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大肠杆菌中腺苷酸环化酶的调控

Regulation of adenylate cyclase in E. coli.

作者信息

Gstrein-Reider E, Schweiger M

出版信息

EMBO J. 1982;1(3):333-7. doi: 10.1002/j.1460-2075.1982.tb01170.x.

Abstract

The intracellular concentrations of cAMP in Escherichia coli are regulated mainly by control of the activity of adenylate cyclase. Withdrawal of the carbon source from the growth medium causes a gradual reduction of cellular energy and a dramatic stimulation of cyclase activity. Manipulations of the proton gradient at the cell membrane of ATP synthase-deficient E. coli (unc-) revealed that this part of the energy compartment is not responsible for the starvation-induced stimulation of cyclase. Neither is the ATP pool involved in regulation of the activity of the cyclase. The intracellular concentrations of ATP were experimentally lowered by purine starvation of auxotrophs, by inhibition of purine synthesis using amethopterin, or by affecting ATP synthesis using arsenate. None of these conditions led to stimulation of cyclase activity. The control of cyclase is exerted not via the energy pools but via uptake systems of energy substrates independent of whether the substrate can be metabolized or not, or how the transport is energized. The stringent coupling between these transport systems and cyclase activity enables the cell to react instantaneously to changes in its environment.

摘要

大肠杆菌中细胞内cAMP的浓度主要通过控制腺苷酸环化酶的活性来调节。从生长培养基中去除碳源会导致细胞能量逐渐减少,并显著刺激环化酶活性。对缺乏ATP合酶的大肠杆菌(unc-)细胞膜上质子梯度的操作表明,这部分能量区室与饥饿诱导的环化酶刺激无关。ATP池也不参与环化酶活性的调节。通过对营养缺陷型进行嘌呤饥饿处理、使用氨甲蝶呤抑制嘌呤合成或使用砷酸盐影响ATP合成,实验性地降低了细胞内ATP的浓度。这些条件均未导致环化酶活性的刺激。环化酶的控制不是通过能量池,而是通过能量底物的摄取系统,与底物是否可以代谢、运输如何供能无关。这些运输系统与环化酶活性之间的严格耦合使细胞能够对其环境变化立即做出反应。

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