Directed evolution for enzyme development in biocatalysis

Curr Opin Chem Biol. 2021 Apr:61:107-113. doi: 10.1016/j.cbpa.2020.11.006. Epub 2020 Dec 29.

Abstract

As an important sector of the chemical industry, biocatalysis requires the continuous development of enzymes with tailor-made activity, selectivity, stability, or tolerance to unnatural environments. This is now routinely achieved by directed evolution based on iterative cycles of genetic diversification and activity screening. Here, we highlight its recent developments. First, the design of "smarter" libraries by focused mutagenesis may be a crucial start-up for a fast and successful outcome. Then library assembly and expression are also key steps that benefits from modern molecular biology progresses. Finally, various strategies may be considered for library screening depending on the final objective: while low-throughput direct assays have been very successful in generating enzymes for important biocatalytic processes, even in bringing completely new chemistries to the enzyme world, ultrahigh-throughput screening methods are emerging as powerful approaches for engineering the next generation of industrial enzymes.

Keywords: Cell display; Enzyme assay; Library; Microdroplet; Microfluidics; Mutagenesis; Screening.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biocatalysis*
  • Directed Molecular Evolution*
  • High-Throughput Screening Assays
  • Protein Engineering