Carly Masonheimer, Michael Rourke, Reece S. Gardner, Ryan Hall, Lydia J. Perkins, Thomas C. Brunold, Andrew R. Buller
Introduction of unnatural cofactors in biocatalysis may open the door to new reactive enzymatic intermediates, and in turn, new biochemical reactions. Here, we employed a de novo biosynthesized, non-natural cofactor, cobalt protoporphyrin IX (CoPPIX), to generate a mononuclear cobalt hydride in the active site of CYP119, a model P450 enzyme. We show that this cobalt hydride intermediate engages in metal-hydrogen atom transfer (MHAT) reactivity, a well-studied and highly utilized reactivity pattern in synthetic chemistry, but which is not known to operate in Nature. We paired convenient in vivo CoPPIX biosynthesis with a colorimetric screen to enable rapid directed evolution. Thus, we engineered CYP119 for MHAT-mediated deallylation of nitrophenols, with the goal of generating not one prolific catalysis, but a diverse set of MHAT-compatible enzymes. Because many silanes hydrolyze quickly, we additionally sought enzymes that accelerate metal-hydride formation from a more persistent silane. This evolution yielded 80 diverse active site recombinants that catalyze MHAT. Serendipitously, we found many variants reduced the aromatic ring of the colorimetric probe, a reaction not previously known. Detailed mechanistic analysis established this is a radical, MHAT-mediated reductive dearomatization that occurs efficiently under aerobic conditions, albeit on a limited suite of nitrophenyl ethers. These results lay a framework for further engineering and study of biocatalytic MHAT and the unique role of metal substitution to tune reactivity.