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Published April 2014 | Accepted Version
Journal Article Open

Expanding P450 catalytic reaction space through evolution and engineering

Abstract

Advances in protein and metabolic engineering have led to wider use of enzymes to synthesize important molecules. However, many desirable transformations are not catalyzed by any known enzyme, driving interest in understanding how new enzymes can be created. The cytochrome P450 enzyme family, whose members participate in xenobiotic metabolism and natural products biosynthesis, catalyzes an impressive range of difficult chemical reactions that continues to grow as new enzymes are characterized. Recent work has revealed that P450-derived enzymes can also catalyze useful reactions previously accessible only to synthetic chemistry. The evolution and engineering of these enzymes provides an excellent case study for how to genetically encode new chemistry and expand biology's reaction space.

Additional Information

© 2014 Elsevier Ltd. The authors acknowledge the support of the Jacobs Institute of Molecular Medicine at Caltech and the Office of Naval Research (grant N00014-11-1-0205). JAM is supported by an NIH Ruth L. Kirschstein National Research Service Award (F32GM101792) and CCF is supported by an NSF Graduate Research Fellowship. The content is solely the responsibility of the authors and does not represent the official views of any of the funding agencies. We thank Devin Trudeau, Jackson Cahn, Jane Wang, Ryan Lauchli, Sabine Brinkmann-Chen, Sheel Dodani, Tillman Heinisch, Todd Hyster, and Martin Enqvist for helpful comments on several versions of this review. The authors are aware of no conflicts of interest regarding the preparation and submission of this manuscript.

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August 20, 2023
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October 26, 2023