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代谢控制及其分析。理论与矩阵方法的扩展。

Metabolic control and its analysis. Extensions to the theory and matrix method.

作者信息

Sauro H M, Small J R, Fell D A

出版信息

Eur J Biochem. 1987 May 15;165(1):215-21. doi: 10.1111/j.1432-1033.1987.tb11214.x.

Abstract

The matrix algebra procedure for determining the flux control coefficients of enzymes in metabolic pathways has been extended to allow determination of the concentration control coefficients. Although it is shown that the procedure is essentially unchanged in most cases, the presence of moiety-conserved cycles in a pathway places additional limitations on the form of the equations that can be used in the matrix formulation for concentration control coefficients. In the case of branched pathways, a new coefficient has been defined, the branch distribution control coefficient, which can be obtained via the matrix procedure. Thus a single matrix equation permits calculation or algebraic evaluation of the control coefficients for flux, concentration and distribution of flux at branches, so that the complete response of a pathway to alteration of enzyme content, or to modulation by an effector, can be determined. The relationships have been determined between flux control coefficients in isolated sections of metabolic pathways and the coefficients for the same enzymes when part of a larger metabolic system. It is shown that the control analysis of the isolated system provides useful information towards determining the control properties of the extended system.

摘要

用于确定代谢途径中酶的通量控制系数的矩阵代数程序已得到扩展,以允许确定浓度控制系数。尽管结果表明在大多数情况下该程序基本不变,但途径中部分守恒循环的存在对可用于浓度控制系数矩阵公式的方程形式施加了额外限制。在分支途径的情况下,定义了一个新的系数,即分支分布控制系数,它可以通过矩阵程序获得。因此,一个单一的矩阵方程允许计算或代数评估分支处通量、浓度和通量分布的控制系数,从而可以确定途径对酶含量变化或效应物调节的完整响应。已经确定了代谢途径孤立部分中的通量控制系数与同一酶在更大代谢系统中作为一部分时的系数之间的关系。结果表明,孤立系统的控制分析为确定扩展系统的控制特性提供了有用信息。

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