Elling L, Kula M R
Institut für Enzymtechnologie, Heinrich-Heine Universität Düsseldorf im Forschungszentrum Jülich, Germany.
Biotechnol Appl Biochem. 1991 Dec;14(3):306-16.
An optimized coupled enzyme assay for UDP-glucose pyrophosphorylase (EC 2.7.7.9) using UDP-glucose dehydrogenase (EC 1.1.1.22) is presented. This optimized assay was developed by a detailed investigation of the kinetics of the UDP-glucose dehydrogenase reaction. In addition the data provide a basis for the enzymatic synthesis of UDP-glucuronic acid. The results demonstrate that the two binding sites of the dehydrogenase differ since a different modulation of the enzyme activity and stability is observed after preincubation with UDP-glucose or NAD+ at various pH values. This is of general interest for the preparation of assay mixtures where UDP-glucose dehydrogenase is used as an auxiliary enzyme.
本文介绍了一种使用UDP-葡萄糖脱氢酶(EC 1.1.1.22)对UDP-葡萄糖焦磷酸化酶(EC 2.7.7.9)进行优化的偶联酶测定法。这种优化的测定法是通过对UDP-葡萄糖脱氢酶反应动力学的详细研究而开发的。此外,这些数据为UDP-葡萄糖醛酸的酶促合成提供了基础。结果表明,脱氢酶的两个结合位点不同,因为在不同pH值下用UDP-葡萄糖或NAD+预孵育后,观察到酶活性和稳定性的调节不同。这对于制备使用UDP-葡萄糖脱氢酶作为辅助酶的测定混合物具有普遍意义。