State Key Laboratory of Materials-Oriented Chemical Engineering, School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing 210009, China; School of Pharmacy, Liaocheng University, Liaocheng 252059, China.
School of Pharmacy, Liaocheng University, Liaocheng 252059, China.
Carbohydr Polym. 2020 Apr 15;234:115914. doi: 10.1016/j.carbpol.2020.115914. Epub 2020 Jan 24.
In this work, ionic liquids-modified magnetic carboxymethyl cellulose nanoparticles (IL-MCMC) were prepared and used as supports for enzyme immobilization. The specific activity of immobilized lipase PPL-IL-MCMC was 1.43 and 2.81 folds higher than that of free PPL and PPL-MCMC, respectively. Water contact angle analysis indicated that the introduction of ionic liquids increased the hydrophobicity of supports, which in tune induced the lid-opening of lipase, allowing its active sites to become more accessible. In addition, the affinity between lipase and substrate immobilized on the prepared supports was enhanced. The same method was also applied to analyze immobilize penicillin G acylase (PGA) to further investigate the general applicability of the method. The results showed that the immobilized PGA exhibited higher stability than many other reported PGAs. The developed composites may be utilized as excellent supports for enzyme immobilization in industrial application.
在这项工作中,制备了离子液体修饰的磁性羧甲基纤维素纳米粒子(IL-MCMC),并将其用作酶固定化的载体。固定化脂肪酶 PPL-IL-MCMC 的比活性分别比游离 PPL 和 PPL-MCMC 高 1.43 和 2.81 倍。水接触角分析表明,离子液体的引入增加了载体的疏水性,从而诱导脂肪酶的盖打开,使其活性位点更容易接近。此外,固定在制备的载体上的脂肪酶和底物之间的亲和力增强。同样的方法也被应用于分析固定化青霉素 G 酰化酶(PGA),以进一步研究该方法的通用性。结果表明,固定化 PGA 表现出比许多其他报道的 PGA 更高的稳定性。开发的复合材料可用作工业应用中酶固定化的优良载体。