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睾丸酮假单胞菌的3β,17β-羟基类固醇脱氢酶。在一个共同催化位点上双功能活性的动力学证据。

3 beta, 17 beta-hydroxysteroid dehydrogenase of Pseudomonas testosteroni. Kinetic evidence for the bifunctional activity at a common catalytic site.

作者信息

Minard P, Legoy M D, Thomas D

出版信息

FEBS Lett. 1985 Aug 19;188(1):85-90. doi: 10.1016/0014-5793(85)80880-2.

Abstract

3 beta, 17 beta-Hydroxysteroid dehydrogenase (3 beta 17 beta HSDH) is an NAD-dependent dehydrogenase which has a double specificity for the 3- and 17-positions on the steroid skeleton. When dehydroepiandrosterone (DHEA) is used as steroid substrate, and the assay coupled with ketosteroid-isomerase, the two reactions occur alternately and each reaction on the 3-position produces a chromophoric molecule. These two reactions can follow one another without dissociation of the coenzyme from the enzyme binding site. This is confirmed by competition experiments with another dehydrogenase.

摘要

3β,17β-羟基类固醇脱氢酶(3β17βHSDH)是一种依赖烟酰胺腺嘌呤二核苷酸(NAD)的脱氢酶,对类固醇骨架上的3位和17位具有双重特异性。当以脱氢表雄酮(DHEA)作为类固醇底物,并将该测定与酮类固醇异构酶偶联时,这两个反应交替发生,并且3位上的每个反应都会产生一个发色分子。这两个反应可以相继进行,而辅酶不会从酶结合位点解离。这一点通过与另一种脱氢酶的竞争实验得到了证实。

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