Horák D, Karpísek M, Turková J, Benes M
Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovský Sq. 2, 162 06 Prague 6, Czech Republic.
Biotechnol Prog. 1999 Mar-Apr;15(2):208-15. doi: 10.1021/bp990006w.
Nonporous cross-linked poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate) (poly(HEMA-co-EDMA)) microspheres were prepared by dispersion polymerization of HEMA and EDMA. The polymerization was performed in toluene/2-methylpropan-1-ol in the presence of cellulose acetate butyrate as a steric stabilizer and dibenzoyl peroxide initiator. The particle size may be increased by decreasing the toluene/2-methylpropan-1-ol ratio and by increasing polymerization temperature. Adipohydrazide was attached to the microspheres activated with 2,4,6-trichloro-1,3,5-triazine. After periodate oxidation of its carbohydrate moieties, horseradish peroxidase was coupled to the hydrazide-functionalized poly(HEMA-co-EDMA) microparticles up to 7.3 microgram of enzyme/g of carrier without a significant loss of its activity. Immobilized peroxidase was found to be stable, retaining more than 97% of its initial activity when stored for 23 days after the preparation.
通过甲基丙烯酸2-羟乙酯与二甲基丙烯酸乙烯酯(聚(甲基丙烯酸2-羟乙酯-共-二甲基丙烯酸乙烯酯))的分散聚合反应制备了无孔交联微球。聚合反应在甲苯/2-甲基-1-丙醇中进行,以醋酸丁酸纤维素作为空间稳定剂,过氧化二苯甲酰作为引发剂。通过降低甲苯/2-甲基-1-丙醇的比例和提高聚合温度,可以增大粒径。己二酰肼连接到用2,4,6-三氯-1,3,5-三嗪活化的微球上。在其碳水化合物部分经高碘酸盐氧化后,辣根过氧化物酶与酰肼功能化的聚(甲基丙烯酸2-羟乙酯-共-二甲基丙烯酸乙烯酯)微粒偶联,每克载体可偶联高达7.3微克的酶,且酶活性没有显著损失。发现固定化过氧化物酶很稳定,制备后储存23天,仍保留其初始活性的97%以上。