Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution

Angew Chem Int Ed Engl. 2015 Mar 9;54(11):3351-67. doi: 10.1002/anie.201409470. Epub 2015 Feb 3.

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.

Keywords: biocatalysis; enzymes; non-natural activity; promiscuity; protein engineering.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Enzymes / metabolism*
  • Genetic Techniques*
  • Protein Engineering / methods*

Substances

  • Enzymes