Levy H R, Daouk G H
J Biol Chem. 1979 Jun 10;254(11):4843-7.
A method is described which enables one to assay simultaneously the NAD- and NADP-linked reactions of dehydrogenases which can utilize both coenzymes. The method is based on the fact that the thionicotinamide analogs of NADH and NADPH absorb light maximally at 400 nm, a wavelength sufficiently far removed from the absorbance maximum of NADH and NADPH to permit measurements of the simultaneous reduction of NAD+ (or NADP+) and the thionicotinamide analog of NADP+ (or NAD+). Application of the method to glucose-6-phosphate dehydrogenase from Leuconostoc mesenteroides reveals differential effects of glucose 6-phosphate concentration on the NAD- and NADP-linked reactions catalyzed by this enzyme which can not be detected by conventional assay procedures and which may have regulatory significance.
本文描述了一种方法,该方法能够同时测定可利用两种辅酶的脱氢酶的NAD和NADP连接反应。该方法基于以下事实:NADH和NADPH的硫代烟酰胺类似物在400nm处有最大吸光度,该波长与NADH和NADPH的最大吸光度相距足够远,从而允许同时测量NAD⁺(或NADP⁺)和NADP⁺(或NAD⁺)的硫代烟酰胺类似物的还原。将该方法应用于肠系膜明串珠菌的葡萄糖-6-磷酸脱氢酶,结果显示葡萄糖6-磷酸浓度对该酶催化的NAD和NADP连接反应有不同影响,而传统检测方法无法检测到这些影响,这些影响可能具有调节意义。