溶解
大肠杆菌
无细胞蛋白质合成
无氧运动
生物化学
绿色荧光蛋白
化学
突变体
无氧呼吸
蛋白质生物合成
产量(工程)
细胞
细菌
生物
基因
遗传学
冶金
材料科学
生理学
作者
By Denis Tamiev,Jared L. Dopp,Nigel F. Reuel
标识
DOI:10.1021/acssynbio.0c00501
摘要
Cell-free protein expression (CFPS) from E. coli cell lysate is an established chemical biology technique. Common efforts to improve synthesis capacity, such as strain engineering and process improvements, have overlooked the opportunity to increase productivity by reducing the dependence on limited, dissolved oxygen. Here we demonstrate conditioning E. coli cells for anaerobic respiration which increases the initial protein expression rate up to 4-fold and increases titer by 50% as compared to traditional aerobic cell lysate when using sfGFP as a reporter protein in CFPS reactions run at atmospheric conditions. This enhancement is even more significant when run in an oxygen-depleted environment, where anaerobic respiration preconditioned cells increase yield when supplemented with nitrite as a terminal electron acceptor (TEA). Furthermore, we test knockout mutants to determine key proteins responsible for enhancing the anaerobically prepared CFPS lysate. Further improvements could be made in preconditioning cells by increasing expression levels of critical pathway enzymes or by screening other TEA.
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