Schneider H, Fiechter A, Fuhrmann G F
Biochim Biophys Acta. 1978 Oct 4;512(3):495-507. doi: 10.1016/0005-2736(78)90160-8.
Plasma membranes from Candida tropicalis grown on glucose or hexadecane were isolated using a method based on the difference in surface charge of mitochondria and plasma membranes. After mechanical disruption of the cells, a fraction consisting of mitochondrial and plasma membrane vesicles was obtained by differential centrifugation. Subsequently the mitochondria were separated from the plasma membrane vesicles by aggregation of the mitochondria at a pH corresponding to their isoelectric point. Additional purification of the isolated plasma membrane vesicles was achieved by osmolysis. Surface charge densities of mitochondria and plasma membranes were determined and showed substrate-dependent differences. The isolated plasma membranes were morphologically characterized by electron microscopy and, as a marker enzyme, the activity of Mg2+-dependent ATPase was determine. By checking for three mitochondrial marker enzymes the plasma membrane fractions were estimated to be 94% pure with regard to mitochondrial contamination.
使用一种基于线粒体和质膜表面电荷差异的方法,分离在葡萄糖或十六烷上生长的热带假丝酵母的质膜。细胞经机械破碎后,通过差速离心获得由线粒体和质膜囊泡组成的部分。随后,通过在对应于线粒体等电点的pH值下使线粒体聚集,将线粒体与质膜囊泡分离。通过渗透裂解实现对分离的质膜囊泡的进一步纯化。测定了线粒体和质膜的表面电荷密度,并显示出底物依赖性差异。通过电子显微镜对分离的质膜进行形态学表征,并测定了作为标记酶的Mg2+依赖性ATP酶的活性。通过检测三种线粒体标记酶,估计质膜部分的线粒体污染率为94%纯。