PHASE-PLANE GEOMETRIES IN ENZYME-KINETICS

被引:22
作者
FRASER, SJ [1 ]
ROUSSEL, MR [1 ]
机构
[1] UNIV TORONTO,SCARBOROUGH COLL,TORONTO M5S 1A1,ON,CANADA
来源
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1994年 / 72卷 / 03期
关键词
D O I
10.1139/v94-107
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The transient and steady-state behaviour of the reversible Michaelis-Menten mechanism [R] and Competitive Inhibition (CI) mechanism is studied by analysis in the phase plane. Usually, the kinetics of both mechanisms is simplified to give a modified Michaelis-Menten velocity expression; this applies to the CI mechanism with excess inhibitor and to mechanism [R] in the product inhibition limit. In this paper, [R] is treated exactly as a plane autonomous system of differential equations and its true (dynamical) steady state is described by a line-like slow manifold M. Initial velocity experiments for [R] no longer strictly correspond to the hyperbolic law (as in the irreversible Michaelis-Menten mechanism) and this leads to corrections to the standard integrated rate law. Using a new analysis, the slow dynamics of the CI mechanism is reduced from a three-dimensional system to a planar system. In this mechanism transient decay collapses the trajectory flow onto a two-dimensional ''slow'' surface Sigma; motion on Sigma can be treated exactly as projected dynamics in the plane. This projected flow may differ in important ways from that of two-step mechanisms, e.g., it may lack a proper steady state. The relevance of these more accurate dynamical descriptions is discussed in relation to experimental design and metabolic function.
引用
收藏
页码:800 / 812
页数:13
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