Delgado J, Liao J C
Department of Chemical Engineering, Texas A&M University, College Station 77843-3122.
Biochem J. 1992 Mar 15;282 ( Pt 3)(Pt 3):919-27. doi: 10.1042/bj2820919.
Flux Control Coefficients have been used in the analysis of metabolic regulation for quantifying the effect of an enzyme on the overall steady-state flux. However, the experimental determination of these coefficients is very time-consuming, involving either determining the individual enzyme kinetics or perturbing the enzyme activity by genetic or other means. We developed a methodology that enables the determination of the Flux Control Coefficients from transient metabolite concentrations without knowing kinetic parameters. The transient states can be generated by changing the incubation conditions or adding the initial substrate. This approach is suitable for investigating metabolic regulation in vivo or multiple enzyme systems in vitro. It is particularly helpful if used in conjunction with n.m.r. measurements. The approach is based on a relationship between transient metabolite concentrations and the Flux Control Coefficients. The methodology has been improved from our previous results, and it is illustrated by three examples with simple pathway topologies.
通量控制系数已被用于代谢调控分析,以量化一种酶对整体稳态通量的影响。然而,这些系数的实验测定非常耗时,涉及确定单个酶的动力学或通过遗传或其他手段干扰酶活性。我们开发了一种方法,能够在不知道动力学参数的情况下,根据瞬态代谢物浓度来确定通量控制系数。瞬态状态可以通过改变孵育条件或添加初始底物来产生。这种方法适用于研究体内的代谢调控或体外的多酶系统。如果与核磁共振测量结合使用,它会特别有帮助。该方法基于瞬态代谢物浓度与通量控制系数之间的关系。该方法在我们之前的结果基础上得到了改进,并通过三个具有简单途径拓扑结构的例子进行了说明。