Jacquot Jean-Pierre, Lancelin Jean-Marc, Meyer Yves
Institut de Biotechnologie des Plantes, URA 1128 CNRS, Université de Paris-Sud, Bâilment 630, 91405 Orsay Cedex, France.
Laboratoire de RMN Biomoléculaire, ESA 5078 CNRS, Université de Lyon 1 et CPE-Lyon, Bâilment 308, 69622 Villeurbanne Cedex France.
New Phytol. 1997 Aug;136(4):543-570. doi: 10.1046/j.1469-8137.1997.00784.x.
Thioredoxins are ubiquitous small-molecular-weight proteins (typically 100-120 amino-acid residues) containing an extremely reactive disulphide bridge with a highly conserved sequence -Cys-Gly(Ala/Pro)-Pro-Cys-. In bacteria and animal cells, thioredoxins participate in multiple reactions which require reduction of disulphide bonds on selected target proteins/ enzymes. There is now ample biochemical evidence that thioredoxins exert very specific functions in plants, the best documented being the redox regulation of chloroplast enzymes. Another area in which thioredoxins are believed to play a prominent role is in reserve protein mobilization during the process of germination. It has been discovered that thioredoxins constitute a large multigene family in plants with different-subcellular localizations, a unique feature in living cells so far. Evolutionary studies based on these molecules will be discussed, as well as the available biochemical and genetic evidence related to their functions in plant cells. Eukaryotic photosynthetic plant cells are also unique in that they possess two different reducing systems, one extrachloroplastic dependent on NADPH as an electron donor, and the other one chloroplastic, dependent on photoreduced ferredoxin. This review will examine in detail the latest progresses in the area of thioredoxin structural biology in plants, this protein being an excellent model for this purpose. The structural features of the reducing enzymes ferredoxin thioredoxin reductase and NADPH thioredoxin reductase will also be described. The properties of the target enzymes known so far in plants will be detailed with special emphasis on the structural features which make them redox regulatory. Based on sequence analysis, evidence will be presented that redox regulation of enzymes of the biosynthetic pathways first appeared in cyanobacteria possibly as a way to cope with the oxidants produced by oxygenic photosynthesis. It became more elaborate in the chloroplasts of higher plants where a co-ordinated functioning of the chloroplastic and extra chloroplastic metabolisms is required. CONTENTS Summary 543 I. Introduction 544 II. Thioredoxins from photosynthetic organisms as a structural model 545 III. Physiological functions 552 IV. The thioredoxin reduction systems 556 V. Structural aspects of target enzymes 558 VI. Concluding remarks 563 Acknowledgements 564 References 564.
硫氧还蛋白是普遍存在的小分子蛋白质(通常含有100 - 120个氨基酸残基),其含有一个具有高度保守序列-Cys-Gly(Ala/Pro)-Pro-Cys-的极具反应性的二硫键。在细菌和动物细胞中,硫氧还蛋白参与多种需要还原特定靶蛋白/酶上二硫键的反应。现在有充分的生化证据表明硫氧还蛋白在植物中发挥着非常特定的功能,其中记载最详尽的是对叶绿体酶的氧化还原调节。硫氧还蛋白被认为发挥重要作用的另一个领域是在种子萌发过程中储备蛋白的动员。现已发现硫氧还蛋白在植物中构成一个具有不同亚细胞定位的多基因大家族,这是迄今为止活细胞中的一个独特特征。将讨论基于这些分子的进化研究,以及与其在植物细胞中的功能相关的现有生化和遗传证据。真核光合植物细胞的独特之处还在于它们拥有两个不同的还原系统,一个是依赖NADPH作为电子供体的叶绿体外部系统,另一个是依赖光还原铁氧还蛋白的叶绿体系统。本综述将详细探讨植物硫氧还蛋白结构生物学领域的最新进展,该蛋白为此提供了一个绝佳模型。还将描述还原酶铁氧还蛋白硫氧还蛋白还原酶和NADPH硫氧还蛋白还原酶的结构特征。将详细阐述目前已知的植物靶酶的特性,特别强调使其具有氧化还原调节作用的结构特征。基于序列分析,将提供证据表明生物合成途径中酶的氧化还原调节最早可能出现在蓝细菌中,作为应对光合放氧产生的氧化剂的一种方式。在高等植物的叶绿体中,这种调节变得更加精细,因为需要叶绿体和叶绿体外部代谢的协调运作。目录摘要543一、引言544二、光合生物中的硫氧还蛋白作为结构模型545三、生理功能552四、硫氧还蛋白还原系统556五、靶酶的结构方面558六、结束语563致谢564参考文献564