van der Loos C M, van Breda A J, Meijer A E, Jöbsis A C
Histochemistry. 1981;73(2):161-4. doi: 10.1007/BF00493015.
Polyacrylamide gel-electrophoresis was performed with an extract from cultivated skin fibroblasts. Arylsulphatase activity is measured and visualised using the biochemical substrate dehydroepiandrosterone sulphate and the histochemical substrate 6-bromo-2-naphthyl sulphate respectively. The histochemical substrate was hydrolysed at Rf = 0.49 and 0.58 while the biochemical substrate was hydrolysed only at 0.49. We conclude that two different microsomal arylsulphatases exist: a sulphatase able to hydrolyse steroid sulphatases (Rf = 0.49) and one unable to hydrolyse steroid sulphatases (RF = 0.58). In consequence if is recommended to carry out an electrophoresis experiment after the histochemical investigation, in order to discriminate between these two types of sulphatase.
使用培养的皮肤成纤维细胞提取物进行聚丙烯酰胺凝胶电泳。分别使用生化底物硫酸脱氢表雄酮和组织化学底物6-溴-2-萘基硫酸盐来测量和可视化芳基硫酸酯酶活性。组织化学底物在Rf = 0.49和0.58处被水解,而生化底物仅在0.49处被水解。我们得出结论,存在两种不同的微粒体芳基硫酸酯酶:一种能够水解类固醇硫酸酯酶(Rf = 0.49),另一种不能水解类固醇硫酸酯酶(RF = 0.58)。因此,建议在组织化学研究后进行电泳实验,以区分这两种类型的硫酸酯酶。