Gierow P, Jergil B
Department of Biochemistry, University of Lund, Sweden.
Biochem J. 1989 Aug 15;262(1):55-61. doi: 10.1042/bj2620055.
Smooth microsomal membranes, prepared from rat liver by sucrose-density-gradient centrifugation, were subfractionated by counter-current distribution in an aqueous two-phase system consisting of poly(ethylene glycol) and Dextran T500. A comparison of the distribution curves of marker enzymes, together with theoretically calculated curves, indicated the presence of at least five membrane subfractions, differing in the ratios of the marker enzymes. Glucose-6-phosphatase and arylesterase distributed in one manner, and NADPH-cytochrome c reductase and NADH-ferricyanide reductase in another. Evidence for further heterogeneities in the distribution of marker enzymes in smooth microsomes was obtained by analysing the membrane domain structure using a recently described method [Albertsson (1988) Q. Rev. Biophys. 21, 61-98]. Phenobarbital treatment did not influence the behaviour of the marker enzymes.
通过蔗糖密度梯度离心从大鼠肝脏制备的光滑微粒体膜,在由聚乙二醇和葡聚糖T500组成的水两相系统中通过逆流分配进行亚分级分离。标记酶分布曲线与理论计算曲线的比较表明存在至少五个膜亚组分,其标记酶的比例不同。葡萄糖-6-磷酸酶和芳基酯酶以一种方式分布,而NADPH-细胞色素c还原酶和NADH-铁氰化物还原酶以另一种方式分布。通过使用最近描述的方法[阿尔伯特松(1988年)《生物物理学季评》21,61 - 98]分析膜结构域结构,获得了光滑微粒体中标记酶分布进一步异质性的证据。苯巴比妥处理不影响标记酶的行为。