| Literature DB >> 32589835 |
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.Entities:
Keywords: 1,6-hexanediol; 2-methoxybenzoate; adipate; carboxylic acid reductase; enzyme engineering; redox growth coupling
Mesh:
Substances:
Year: 2020 PMID: 32589835 DOI: 10.1021/acssynbio.0c00290
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110