Literature DB >> 22579412

Directed enzyme evolution: beyond the low-hanging fruit.

Moshe Goldsmith1, Dan S Tawfik.   

Abstract

The field of directed evolution has progressed to the point where it is feasible to engineer enzymes for unnatural substrates and reactions with catalytic efficiencies and regio-specificity or stereo-specificity that rival those of natural enzymes. Here, we describe the conceptual and methodological advances that have enabled this progress. We address methodologies based on small libraries enriched with improved variants and carrying compensatory stabilizing mutations. Such libraries can be combined with low-throughput screens that provide high accuracy and directly target the desired substrate and reaction conditions, and thereby provide highly improved variants.
Copyright © 2012. Published by Elsevier Ltd.

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Year:  2012        PMID: 22579412     DOI: 10.1016/j.sbi.2012.03.010

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  50 in total

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7.  Quantitative mapping of binding specificity landscapes for homologous targets by using a high-throughput method.

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Journal:  Biochem J       Date:  2020-05-15       Impact factor: 3.857

8.  High-throughput evaluation of synthetic metabolic pathways.

Authors:  Justin R Klesmith; Timothy A Whitehead
Journal:  Technology (Singap World Sci)       Date:  2015-12-16

9.  Monobody-mediated alteration of enzyme specificity.

Authors:  Shun-Ichi Tanaka; Tetsuya Takahashi; Akiko Koide; Satoru Ishihara; Satoshi Koikeda; Shohei Koide
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10.  Engineering of isoamylase: improvement of protein stability and catalytic efficiency through semi-rational design.

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