Straka J G, Kushner J P, Pryor M A
Enzyme. 1982;28(2-3):170-85.
A method for measuring the activity of uroporphyrinogen decarboxylase from a variety of sources is described. Porphyrinogen substrates are generated by enzymic synthesis or chemical reduction. Substrates and enzyme are incubated under standardized conditions. The reactions are then stopped and the reaction products, as well as unmetabolized substrate, are absorbed on tale, eluted and esterified. Porphyrin esters are then separated and quantified using high performance liquid chromatography.
描述了一种用于测量来自多种来源的尿卟啉原脱羧酶活性的方法。卟啉原底物通过酶促合成或化学还原产生。底物和酶在标准化条件下孵育。然后终止反应,反应产物以及未代谢的底物被吸附在滑石粉上,洗脱并酯化。然后使用高效液相色谱法分离和定量卟啉酯。