Institute of Biotechnology, RWTH Aachen University, Worringer Weg 3, 52074, Aachen, Germany.
DWI Leibniz-Institute for Interactive Materials, Forckenbeckstrasse 50, 52074, Aachen, Germany.
Angew Chem Int Ed Engl. 2019 Mar 26;58(14):4562-4565. doi: 10.1002/anie.201814069. Epub 2019 Mar 6.
Escherichia coli's copper efflux oxidase (CueO) has rarely been employed in the cathodic compartment of enzymatic biofuel cells (EBFCs) due to its low redox potential (0.36 V vs. Ag/AgCl, pH 5.5) towards O reduction. Herein, directed evolution of CueO towards a more positive onset potential was performed in an electrochemical screening system. An improved CueO variant (D439T/L502K) was obtained with a significantly increased onset potential (0.54 V), comparable to that of high-redox-potential fungal laccases. Upon coupling with an anodic compartment, the EBFC exhibited an open-circuit voltage (V ) of 0.56 V. Directed enzyme evolution by tailoring enzymes to application conditions in EBFCs has been validated and might, in combination with molecular understanding, enable future breakthroughs in EBFC performance.
大肠杆菌的铜外排氧化酶(CueO)由于其对 O 还原的低氧化还原电位(0.36 V 与 Ag/AgCl,pH 5.5),很少在酶生物燃料电池(EBFC)的阴极室中使用。在此,通过电化学筛选系统对 CueO 进行了定向进化,以获得更正向的起始电位。得到了一个改进的 CueO 变体(D439T/L502K),其起始电位显著增加(0.54 V),与高氧化还原电位真菌漆酶相当。与阳极室耦合后,EBFC 的开路电压(V )为 0.56 V。通过将酶调整为 EBFC 中的应用条件进行定向酶进化已经得到验证,并且可能与分子理解相结合,为 EBFC 性能的未来突破提供可能。