Eichler K, Bourgis F, Buchet A, Kleber H P, Mandrand-Berthelot M A
Laboratoire de Génétique Moléculaire des Microorganismes et des Interactions Cellulaires URA 1486 du CNRS, Institut National des Sciences Appliquées, Villeurbanne, France.
Mol Microbiol. 1994 Sep;13(5):775-86. doi: 10.1111/j.1365-2958.1994.tb00470.x.
The sequence encompassing the cai genes of Escherichia coli, which encode the carnitine pathway, has been determined. Apart from the already identified caiB gene coding for the carnitine dehydratase, five additional open reading frames were identified. They belong to the caiTABCDE operon, which was shown to be located at the first minute on the chromosome and transcribed during anaerobic growth in the presence of carnitine. The activity of carnitine dehydratase was dependent on the CRP regulatory protein and strongly enhanced in the absence of a functional H-NS protein, in relation to the consensus sequences detected in the promoter region of the cai operon. In vivo expression studies led to the synthesis of five polypeptides in addition to CaiB, with predicted molecular masses of 56,613 Da (CaiT), 42,564 Da (CaiA), 59,311 Da (CaiC), 32,329 Da (CaiD) and 21,930 Da (CaiE). Amino acid sequence similarity or enzymatic analysis supported the function assigned to each protein. CaiT was suggested to be the transport system for carnitine or betaines, CaiA an oxidoreduction enzyme, and CaiC a crotonobetaine/carnitine CoA ligase. CaiD bears strong homology with enoyl hydratases/isomerases. Overproduction of CaiE was shown to stimulate the carnitine racemase activity of the CaiD protein and to markedly increase the basal level of carnitine dehydratase activity. It is inferred that CaiE is an enzyme involved in the synthesis or the activation of the still unknown cofactor required for carnitine dehydratase and carnitine racemase activities. Taken together, these data suggest that the carnitine pathway in E. coli resembles that found in a strain situated between Agrobacterium and Rhizobium.
已确定了大肠杆菌中包含编码肉碱途径的cai基因的序列。除了已鉴定出的编码肉碱脱水酶的caiB基因外,还鉴定出另外五个开放阅读框。它们属于caiTABCDE操纵子,该操纵子位于染色体的第一分钟处,并在肉碱存在下厌氧生长期间转录。肉碱脱水酶的活性依赖于CRP调节蛋白,并且相对于在cai操纵子启动子区域检测到的共有序列,在缺乏功能性H-NS蛋白的情况下其活性强烈增强。体内表达研究除了产生CaiB外,还导致了另外五种多肽的合成,其预测分子量分别为56,613 Da(CaiT)、42,564 Da(CaiA)、59,311 Da(CaiC)、32,329 Da(CaiD)和21,930 Da(CaiE)。氨基酸序列相似性或酶促分析支持了赋予每种蛋白质的功能。推测CaiT是肉碱或甜菜碱的转运系统,CaiA是一种氧化还原酶,CaiC是巴豆甜菜碱/肉碱CoA连接酶。CaiD与烯酰水合酶/异构酶具有很强的同源性。已表明过量生产CaiE会刺激CaiD蛋白的肉碱消旋酶活性,并显著提高肉碱脱水酶活性的基础水平。据推测,CaiE是一种参与合成或激活肉碱脱水酶和肉碱消旋酶活性所需的仍未知辅因子的酶。综上所述,这些数据表明大肠杆菌中的肉碱途径类似于在农杆菌和根瘤菌之间的菌株中发现的途径。