Ukeda Hiroyuki, Adachi Yukiko, Sawamura Masayoshi
Department of Bioresources Science, Faculty of Agriculture, Kochi University, Monobe B-200, Nankoku 783-8502, Japan.
Anal Sci. 2004 Mar;20(3):471-4. doi: 10.2116/analsci.20.471.
A novel flow-injection assay (FIA) system with a double line for catalase activity was constructed in which an oxidase is immobilized and the substrate is continuously pumped to reduce the dissolved oxygen and to generate a given level of hydrogen peroxide. The catalase in a sample decomposed the hydrogen peroxide, and thus the increase in dissolved oxygen dependent on the activity was amperometrically monitored using a Clark-type oxygen electrode. Among the examined several oxidases, uricase was most suitable for the continuous formation of hydrogen peroxide from a consideration of the stability and the conversion efficiency. Under the optimum conditions, a linear calibration curve was obtained in the range from 21 to 210 units/mg and the reproducibility (CV) was better than 2% by 35 successive determinations of 210 units/ml catalase preparation. The sampling frequency was about 15 samples/h. The present FIA system was applicable to monitor the inactivation of catalase by glycation.
构建了一种用于过氧化氢酶活性检测的新型双管路流动注射分析(FIA)系统,其中固定化了一种氧化酶,并持续泵入底物以降低溶解氧并生成一定水平的过氧化氢。样品中的过氧化氢酶分解过氧化氢,因此,利用克拉克型氧电极通过安培法监测因活性而导致的溶解氧增加。在所研究的几种氧化酶中,从稳定性和转化效率方面考虑,尿酸酶最适合用于过氧化氢的连续生成。在最佳条件下,得到了21至210单位/毫克范围内的线性校准曲线,通过对210单位/毫升过氧化氢酶制剂进行35次连续测定,重现性(CV)优于2%。采样频率约为每小时15个样品。本FIA系统适用于监测糖化作用对过氧化氢酶的失活情况。