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大肠杆菌中不依赖磷酸核糖焦磷酸合成酶的NAD从头合成:磷酸盐调节子突变体的一种新表型

Phosphoribosyl diphosphate synthetase-independent NAD de novo synthesis in Escherichia coli: a new phenotype of phosphate regulon mutants.

作者信息

Hove-Jensen B

机构信息

Department of Biological Chemistry, University of Copenhagen, Denmark.

出版信息

J Bacteriol. 1996 Feb;178(3):714-22. doi: 10.1128/jb.178.3.714-722.1996.

Abstract

Phosphoribosyl diphosphate-lacking (delta prs) mutant strains of Escherichia coli require NAD, guanosine, uridine, histidine, and tryptophan for growth. NAD is required by phosphoribosyl diphosphate-lacking mutants because of lack of one of the substrates for the quinolinate phosphoribosyltransferase reaction, an enzyme of the NAD de novo pathway. Several NAD-independent mutants of a host from which prs had been deleted were isolated; all of them were shown to have lesions in the pstSCAB-phoU operon, in which mutations lead to derepression of the Pho regulon. In addition NAD-independent growth was dependent on a functional quinolinate phosphoribosyltransferase. The prs suppressor mutations led to the synthesis of a new phosphoryl compound that may act as a precursor for a new NAD biosynthetic pathway. This compound may be synthesized by the product of an unknown phosphate starvation-inducible gene of the Pho regulon because the ability of pst or phoU mutations to suppress the NAD requirement requires PhoB, the transcriptional activator of the Pho regulon.

摘要

缺乏磷酸核糖焦磷酸(delta prs)的大肠杆菌突变菌株生长需要烟酰胺腺嘌呤二核苷酸(NAD)、鸟苷、尿苷、组氨酸和色氨酸。缺乏磷酸核糖焦磷酸的突变体需要NAD,因为喹啉酸磷酸核糖转移酶反应(NAD从头合成途径中的一种酶)的一种底物缺失。从缺失prs的宿主中分离出了几个不依赖NAD的突变体;结果表明,它们在pstSCAB-phoU操纵子中都有损伤,该操纵子中的突变会导致Pho调控子的去阻遏。此外,不依赖NAD的生长依赖于功能性喹啉酸磷酸核糖转移酶。prs抑制突变导致一种新的磷酰化合物的合成,该化合物可能作为新的NAD生物合成途径的前体。这种化合物可能由Pho调控子中一个未知的磷酸盐饥饿诱导基因的产物合成,因为pst或phoU突变抑制NAD需求的能力需要PhoB,即Pho调控子的转录激活因子。

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