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大肠杆菌中高亲和力亮氨酸转运的调控

Regulation of high-affinity leucine transport in Escherichia coli.

作者信息

Landick R, Anderson J J, Mayo M M, Gunsalus R P, Mavromara P, Daniels C J, Oxender D L

出版信息

J Supramol Struct. 1980;14(4):527-37. doi: 10.1002/jss.400140410.

Abstract

Leucine is transported into E coli by two osmotic shock-sensitive, high-affinity systems (LIV-I and leucine-specific systems) and one membrane bound, low-affinity system (LIV-II). Expression of the high-affinity transport systems is altered by mutations in livR and 1stR, genes for negatively acting regulatory elements, and by mutations in rho, the gene for transcription termination. All four genes for high-affinity leucine transport (livJ, livK, livH, and livG) are closely linked and have been cloned on a plasmid vector, pOX1. Several subcloned fragments of this plasmid have been prepared and used in complementation and regulation studies. The results of these studies suggest that livJ and livK are separated by approximately one kilobase and give a gene order of livJ-livK-livH. livJ and livK appear to be regulated in an interdependent fashion; livK is expressed maximally when the livJ gene is activated by mutation or deletion. The results support the existence of separate promotors for the livJ and livK genes. The effects of mutations in the rho and livR genes are additive on one another and therefore appear to be involved in independent regulatory mechanisms. Mutations in the rho gene affect both the LIV-I and leucine-specific transport systems by increasing the expression of livJ and livK, genes for the LIV-specific and leucine-specific binding proteins, respectively.

摘要

亮氨酸通过两种对渗透休克敏感的高亲和力系统(LIV-I和亮氨酸特异性系统)以及一种膜结合的低亲和力系统(LIV-II)转运到大肠杆菌中。高亲和力转运系统的表达会因livR和1stR(负向作用调节元件的基因)的突变以及rho(转录终止基因)的突变而改变。高亲和力亮氨酸转运的所有四个基因(livJ、livK、livH和livG)紧密相连,并已克隆到质粒载体pOX1上。已制备了该质粒的几个亚克隆片段,并用于互补和调节研究。这些研究结果表明,livJ和livK相隔约1千碱基,基因顺序为livJ-livK-livH。livJ和livK似乎以相互依赖的方式受到调节;当livJ基因通过突变或缺失被激活时,livK表达达到最大。结果支持livJ和livK基因存在独立的启动子。rho和livR基因的突变彼此具有累加效应,因此似乎参与独立的调节机制。rho基因的突变通过增加livJ和livK的表达来影响LIV-I和亮氨酸特异性转运系统,livJ和livK分别是LIV特异性和亮氨酸特异性结合蛋白的基因。

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