青霉素G酰化酶固定化用热敏靶段树脂的设计与合成

Yangdong Liu, Siyuan Lu, Hongyi Tu, Boyuan Zhang, Yaqin Zhao, Jiasheng He, Liangliang He, Z. Chen
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摘要

目的为节约经济成本,提高企业效益,本研究旨在通过相应的理论指导和实验探索,合成反应速度快、酶活性回收率高、可重复使用性好的固定化青霉素G酰化酶(PGA)载体。以N, N-二乙基丙烯酰胺(DEA)和β-甲基丙烯酸羟乙酯(HEMA)为功能单体,采用可逆加成-破碎链转移聚合法制备了双嵌段树脂,得到了N, N-二乙基丙烯酰胺-b-聚(β-甲基丙烯酸羟乙酯)(PDEA-b-PHEMA),并考察了DEA和HEMA的配比对PGA活性的影响,得到了合适的DEA和HEMA的嵌段比例。然后,研究了在载体制备条件下HEMA和甲基丙烯酸缩水甘油酯(GMA)的竞争率。在此基础上,合成了具有不同靶距的热敏树脂载体PDEA-b-PHEMA-b-P(HEMA-co-GMA),并用氢核磁共振(1H NMR)研究了共聚物的化学结构和分子量。发现:在无规共聚过程中,随着单体HEMA用量的增加,树脂载体的下临界溶解温度降低;催化性能研究表明,固定化PGA反应速度快,且固定化PGA酶活性的恢复速率随靶标距离的变化而变化。当树脂块中HEMA与GMA的摩尔比为8.15:1[即树脂PDEA100-b-PHEMA10-b-P(HEMA65-co-GMA8)]时,固定化PGA的活性回收率可达50.51%,比纯GMA固定化PGA的活性回收率高15.49%。这一贡献为固定化PGA提供了一种新的载体。在最佳摩尔比下,固定化PGA的酶活回收率可达50.51%,比固定化距离不受调节的载体固定化PGA的酶活回收率高15.49%。
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Design and synthesis of thermosensitive target segment resin with precisely controlled distance between immobilization sites for immobilization of penicillin G acylase
Purpose To save the economic cost and improve the performance of enterprises, this study aims to synthesize high performance immobilized penicillin G acylase (PGA) carriers with fast reaction speed, high recovery rate of enzyme activity and good reusability through corresponding theoretical guidance and experimental exploration. Design methodology approach A diblock resin was synthesized by reversible addition-fragmentation chain transfer polymerization method using N, N-diethylacrylamide (DEA) and β-hydroxyethyl methacrylate (HEMA) as functional monomers poly(N, N-diethylacrylamide)-b-poly(β-hydroxyethyl methacrylate) (PDEA-b-PHEMA) was obtained, and the effect of the ratio of DEA and HEMA on the activity of PGA was investigated, and the appropriate block ratio of DEA and HEMA was obtained. After that, the competitive rate of HEMA and glycidyl methacrylate (GMA) under the carrier preparation conditions was investigated. Based on the above work, a thermosensitive resin carrier PDEA-b-PHEMA-b-P(HEMA-co-GMA) with different target distances was synthesized, and the chemical structures and molecular weight of copolymers were investigated by hydrogen NMR (1H NMR). Findings The lower critical solution temperature of the resin support decreases with the increase of the monomer HEMA in the random copolymerization; the catalytic performance study indicated that the response rate of the immobilized PGA is fast, and the recovery rate of the enzyme activity of the immobilized PGA varies with the distance between the targets. When the molar ratio of HEMA to GMA in the resin block is 8.15:1 [i.e. resin PDEA100-b-PHEMA10-b-P(HEMA65-co-GMA8)], the activity recovery rate of immobilized PGA can reach 50.51%, which was 15.49% higher than that of pure GMA immobilized PGA. Originality value This contribution provides a novel carrier for immobilizing PGA. Under the optimal molar ratio, the enzyme activity recovery could be up to 50.51%, which was 15.49% higher than that of PGA immobilized on the carrier with nonregulated distance between two immobilization sites.
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