首页> 美国卫生研究院文献>Biochemical Journal >Escherichia coli engineered to synthesize isopentenyl diphosphate and dimethylallyl diphosphate from mevalonate: a novel system for the genetic analysis of the 2-C-methyl-d-erythritol 4-phosphate pathway for isoprenoid biosynthesis.
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Escherichia coli engineered to synthesize isopentenyl diphosphate and dimethylallyl diphosphate from mevalonate: a novel system for the genetic analysis of the 2-C-methyl-d-erythritol 4-phosphate pathway for isoprenoid biosynthesis.

机译:大肠杆菌经过工程改造从甲羟戊酸酯合成了异戊烯基二磷酸酯和二甲基烯丙基二磷酸酯:用于类异戊二烯生物合成的2-C-甲基-d-赤藓糖醇4-磷酸酯途径的遗传分析新系统。

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摘要

Isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP) constitute the basic building block of isoprenoids, a family of compounds that is extraordinarily diverse in structure and function. IPP and DMAPP can be synthesized by two independent pathways: the mevalonate pathway and the recently discovered 2-C-methyl-d-erythritol 4-phosphate (MEP) pathway. Although the MEP pathway is essential in most eubacteria, algae and plants and has enormous biotechnological interest, only some of its steps have been determined. We devised a system suitable for the genetic analysis of the MEP pathway in Escherichia coli. A synthetic operon coding for yeast 5-diphosphomevalonate decarboxylase, human 5-phosphomevalonate kinase, yeast mevalonate kinase and E. coli isopentenyl diphosphate isomerase was incorporated in the chromosome of this bacterium. The expression of this operon allowed the synthesis of IPP and DMAPP from mevalonate added exogenously and complementation of lethal mutants of the MEP pathway. We used this system to show that the ygbP, ychB and ygbB genes are essential in E. coli and that the steps catalysed by the products of these genes belong to the trunk line of the MEP pathway.
机译:异戊烯基二磷酸酯(IPP)及其异构体二甲基烯丙基二磷酸酯(DMAPP)构成了类异戊二烯的基本组成部分,类异戊二烯是一类结构和功能各异的化合物。 IPP和DMAPP可以通过两个独立的途径合成:甲羟戊酸途径和最近发现的2-C-甲基-d-赤藓糖醇4-磷酸(MEP)途径。尽管MEP途径在大多数真细菌,藻类和植物中必不可少,并且具有巨大的生物技术意义,但仅确定了其中的一些步骤。我们设计了一种适用于大肠杆菌中MEP途径遗传分析的系统。编码酵母5-二磷酸甲戊二酸脱羧酶,人5-磷酸戊二酸激酶,酵母甲羟戊酸激酶和大肠杆菌异戊烯基二磷酸异构酶的合成操纵子被掺入该细菌的染色体中。该操纵子的表达允许由外源性添加的甲羟戊酸酯合成IPP和DMAPP,并互补MEP途径的致死突变体。我们使用该系统显示ygbP,ychB和ygbB基因在大肠杆菌中必不可少,并且这些基因的产物催化的步骤属于MEP途径的干线。

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