Rangheard M S, Langrand G, Triantaphylides C, Baratti J
Ecole Supérieure de Chimie de Marseille, France.
Biochim Biophys Acta. 1989 Jul 17;1004(1):20-8. doi: 10.1016/0005-2760(89)90207-5.
Multiple substrate competition was kinetically analyzed to study lipase-catalyzed reactions in organic media. For each substrate, a competitive factor (the ratio of the specificity constants kcat/Km) was measured by reference to the best substrate using a mixture of fatty acid ethyl esters submitted to a solvolysis reaction by n-propanol. A scale of competitive factors was established which quantitatively described the lipase specificity. This principle was applied to the determination of the specificity of four commercial lipase preparations towards fatty acid chain length and degree of unsaturation. The results were not affected by changes in the physicochemical conditions of the reaction (water content, substrate concentration, nature of nucleophile, etc.). The simple test will be a useful tool to characterize lipase specificity.
通过动力学分析多底物竞争来研究有机介质中脂肪酶催化的反应。对于每种底物,通过使用正丙醇进行溶剂解反应的脂肪酸乙酯混合物,以最佳底物为参照测量竞争因子(特异性常数kcat/Km的比值)。建立了一个竞争因子量表,定量描述脂肪酶的特异性。该原理应用于测定四种商业脂肪酶制剂对脂肪酸链长度和不饱和度的特异性。反应的物理化学条件(含水量、底物浓度、亲核试剂性质等)的变化不会影响结果。这个简单的测试将成为表征脂肪酶特异性的有用工具。