Zherebtsov N A, Zabelina L F, Ektoba A I
Biokhimiia. 1976 Dec;41(12):2119-25.
Functional groups of glucoamylase and alpha-amylase from Asp. awamori, alpha-amylase from Asp. oryzae and alpha- and beta-amylases from barley malt are identified. Kinetic curves of the activity dependency on pH, values of ionization heats and photooxidative inactivation draw to the conclusion that carboxyl-imidazole system enters into the active site of the enzymes. A hypothetic mechanism of hydrolysis of alpha-1,4-glucoside bond in starch molecule by alpha- and beta-amylases and of alpha-1,4- and alpha-1,6-glucoside bonds by glucoamylase is given. A theory of induced correspondence of enzyme and substrate satisfactorily explains the specificity of the enzyme action and the cause of complete starch convertion into glucose under glucoamylase action and of terminal starch hydrolysis by alpha- and beta-amylases.
鉴定了泡盛曲霉葡糖淀粉酶和α-淀粉酶、米曲霉α-淀粉酶以及大麦芽α-淀粉酶和β-淀粉酶的官能团。活性对pH依赖性的动力学曲线、电离热值和光氧化失活得出结论:羧基-咪唑体系进入酶的活性位点。给出了α-淀粉酶和β-淀粉酶水解淀粉分子中α-1,4-糖苷键以及葡糖淀粉酶水解α-1,4-和α-1,6-糖苷键的假设机制。酶与底物的诱导契合理论令人满意地解释了酶作用的特异性以及在葡糖淀粉酶作用下淀粉完全转化为葡萄糖的原因和α-淀粉酶与β-淀粉酶对淀粉进行末端水解的原因。