A soluble phosphodiesterase is present in mammalian tissues which rapidly hydrolyses enantiomorphs of rac-glycerol 1:2-cyclic phosphate, producing rac-glycerol 1-phosphate. 2. The enzyme has been purified up to 1700-fold by a combination of acetone precipitation and chromatography on DEAE-Sephadex A-50, Sephadex G-150 and hydroxyapatite. 3. The Km with glycerol cyclic phosphate as substrate is 7.2 mM, and the pH optimum broad (6.9--7.5). The molecular weight (by gel filtration) of the enzyme is approx. 35500. 4. The phosphodiesterase has no requirement for Ca2+ or Mg2+, but is stimulated by reducing agents (cysteine, dithiothreitol) and Fe2+. 5. The purified phosphodiesterase preparation also hydrolysed 3':5'-cyclic AMP, producing 5'-AMP exclusively, and 2':3'-cyclic AMP, forming 3'-AMP and 2'-AMP in the ratio 7:3. Bis-(p-nitrophenyl) phosphate was slowly hydrolysed, but other phosphodiesters tested were not attacked. 6. The phosphodiesterase is inhibited by theophylline and o-phenanthroline. It is inhibited by Pi and by a variety of phosphomonoesters, of which certain aromatic primary phosphates are particularly effective.
摘要
哺乳动物组织中存在一种可溶性磷酸二酯酶,它能迅速水解消旋甘油1:2 -环磷酸酯的对映体,生成消旋甘油1 -磷酸。2. 通过丙酮沉淀以及在DEAE - Sephadex A - 50、Sephadex G - 150和羟基磷灰石上进行色谱分离相结合的方法,该酶已被纯化至1700倍。3. 以甘油环磷酸为底物时,Km为7.2 mM,最适pH范围较宽(6.9 - 7.5)。该酶的分子量(通过凝胶过滤法测定)约为35500。4. 该磷酸二酯酶不需要Ca2+或Mg2+,但可被还原剂(半胱氨酸、二硫苏糖醇)和Fe2+激活。5. 纯化后的磷酸二酯酶制剂还能水解3':5'-环磷酸腺苷,仅产生5'-腺苷酸,以及水解2':3'-环磷酸腺苷,生成3'-腺苷酸和2'-腺苷酸的比例为7:3。双(对硝基苯基)磷酸酯被缓慢水解,但所测试的其他磷酸二酯未受攻击。6. 该磷酸二酯酶被茶碱和邻菲罗啉抑制。它被无机磷酸盐和多种磷酸单酯抑制,其中某些芳香族伯磷酸盐特别有效。