Brown G C, Cooper C E
Department of Biochemistry and Molecular Biology, University College London, U.K.
Biochem J. 1993 Aug 15;294 ( Pt 1)(Pt 1):87-94. doi: 10.1042/bj2940087.
Control analysis is used to analyse and quantify the concept of a rate-limiting step within an enzyme. The extent to which each rate constant within the enzyme limits the steady-state rate of the enzyme and the levels of enzyme intermediate species are quantified as flux and concentration control coefficients. These coefficients are additive and obey summation theorems. The control coefficients of triose phosphate isomerase, carbamate kinase and lactate dehydrogenase are calculated from literature values of the rate constants. It is shown that, contrary to previous assumption, these enzymes do not have a unique rate-limiting step, but rather flux control is shared by several rate constants and varies with substrate, product and effector concentrations, and with the direction of the reaction. Thus the general assumption that an enzyme will have a unique rate-limiting step is unjustified.
控制分析用于分析和量化酶中限速步骤的概念。酶内每个速率常数限制酶稳态速率的程度以及酶中间物种的水平被量化为通量控制系数和浓度控制系数。这些系数是可加的,并遵循求和定理。磷酸丙糖异构酶、氨基甲酸激酶和乳酸脱氢酶的控制系数是根据速率常数的文献值计算得出的。结果表明,与先前的假设相反,这些酶没有唯一的限速步骤,而是通量控制由几个速率常数共同分担,并随底物、产物和效应物浓度以及反应方向而变化。因此,认为一种酶会有唯一限速步骤的一般假设是不合理的。