CaltechAUTHORS
  A Caltech Library Service

Improved Cyclopropanation Activity of Histidine-Ligated Cytochrome P450 Enables the Enantioselective Formal Synthesis of Levomilnacipran

Wang, Jane Z. and Renata, Hans and Peck, Nicole E. and Farwell, Christopher C. and Coelho, Pedro S. and Arnold, Frances H. (2014) Improved Cyclopropanation Activity of Histidine-Ligated Cytochrome P450 Enables the Enantioselective Formal Synthesis of Levomilnacipran. Angewandte Chemie International Edition, 53 (26). pp. 6810-6813. ISSN 1433-7851. PMCID PMC4120663. http://resolver.caltech.edu/CaltechAUTHORS:20140512-091600678

[img] PDF - Accepted Version
See Usage Policy.

1105Kb

Use this Persistent URL to link to this item: http://resolver.caltech.edu/CaltechAUTHORS:20140512-091600678

Abstract

Engineering enzymes capable of modes of activation unprecedented in nature will increase the range of industrially important molecules that can be synthesized through biocatalysis. However, low activity for a new function is often a limitation in adopting enzymes for preparative-scale synthesis, reaction with demanding substrates, or when a natural substrate is also present. By mutating the proximal ligand and other key active-site residues of the cytochrome P450 enzyme from Bacillus megaterium (P450-BM3), a highly active His-ligated variant of P450-BM3 that can be employed for the enantioselective synthesis of the levomilnacipran core was engineered. This enzyme, BM3-Hstar, catalyzes the cyclopropanation of N,N-diethyl-2-phenylacrylamide with an estimated initial rate of over 1000 turnovers per minute and can be used under aerobic conditions. Cyclopropanation activity is highly dependent on the electronic properties of the P450 proximal ligand, which can be used to tune this non-natural enzyme activity.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://onlinelibrary.wiley.com/doi/10.1002/anie.201402809/abstractPublisherArticle
http://dx.doi.org/10.1002/anie.201402809DOIArticle
http://onlinelibrary.wiley.com/doi/10.1002/anie.201402809/suppinfoPublisherSupporting Information
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120663PubMed CentralArticle
ORCID:
AuthorORCID
Arnold, Frances H.0000-0002-4027-364X
Additional Information:© 2014 Wiley-VCH Verlag GmbH & Co. Article first published online: 6 May 2014. Manuscript Received: 26 Feb 2014. We thank Dr. S. Virgil and the Center for Catalysis and Chemical Synthesis (3CS) at Caltech for assistance with HPLC, Dr. J. McIntosh and Dr. T. Heel for helpful discussions, and R. Kitto for help during preparative-scale reactions. This work was supported by the Gordon and Betty Moore Foundation through Grant GBMF2809 to the Caltech Programmable Molecular Technology Initiative. Z.J.W. was supported by a Ruth L. Kirschstein Fellowship from the National Institutes of Health, award number F32EB015846-01.
Funders:
Funding AgencyGrant Number
Gordon and Betty Moore FoundationGBMF2809
NIH Predoctoral FellowshipF32EB015846-01
Subject Keywords:biocatalysis; cyclopropanation; cytochrome P450; enzymes; protein engineering
PubMed Central ID:PMC4120663
Record Number:CaltechAUTHORS:20140512-091600678
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:20140512-091600678
Official Citation:Wang, Z. J., Renata, H., Peck, N. E., Farwell, C. C., Coelho, P. S. and Arnold, F. H. (2014), Improved Cyclopropanation Activity of Histidine-Ligated Cytochrome P450 Enables the Enantioselective Formal Synthesis of Levomilnacipran. Angew. Chem. Int. Ed., 53: 6810–6813. doi: 10.1002/anie.201402809
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:45663
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:12 May 2014 17:54
Last Modified:21 Jul 2017 14:59

Repository Staff Only: item control page