苯胺
漆酶
氧化还原
生物催化
基质(水族馆)
化学
组合化学
聚苯胺
蛋白质工程
电子转移
酶动力学
催化作用
纳米技术
材料科学
反应机理
活动站点
有机化学
酶
聚合物
地质学
海洋学
聚合
作者
Gerard Santiago,Felipe de Salas,Maria Fátima Lucas,Emanuele Monza,Sandra Acebes,Ángel T. Martı́nez,Susana Camarero,Vı́ctor Guallar
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2016-07-08
卷期号:6 (8): 5415-5423
被引量:61
标识
DOI:10.1021/acscatal.6b01460
摘要
Oxidation of arylamines, such as aniline, is of high industrial interest, and laccases have been proposed as biocatalysts to replace harsh chemical oxidants. However, the reaction is hampered by the redox potential of the substrate at acid pH, and enzyme engineering is required to improve the oxidation. In this work, instead of trying to improve the redox potential of the enzyme, we aim toward the (transient) substrate's potential and propose this as a more reliable strategy. We have successfully combined a computational approach with experimental validation to rationally design an improved biocatalyst. The in silico protocol combines classical and quantum mechanics to deliver atomic and electronic level detail on the two main processes involved: substrate binding and electron transfer. After mutant expression and comparison to the parent type, kinetic results show that the protocol accurately predicts aniline's improved oxidation (2-fold kcat increase) in the engineered variant for biocatalyzed polyaniline production.
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