Scragg A H, Thomas D Y
Mol Gen Genet. 1977 Jan 7;150(1):81-6. doi: 10.1007/BF02425328.
Using purified yeast mitochondrial DNA as a template for E. coli RNA polymerase (holoenzyme) complementary mitochondrial RNA has been synthesized in vitro. This RNA has been used to direct a low background E. coli S-30 protein-synthesizing system. The synthesis of mitochondrial polypeptides has been detected by using antiserum raised against purified cytochrome c oxidase holoenzyme and shown to be specific for this antigen. The antiserum-antigen complex was dissociated and subject to SDS-polyacrylamide gel electrophoresis and the presence of 3 polypeptides of 39, 31, and 26 X 10(3) daltons molecular weight demonstrated, which correspond to the subunits synthesized by mitochondria in whole cells which are inhibited with cycloheximide.
以纯化的酵母线粒体DNA为模板,用大肠杆菌RNA聚合酶(全酶)在体外合成了互补的线粒体RNA。该RNA已用于指导低背景的大肠杆菌S-30蛋白质合成系统。通过使用针对纯化的细胞色素c氧化酶全酶产生的抗血清检测到了线粒体多肽的合成,并证明其对该抗原具有特异性。将抗血清-抗原复合物解离并进行SDS-聚丙烯酰胺凝胶电泳,结果表明存在分子量分别为39、31和26×10³道尔顿的3种多肽,它们对应于完整细胞中线粒体合成的、被环己酰亚胺抑制的亚基。