Burnap R L, Trench R K
Department of Biological Sciences, University of California, Santa Barbara 93106.
Proc R Soc Lond B Biol Sci. 1989 Oct 23;238(1290):89-102. doi: 10.1098/rspb.1989.0068.
RNA from Cyanophora paradoxa was separated into cytoplasmic and cyanellar fractions by using a combination of subcellular fractionation and oligo-dT chromatography. In vitro translation of the separated cytoplasmic and cyanellar RNAs in a rabbit reticulocyte lysate system in the presence of [35S]methionine resulted in the incorporation of radiolabel into electrophoretically distinct sets of polypeptides. Monospecific and polyspecific antibodies that react with cyanellar polypeptides were used to probe the in vitro translation products by indirect immunoprecipitation by using Staphylococcus protein A conjugated to Sepharose beads. The results indicate that linker polypeptide L1 of the phycobilisome, the gamma subunit of coupling factor CF1, and subunit II of PS I are synthesized in the cytoplasm as precursor molecules that are 5-8 kDa larger than their mature sizes. Antibodies directed against the psbA gene product (the D1 protein) precipitated a polypeptide found in the translation products of the cyanellar RNA-directed reactions, which is about 1.5 kDa larger than the mature protein.
通过亚细胞分级分离和寡聚 -dT 层析相结合的方法,将来自蓝氏贾第鞭毛虫(Cyanophora paradoxa)的 RNA 分离为细胞质和蓝藻细胞器组分。在含有[35S]甲硫氨酸的兔网织红细胞裂解物系统中,对分离出的细胞质和蓝藻细胞器 RNA 进行体外翻译,结果导致放射性标记掺入到电泳上不同的多肽组中。使用与蓝藻细胞器多肽反应的单特异性和多特异性抗体,通过使用与琼脂糖珠偶联的葡萄球菌蛋白 A 进行间接免疫沉淀,来探测体外翻译产物。结果表明,藻胆体的连接多肽 L1、偶联因子 CF1 的γ亚基和光系统 I 的亚基 II 在细胞质中作为前体分子合成,其比成熟大小大 5 - 8 kDa。针对 psbA 基因产物(D1 蛋白)的抗体沉淀了在蓝藻细胞器 RNA 指导反应的翻译产物中发现的一种多肽,该多肽比成熟蛋白大约大 1.5 kDa。