Grossman A R, Bartlett S G, Schmidt G W, Mullet J E, Chua N H
J Biol Chem. 1982 Feb 10;257(3):1558-63.
Many polypeptides translated in the cytosol enter the chloroplast where they assemble into macromolecular complexes. The transport of these polypeptides into the plastid can be examined in vitro by mixing isolated chloroplasts with pea poly(A) RNA translation products. Following optimization of both translation in the wheat germ system and the conditions during in vitro uptake, we observe the post-translational transport of over 100 polypeptides; many remain in the soluble phase of the organelle while others integrate into the thylakoid membranes. Most products transported in vitro co-migrate with in vivo products on sodium dodecyl sulfate-polyacrylamide gels. Furthermore, with the improved conditions, we demonstrate the transport of plastocyanin, ferredoxin-NADP+ oxidoreductase, and fructose-1,6-bisphosphatase into isolated plastids. While we have not been able to detect any cell-free translation product that is immunologically related to fructose-1,6-bisphosphatase, both plastocyanin and ferredoxin-NADP+ oxidoreductase are synthesized as precursors in vitro. These precursors are imported into the organelle where they are processed to the size of their mature counterparts. As determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the molecular weight of the precursor to plastocyanin is 15,000 larger than the mature product and the precursor to ferredoxin-NADP+ oxidoreductase is 8,000 larger than the mature product.
许多在细胞质中翻译的多肽进入叶绿体,在那里它们组装成大分子复合物。这些多肽向质体的转运可以通过将分离的叶绿体与豌豆多聚腺苷酸(poly(A))RNA翻译产物混合在体外进行检测。在优化了小麦胚系统中的翻译以及体外摄取过程中的条件后,我们观察到100多种多肽的翻译后转运;许多多肽留在细胞器的可溶性相中,而其他多肽则整合到类囊体膜中。在十二烷基硫酸钠-聚丙烯酰胺凝胶上,大多数体外转运的产物与体内产物共迁移。此外,在改进的条件下,我们证明了质体蓝素、铁氧还蛋白-NADP⁺氧化还原酶和果糖-1,6-二磷酸酶向分离的质体的转运。虽然我们未能检测到任何与果糖-1,6-二磷酸酶免疫相关的无细胞翻译产物,但质体蓝素和铁氧还蛋白-NADP⁺氧化还原酶在体外均以前体形式合成。这些前体被导入细胞器,在那里它们被加工成与成熟对应物大小相同的产物。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定,质体蓝素前体的分子量比成熟产物大15000,铁氧还蛋白-NADP⁺氧化还原酶前体的分子量比成熟产物大8000。