Piccioni R G, Bennoun P, Chua N H
Eur J Biochem. 1981 Jun;117(1):93-102. doi: 10.1111/j.1432-1033.1981.tb06307.x.
Use of the Flagyl selection procedure [Schmidt et al. (1977) Proc. Natl Acad. Sci. USA, 74, 610-614] led to the isolation of a nuclear mutant of Chlamydomonas reinhardtii designated thm-24. This mutant displays normal electron transport rates in vitro, possesses high latent ATPase activity bound to the thylakoid membrane, but is incapable of photophosphorylation. Decay of the transmembrane potential, as indicated by the kinetics of the 520-nm absorption change after illumination, is unusually slow and markedly biphasic. Sodium dodecylsulfate/polyacrylamide gel electrophoresis of purified thylakoid membranes shows mutant thm-24 to be lacking a number of polypeptides including those previously designated 4.1, 4.2 and 8.1. Treatment of purified thylakoid membranes of wild-type and mutant algae, using the chloroform-release procedure of Beechey et al. [(1975) Biochem. J. 148, 533-537] resulted in the removal of ATPase activity from each strain. In wild-type cells, the ATPase activity was of heterogeneous enzymatic origin; fractionation of the chloroform-release extracts by non-denaturing polyacrylamide gel electrophoresis yielded three distinct bands displaying ATPase activity, designated ATPases I, II and III. In contrast, extracts from membranes of mutant thm-24 yielded only one ATPase-containing fraction, co-migrating with ATPase I from wild-type. Use of electrophoretic, immunological and enzymatic methods established a correspondence of the polypeptide subunits of ATPases II and III and those of spinach coupling factor, CF1. ATPase I from either algal strain was shown to be structurally distinct from high plant CF1 and to C. reinhardtii ATPases II and III.
使用甲硝唑筛选程序[施密特等人(1977年),《美国国家科学院院刊》,74卷,610 - 614页]导致莱茵衣藻的一个核突变体被分离出来,命名为thm - 24。该突变体在体外显示出正常的电子传递速率,具有与类囊体膜结合的高潜在ATP酶活性,但不能进行光合磷酸化。光照后520纳米吸收变化的动力学表明,跨膜电位的衰减异常缓慢且明显呈双相。纯化的类囊体膜的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳显示,突变体thm - 24缺少许多多肽,包括先前命名为4.1、4.2和8.1的那些多肽。使用比奇等人[(1975年),《生物化学杂志》,148卷,533 - 537页]的氯仿释放程序处理野生型和突变型藻类的纯化类囊体膜,导致每个菌株的ATP酶活性被去除。在野生型细胞中,ATP酶活性源于多种酶;通过非变性聚丙烯酰胺凝胶电泳对氯仿释放提取物进行分级分离,产生了三条显示ATP酶活性的不同条带,分别命名为ATP酶I、II和III。相比之下,突变体thm - 24膜的提取物只产生了一个含ATP酶的组分,与野生型的ATP酶I共迁移。电泳、免疫和酶学方法的使用确定了ATP酶II和III的多肽亚基与菠菜偶联因子CF1的多肽亚基相对应。任一藻类菌株的ATP酶I在结构上与高等植物CF1以及莱茵衣藻的ATP酶II和III不同。