Modeling Alcohol Dehydrogenase Catalysis in Deep Eutectic Solvent/Water Mixtures

被引:33
作者
Huang, Lei [1 ]
Bittner, Jan Philipp [2 ]
Dominguez de Maria, Pablo [3 ]
Jakobtorweihen, Sven [2 ]
Kara, Selin [1 ]
机构
[1] Aarhus Univ, Dept Engn, Biocatalysis & Bioproc Grp, Gustav Wieds Vej 10, DK-8000 Aarhus, Denmark
[2] Hamburg Univ Technol, Inst Thermal Separat Proc, Eissendorfer Str 38, D-21073 Hamburg, Germany
[3] Sustainable Momentum SL, Av Ansite 3,4-6, Las Palmas Gran Canaria 35011, Canary Islands, Spain
关键词
alcohol dehydrogenase; deep eutectic solvents; molecular dynamics; solvent effects; thermodynamics; WHOLE-CELL BIOCATALYSIS; ANTARCTICA LIPASE B; ONE-POT SYNTHESIS; WATER ACTIVITY; CHOLINE CHLORIDE; BIOTRANSFORMATIONS; STABILITY; INSIGHTS; DYNAMICS; PROTEIN;
D O I
10.1002/cbic.201900624
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
The use of oxidoreductases (EC1) in non-conventional reaction media has been increasingly explored. In particular, deep eutectic solvents (DESs) have emerged as a novel class of solvents. Herein, an in-depth study of bioreduction with an alcohol dehydrogenase (ADH) in the DES glyceline is presented. The activity and stability of ADH in mixtures of glyceline/water with varying water contents were measured. Furthermore, the thermodynamic water activity and viscosity of mixtures of glyceline/water have been determined. For a better understanding of the observations, molecular dynamics simulations were performed to quantify the molecular flexibility, hydration layer, and intraprotein hydrogen bonds of ADH. The behavior of the enzyme in DESs follows the classic dependence of water activity (a(W)) in non-conventional media. At low a(W) values (<0.2), ADH does not show any activity; at higher a(W) values, the activity was still lower than that in pure water due to the high viscosities of the DES. These findings could be further explained by increased enzyme flexibility with increasing water content.
引用
收藏
页码:811 / 817
页数:7
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