Enabling Regiospecific Di-halogenation in One-Pot Reactions Using an Engineered Single-Component Flavin-Dependent Tryptophan Halogenase

This is the authors' abstract. We don't add key points for this paper.

The installation of halogen atoms into organic compounds through flavin-dependent halogenase (FDH)-catalyzed reactions has emerged as an attractive strategy in organic biochemistry and synthetic biology. A cyanobacterial FDH termed AetF that contains FDH and flavin reductase in the same polypeptide chain could become a useful tool enzyme as the need for including a reductase is omitted. Notably, AetF exploits a specific substrate-interaction network to consecutively brominate tryptophan (Trp) at C5 and then C7 to generate dibrominated Trp. In this study, structure-based engineering is used to eliminate the C7-halogenation capacity of AetF. The resulting variant, AetF-AIF, which contains three residue substitutions, mainly catalyzes bromination or iodination at C5 of Trp. We also show that combining AetF-AIF in tandem with wild-type AetF enables the generation of heterogeneously halogenated Trp in a one-pot reaction. The final products, 5-Br-7-I-Trp or 5-I-7-Br-Trp, depending on the order of halide addition, account for a high ratio in the reaction mixture without an additional purification step. These results demonstrate the potential of single-component Trp-FDHs for a wide range of halogenation reactions.