Simakova I M, Ostrovskiĭ D N
Biokhimiia. 1980 Feb;45(2):363-70.
Treatment of M. lysodeikticus protoplasts with subtilisin or pronase did not affect their permeability and led to a digestion of 20--30% of protein. DS-Na electrophoresis of protoplast membranes resulted in disappearance of three protein bands. This suggests that the outer surface of M. lysodeikticus protoplasts contains three proteins other than respiratory chain enzymes, which are subjected to an attack by proteinases. Treatment of the M. lysodeikticus membranes, isolated by osmotic shock, with proteinases resulted in a digestion of 20--50% of protein. The factors preventing the interaction between the membrane components (e.g. decrease of Mg2+ concentration, ultrasound, KCl, EDTA and particularly detergents) favoured the proteolysis; however, the bulk of the proteins remained insensitive to the effect of proteinases. The membranes pretreated with DS-Na or chlorophorm--methanol mixture proved to be good substrates for proteinases. Treatment of the membrane fraction with proteolytic enzymes allowed to obtain some data on localization of respiratory chain enzymes in the membrane stroma of M. lysodeikticus. Thus, cytochrome c is localized nearer to the membrane surface than cytochromes a and b, while malate dehydrogenase is plunged deeper into the membrane stroma as compared to NADH dehydrogenase.
用枯草杆菌蛋白酶或链霉蛋白酶处理溶壁微球菌原生质体不会影响其通透性,且会导致20% - 30%的蛋白质被消化。原生质体膜的十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳导致三条蛋白带消失。这表明溶壁微球菌原生质体的外表面除了呼吸链酶之外还含有三种蛋白质,它们会受到蛋白酶的攻击。用蛋白酶处理通过渗透休克分离得到的溶壁微球菌膜,会导致20% - 50%的蛋白质被消化。阻止膜成分之间相互作用的因素(例如Mg2 +浓度降低、超声、KCl、EDTA,尤其是去污剂)有利于蛋白水解;然而,大部分蛋白质对蛋白酶的作用不敏感。用十二烷基硫酸钠或氯仿 - 甲醇混合物预处理的膜被证明是蛋白酶的良好底物。用蛋白水解酶处理膜部分能够获得一些关于呼吸链酶在溶壁微球菌膜基质中定位的数据。因此,细胞色素c比细胞色素a和b更靠近膜表面定位,而与NADH脱氢酶相比,苹果酸脱氢酶更深地嵌入膜基质中。