Abstract
The multidomain, catalytically self-sufficient cytochrome P450 BM-3 from Bacillus megaterium (P450(BM3) ) constitutes a versatile enzyme for the oxyfunctionalization of organic molecules and natural products. However, the limited stability of the diflavin reductase domain limits the utility of this enzyme for synthetic applications. In this work, a consensus-guided mutagenesis approach was applied to enhance the thermal stability of the reductase domain of P450(BM3) . Upon phylogenetic analysis of a set of distantly related P450s (>38 % identity), a total of 14 amino acid substitutions were identified and evaluated in terms of their stabilizing effects relative to the wild-type reductase domain. Recombination of the six most stabilizing mutations generated two thermostable variants featuring up to tenfold longer half-lives at 50 °C and increased catalytic performance at elevated temperatures. Further characterization of the engineered P450(BM3) variants indicated that the introduced mutations increased the thermal stability of the FAD-binding domain and that the optimal temperature (T(opt) ) of the enzyme had shifted from 25 to 40 °C. This work demonstrates the effectiveness of consensus mutagenesis for enhancing the stability of the reductase component of a multidomain P450. The stabilized P450(BM3) variants developed here could potentially provide more robust scaffolds for the engineering of oxidation biocatalysts.