Peterkofsky A, Gazdar C
J Supramol Struct. 1978;9(2):219-30. doi: 10.1002/jss.400090207.
A model for the regulation of the activity of Escherichia coli adenylate cyclase is presented. It is proposed that Enzyme I of the phosphoenolpyruvate:sugar phosphotransferase system (PTS) interacts in a regulatory sense with the catalytic unit of adenylate cyclase. The phosphoenolpyruvate (PEP)-dependent phosphorylation of Enzyme I is assumed to be associated with a high activity state of adenylate cyclase. The pyruvate or sugar-dependent dephosphorylation of Enzyme I is correlated with a low activity state of adenylate cyclase. Evidence in support of the proposed model involves the observation that Enzyme I mutants have low cAMP levels and that PEP increases cellular cAMP levels and, under certain conditions, activates adenylate cyclase, Kinetic studies indicate that various ligands have opposing effects on adenylate cyclase. While PEP activates the enzyme, either glucose or pyruvate inhibit it. The unique relationships of PEP and Enzyme I to adenylate cyclase activity are discussed.
本文提出了一种大肠杆菌腺苷酸环化酶活性调节模型。有人提出,磷酸烯醇式丙酮酸:糖磷酸转移酶系统(PTS)的酶I在调节意义上与腺苷酸环化酶的催化单元相互作用。酶I的磷酸烯醇式丙酮酸(PEP)依赖性磷酸化被认为与腺苷酸环化酶的高活性状态相关。酶I的丙酮酸或糖依赖性去磷酸化与腺苷酸环化酶的低活性状态相关。支持该模型的证据包括观察到酶I突变体的cAMP水平较低,以及PEP可提高细胞cAMP水平,并在某些条件下激活腺苷酸环化酶。动力学研究表明,各种配体对腺苷酸环化酶有相反的作用。虽然PEP激活该酶,但葡萄糖或丙酮酸会抑制它。文中讨论了PEP和酶I与腺苷酸环化酶活性的独特关系。