decarboxylase was induced, indicating that MdcY is a transcriptional repressor and that malonate or a product resulting from malonate metabolism should be the intracellular inducer of the mdc operon.

摘要

在醋酸钙不动杆菌KCCM 40902中,发现一个与mdcL方向相反的调控基因样开放阅读框,命名为mdcY,位于mdcLMACDEGBH操纵子结构基因的上游。为阐明该基因的功能,在大肠杆菌中表达了mdcY,并将MdcY蛋白纯化至同质。通过体外凝胶阻滞和足迹分析以及体内结合位点的定点诱变来检测其DNA结合活性和结合位点。无论丙二酸是否存在,该调节因子均能结合靶DNA,并且发现结合位点位于相对于mdcL转录起始位点-65处的中心位置,包含一个12bp的回文结构(5'-ATTGTA/TACAAT-3')。使用与报告基因luc的启动子融合,我们发现启动子P(mdcY)受MdcY负调控,且与丙二酸无关。然而,在丙二酸存在的情况下,启动子P(mdcL)恢复了其活性。当将mdcY导入因IS3家族元件而使该基因失活的醋酸钙不动杆菌KCCM 40902中时,在以乙酸盐、琥珀酸盐或Luria-Bertani培养基生长的培养物中,丙二酸脱羧酶受到显著抑制。然而,在以丙二酸生长的细胞中,丙二酸脱羧酶被诱导,这表明MdcY是一种转录抑制因子,并且丙二酸或丙二酸代谢产生的产物应该是mdc操纵子的细胞内诱导物。

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