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多酶系统的数学分析。II. 稳态与瞬态控制。

Mathematical analysis of multienzyme systems. II. Steady state and transient control.

作者信息

Heinrich R, Rapoport T A

出版信息

Biosystems. 1975 Jul;7(1):130-6. doi: 10.1016/0303-2647(75)90050-7.

Abstract

The control theory of steady states, previously presented for linear enzymatic systems (Heinrich and Rapoport, 1974) is extended to nonlinear systems. On the basis of three theorems a new procedure for the calculation of the control strength and of the control matrix is developed. The theory is applied to the extended model of glycolysis of erythrocytes, which includes also ATP-consuming processes. Also in this model the glycolytic flux is mainly controlled by the hexokinase-phosphofructokinase-system. The control strengths of the pyruvate kinase and of the enzymes of the 2.3 P2G-bypass are negligibly small. The control strength of the ATPase is negative, i.e. an activation of this enzyme leads to a decrease of the flux. For transition states of multienzyme systems definitions are given for the mean time required for the transition of the metabolites and for the "transient control" of enzymes. Enzymes with a pronounced influence on the transition time are called time-limiting enzymes. Enzymes which excert strong control on the time-dependent processes may have little influence under steady state conditions and vice versa. The transition times of ATP have been calculated for transient states of glycolysis.

摘要

先前针对线性酶系统提出的稳态控制理论(海因里希和拉波波特,1974年)被扩展到非线性系统。基于三个定理,开发了一种计算控制强度和控制矩阵的新方法。该理论应用于红细胞糖酵解的扩展模型,该模型还包括ATP消耗过程。在这个模型中,糖酵解通量主要由己糖激酶 - 磷酸果糖激酶系统控制。丙酮酸激酶和2,3 - 二磷酸甘油酸支路酶的控制强度小到可以忽略不计。ATP酶的控制强度为负,即该酶的激活会导致通量下降。对于多酶系统的过渡态,给出了代谢物过渡所需平均时间和酶的“瞬态控制”的定义。对过渡时间有显著影响的酶称为限时酶。对时间依赖性过程有强控制作用的酶在稳态条件下可能影响很小,反之亦然。已经计算了糖酵解瞬态状态下ATP的过渡时间。

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