Campbell N R, Van Loon J A, Weinshilboum R M
Biochem Pharmacol. 1987 May 1;36(9):1435-46. doi: 10.1016/0006-2952(87)90108-0.
Phenol sulfotransferase (PST) catalyzes the sulfate conjugation of phenolic and catechol drugs and neurotransmitters. Human platelets and brain contain at least two forms of PST. One form is relatively thermolabile (TL) and catalyzes the sulfate conjugation of monoamines such as dopamine. The other is thermostable (TS) and catalyzes the sulfation of "simple" phenols such as phenol and p-nitrophenol. We found that homogenates of human liver also contain two forms of PST that are similar to brain and platelet TL and TS PST with regard to substrate specificities, thermal stabilities and sensitivities to inhibitors. Optimal conditions were determined for the assay of these two activities in human liver homogenates. The apparent Km of liver homogenate TL PST for dopamine was 27 microM. The apparent Km of the TS form of the enzyme for p-nitrophenol was 0.94 microM. Human liver TS PST also catalyzed the sulfate conjugation of dopamine, but with an apparent Km of 5 mM, over two orders of magnitude higher than that of TL PST. Two different peaks of TS PST activity were separated from the TL activity by ion exchange chromatography of human liver preparations. Both peaks of TS PST activity were partially purified and characterized. Both had similar substrate specificities and inhibitor sensitivities. Km values of TS PST peak I for p-nitrophenol and for 3'-phosphoadenosine-5'-phosphosulfate were 0.91 and 0.86 microM, respectively, while the Km values of TS PST peak II for these two cosubstrates for the reaction were 0.43 and 0.64 microM, respectively. However, the TS PST activity in peak II was significantly more thermolabile than was the activity in peak I. These results are compatible with the conclusion that human liver homogenates contain at least two forms of PST, forms with properties similar to those of TS and TL PST in homogenates of human cerebral cortex and platelets. In addition, human liver contains two isozymes of TS PST.
酚磺基转移酶(PST)催化酚类和儿茶酚类药物及神经递质的硫酸结合反应。人血小板和大脑中至少含有两种形式的PST。一种形式相对热不稳定(TL),催化单胺如多巴胺的硫酸结合反应。另一种是热稳定的(TS),催化“简单”酚类如苯酚和对硝基苯酚的硫酸化反应。我们发现人肝脏匀浆中也含有两种形式的PST,它们在底物特异性、热稳定性和对抑制剂的敏感性方面与大脑和血小板的TL和TS PST相似。确定了在人肝脏匀浆中测定这两种活性的最佳条件。肝脏匀浆TL PST对多巴胺的表观Km值为27μM。该酶TS形式对对硝基苯酚的表观Km值为0.94μM。人肝脏TS PST也催化多巴胺的硫酸结合反应,但其表观Km值为5 mM,比TL PST高两个数量级以上。通过对人肝脏制剂进行离子交换色谱,从TL活性中分离出两个不同的TS PST活性峰。TS PST活性的两个峰均经过部分纯化和表征。两者具有相似的底物特异性和抑制剂敏感性。TS PST峰I对对硝基苯酚和3'-磷酸腺苷-5'-磷酸硫酸酯的Km值分别为0.91和0.86μM,而TS PST峰II对这两种共底物的Km值分别为0.43和0.64μM。然而,峰II中的TS PST活性比峰I中的活性热稳定性明显更低。这些结果与以下结论一致,即人肝脏匀浆中至少含有两种形式的PST,其性质与人类大脑皮层和血小板匀浆中的TS和TL PST相似。此外,人肝脏含有两种TS PST同工酶。