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为蔡氏推导速率方程方法的普遍有效性辩护。明确认识酶动力学中热力学框的重要性。

In defence of the general validity of the Cha method of deriving rate equations. The importance of explicit recognition of the thermodynamic box in enzyme kinetics.

作者信息

Topham C M, Brocklehurst K

机构信息

Department of Crystallography, Birkbeck College, University of London, U.K.

出版信息

Biochem J. 1992 Feb 15;282 ( Pt 1)(Pt 1):261-5. doi: 10.1042/bj2820261.

Abstract
  1. The suggestion by Segel & Martin [(1988) J. Theor. Biol. 135, 445-453] that the well-known schematic method for the derivation of rate equations for combined quasi-equilibrium-steady-state models proposed by Cha [(1968) J. Biol. Chem. 243, 820-825] may not be generally applicable was shown to be incorrect. By contrast, Cha's method was shown (a) to yield correct initial-rate equations that are exact and (b) not to require any constraints on the relative magnitudes of rate constants for slow steps outside the quasi-equilibrium segments of the kinetic model, including those suggested by Segel & Martin. 2. Examination of residual King-Altman patterns for the general modifier model of Botts & Morales [(1953) Trans. Faraday Soc. 49, 696-707] revealed the reasons for the erroneous conclusions reached by Segel & Martin. The errors arise from the failure to take account of fluxes in parallel pathways that connect the two isolated groups of enzyme species existing in quasi-equilibrium with the modifier. 3. A similar failure to take explicit account of parallel pathways in a thermodynamic box that delayed proper appreciation of the form of pH-dependence of kcat/Km is briefly discussed.
摘要
  1. 西格尔和马丁[(1988年)《理论生物学杂志》135卷,445 - 453页]提出,查[(1968年)《生物化学杂志》243卷,820 - 825页]提出的用于推导组合准平衡 - 稳态模型速率方程的著名图解法可能并不普遍适用,但事实证明这一观点是错误的。相比之下,查的方法被证明:(a)能得出准确的初始速率方程,这些方程是精确的;(b)对于动力学模型准平衡段之外慢步骤的速率常数相对大小,包括西格尔和马丁所建议的那些,不需要任何限制。2. 对博茨和莫拉莱斯[(1953年)《法拉第学会会报》49卷,696 - 707页]的一般修饰剂模型的剩余金 - 阿尔特曼模式进行研究,揭示了西格尔和马丁得出错误结论的原因。这些错误源于未能考虑连接与修饰剂处于准平衡状态的两组孤立酶物种的平行途径中的通量。3. 简要讨论了在一个热力学框中类似的未能明确考虑平行途径的情况,这种情况延迟了对kcat/Km的pH依赖性形式的正确认识。

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本文引用的文献

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Some aspects of the kinetics of enzymic reactions.酶促反应动力学的某些方面。
Biochim Biophys Acta. 1953 Jan;10(1):27-34. doi: 10.1016/0006-3002(53)90206-6.
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PK of the lysine amino group at the active site of acetoacetate decarboxylase.
Biochemistry. 1971 Mar 30;10(7):1249-53. doi: 10.1021/bi00783a023.

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