Expanding the Enzyme Universe: Accessing Non-Natural Reactions by Mechanism-Guided Directed Evolution
- Creators
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Renata, Hans
- Wang, Z. Jane
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Arnold, Frances H.
Abstract
High selectivity and exquisite control over the outcome of reactions entice chemists to use biocatalysts in organic synthesis. However, many useful reactions are not accessible because they are not in nature's known repertoire. In this Review, we outline an evolutionary approach to engineering enzymes to catalyze reactions not found in nature. We begin with examples of how nature has discovered new catalytic functions and how such evolutionary progression has been recapitulated in the laboratory starting from extant enzymes. We then examine non-native enzyme activities that have been exploited for chemical synthesis, with an emphasis on reactions that do not have natural counterparts. Non-natural activities can be improved by directed evolution, thus mimicking the process used by nature to create new catalysts. Finally, we describe the discovery of non-native catalytic functions that may provide future opportunities for the expansion of the enzyme universe.
Additional Information
© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. Received: September 25, 2014. Article first published online: 3 Feb. 2015. Our research is supported by the Department of the Navy, Office of Naval Research (grant N00014-11-10205), the Jacobs Institute for Molecular Engineering for Medicine at Caltech, the Gordon and Betty Moore Foundation through grant GBMF2809 to the Caltech Programmable Molecular Technology Initiative, and the National Science Foundation, Office of Chemical, Bioengineering, Environmental and Transport Systems SusChEM Initiative (grant CBET-1403077). Z.J.W. was supported by a Ruth L. Kirschstein Fellowship from the National Institutes of Health (F32EB015846). We thank Prof. Dan S. Tawfik, Prof. Bernhard Hauer, Dr. John A. McIntosh, Dr. Andrew R. Buller, Dr. Sheel C. Dodani, and Dr. Christopher K. Prier for helpful suggestions and discussions. The content of this Review is solely the responsibility of the authors and does not represent the official views of the funding agencies.Attached Files
Accepted Version - nihms678535.pdf
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Additional details
- PMCID
- PMC4404643
- Eprint ID
- 54521
- DOI
- 10.1002/anie.201409470
- Resolver ID
- CaltechAUTHORS:20150209-090308645
- Office of Naval Research (ONR)
- N00014-11-10205
- Jacobs Institute for Molecular Engineering for Medicine
- Gordon and Betty Moore Foundation
- GBMF2809
- NSF
- CBET-1403077
- NIH Predoctoral Fellowship
- F32EB015846-01
- Created
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2015-02-09Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field