Cascante M, Meléndez-Hevia E, Kholodenko B, Sicilia J, Kacser H
Universitat de Barcelona, Departament de Bioquímica i Fisiologia, Facultat de Química, Spain.
Biochem J. 1995 Jun 15;308 ( Pt 3)(Pt 3):895-9. doi: 10.1042/bj3080895.
Control analysis of transit time, defined as tau = delta/J, has previously been considered with the constraint of low enzyme concentrations compared with free pools of metabolites [Meléndez-Hevia, Torres, Sicilia and Kacser (1990) Biochem. J. 265, 195-202]. One of the conclusions was that the sum of the control coefficients of the transition time with respect to enzyme concentration was -1. Here we demonstrate that, if the enzyme-bound pools are taken into consideration (which would be important at high enzyme concentrations and high affinities), the sum lies between 0 and -1. The transition time between two steady states, which are frequent physiological events, is mainly governed by time constants involved in changing the enzyme concentrations. Some physiological and evolutionary aspects are discussed.
转运时间的控制分析,定义为τ=δ/J,此前在与游离代谢物池相比酶浓度较低的约束条件下进行过研究[梅伦德斯 - 埃维亚、托雷斯、西西里亚和卡克瑟(1990年)《生物化学杂志》265卷,195 - 202页]。其中一个结论是,转运时间相对于酶浓度的控制系数之和为 -1。在此我们证明,如果考虑酶结合池(这在高酶浓度和高亲和力时很重要),该和值介于0和 -1之间。两个稳态之间的转运时间是常见的生理事件,主要由改变酶浓度所涉及的时间常数决定。文中讨论了一些生理和进化方面的问题。