Schulz A R, Südi J
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis 46202-5122, USA.
J Theor Biol. 1996 Oct 7;182(3):397-403. doi: 10.1006/jtbi.1996.0179.
Single-enzyme reactions involving abortive complexes, and random sequences, respectively, are subjected to control analysis. Explicit analytical expressions are presented which cover these kinetic behaviors. The latter are based (1) on the concept of control coefficients which measure the sensitivity of flux with respect to rate constants, and (2) on the classical steady state rate equations. The methods include both a graph theoretic approach and computer-aided derivation of algebraic expressions. Some conclusions are derived from the analysis of simple models. It is demonstrated (1) that abortive complexes exert no kinetic (as opposed to equilibrium) control over steady state flux; (2) the sum of the paired flux control coefficients for each step in the catalytic cycle, as well as the sum of the flux control coefficients for the unidirectional steps which emanate from each enzyme species, is equal to unity in a random sequence; (3) in the case of a random reaction sequence, the numerator terms of the rate equation exert an effect in the paired flux control coefficients for those steps in the random portion of the reaction sequence.
分别涉及流产复合物和随机序列的单酶反应接受控制分析。给出了涵盖这些动力学行为的明确解析表达式。后者基于:(1)测量通量相对于速率常数敏感性的控制系数概念;(2)经典稳态速率方程。这些方法包括图论方法和代数表达式的计算机辅助推导。从简单模型的分析中得出了一些结论。结果表明:(1)流产复合物对稳态通量没有动力学(与平衡相反)控制作用;(2)在随机序列中,催化循环中每一步的成对通量控制系数之和,以及源自每种酶物种的单向步骤的通量控制系数之和等于1;(3)在随机反应序列的情况下,速率方程的分子项对反应序列随机部分中那些步骤的成对通量控制系数有影响。