Robinson C, Klösgen R B, Herrmann R G, Shackleton J B
Department of Biological Sciences, University of Warwick, Coventry, UK.
FEBS Lett. 1993 Jun 28;325(1-2):67-9. doi: 10.1016/0014-5793(93)81415-v.
In vitro reconstitution assays have been used in recent years to probe the mechanisms by which a variety of cytosolically synthesised proteins are transported across the thylakoid membrane within higher plant chloroplasts. The emerging data suggest that two distinct mechanisms operate. Translocation of a subset of lumenal proteins, namely the 23 kDa and 16 kDa proteins of the oxygen-evolving complex, and of the CFo2 protein (an integral membrane protein), requires only the presence of the thylakoidal delta pH. In contrast, two other lumenal proteins, the 33 kDa oxygen-evolving complex protein and plastocyanin, require also the presence of ATP and at least one stromal factor for efficient transport into isolated thylakoids to take place.
近年来,体外重组分析已被用于探究多种在细胞质中合成的蛋白质跨高等植物叶绿体类囊体膜运输的机制。新出现的数据表明存在两种不同的机制。一类腔蛋白的转运,即放氧复合体的23 kDa和16 kDa蛋白以及CFo2蛋白(一种整合膜蛋白),仅需要类囊体膜质子动力势差(ΔpH)的存在。相比之下,另外两种腔蛋白,即33 kDa放氧复合体蛋白和质体蓝素,还需要ATP的存在以及至少一种基质因子,才能有效地转运到分离的类囊体中。