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蛋白质靶向次生质体。

Protein targeting into secondary plastids.

作者信息

Bolte Kathrin, Bullmann Lars, Hempel Franziska, Bozarth Andrew, Zauner Stefan, Maier Uwe-G

机构信息

Laboratory for Cell Biology, Philipps-University of Marburg, Karl-von-Frisch Strasse 8, D-35032 Marburg, Germany.

出版信息

J Eukaryot Microbiol. 2009 Jan-Feb;56(1):9-15. doi: 10.1111/j.1550-7408.2008.00370.x.

Abstract

Most of the coding capacity of primary plastids is reserved for expressing some central components of the photosynthesis machinery and the translation apparatus. Thus, for the bulk of biochemical and cell biological reactions performed within the primary plastids, many nucleus-encoded components have to be transported posttranslationally into the organelle. The same is true for plastids surrounded by more than two membranes, where additional cellular compartments have to be supplied with nucleus-encoded proteins, leading to a corresponding increase in complexity of topogenic signals, transport and sorting machineries. In this review, we summarize recent progress in elucidating protein transport across up to five plastid membranes in plastids evolved in secondary endosymbiosis. Current data indicate that the mechanisms for protein transport across multiple membranes have evolved by altering pre-existing ones to new requirements in secondary plastids.

摘要

初级质体的大部分编码能力用于表达光合作用机制和翻译装置的一些核心组件。因此,对于在初级质体内进行的大部分生化和细胞生物学反应,许多核编码组件必须在翻译后转运到该细胞器中。对于被两层以上膜包围的质体也是如此,在这些质体中,额外的细胞区室必须被供应核编码蛋白质,这导致了拓扑信号、转运和分选机制的复杂性相应增加。在这篇综述中,我们总结了在阐明次生内共生进化而来的质体中跨多达五层质体膜的蛋白质转运方面的最新进展。目前的数据表明,跨多膜的蛋白质转运机制是通过将已有的机制改变以适应次生质体中的新需求而进化的。

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