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Encapsulation of Photosystem I in Organic MicroparticlesIncreases Its Photochemical Activity and Stability for Ex Vivo Photocatalysis

机译:光系统I在有机微粒中的封装增加其光化学活性和离体光催化稳定性

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摘要

Photosystem I (PSI) is a pigment binding multisubunit protein complex involved in the light phase of photosynthesis, catalyzing a light-dependent electron transfer reaction from plastocyanin to ferredoxin. PSI is characterized by a photochemical efficiency close to one, suggesting its possible application in light-dependent redox reaction in an extracellular context. The stability of PSI complexes isolated from plant cells is however limited if not embedded in a protective environment. Here we show an innovative solution for exploiting the photochemical properties of PSI, by encapsulation of isolated PSI complexes in PLGA (poly lactic-co-glycolic acid) organic microparticles. These encapsulated PSI complexes were able to catalyze light-dependent redox reactions with electron acceptors and donors outside the PLGA microparticles. Moreover, PSI complexes encapsulated in PLGA microparticles were characterized by a higher photochemical activity and stability compared with PSI complexes in detergent solution, suggesting their possible application for ex vivo photocatalysis.
机译:光系统I(PSI)是一种色素结合型多亚基蛋白复合物,参与光合作用的光相,催化从质体蓝素到铁氧还蛋白的光依赖性电子转移反应。 PSI的特征是光化学效率接近一个,表明其可能在细胞外环境中应用于光依赖性氧化还原反应。但是,如果不包埋在保护性环境中,则从植物细胞中分离出的PSI复合物的稳定性会受到限制。在这里,我们展示了一种通过将孤立的PSI复合物封装在PLGA(聚乳酸-乙醇酸共聚物)有机微粒中来开发PSI的光化学特性的创新解决方案。这些封装的PSI复合物能够催化PLGA微粒外部的电子受体和供体的光依赖性氧化还原反应。此外,与洗涤剂溶液中的PSI配合物相比,封装在PLGA微粒中的PSI配合物具有更高的光化学活性和稳定性,这表明它们可能用于离体光催化。

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