Siegel S A, Woods K L, Dreyer R N
J Chromatogr. 1985 Feb 20;319(3):351-8. doi: 10.1016/s0021-9673(01)90571-0.
A new assay for pyrimidine nucleoside phosphorylase is reported. This method utilizes an isocratic reversed-phase high-performance liquid chromatographic system for separation of nucleosides and bases. Product detection is accompanied by ultraviolet monitoring and radioactive flow detection. Use of an automated sample injector allows for the analysis of a series of samples, with data recorded onto a microprocessor-based cassette recorder. Data can then be downloaded into computer memory. The velocity of uridine phosphorylase (E.C. 2.4.2.3) was a linear function of enzyme concentration. The Michaelis constant for uridine at pH 8.0 was found to be in close agreement with the value obtained by a thin-layer chromatographic assay method.
报道了一种新的嘧啶核苷磷酸化酶检测方法。该方法利用等度反相高效液相色谱系统分离核苷和碱基。产物检测采用紫外监测和放射性流动检测。使用自动进样器可对一系列样品进行分析,数据记录在基于微处理器的盒式记录仪上。然后数据可下载到计算机内存中。尿苷磷酸化酶(E.C. 2.4.2.3)的活性是酶浓度的线性函数。发现在pH 8.0时尿苷的米氏常数与通过薄层色谱检测方法获得的值非常一致。