4.7 Article

Efficient whole-cell oxidation of α,β-unsaturated alcohols to α,β-unsaturated aldehydes through the cascade biocatalysis of alcohol dehydrogenase, NADPH oxidase and hemoglobin

Journal

MICROBIAL CELL FACTORIES
Volume 20, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12934-021-01511-8

Keywords

alpha; beta-Unsaturated aldehydes; Alcohol dehydrogenase; NADPH oxidase; NADP(+) regeneration; Enzyme fusion

Funding

  1. Natural Science Foundation of Zhejiang Province, China [LY17B020012]
  2. Xinmiao Talents Program of Zhejiang Province [2020R403072]

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The study successfully constructed a strain expressing a fusion enzyme that achieved efficient NADP(+) regeneration and the selective oxidation of various alpha, beta-unsaturated alcohols. The researchers also optimized reaction conditions and established a platform for synthesizing valuable alpha, beta-unsaturated aldehydes.
Background alpha,beta -Unsaturated aldehydes are widely used in the organic synthesis of fine chemicals for application in products such as flavoring agents, fragrances and pharmaceuticals. In the selective oxidation of alpha,beta -unsaturated alcohols to the corresponding alpha,beta -unsaturated aldehydes, it remains challenging to overcome poor selectivity, overoxidation and a low atom efficiency in chemical routes.ResultsAn E. coli strain coexpressing the NADP(+)-specific alcohol dehydrogenase YsADH and the oxygen-dependent NADPH oxidase TkNOX was constructed; these components enabled the NADP(+) regeneration and catalyzed the oxidation of 100 mM 3-methyl-2-buten-1-ol to 3-methyl-2-butenal with a yield of 21.3%. The oxygen supply was strengthened by introducing the hemoglobin protein VsHGB into recombinant E. coli cells and replacing the atmosphere of the reactor with pure oxygen, which increased the yield to 51.3%. To further improve catalytic performance, the E. coli cells expressing the multifunctional fusion enzyme YsADH-(GSG)-TkNOX-(GSG)-VsHGB were generated, which completely converted 250 mM 3-methyl-2-buten-1-ol to 3-methyl-2-butenal after 8 h of whole-cell oxidation. The reaction conditions for the cascade biocatalysis were optimized, in which supplementation with 0.2 mM FAD and 0.4 mM NADP(+) was essential for maintaining high catalytic activity. Finally, the established whole-cell system could serve as a platform for the synthesis of valuable alpha,beta -unsaturated aldehydes through the selective oxidation of various alpha,beta -unsaturated alcohols.ConclusionsThe construction of a strain expressing the fusion enzyme YsADH-(GSG)-TkNOX-(GSG)-VsHGB achieved efficient NADP(+) regeneration and the selective oxidation of various alpha,beta -unsaturated alcohols to the corresponding alpha,beta -unsaturated aldehydes. Among the available redox enzymes, the fusion enzyme YsADH-(GSG)-TkNOX-(GSG)-VsHGB has become the most recent successful example to improve catalytic performance in comparison with its separate components.

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