Ovádi J, Tompa P, Vértessy B, Orosz F, Keleti T, Welch G R
Institute of Enzymology, Hungarian Academy of Sciences, Budapest.
Biochem J. 1989 Jan 1;257(1):187-90. doi: 10.1042/bj2570187.
The kinetics of dynamically interacting enzyme systems is examined, in the light of increasing evidence attesting to the widespread occurrence of this mode of organization in vivo. The transient time, a key phenomenological parameter for the coupled reaction, is expressed as a function of the lifetime of the intermediate substrate. The relationships between the transient time and the pseudo-first-order rate constants for the coupled reaction by the complexed and uncomplexed enzyme species are indicative of the mechanism of intermediate transfer ('channelling'). In a dynamically interacting enzyme system these kinetic parameters are composite functions of those for the processes catalysed by the complex and by the separated enzymes. The mathematical paradigm can be extended to a linear sequence of N coupled reactions catalysed by dynamically (pair-wise) interacting enzymes.
鉴于越来越多的证据证明这种组织模式在体内广泛存在,我们对动态相互作用酶系统的动力学进行了研究。瞬态时间是偶联反应的一个关键现象学参数,它被表示为中间底物寿命的函数。复合物和未复合酶物种进行偶联反应的瞬态时间与伪一级速率常数之间的关系表明了中间产物转移(“通道化”)的机制。在动态相互作用酶系统中,这些动力学参数是复合物和分离酶催化过程动力学参数的复合函数。该数学范式可以扩展到由动态(两两)相互作用酶催化的N个偶联反应的线性序列。