Faculty of Natural Sciences, Institute of Plant Genetics, Leibniz Universität Hannover, 30419 Hannover, Germany.
Plant Mol Biol. 2012 Jun;79(3):273-84. doi: 10.1007/s11103-012-9911-4. Epub 2012 Apr 17.
In most studies, amounts of protein complexes of the oxidative phosphorylation (OXPHOS) system in different organs or tissues are quantified on the basis of isolated mitochondrial fractions. However, yield of mitochondrial isolations might differ with respect to tissue type due to varying efficiencies of cell disruption during organelle isolation procedures or due to tissue-specific properties of organelles. Here we report an immunological investigation on the ratio of the OXPHOS complexes in different tissues of Arabidopsis thaliana which is based on total protein fractions isolated from five Arabidopsis organs (leaves, stems, flowers, roots and seeds) and from callus. Antibodies were generated against one surface exposed subunit of each of the five OXPHOS complexes and used for systematic immunoblotting experiments. Amounts of all complexes are highest in flowers (likewise with respect to organ fresh weight or total protein content of the flower fraction). Relative amounts of protein complexes in all other fractions were determined with respect to their amounts in flowers. Our investigation reveals high relative amounts of complex I in green organs (leaves and stems) but much lower amounts in non-green organs (roots, callus tissue). In contrast, complex II only is represented by low relative amounts in green organs but by significantly higher amounts in non-green organs, especially in seeds. In fact, the complex I-complex II ratio differs by factor 37 between callus and leaf, indicating drastic differences in electron entry into the respiratory chain in these two fractions. Variation in amounts concerning complexes III, IV and V was less pronounced in different Arabidopsis tissues (quantification of complex V in leaves was not meaningful due to a cross-reaction of the antibody with the chloroplast form of this enzyme). Analyses were complemented by in gel activity measurements for the protein complexes of the OXPHOS system and comparative 2D blue native/SDS PAGE analyses using isolated mitochondria. We suggest that complex I has an especially important role in the context of photosynthesis which might be due to its indirect involvement in photorespiration and its numerous enzymatic side activities in plants.
在大多数研究中,不同器官或组织的氧化磷酸化(OXPHOS)系统的蛋白质复合物的量是基于分离的线粒体部分进行定量的。然而,由于细胞器分离过程中细胞破坏的效率不同,或者由于细胞器的组织特异性,线粒体分离的产量可能会因组织类型而异。在这里,我们报告了一种基于从五个拟南芥器官(叶、茎、花、根和种子)和愈伤组织分离的总蛋白部分对拟南芥不同组织的 OXPHOS 复合物的比例进行的免疫学研究。针对五个 OXPHOS 复合物中的每个复合物的一个表面暴露亚基产生了抗体,并用于系统的免疫印迹实验。所有复合物的量在花中最高(相对于器官鲜重或花部分的总蛋白含量也是如此)。所有其他部分的蛋白质复合物的相对量相对于它们在花中的量来确定。我们的研究表明,在绿色器官(叶和茎)中复合物 I 的相对量较高,但在非绿色器官(根、愈伤组织)中复合物 I 的相对量较低。相反,复合物 II 仅在绿色器官中以相对较低的量表示,但在非绿色器官中以显著较高的量表示,特别是在种子中。事实上,在愈伤组织和叶之间,复合物 I-复合物 II 的比例差异为 37,表明这两个部分的电子进入呼吸链的差异很大。不同拟南芥组织中复合物 III、IV 和 V 的量变化不明显(由于抗体与该酶的叶绿体形式发生交叉反应,因此叶片中复合物 V 的定量没有意义)。分析结果通过凝胶活性测定和使用分离的线粒体进行的比较 2D 蓝色天然/SDS PAGE 分析得到补充。我们认为,复合物 I 在光合作用的背景下具有特别重要的作用,这可能是由于其间接参与光呼吸以及其在植物中的许多酶的副活性。