Magnetic macroporous chitin microsphere as a support for covalent enzyme immobilization

被引:7
|
作者
Wang, Wei [1 ,3 ,4 ]
Liu, Jiayuan [1 ]
Khan, Muhammad Junaid [1 ,3 ,4 ]
Wang, Rong [1 ]
Francesco, Secundo [5 ]
Sun, Jianan [1 ,3 ,4 ]
Mao, Xiangzhao [1 ,2 ,3 ,4 ]
Huang, Wen-Can [1 ,3 ,4 ]
机构
[1] Ocean Univ China, Coll Food Sci & Engn, State Key Lab Marine Food Proc & Safety Control, Qingdao 266404, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
[3] Qingdao Key Lab Food Biotechnol, Qingdao 266404, Peoples R China
[4] China Natl Light Ind, Key Lab Biol Proc Aquat Prod, Qingdao 266404, Peoples R China
[5] CNR, Ist Sci & Tecnol Chim Giulio Natta, Via Mario Bianco 9, I-20131 Milan, Italy
基金
国家重点研发计划;
关键词
Chitin nanofiber; Magnetic macroporous carrier; Enzyme immobilization; NANOFIBERS; CELLULOSE; BIOCATALYSIS; SIZE; NANOPARTICLES; IMPROVEMENT; COMPOSITES; STRATEGIES; STABILITY; LIPASE;
D O I
10.1016/j.ijbiomac.2023.128214
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
In this study, a novel magnetic macroporous chitin microsphere (MMCM) was developed for enzyme immobilization. Chitin nanofibers were prepared and subsequently subjected to self-assembly with magnetic nanoparticles and PMMA (polymethyl methacrylate). Following this, microspheres were formed through spray drying, achieving a porous structure through etching. The MMCM serves as an effective support for immobilizing enzymes, allowing for their covalent immobilization both on the microsphere's surface and within its pores. The substantial surface area resulting from the porous structure leads to a 2.1-fold increase in enzyme loading capacity compared to non-porous microspheres. The MMCM enhances stability of the immobilized enzymes under various pH and temperature conditions. Furthermore, after 20 days of storage at 4 degrees C, the residual activity of the immobilized enzyme was 2.93 times that of the free enzyme. Even after being recycled 10 times, the immobilized enzyme retained 56.7 % of its initial activity. It's noteworthy that the active sites of the enzymes remained unchanged after immobilization using the MMCM, and kinetic analysis revealed that the affinity of the immobilized enzymes rivals that of the free enzymes.
引用
收藏
页数:7
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