Serological Investigations of the Function of Galactolipids in the Thylakoid Membrane

A. Radunz, K.P. Bader, G.H. Schmid
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引用次数: 11

Abstract

We investigated the influence of monospecific antisera to monogalactosyl diglyceride and to digalactosyl diglyceride on the photosynthetic electron transport in chloroplasts of higher plants. Both antisera inhibit the photoreduction of dichlorophenolindophenol (DCPiP) with water as the native electron donor as well as the reduction of anthraquinone-2-sulfonate with the electron donor couple DCPiP/ascorbate. The degree of inhibition of the galactolipid antisera in the region of photosystem I depends on the pH and the temperature of the reaction assay. Treatment of the chloroplasts with sodium periodate or with lipase results in a complete loss of any inhibition by the galactolipid antisera. Treatment with β-galactosidase, however, had no influence on the reactions with galactolipid antisera. The sites of inhibition of the galactolipid antisera could be localized on the donor side of photosystem I as well as on the donor side of photosystem II. From this we conclude that the mono- and digalactosyl diglyceride molecules that are localized on the stroma side of the membrane are components of the photosystem I- and also of the photosystem II-protein-lipid-complex. We may conclude that there are obviously interactions between the galactolipid molecules and the photosynthetically active proteins, since the binding of antibodies leads to a partial blocking of electron transport.

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类囊体膜中半乳糖脂功能的血清学研究
研究了单半乳糖二甘油酯和双半乳糖二甘油酯单抗血清对高等植物叶绿体光合电子传递的影响。两种抗血清均能抑制以水为电子给体光还原二氯酚吲哚酚(DCPiP),以及DCPiP/抗坏血酸对电子给体光还原蒽醌-2-磺酸盐。半乳糖脂抗血清在光系统I区的抑制程度取决于反应测定的pH值和温度。用高碘酸钠或脂肪酶处理叶绿体导致半乳糖脂抗血清完全丧失任何抑制作用。然而,用β-半乳糖苷酶治疗对半乳糖脂抗血清的反应没有影响。半乳糖脂抗血清的抑制位点既可定位于光系统I的供体侧,也可定位于光系统II的供体侧。由此我们得出结论,位于膜基质侧的单半乳糖和双半乳糖双甘油酯分子是光系统I-和光系统ii -蛋白质-脂质复合物的组成部分。我们可以得出结论,在半乳脂分子和光合活性蛋白之间存在明显的相互作用,因为抗体的结合导致电子传递的部分阻断。
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Die Zelle als gengesteuertes System Die Zelle als gengesteuertes System Foreword Contents Transport and Metabolism of Labelled Zeatin Applied to the Stems of Phaseolus vulgaris at Different Stages of Development
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