| Literature DB >> 29741801 |
Michael R Chapman1, Sebastian C Cosgrove2, Nicholas J Turner2, Nikil Kapur3, A John Blacker1.
Abstract
We report a simple, mild, and synthetically clean approach to accelerate the rate of enzymatic oxidation reactions by a factor of up to 100 when compared to conventional batch gas/liquid systems. Biocatalytic decomposition of H2 O2 is used to produce a soluble source of O2 directly in reaction media, thereby enabling the concentration of aqueous O2 to be increased beyond equilibrium solubility under safe and practical conditions. To best exploit this method, a novel flow reactor was developed to maximize productivity (g product L-1 h-1 ). This scalable benchtop method provides a distinct advantage over conventional bio-oxidation in that no pressurized gas or specialist equipment is employed. The method is general across different oxidase enzymes and compatible with a variety of functional groups. These results culminate in record space-time yields for bio-oxidation.Entities:
Keywords: biocatalysis; continuous flow; flow reactors; oxidation; space-time yields
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Year: 2018 PMID: 29741801 DOI: 10.1002/anie.201803675
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336