Krstulovic A M, Matzura C
J Chromatogr. 1979 Aug 11;176(2):217-24. doi: 10.1016/s0021-9673(00)85653-8.
A rapid and sensitive high-performance liquid-chromatographic assay for tryptophanase based upon the fluorometric measurement of the enzymatically liberated indole was developed. The total incubation time is 20 min, and the reversed-phase separation is fast (elution time of indole in 8 min) and reproducible. The sensitivity of the method is in the nanomole range. This method was tested in the assay of tryptophanase activity in E. coli, giving an average activity of 6589.6 U/g of cells. Because of its speed, high sensitivity and minimal sample preparation, this method circumvents several problems commonly encountered in standard spectrophotometric methods of analysis.
基于对酶促释放的吲哚进行荧光测定,开发了一种快速灵敏的高效液相色谱法用于测定色氨酸酶。总孵育时间为20分钟,反相分离快速(吲哚洗脱时间为8分钟)且可重复。该方法的灵敏度在纳摩尔范围内。该方法用于检测大肠杆菌中色氨酸酶的活性,测得细胞平均活性为6589.6 U/g。由于其速度快、灵敏度高且样品制备最少,该方法避免了标准分光光度分析方法中常见的几个问题。