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参与乳酸脱氢酶周转的两个核心酶 - 底物复合物形成和相互转化的宏观速率常数。

Macroscopic rate constants involved in the formation and interconversion of the two central enzyme--substrate complexes of the lactate dehydrogenase turnover.

作者信息

Südi J

出版信息

Biochem J. 1974 Apr;139(1):261-71. doi: 10.1042/bj1390261.

Abstract

The preceding paper (Südi, 1974) reports partial success in describing the conversion of E(NADH) plus pyruvate into E(NAD+) plus lactate in terms of a simple Haldane-type scheme which involves two intermediates (E(NADH) (Pyr) and E(NAD+) (Lac)), where E represents lactate dehydrogenase. This information is completed here by reporting kinetic results obtained by carrying out the same reaction in the opposite direction. The combined results of these two papers confirm the findings of Holbrook & Gutfreund (1973) that the observed spectral changes do take place at the level of resolution of this simple two-intermediate scheme. The following numerical values for the rate (and equilibrium) constants involved in their formation and decomposition are reported: [Formula: see text] It is shown that although the precision of estimation of some of these numerical values is subject to some experimental uncertainty, their derivation from direct experimental observations only involves the principle of microscopic reversibility. This paper describes stopped-flow kinetic observations made with E(NAD+) and lactate as the two reactants. It is shown that fluorescence and u.v.-absorption measurements yield the same experimental rate constant for the last reaction step in which E(NADH) is generated. On the other hand, the generation of E(NADH) (Pyr) can only be indirectly observed, as a less than stoicheiometric ;burst', and by u.v.-absorption measurements only. It is shown that the stoicheiometry of this partial ;burst reaction', and a pre-equilibrium factor in the directly observed rate of E(NADH)-production, yield equivalent information about the reversible oxidation-reduction step. It is further shown that the pre-equilibrium factor that is involved in the generation of E(NADH) can be determined because k(+4)=222s(-1) is already known (Südi, 1974). Since the fluorescence measurements yield much more precise estimations, and their interpretation is considered by the author to be free of ambiguity, the presented quantitative analysis is based on the fluorescence observations.

摘要

前文(苏迪,1974年)报道了在描述E(NADH)加丙酮酸转化为E(NAD+)加乳酸的过程中取得的部分成功,该过程采用了一种简单的哈代型反应机制,涉及两个中间体(E(NADH)(Pyr)和E(NAD+)(Lac)),其中E代表乳酸脱氢酶。本文通过报道在相反方向进行相同反应所获得的动力学结果来完善这一信息。这两篇论文的综合结果证实了霍尔布鲁克和古特弗罗因德(1973年)的发现,即在这个简单的双中间体反应机制的分辨率水平上确实发生了所观察到的光谱变化。报告了以下参与其形成和分解的速率(和平衡)常数的数值:[公式:见原文]结果表明,尽管其中一些数值的估计精度存在一定的实验不确定性,但它们直接从实验观察中推导出来仅涉及微观可逆性原理。本文描述了以E(NAD+)和乳酸作为两种反应物进行的停流动力学观察。结果表明,荧光和紫外吸收测量对于生成E(NADH)的最后反应步骤给出了相同的实验速率常数。另一方面,E(NADH)(Pyr)的生成只能间接观察到,表现为小于化学计量的“爆发”,且只能通过紫外吸收测量来观察。结果表明,这个部分“爆发反应”的化学计量以及直接观察到的E(NADH)生成速率中的预平衡因子,提供了关于可逆氧化还原步骤的等效信息。进一步表明,由于k(+4)=222s(-1)已经已知(苏迪,1974年),所以可以确定参与E(NADH)生成的预平衡因子。由于荧光测量给出了更精确的估计值,并且作者认为对其解释不存在歧义,所以本文给出的定量分析基于荧光观察结果。

相似文献

本文引用的文献

1
Approaches to the study of enzyme mechanisms lactate dehydrogenase.乳酸脱氢酶的酶机制研究方法
FEBS Lett. 1973 Apr 15;31(2):157-169. doi: 10.1016/0014-5793(73)80095-x.
7
Structure-function relationships in lactate dehydrogenase.乳酸脱氢酶的结构-功能关系
Proc Natl Acad Sci U S A. 1973 Jul;70(7):1968-72. doi: 10.1073/pnas.70.7.1968.

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