Milner Y, Wood H G
J Biol Chem. 1976 Dec 25;251(24):7920-8.
Evidence is presented based on requirements for exchange in the partial reactions, initial velocity and exchange kinetics and product inhibition, that the pyruvate, phosphate dikinase reaction of propionibacteria occurs by a nonclassical Tri Uni Uni Ping Pong mechanism. The mechanism involves a pyrophosphoryl enzyme, a phosphoryl enzyme, and the free enzyme, and three functionally distinct and independent substrate sites. On the first site, there is pyrophosphorylation of the enzyme by ATP with subsequent release of AMP. The pyrophosphoryl moiety then reacts at the second site with Pi yielding the product PPi and the phosphoryl from of the enzyme. At the third site pyruvate is phosphorylated yielding P-enolpyruvate and the free enzyme. The three catalytic sites are proposed to be linked by a histidyl residue which functions as a pyrophosphoyrl- and phosphoryl-carrier between the three sites. This proposal is based on the following observations. (A) The patterns of the double reciprocal plots of the initial velocities were all parallel; (b) product inhibition between each pair of substrates and products of the three partial reactions were competitive, i.e. ATP against AMP, Pi against PPi, and pyruvate against P-enolpyruvate; (c) the other product inhibitions, with one exception, were noncompetitive as required by the nonclassical ping-pong mechanism; (d) ATP or P-enolpyruvate was required for the Pi in equilibrium PPi exchange reaction which is in accord with the participation of a pyrosphosphoryl or phosphoryl form of the enzyme in this exchange; (e) the ATP in equilibrium AMP exchange and pyruvate in equilibrium P-enolpyruvate exchange did not require additional substrates. In addition, the inhibition and participation in the exchange reactions of the alpha,beta and beta,gamma-methylene analogues of ATP and of the methylene analogue of inorganic pyrophosphate were investigated and the results were in accord with the proposed mechanism. The combined evidence provides a well documented example of a three site nonclassical Tri Uni Uni Ping Pong mechanism.
基于部分反应中的交换要求、初速度、交换动力学和产物抑制等方面的证据表明,丙酸杆菌的丙酮酸磷酸二激酶反应是通过一种非经典的三底物-单底物-单底物-乒乓机制进行的。该机制涉及一种焦磷酸化酶、一种磷酸化酶和游离酶,以及三个功能不同且独立的底物位点。在第一个位点,ATP使酶发生焦磷酸化,随后释放出AMP。然后,焦磷酸基团在第二个位点与Pi反应,生成产物PPi和酶的磷酸化形式。在第三个位点,丙酮酸被磷酸化,生成磷酸烯醇式丙酮酸和游离酶。提出这三个催化位点由一个组氨酸残基相连,该组氨酸残基在三个位点之间作为焦磷酸基团和磷酸基团的载体发挥作用。这一推测基于以下观察结果:(A)初速度的双倒数图模式均为平行;(b)三个部分反应中每对底物和产物之间的产物抑制是竞争性的,即ATP对AMP、Pi对PPi、丙酮酸对磷酸烯醇式丙酮酸;(c)除一个例外,其他产物抑制符合非经典乒乓机制的要求,是非竞争性的;(d)Pi在平衡PPi交换反应中需要ATP或磷酸烯醇式丙酮酸,这与酶的焦磷酸化或磷酸化形式参与该交换一致;(e)平衡AMP交换中的ATP和平衡磷酸烯醇式丙酮酸交换中的丙酮酸不需要额外的底物。此外,还研究了ATP的α,β-和β,γ-亚甲基类似物以及无机焦磷酸的亚甲基类似物对交换反应的抑制作用和参与情况,结果与所提出的机制相符。综合证据提供了一个有充分记录的三位点非经典三底物-单底物-单底物-乒乓机制的例子。