Complete Enzymatic Oxidation of Methanol to Carbon Dioxide: Towards More Eco-Efficient Regeneration Systems for Reduced Nicotinamide Cofactors

被引:22
|
作者
Kara, Selin [1 ,2 ]
Schrittwieser, Joerg H. [1 ]
Gargiulo, Serena [1 ]
Ni, Yan [1 ]
Yanase, Hideshi [3 ]
Opperman, Diederik J. [4 ]
van Berkel, Willem J. H. [5 ]
Hollmann, Frank [1 ]
机构
[1] Delft Univ Technol, Dept Biotechnol, NL-2628 BL Delft, Netherlands
[2] Tech Univ Dresden, Chair Mol Biotechnol, Inst Microbiol, D-01062 Dresden, Germany
[3] Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
[4] Univ Orange Free State, Dept Microbial Biochem & Food Biotechnol, ZA-9300 Bloemfontein, South Africa
[5] Wageningen Univ, Biochem Lab, NL-6703 HA Wageningen, Netherlands
关键词
cofactor regeneration; complete methanol oxidation; enzymatic cascades; oxidoreductases; FORMALDEHYDE DISMUTASE; BIOCATALYSIS; REDUCTIONS; ALDEHYDES; REDUCTASE;
D O I
10.1002/adsc.201500173
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel system for in situ regeneration of reduced nicotinamide cofactors (NADH) is proposed: through a cascade of alcohol dehydrogenase (ADH), formaldehyde dismutase (FDM) and formate dehydrogenase (FDH) complete oxidation of methanol to carbon dioxide (CO2) is coupled to the regeneration of NADH. As a consequence, from one equivalent of methanol three equivalents of NADH can be obtained. The feasibility of this cascade is demonstrated at the examples of an NADH-dependent reduction of conjugated C=C-double bonds (catalysed by an enoate reductase) and the NADH-dependent hydroxylation of phenols (catalysed by a monooxygenase). The major limitation of the current regeneration system is the comparably poor catalytic efficiency of the methanol oxidation step (low k(cat) and high K-M value of the ADH used) necessitating higher than theoretical methanol concentrations.
引用
收藏
页码:1687 / 1691
页数:5
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