首页> 外文OA文献 >Psb28 Protein Is Involved in the Biogenesis of the Photosystem II Inner Antenna CP47 (PsbB) in the Cyanobacterium Synechocystis sp. PCC 68031[W][OA]
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Psb28 Protein Is Involved in the Biogenesis of the Photosystem II Inner Antenna CP47 (PsbB) in the Cyanobacterium Synechocystis sp. PCC 68031[W][OA]

机译:Psb28蛋白参与蓝藻蓝藻中光系统II内部天线CP47(PsbB)的生物发生。 PCC 68031 [W] [OA]

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摘要

The role of the Psb28 protein in the structure and function of the photosystem II (PSII) complex has been studied in the cyanobacterium Synechocystis sp. PCC 6803. The protein was localized in the membrane fraction and, whereas most of the protein was detected as an unassembled protein, a small portion was found in the PSII core complex lacking the CP43 antenna (RC47). The association of Psb28 with RC47 was further confirmed by preferential isolation of RC47 from the strain containing a histidine-tagged derivative of Psb28 using nickel-affinity chromatography. However, the affinity-purified fraction also contained a small amount of the unassembled PSII inner antenna CP47 bound to Psb28-histidine, indicating a structural relationship between Psb28 and CP47. A psb28 deletion mutant exhibited slower autotrophic growth than wild type, although the absence of Psb28 did not affect the functional properties of PSII. The mutant showed accelerated turnover of the D1 protein, faster PSII repair, and a decrease in the cellular content of PSI. Radioactive labeling revealed a limitation in the synthesis of both CP47 and the PSI subunits PsaA/PsaB in the absence of Psb28. The mutant cells contained a high level of magnesium protoporphyrin IX methylester, a decreased level of protochlorophyllide, and released large quantities of protoporphyrin IX into the medium, indicating inhibition of chlorophyll (Chl) biosynthesis at the cyclization step yielding the isocyclic ring E. Overall, our results show the importance of Psb28 for synthesis of Chls and/or apoproteins of Chl-binding proteins CP47 and PsaA/PsaB.
机译:Psb28蛋白在光系统II(PSII)复合体的结构和功能中的作用已在蓝藻Synechocystis sp。中进行了研究。 PCC6803。该蛋白质位于膜级分中,而大多数蛋白质被检测为未组装的蛋白质,而在缺少CP43天线(RC47)的PSII核心复合物中发现了一小部分。通过使用镍亲和色谱法从含有Psb28组氨酸标签衍生物的菌株中优先分离RC47,进一步证实了Psb28与RC47的缔合。但是,亲和纯化级分还包含少量未结合到Psb28-组氨酸的PSII内部天线CP47,表明Psb28和CP47之间存在结构关系。 psb28缺失突变体表现出比野生型慢的自养生长,尽管缺少Psb28并不影响PSII的功能特性。该突变体显示出D1蛋白的更新加速,PSII修复更快,PSI的细胞含量减少。放射性标记显示在不存在Psb28的情况下,CP47和PSI亚基PsaA / PsaB的合成均受到限制。突变细胞含有高水平的原卟啉IX甲酯,降低的原叶绿素内酯水平,并向培养基中释放了大量的原卟啉IX,表明在环化步骤中叶绿素(Chl)的生物合成受到抑制,从而产生了等环E。我们的结果表明,Psb28对于合成Chl和/或Chl结合蛋白CP47和PsaA / PsaB的载脂蛋白的重要性。

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