Shih J C, Teulings E P
Clin Chem. 1978 Dec;24(12):2176-8.
With a radial diffusion assay we measured the activity of six NAD- and NADP-dependent oxidoreductases: alcohol, glucose-6-phosphate, hydroxysteroid, lactate and malate dehydrogenases, and glutathione reductase. The enzyme was allowed to diffuse for 24h in an agarose gel in which the substrate was incorporated, then reacted the pyridine nucleotide coenzyme. The size of an enzyme diffusion zone could be made visible by the change of the fluorescence of the coenzyme against the background when the coenzyme was either oxidized or reduced. The procedure for each enzyme is reported. The results indicate that this new technique may be applicable to all NAD- and NADP-dependent enzymes. Because of its simplicity and potentiality for screening many samples, we think this method has applications in the clinical laboratory and in nutrition studies.
我们使用径向扩散测定法测量了六种依赖NAD和NADP的氧化还原酶的活性:乙醇脱氢酶、葡萄糖-6-磷酸脱氢酶、羟类固醇脱氢酶、乳酸脱氢酶、苹果酸脱氢酶和谷胱甘肽还原酶。使酶在掺入底物的琼脂糖凝胶中扩散24小时,然后与吡啶核苷酸辅酶反应。当辅酶被氧化或还原时,辅酶荧光相对于背景的变化可使酶扩散区的大小可见。报告了每种酶的操作步骤。结果表明,这项新技术可能适用于所有依赖NAD和NADP的酶。由于其简单性和筛选大量样品的潜力,我们认为该方法在临床实验室和营养研究中具有应用价值。