van Leeuwen L
Clin Chem. 1979 Feb;25(2):215-7.
I describe a new kinetic enzymatic saccharogenic method for assaying alpha-amylase in human serum and urine. alpha-Amylase liberates maltose from starch. This is successively acted on by alpha-glucosidase, mutarotase, and glucose dehydrogenase. The resulting conversion of NAD+ to NADH, measured at 340 nm, during a 20-min incubation reflects amylase activity. Endogenous glucose is destroyed before measurement of amylase activity is begun.
我描述了一种用于检测人血清和尿液中α-淀粉酶的新的动力学酶促糖化方法。α-淀粉酶从淀粉中释放出麦芽糖。麦芽糖依次受到α-葡萄糖苷酶、变旋酶和葡萄糖脱氢酶的作用。在20分钟孵育期间,在340nm处测量由此产生的NAD⁺向NADH的转化,反映淀粉酶活性。在开始测量淀粉酶活性之前,内源性葡萄糖被破坏。