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Published January 2015 | public
Journal Article

P450_(BM3)-Axial Mutations: A Gateway to Non-Natural Reactivity

Abstract

Enzymes capable of catalyzing non-natural reactions have the potential to alter the way relevant molecules are prepared on-scale. Efforts to this end have largely focused on combining non-natural cofactors with proteins lacking catalytic function to obtain non-natural reactivity. An alternative approach is to utilize a native cofactor to catalyze non-natural reactions. Recently, our group demonstrated that heme-containing cytochrome P450s are able to catalyze the highly selective cyclopropanation of alkenes. Superior activity was observed upon changing the axial cysteine to serine ("P411"). Mutation at the conserved axial ligand has enabled P450s to catalyze other non-natural reactions such as N—H insertion and C—H amination.

Additional Information

© 2014 Wiley-VCH Verlag GmbH & Co. Received: May 1, 2014. Accepted: May 27, 2014. Article first published online: 20 Aug 2014. We have described the work of many former and current Arnold Lab students and postdoctoral fellows, including Pedro Coelho, Eric Brustad, John McIntosh, Jane Z. Wang, Chris Farwell, Hans Renata, Todd Hyster, and Nicole Peck. The authors also gratefully acknowledge support from the Jacobs Institute for Molecular Engineering for Medicine, at Caltech, and the Department of the Navy, Office of Naval Research (grant N00014-11-1-0205). T. K. H. is supported by a Ruth L. Kirschstein NRSA postdoctoral fellowship (1F32GM108143). The content of this paper is solely the responsibility of the authors and does not represent the official views of the funding agencies. We also thank John McIntosh and Sheel Dodani for helpful comments on this manuscript. Early View (Online Version of Record published before inclusion in an issue).

Additional details

Created:
August 22, 2023
Modified:
October 17, 2023