首页|细菌纤维素固定化酶的制备及其水解拆分性能

细菌纤维素固定化酶的制备及其水解拆分性能

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经D-泛解酸内酯酶(D-Lacs)催化水解拆分是制备医药中间体D-泛解酸的绿色催化新技术,但游离酶存在价格昂贵、易失活、难分离等问题.利用椰果源细菌纤维素(BC)的三维纳米纤维网络为支架,以二乙烯三胺将其改性成BC-NH2,吸附纳米酶后,以戊二醛稳定D-泛解酸内酯水解酶固定于BC网络中.结果表明,氨基化修饰改性提高了 BC固定化酶的活性,BC-NH2固定化D-Lacs的酶固载量高达372.5 mg/g,约4.5 h即可完成D,L-泛解酸内酯的水解拆分,均高于未改性BC.经过10次回收循环水解拆分实验,均可保证每批次2 h即可达到一半水解率,是一种有前景的全生物基酶固定化技术.
Preparation and Its Hydrolysis Resolution Properties of Nanofiber D-Lacs@BC-NH2
D-Lactonohydrolase(D-Lacs)catalyzed hydrolysis and resolution is a new green catalytic technology for the preparation of pharmaceutical intermediate D-Lacs.However,free enzymes have problems such as high cost,easy deacti-vation,and difficulty in separation.This article uses a three-dimensional nanofiber network of coconut derived bacterial cellulose(BC)as a scaffold,modified with diethylenetriamine to BC-NH2,adsorbed with nanoenzymes,and immobilized with glutaraldehyde stabilized D-Lactonohydrolase in the BC network.The results showed that the amination modification improved the activity of BC immobilized enzyme.The enzyme load of BC-NH2 immobilized D-Lacs was up to 372.5 mg/g,and the hydrolysis and resolution of DL-pantolactone could be completed in about 4.5 hours,which were higher than un-modified BC.After 10 cycles of recycling,hydrolysis and separation experiments,it can be ensured that each batch reach-es half of the hydrolysis rate within 2 hours,it has been proven to have good cycling stability and is a promising technology for immobilization of all bio-based enzymes.

D-Lactonohydrolasebacterial celluloseimmobilizationhydrolysis

元佳丽、周晓悦、向忠润、王慧庆

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合肥工业大学化学与化工学院,安徽合肥 230009

D-泛解酸内酯水解酶 细菌纤维素 酶固定化 水解

安徽省重点研究与开发计划

2022a05020059

2024

安徽化工
安徽省化工研究院

安徽化工

影响因子:0.229
ISSN:1008-553X
年,卷(期):2024.50(3)