期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 7, 页码 3481-3486出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202012658
关键词
atom efficiency; cofactor; co-product recycling; integrated multienzyme catalysis; lactams; nylon monomers
资金
- Ministry of Trade, Industry and Energy of South Korea (MOTIE, Korea) under the industrial Technology Innovation Program [10076343]
- Basic Science Research program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and future Planning [2020R1A2C2009806]
- Korea Evaluation Institute of Industrial Technology (KEIT) [10076343] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [2020R1A2C2009806] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
A highly atom-efficient integrated cofactor/co-product recycling cascade using cycloalkylamines for the synthesis of nylon building blocks was reported, achieving excellent conversions with E. coli whole cells and purified enzymes. The tandem biocatalytic cascade was demonstrated to produce lactams using engineered biocatalysts, showing promise as an alternative for bio-based production of omega-amino acids and corresponding lactam compounds.
We report a highly atom-efficient integrated cofactor/co-product recycling cascade employing cycloalkylamines as multifaceted starting materials for the synthesis of nylon building blocks. Reactions using E. coli whole cells as well as purified enzymes produced excellent conversions ranging from >80 and 95 % into desired omega-amino acids, respectively with varying substrate concentrations. The applicability of this tandem biocatalytic cascade was demonstrated to produce the corresponding lactams by employing engineered biocatalysts. For instance, epsilon-caprolactam, a valuable polymer building block was synthesized with 75 % conversion from 10 mM cyclohexylamine by employing whole-cell biocatalysts. This cascade could be an alternative for bio-based production of omega-amino acids and corresponding lactam compounds.
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