Jacobs N J, Jacobs J M
Enzyme. 1982;28(2-3):206-19. doi: 10.1159/000459103.
Detailed directions are given for the spectrophotometric and fluorometric assays for protoporphyrinogen oxidation in rat liver mitochondria and other tissues. Linearity of the two assays with enzyme concentration is demonstrated. Some possible assay modifications and sources of error are mentioned. The fluorometric assay appears more sensitive, while the spectrophotometric assay may be more useful for assaying a wider variety of tissues. By both methods, rat liver mitochondria exhibit enzymatic oxidation at the rate of approximately 10 nmol protoporphyrin produced per hour per milligram protein.
文中给出了大鼠肝线粒体及其他组织中原卟啉原氧化的分光光度法和荧光测定法的详细操作说明。证明了这两种测定法与酶浓度的线性关系。文中还提到了一些可能的测定法改进方法及误差来源。荧光测定法似乎更灵敏,而分光光度法可能更适用于多种组织的测定。通过这两种方法,大鼠肝线粒体均表现出酶促氧化作用,每小时每毫克蛋白质产生原卟啉的速率约为10纳摩尔。