化学
生物催化
酶
催化作用
链霉菌
生物化学
代谢途径
卡宾
组合化学
代谢中间体
细胞质
异源的
立体化学
合成生物学
代谢工程
酵母
催化循环
定向进化
大肠杆菌
基因工程
异源表达
酶催化
生物转化
聚酮
反应中间体
生物合成
电子转移
氧化还原
作者
Sukriyo Chakraborty,Soonkyu Hwang,Jing Huang,Dongping Chen,Y Chen,Christopher J. Petzold,Douglas S. Clark,Aindrila Mukhopadhyay,Jay D. Keasling,John F. Hartwig
摘要
Artificial metalloenzymes (ArMs) expand the suite of synthetically valuable, new-to-nature biocatalytic reactions. Integrating these enzymes into biosynthetic pathways enables reactions not found in nature to occur in living cells with the intermediates or products of the metabolic pathways. However, the integration of reactions catalyzed by ArMs into complex metabolic pathways is constrained by the lack of methods to assemble these ArMs in organisms that are commonly used for metabolic engineering. We report the assembly of an iridium-containing artificial metalloenzyme (Ir-ArM) in Streptomyces albus, a Gram-positive bacterial chassis widely used for the heterologous expression of natural products. In this engineered organism, the Ir-ArM assembles in the cytoplasm and catalyzes abiological carbene transfer to the unactivated, disubstituted double bond of an exogenously added terpene with turnover numbers (TONs) that are two times higher than those for the same reaction catalyzed within E. coli cells harboring Ir-ArM and 20 times higher than the TONs for the same reaction catalyzed by the purified holoprotein itself.
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