Abstract
Cytochrome P450 BM3 natively exhibits substrate promiscuity, mainly in hydroxylation and epoxidation reactions. Whereas directed evolution has broadened its scope of reactivity, screening for specific non-native enzymatic reactivity remains challenging, thereby limiting potential applications. In this study, we investigated the predictive potential of indigo production as an indicator of promiscuous hydroxylation in non-native aromatic compounds. Following site- saturation mutagenesis on 42 residues in the active-site region, we rapidly identified 97 previously unreported variants at 18 unique positions, significantly increasing the database of indigo-positive variants. From this expanded pool, we isolated 80 well-expressed indigo-positive variants and evaluated them alongside 46 well-expressed indigo-negative variants for their hydroxylation activity on the representative non-native aromatic compounds, anisole and naphthalene. We observed a strong correlation between indigo formation and aromatic compound hydroxylation, with 73-80% of indigo-positive variants hydroxylating these compounds, compared to 40-45% of indigo-negative variants. Notably, only indigo-positive variants showed greater than 3-fold higher activity than the wild-type P450 BM3. Furthermore, a positive correlation was obtained between promiscuous hydroxylation of anisole and naphthalene. The approach also allowed identification of new variants that hydroxylate a further aromatic compound, 4-phenyl-2-butanone, suggesting generality. Although we did not succeed in identifying the molecular basis underlying the indigo- positive phenotype, our findings demonstrate that indigo production is an effective screening tool, expediting the discovery of novel functional genes for promiscuous aromatic hydroxylation reactions. This method offers a cost-effective and efficient approach to identify and develop new biocatalysts, advancing the potential applications of P450 BM3 in scientific and industrial fields.
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