Kim H Y, Schlictman D, Shankar S, Xie Z, Chakrabarty A M, Kornberg A
Department of Biochemistry, Beckman Center, Stanford University School of Medicine, CA 94305-5307, USA.
Mol Microbiol. 1998 Feb;27(4):717-25. doi: 10.1046/j.1365-2958.1998.00702.x.
The regulatory protein AlgR2 in Pseudomonas aeruginosa positively regulates nucleoside diphosphate kinase (Ndk) and succinyl-CoA synthetase, enzymes critical in nucleoside triphosphate (NTP) formation. AlgR2 positively regulates the production of alginate, GTP, ppGpp and inorganic polyphosphate (poly P). An algR2 mutant with low levels of these metabolites has them restored by introducing and overexpressing either the algR2 or the ndk gene into the algR2 mutant. Thus, Ndk is involved in the formation of these compounds and largely prevents the death of the algR2 mutant, which occurs early in the stationary phase. We demonstrate that the 12 kDa Ndk-pyruvate kinase (Pk) complex, previously shown to generate predominantly GTP instead of all the NTPs, has a low affinity for the deoxynucleoside diphosphates and cannot generate the dNTPs needed for DNA replication and cell division; this complex may thus be involved in regulating the levels of both NTPs and dNTPs that modulate cell division and survival in the stationary phase.
铜绿假单胞菌中的调节蛋白AlgR2正向调节核苷二磷酸激酶(Ndk)和琥珀酰辅酶A合成酶,这两种酶在三磷酸核苷(NTP)形成过程中至关重要。AlgR2正向调节藻酸盐、GTP、ppGpp和无机多聚磷酸盐(多聚P)的产生。通过将algR2或ndk基因导入并过表达于algR2突变体中,可使这些代谢物水平较低的algR2突变体恢复正常。因此,Ndk参与这些化合物的形成,并在很大程度上防止algR2突变体在稳定期早期发生死亡。我们证明,先前显示主要生成GTP而非所有NTP的12 kDa Ndk-丙酮酸激酶(Pk)复合物,对脱氧核苷二磷酸的亲和力较低,无法生成DNA复制和细胞分裂所需的dNTP;因此,该复合物可能参与调节NTP和dNTP的水平,从而调节稳定期的细胞分裂和存活。