Anderson E G, Pratt R F
J Biol Chem. 1983 Nov 10;258(21):13120-6.
The hydrolysis of sodium 3-dansylamidomethyl-7-beta (thienyl-2')-acetamido-ceph-3-em-4-oate, catalyzed by the beta-lactamase of Staphylococcus aureus PC1, has previously been shown (Anderson, E. G., and Pratt, R. F. (1981) J. Biol. Chem. 256, 11401-11404) to follow the reaction scheme Formula; see text. where ES' is an enzyme-substrate complex in which the substrate has undergone nucleophilic attack at the beta-lactam carbonyl group and P is product. Acid quenching of the reaction mixture has now been shown to yield, in amounts predicted by the rate constants, a covalent enzyme-substrate complex. The liability of this complex in alkaline solution is suggestive of that of an ester. Together, all of these results prove that the turnover of this apparently normal substrate by a class A beta-lactamase involves an acyl-enzyme intermediate. In the case of another fluorescent substrate, dansylcephalexin, no intermediate analogous to ES' accumulated during catalysis; presumably here, acylation of the enzyme is rate-determining. The pH profiles (pH 4-9) of the pre-steady state rate constants for hydrolysis of the former substrate have also been determined. Binding (1/K8) is pH invariant except at low pH where it weakens, probably because of substrate protonation and/or a protein conformational change. The rate constants, k2, k-2, and k3, are pH invariant at low pH but decrease at higher pH in a way which can be described by ionization of an essential acid of pKa around 7.7. This may be the same acid for each constant, being either an active participant at the active site, or a more distant acid which controls an essential conformational change.
先前已表明,金黄色葡萄球菌PC1的β-内酰胺酶催化的3-丹磺酰氨基甲基-7-β(噻吩基-2')-乙酰氨基头孢-3-烯-4-酸酯钠的水解反应(Anderson, E. G., and Pratt, R. F. (1981) J. Biol. Chem. 256, 11401 - 11404)遵循反应式(见原文)。其中ES'是一种酶 - 底物复合物,底物在β-内酰胺羰基处发生了亲核攻击,P为产物。现已证明,对反应混合物进行酸淬灭会产生按速率常数预测量的共价酶 - 底物复合物。该复合物在碱性溶液中的不稳定性表明其具有酯的性质。所有这些结果共同证明,A类β-内酰胺酶对这种看似正常的底物的周转涉及酰基酶中间体。对于另一种荧光底物丹磺头孢氨苄,催化过程中没有积累类似于ES'的中间体;据推测,在此处酶的酰化是速率决定步骤。还测定了前一种底物水解的预稳态速率常数的pH谱(pH 4 - 9)。结合常数(1/K8)在pH值不变,除非在低pH值时它会减弱,这可能是由于底物质子化和/或蛋白质构象变化。速率常数k2、k - 2和k3在低pH值时pH不变,但在较高pH值时会下降,其下降方式可用pKa约为7.7的必需酸的电离来描述。对于每个常数,这可能是同一种酸,它要么是活性位点的活性参与者,要么是控制必需构象变化的更远距离的酸。