Combined cross-linked enzyme aggregates of glycerol dehydrogenase and NADH oxidase for high efficiency in situ NAD+ regeneration

被引:50
作者
Xu, Meng-Qiu [1 ]
Li, Fei-Long [1 ]
Yu, Wen-Qian [1 ]
Li, Rui-Fang [1 ]
Zhang, Ye-Wang [1 ]
机构
[1] Jiangsu Univ, Sch Pharm, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cofactor regeneration; Combi-CLEAs; NADH oxidase; Glycerol dehydrogenase; ALCOHOL-DEHYDROGENASE; CLEAS; PROTEIN; 1,3-DIHYDROXYACETONE; IMMOBILIZATION; CLONING; SYSTEM;
D O I
10.1016/j.ijbiomac.2019.09.178
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
Cofactor regeneration is an important method to avoid the consumption of large quantities of oxidized cofactor NAD(+) in enzyme-catalyzed reactions. Herein, glycerol dehydrogenase (GDH) and NADH oxidase preparations by aggregating enzymes with ammonium sulphate followed by cross-linking formed aggregates for effective regeneration of NAD(+). After optimization, the activity of combi-CLEAs and separate CLEAs mixtures were 950 and 580 U/g, respectively. And the catalytic stability of combi-CLEAs against pH and temperature was superior to the free enzyme mixture. After ten cycles of reuse, the catalytic efficiency could still retain 63.3% of its initial activity, indicating that the constructed combi-CLEAs system had excellent reusability. Also, the conversion of glycerol to 1,3-dihydroxyacetone (DHA) was improved by the constructed NAD(+) regeneration system, resulting in 4.6%, which was 2.5 times of the free enzyme system. Thus, wide applications of this co-immobilization method in the production of various chiral chemicals could be expected in the industry for its high efficiency at a low cost. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:1013 / 1021
页数:9
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