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可可链霉菌的β-内酰胺酶:与头孢西丁和β-碘青霉素酸盐的相互作用

The beta-lactamase of Streptomyces cacaoi: interaction with cefoxitin and beta-iodopenicillanate.

作者信息

Lenzini M V, Frère J M

机构信息

Service de Microbiologie, Université de Liège, Sart Tilman, Belgium.

出版信息

J Enzyme Inhib. 1985;1(1):25-34. doi: 10.3109/14756368509031279.

Abstract

Cefoxitin was a very poor substrate for the beta-lactamase of Streptomyces cacaoi (kcat = 2.7 x 10(-4) s-1). In the presence of nitrocefin, a good substrate, cefoxitin behaved as a transient inactivator by immobilizing a large proportion of the enzyme as the acyl enzyme intermediate. The enzyme was also inactivated by beta-iodopenicillanate. In this case, the acyl enzyme rearranged into an alpha-beta unsaturated ester and inactivation was irreversible. In contrast to the situation prevailing with the Streptomyces albus G beta-lactamase, no turn-over of beta-iodopenicillanate was observed.

摘要

头孢西丁是可可链霉菌β-内酰胺酶的一种极差的底物(kcat = 2.7 x 10(-4) s-1)。在存在良好底物头孢硝噻吩的情况下,头孢西丁通过将大部分酶固定为酰基酶中间体而表现为瞬时失活剂。该酶也会被β-碘青霉素酸失活。在这种情况下,酰基酶重排为α-β不饱和酯,失活是不可逆的。与白色链霉菌Gβ-内酰胺酶的情况相反,未观察到β-碘青霉素酸的周转。

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