Baldwin J E, Moroney S E, Ting H H
Anal Biochem. 1985 Feb 15;145(1):183-7. doi: 10.1016/0003-2697(85)90345-8.
The development of a coupled enzyme assay for the determination of isopenicillin N synthetase activity in purified extracts from Cephalosporium acremonium was described. Isopenicillin N formed from its precursor, delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine (ACV), by the synthetase was hydrolyzed by beta-lactamase I to the corresponding penicilloic acid. Automatic titration of the acid with standard sodium hydroxide delivered by a pH-stat gave a continuous plot of product formed vs time. This assay has been used in kinetic studies and to determine the effects of pH, ionic strength, and temperature on the enzyme's activity.
描述了一种用于测定顶头孢霉纯化提取物中异青霉素N合成酶活性的偶联酶测定法。由合成酶从其前体δ-(L-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸(ACV)形成的异青霉素N被β-内酰胺酶I水解为相应的青霉素酸。通过pH计用标准氢氧化钠对酸进行自动滴定,得到产物形成量与时间的连续曲线。该测定法已用于动力学研究以及确定pH、离子强度和温度对该酶活性的影响。