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Metabolic Control Design: Implicatios and Applications

机译:代谢控制设计:意义和应用

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摘要

The introduction of metabolic control analysis by Kacser & Burns (1973) and Heinrich & Rapoport (1974) represented a substantial progress int he quantitative study of metabolism. The new framework had important consequences. Perhaps for the first time, it was rigorously shown that the reductionist approach of traditional enzymology was inadequate (or at least incomplete) to understand metabolic functioning. To fill this gap it put forward an integrated view where the patterns of responses naturally emerged from the interplay of the properties of the components and their interactiosn (Cornish-Bowden & Cardenas, 1990; Fell, 1997). The questions usually addressed by metabolic control analysis are of the type: how does metabolism respond under particular conditions? Or, if we construct a metabolic system with enzyme components of known properties, how would it respond? However, there are other questions that metabolic control analysis was not developed to answer For instance, how do we construct a metabolic system that shows a pre-established pattern of responses? How do the constraints operating during evolution shape metabolic responses? These other questions are not in the domain of analysis, they belong to that of design.
机译:Kacser&Burns(1973)和Heinrich&Rapoport(1974)对代谢控制分析的介绍代表了对代谢定量研究的实质性进展。新框架产生了重要的后果。也许是第一次,它被严格地证明,传统酶学的还原论方法不足以(或至少是不完全的)来理解代谢功能。为了填补这一空白,它提出了一个综合的观点,即响应的模式自然是从组件的属性及其交互作用的相互作用中出现的(Cornish-Bowden&Cardenas,1990; Fell,1997)。代谢控制分析通常解决的问题是:在特定条件下代谢如何反应?或者,如果我们构建具有已知特性的酶成分的代谢系统,它将如何响应?但是,还有其他问题尚未开发出代谢控制分析来回答。例如,我们如何构建一个显示预先建立的反应模式的代谢系统?进化过程中的约束如何影响新陈代谢反应?这些其他问题不在分析领域内,它们属于设计领域。

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