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[用炔脂肪酸使绵羊精囊中的前列腺素H合酶失活]

[Inactivation of prostaglandin H synthase from sheep vesicular glands with acetylenic fatty acids].

作者信息

Sheve Kh, Belosludtsev Iu Iu, Demin P M, Khol'tskhiutter Kh G, Sheve T, Miakova G I, Evstigneeva R P

出版信息

Bioorg Khim. 1993 May;19(5):548-54.

PMID:8318023
Abstract

Acetylenic fatty acids, 8,11,14-eicosatrienoic, 5,8,11,14-eicosatetraenoic and 5,8,11,14,17-eicosapentaenoic acids, were compared with respect to their effects on the particulate prostaglandin H synthase. All the acetylenic acids inactivated the enzyme in a time-dependent manner. The eicosatriynoic and eicosatetraynoic acids exhibited comparable efficacies, whereas the eicosapentaenoic acid proved to be a weaker inactivator. The time-courses of inactivation fitted a kinetic model suggest an enzyme-catalysed conversion of the compounds via alternative suicidal and non-suicidal routes. The characteristics of inactivation of prostaglandin H synthase differ from those of lipoxygenases.

摘要

将炔属脂肪酸、8,11,14-二十碳三烯酸、5,8,11,14-二十碳四烯酸和5,8,11,14,17-二十碳五烯酸对微粒体前列腺素H合酶的作用进行了比较。所有炔属酸均以时间依赖性方式使该酶失活。二十碳三炔酸和二十碳四炔酸表现出相当的效力,而二十碳五烯酸被证明是一种较弱的失活剂。失活的时间进程符合动力学模型,表明这些化合物通过交替的自杀性和非自杀性途径进行酶催化转化。前列腺素H合酶的失活特征与脂氧合酶不同。

相似文献

8
The inactivation of lipoxygenases by acetylenic fatty acids.
Biomed Biochim Acta. 1984;43(8-9):S358-61.

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