TY - JOUR
T1 - Selective Electroenzymatic Oxyfunctionalization by Alkane Monooxygenase in a Biofuel Cell
AU - Yuan, Mengwei
AU - Abdellaoui, Sofiene
AU - Chen, Hui
AU - Kummer, Matthew J.
AU - Malapit, Christian A.
AU - You, Chun
AU - Minteer, Shelley D.
N1 - Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/6/2
Y1 - 2020/6/2
N2 - Aliphatic synthetic intermediates with high added value are generally produced from alkane sources (e.g., petroleum) by inert carbon–hydrogen (C−H) bond activation using classical chemical methods (i.e. high temperature, rare metals). As an alternative approach for these reactions, alkane monooxygenase from Pseudomonas putida (alkB) is able to catalyze the difficult terminal oxyfunctionalization of alkanes selectively and under mild conditions. Herein, we report an electrosynthetic system using an alkB biocathode which produces alcohols, epoxides, and sulfoxides through bioelectrochemical hydroxylation, epoxidation, sulfoxidation, and demethylation. The capacity of the alkB binding pocket to protect internal functional groups is also demonstrated. By coupling our alkB biocathode with a hydrogenase bioanode and using H2 as a clean fuel source, we have developed and characterized a series of enzymatic fuel cells capable of oxyfunctionalization while simultaneously producing electricity.
AB - Aliphatic synthetic intermediates with high added value are generally produced from alkane sources (e.g., petroleum) by inert carbon–hydrogen (C−H) bond activation using classical chemical methods (i.e. high temperature, rare metals). As an alternative approach for these reactions, alkane monooxygenase from Pseudomonas putida (alkB) is able to catalyze the difficult terminal oxyfunctionalization of alkanes selectively and under mild conditions. Herein, we report an electrosynthetic system using an alkB biocathode which produces alcohols, epoxides, and sulfoxides through bioelectrochemical hydroxylation, epoxidation, sulfoxidation, and demethylation. The capacity of the alkB binding pocket to protect internal functional groups is also demonstrated. By coupling our alkB biocathode with a hydrogenase bioanode and using H2 as a clean fuel source, we have developed and characterized a series of enzymatic fuel cells capable of oxyfunctionalization while simultaneously producing electricity.
KW - alkane monooxygenase
KW - biofuel cells
KW - C−H activation
KW - electroenzymatic catalysis
KW - oxyfunctionalization
UR - https://www.scopus.com/pages/publications/85083211525
U2 - 10.1002/anie.202003032
DO - 10.1002/anie.202003032
M3 - Article
C2 - 32198829
AN - SCOPUS:85083211525
SN - 1433-7851
VL - 59
SP - 8969
EP - 8973
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 23
ER -