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Biocatalytic Photosynthesis with Water as an Electron Donor

机译:以水为电子给体的生物催化光合作用

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摘要

Efficient harvesting of unlimited solar energy and its conversion into valuable chemicals is one of the ultimate goals of scientists. With the ever-increasing concerns about sustainable growth and environmental issues, numerous efforts have been made to develop artificial photosynthetic process for the production of fuels and fine chemicals, thus mimicking natural photosynthesis. Despite the research progress made over the decades, the technology is still in its infancy because of the difficulties in kinetic coupling of whole photocatalytic cycles. Herein, we report a new type of artificial photosynthesis system that can avoid such problems by integrally coupling biocatalytic redox reactions with photocatalytic water splitting. We found that photocatalytic water splitting can be efficiently coupled with biocatalytic redox reactions by using tetracobalt polyoxometalate and Rh-based organometallic compound as hole and electron scavengers, respectively, for photoexcited [Ru(bpy)_3]~(2+). Based on these results, we could successfully photosynthesize a model chiral compound (l-glutamate) using a model redox enzyme (glutamate dehydrogenase) upon in situ photoregeneration of cofactors.
机译:有效收集无限的太阳能并将其转化为有价值的化学物质是科学家的最终目标之一。随着对可持续增长和环境问题的日益关注,已经做出了许多努力来开发用于生产燃料和精细化学品的人造光合作用工艺,从而模仿了自然光合作用。尽管数十年来取得了研究进展,但由于整个光催化循环的动力学耦合困难,该技术仍处于起步阶段。在此,我们报告了一种新型的人工光合作用系统,该系统可以通过将生物催化氧化还原反应与光催化水分解整体结合来避免此类问题。我们发现,光催化[Ru(bpy)_3]〜(2+)分别使用四钴多金属氧酸盐和Rh基有机金属化合物作为空穴清除剂和电子清除剂,可以将光催化水分解与生物催化氧化还原反应有效结合。基于这些结果,我们可以在辅助因子的原位光再生后,使用模型氧化还原酶(谷氨酸脱氢酶)成功地光合作用模型手性化合物(1-谷氨酸)。

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