Heinz F, Reckel S, Pilz R, Kalden J R
Enzyme. 1980;25(1):44-9. doi: 10.1159/000459214.
A spectrophotometric method especially suitable for biological materials is described for the determination of purine nucleoside phosphorylase activity. In combination with the enzymes xanthine oxidase, catalase and aldehyde dehydrogenase, and in the presence of ethanol and NAD(P), the purines formed by phosphorylysis of purine nucleosides are oxidized and the absorption of the NAD(P)H formed is taken for the calculation of nucleoside phosphorylase activity.
本文描述了一种特别适用于生物材料的分光光度法,用于测定嘌呤核苷磷酸化酶的活性。在黄嘌呤氧化酶、过氧化氢酶和醛脱氢酶存在的情况下,结合乙醇和NAD(P),嘌呤核苷磷酸解产生的嘌呤被氧化,通过测定生成的NAD(P)H的吸光度来计算核苷磷酸化酶的活性。