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具有靶向间隔的磁热敏聚合物复合载体,用于提高固定化酶性能。

Magnetic thermosensitive polymer composite carrier with target spacing for enhancing immobilized enzyme performance.

机构信息

College of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou, 730050, China; State Key Laboratory of Advanced Progressing and Recycling of Nonferrous Metal Materials, Lanzhou University of Technology, Lanzhou, 730050, China.

College of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou, 730050, China; State Key Laboratory of Advanced Progressing and Recycling of Nonferrous Metal Materials, Lanzhou University of Technology, Lanzhou, 730050, China.

出版信息

Enzyme Microb Technol. 2021 Oct;150:109896. doi: 10.1016/j.enzmictec.2021.109896. Epub 2021 Aug 19.

Abstract

A novel magnetic thermosensitive polymer composite carrier with target spacing was developed. In this strategy, thermosensitive polymer grafted on magnetic FeO for enhancing immobilized penicillin G acylase (PGA) performance and introduce immobilized target spacing into magnetic carriers for the first time. FeO nanoparticles were synthesized by a reverse microemulsion method. The modifier used was the silane coupling agent γ-methylacryloxypropyl trimethoxysilane (KH570) and then reacting with a reversible-adaptive fragmentation chain transfer (RAFT) reagent, 2-cyano-2-propyldodecyl trithiocarbonate (CPDTC). The thermo-sensitive nanoparticle-composite carrier of FeO-grafted-poly N, N-diethyl acrylamide-block-poly β-Hydroxyethyl methacrylate-block-random copolymer of glycidyl methacrylate and methyl methacrylate (FeO-g-PDEA-b-PHEMA-b-P(MMA-co-GMA)) were synthesized by RAFT polymerization technique that used N, N-diethyl acrylamide (DEA), β-Hydroxyethyl methacrylate (HEMA), Glycidyl methacrylate (GMA) and Methyl methacrylate (MMA) as monomer, then which were employed as functional carriers for the immobilization of PGA. Within the carrier, the epoxy group of GMA segment was a target immobilization site for PGA and the introduction of MMA reflected the target space of immobilized PGA to improve catalytic activity and catalytic activity recovery rate of the immobilized PGA. Characterizations demonstrated that the triblock copolymers grafted FeO nanoparticles were successfully fabricated by the structure design. Besides, under these circumstances the enzyme activity (EA), enzyme loading capacity (ELC) and catalytic activity recovery ration (CAR) reached 31235 U/g, 128.39 mg/g and 93.32 %, respectively. The catalytic activity of immobilized PGA maintained 87.4 % of initial value and the recovery ratio (R) of immobilized PGA reached 96.22 % after recycling 12 times. Furthermore, the immobilized PGA exhibited advantages of low temperature homogeneous catalysis and magnetic separation, which indicated broad application prospects in the biocatalysts' field.

摘要

开发了一种具有靶向间隔的新型磁性热敏聚合物复合载体。在该策略中,热敏聚合物接枝到磁性 FeO 上,以提高固定化青霉素 G 酰化酶 (PGA) 的性能,并首次将固定化靶向间隔引入磁性载体中。FeO 纳米粒子通过反相微乳液法合成。使用的修饰剂是硅烷偶联剂γ-甲基丙烯酰氧基丙基三甲氧基硅烷(KH570),然后与可逆自适应碎片化链转移(RAFT)试剂 2-氰基-2-丙基十二硫代碳酸酯(CPDTC)反应。通过 RAFT 聚合技术合成了 FeO 接枝聚 N,N-二乙基丙烯酰胺嵌段-聚β-羟乙基甲基丙烯酸酯嵌段-随机甲基丙烯酸缩水甘油酯和甲基丙烯酸甲酯共聚物(FeO-g-PDEA-b-PHEMA-b-P(MMA-co-GMA))热敏纳米粒子复合载体,使用 N,N-二乙基丙烯酰胺(DEA)、β-羟乙基甲基丙烯酸酯(HEMA)、甲基丙烯酸缩水甘油酯(GMA)和甲基丙烯酸甲酯(MMA)作为单体,然后用作固定化 PGA 的功能载体。在载体中,GMA 段的环氧基团是 PGA 的靶向固定化位点,引入 MMA 反映了固定化 PGA 的靶向空间,以提高固定化 PGA 的催化活性和催化活性回收率。表征表明,通过结构设计成功制备了接枝 FeO 纳米粒子的三嵌段共聚物。此外,在这些情况下,酶活性(EA)、酶载量(ELC)和催化活性回收率(CAR)分别达到 31235 U/g、128.39 mg/g 和 93.32%。固定化 PGA 的催化活性保持初始值的 87.4%,固定化 PGA 的回收率(R)在 12 次回收后达到 96.22%。此外,固定化 PGA 表现出低温均相催化和磁分离的优势,这表明在生物催化剂领域具有广阔的应用前景。

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