Hinman L M, Blass J P
J Biol Chem. 1981 Jul 10;256(13):6583-6.
A spectrophotometric assay for the pyruvate dehydrogenase complex has been developed, which measures NADH production by coupling it to the reduction of a tetrazolium dye via an intermediate electron carrier. The procedure uses only commercial reagents. Dependence on pyruvate, coenzyme A, and NAD is complete, and activities are comparable to those obtained by other procedures with both purified (rat kidney mitochondria) and crude (mouse brain homogenate) preparations. These dye-coupled procedures are potentially applicable to assays of other NADH-producing dehydrogenases in crude preparations.
已开发出一种用于丙酮酸脱氢酶复合体的分光光度测定法,该方法通过中间电子载体将其与四唑盐染料的还原偶联来测量NADH的产生。该程序仅使用商业试剂。对丙酮酸、辅酶A和NAD的依赖性是完全的,并且活性与通过其他程序在纯化的(大鼠肾线粒体)和粗制的(小鼠脑匀浆)制剂中获得的活性相当。这些染料偶联程序可能适用于粗制制剂中其他产生NADH的脱氢酶的测定。