Literature DB >> 32589835

Engineering Carboxylic Acid Reductase (CAR) through a Whole-Cell Growth-Coupled NADPH Recycling Strategy.

Levi Kramer1, Xuan Le1, Marisa Rodriguez1, Mark A Wilson2, Jiantao Guo3, Wei Niu1.   

Abstract

Rapid evolution of enzyme activities is often hindered by the lack of efficient and affordable methods to identify beneficial mutants. We report the development of a new growth-coupled selection method for evolving NADPH-consuming enzymes based on the recycling of this redox cofactor. The method relies on a genetically modified Escherichia coli strain, which overaccumulates NADPH. This method was applied to the engineering of a carboxylic acid reductase (CAR) for improved catalytic activities on 2-methoxybenzoate and adipate. Mutant enzymes with up to 17-fold improvement in catalytic efficiency were identified from single-site saturated mutagenesis libraries. Obtained mutants were successfully applied to whole-cell conversions of adipate into 1,6-hexanediol, a C6 monomer commonly used in polymer industry.

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Keywords:  1,6-hexanediol; 2-methoxybenzoate; adipate; carboxylic acid reductase; enzyme engineering; redox growth coupling

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Year:  2020        PMID: 32589835     DOI: 10.1021/acssynbio.0c00290

Source DB:  PubMed          Journal:  ACS Synth Biol        ISSN: 2161-5063            Impact factor:   5.110


  1 in total

1.  Change in Cofactor Specificity of Oxidoreductases by Adaptive Evolution of an Escherichia coli NADPH-Auxotrophic Strain.

Authors:  Madeleine Bouzon; Volker Döring; Ivan Dubois; Anne Berger; Gabriele M M Stoffel; Liliana Calzadiaz Ramirez; Sophia N Meyer; Marion Fouré; David Roche; Alain Perret; Tobias J Erb; Arren Bar-Even; Steffen N Lindner
Journal:  mBio       Date:  2021-08-17       Impact factor: 7.867

  1 in total

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