大肠杆菌
合成生物学
生物合成
生物化学
化学
酶
辅因子
微生物
代谢工程
生物催化
细菌
新陈代谢
大肠杆菌蛋白质类
细胞代谢
微生物代谢
催化作用
生物
计算生物学
细胞生物学
体内
原位
酶催化
体外
化学合成
组合化学
生物转化
代谢途径
桥接(联网)
辅酶A
糖酵解
作者
Yuan, Yujie,Li, Maolin,Harrison, Wesley,Zhang, Zhengyi,Zhao, Huimin
标识
DOI:10.5061/dryad.ns1rn8q54
摘要
Photoenzymatic catalysis enables new-to-nature transformations, but its scalability is limited by high enzyme loading, costly cofactors, and radical-induced instability. Here we report the integration of light-driven photoenzymatic reactions into the cellular metabolism of Escherichia coli, bridging flavin-based photobiocatalysis with biosynthesis. Using synthetic biology strategies, we engineered microbial cells to continuously produce olefin substrates and ene-reductase photoenzyme while regenerating cofactors directly from glucose. By externally supplying radical precursors or by introducing synthetic pathways for their in situ production, we enabled fermentation-based microbial photobiosynthesis, achieving high titers and demonstrating its feasibility for scale-up in bioreactor. This approach extends photobiocatalysis from in vitro applications to in vivo semi-biosynthesis and complete biosynthesis, revealing its full potential for integrating light-driven reactions into cellular metabolism.
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