Hove-Jensen B
Department of Biological Chemistry, University of Copenhagen, Denmark.
J Bacteriol. 1996 Feb;178(3):714-22. doi: 10.1128/jb.178.3.714-722.1996.
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.
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。