Munujos P, Coll-Cantí J, González-Sastre F, Gella F J
Departament de Bioquímica i Biologia Molecular, Hospital de Sant Pau, Universitat Autònoma de Barcelona, Catalonia, Spain.
Anal Biochem. 1993 Aug 1;212(2):506-9. doi: 10.1006/abio.1993.1360.
A spectrophotometric assay method for determining succinate dehydrogenase activity is described in which iodonitrotetrazolium chloride is used as a final electron acceptor. The enzyme activity is determined by measuring the formation of formazan due to the tetrazolium salt reduction. The assay is continuous, rapid, simple, and sensitive, and may be used in the determination of enzyme activity either in tissue homogenates or as a marker of the mitochondrial fraction in cell fractionation procedures.
本文描述了一种用于测定琥珀酸脱氢酶活性的分光光度测定方法,该方法使用氯化碘硝基四氮唑蓝作为最终电子受体。通过测量由于四氮唑盐还原而形成的甲臜来确定酶活性。该测定方法具有连续性、快速、简单且灵敏的特点,可用于测定组织匀浆中的酶活性,或作为细胞分级分离过程中线粒体部分的标志物。