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Computational Approaches to the Study of Biochemical Pathways and Metabolic Control

机译:生化途径和代谢控制研究的计算方法

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Metabolic control analysis as developed by Kacser & Burns (1973) and Heinrich & Rapoport (1974) and further developed by many others (reviewed ten years ago in this series, Cornish-Bowden & Cardenas, 1990) is concerned mainly with providing a quantitative measure of the control exerted by each step of a pathway on a system variable, such as a flux. Metabolic control analysis is much more successful in describing control than the older theory of rate-limiting steps (Blackman, 1905) or the crossover theorem (Chance et al., 1958). Metabolic control analysis is based on quantifying the change in a pathway property of interest as a function of variation in a manipulated parameter-the sensitivity of the pathway to that parameter. One of the strengths of metabolic control analysis is that it is exact, due to its formulation based on infinitesimal changes. In its most popular formalism it uses relative changes and so its coefficients are dimensionless. This is important, as it allows one to compare the properties of the same pathway under different environmental conditions and even, to some extent, different pathways.
机译:由Kacser&Burns(1973)和Heinrich&Rapoport(1974)提出并由其他许多人进一步发展的代谢控制分析(十年前在本系列中进行的回顾,Cornish-Bowden&Cardenas,1990)主要涉及提供定量方法路径的每个步骤对系统变量(例如通量)施加的控制量。与较早的限速步骤理论(Blackman,1905)或交叉定理(Chance等,1958)相比,代谢控制分析在描述控制方面要成功得多。代谢控制分析是基于量化目标途径特性随操纵参数(途径对该参数的敏感性)变化的函数而变化的。代谢控制分析的优点之一是精确,这是由于其基于无穷小变化而制定的。在其最流行的形式主义中,它使用相对变化,因此其系数是无量纲的。这很重要,因为它允许人们比较不同环境条件下甚至在某种程度上不同途径下同一途径的特性。

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