Crosslinked Aggregates of Fusion Enzymes in Microaqueous Organic Media

被引:8
|
作者
Vernet, Guillem [1 ]
Ma, Yu [1 ,2 ]
Zhang, Ningning [1 ]
Kara, Selin [1 ,2 ]
机构
[1] Leibniz Univ Hannover, Inst Tech Chem, Callinstr 5, D-30167 Hannover, Germany
[2] Aarhus Univ, Dept Biol & Chem Engn, Biocatalysis & Bioproc Grp, Gustav Wieds Vej 10, DK-8000 Aarhus, Denmark
关键词
biotransformations; crosslinked enzyme aggregates; cyclohexanone monooxygenase; enzyme immobilization; fusion enzymes; BAEYER-VILLIGER MONOOXYGENASES; EPSILON-CAPROLACTONE; DEHYDROGENASE; BIOCATALYSIS; CASCADE; REGENERATION; OXIDATIONS; COENZYMES; OXYGEN; GREEN;
D O I
10.1002/cbic.202200794
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Baeyer-Villiger monooxygenases (BVMOs) are attractive for selectively oxidizing various ketones using oxygen into valuable esters and lactones. However, the application of BVMOs is restrained by cofactor dependency and enzyme instability combined with water-related downsides such as low substrate loading, low oxygen capacity, and water-induced side reactions. Herein, we described a redox-neutral linear cascade with in-situ cofactor regeneration catalyzed by fused alcohol dehydrogenase and cyclohexanone monooxygenase in aqueous and microaqueous organic media. The cascade conditions have been optimized regarding substrate concentrations as well as the amounts of enzymes and cofactors with the Design of Experiments (DoE). The carrier-free immobilization technique, crosslinked enzyme aggregates (CLEAs), was applied to fusion enzymes. The resultant fusion CLEAs were proven to function in microaqueous organic systems, in which the enzyme ratios, water contents (0.5-5 vol. %), and stability have been systematically studied. The fusion CLEAs showed promising operational (up to 5 cycles) and storage stability.
引用
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页数:8
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