Reading C, Hepburn P
Biochem J. 1979 Apr 1;179(1):67-76. doi: 10.1042/bj1790067.
Clavulanic acid inhibited both the extracellular and cell-extract beta-lactamases of the four Staphylococcus aureus strains tested. The inhibition of S. aureus Russell cell-extract enzyme appeared to be active-site-directed and proceeded in a first-order fashion consistent with the formation of a covalent intermediate. Inhibited enzyme free of excess clavulanic acid was shown to regenerate enzyme activity slowly at pH 7.0, but the rate of reactivation increased at acid pH. When the enzyme was incubated with excess clavulanic acid complete inhibition was rapidly obtained, during further incubation clavulanic acid was shown to disappear slowly and complete loss of clavulanic acid from the reaction mixture coincided with the onset of the return of enzyme activity. A reactive enamine resulting from enzymic hydrolysis of the beta-lactam ring of clavulanic acid has been proposed as a possible intermediate in the inhibitory mechanism.
克拉维酸抑制了所测试的四种金黄色葡萄球菌菌株的细胞外和细胞提取物中的β-内酰胺酶。对金黄色葡萄球菌拉塞尔细胞提取物酶的抑制似乎是活性位点导向的,并且以一级反应方式进行,这与共价中间体的形成一致。不含过量克拉维酸的受抑制酶在pH 7.0时显示出缓慢恢复酶活性,但在酸性pH下再活化速率增加。当酶与过量克拉维酸一起孵育时,迅速获得完全抑制,在进一步孵育期间,克拉维酸显示出缓慢消失,反应混合物中克拉维酸的完全消失与酶活性恢复的开始同时发生。有人提出,克拉维酸β-内酰胺环酶促水解产生的反应性烯胺可能是抑制机制中的中间体。