Veser J
Abteilung Humangenetik, Universität Ulm, Federal Republic of Germany.
Anal Biochem. 1989 Nov 1;182(2):217-21. doi: 10.1016/0003-2697(89)90582-4.
A free solution electrofocusing method for uroporphyrinogen I synthase (EC 4.3.1.8) in an Ampholine pH gradient on a preparative scale is described. Partial purification of the enzyme was achieved in a 4-h focusing run. Enzyme activity was found in the pH range of pH 5.1 to pH 7.0. Complete separation of the most basic and most acidic isozyme from the control and the acute intermittent porphyria (AIP) patient was obtained in this single-step procedure. The level of enzyme activity has been shown to be reduced to about half the normal value in erythrocytes of two patients from a family with AIP. A shift of maximal activity toward the acidic side of the pH gradient was observed with the abnormal enzyme. In contrast to the normal isozyme set with seven isozyme bands, the fluorescence of the three basic bands and the second acidic band was greatly reduced, whereas the intermediate forms showed increased fluorescence intensity.
本文描述了一种在制备规模下,于两性电解质pH梯度中对尿卟啉原I合酶(EC 4.3.1.8)进行自由溶液电聚焦的方法。在4小时的聚焦运行中实现了该酶的部分纯化。在pH 5.1至pH 7.0的范围内发现了酶活性。通过此单步程序,从对照和急性间歇性卟啉病(AIP)患者中完全分离出了最碱性和最酸性的同工酶。在一个AIP家族的两名患者的红细胞中,酶活性水平已被证明降至正常值的约一半。观察到异常酶的最大活性向pH梯度的酸性侧偏移。与具有七条同工酶带的正常同工酶组相比,三条碱性带和第二条酸性带的荧光大大降低,而中间形式的荧光强度增加。