Biochemical Processing and Biomaterial Research Laboratory, Faculty of Arts and Sciences, Gazi University, Teknik Okullar, Ankara, Turkey.
Bioprocess Biosyst Eng. 2010 Feb;33(2):227-36. doi: 10.1007/s00449-009-0316-y. Epub 2009 Apr 7.
Poly(2-hydroxyethyl methacrylate/ethylenglycol dimethacrylate) beads were grafted with poly(glycidylmethacrylate) via surface initiated atom transfer radical polymerization. Epoxy groups of the grafted polymer were modified in to sulfone groups. Sulfonated beads were characterized by swelling studies, FT-IR, SEM and elemental analysis, and were used for reversible immobilization of lipase. Under given experimental conditions, the beads had an adsorption capacity of 44.7 mg protein/g beads. The adsorbed lipase on beads retained up to 67.4% of its initial activity. The immobilized lipase exhibited improved thermal and storage stabilities over those of the free enzyme. The immobilized lipase could desorb 1.0 M NaCl solution at pH 8.0, and the sulfonated beads can be repeatedly charged with fresh enzyme after inactivation upon use.
聚(2-羟乙基甲基丙烯酸酯/乙二醇二甲基丙烯酸酯)珠粒通过表面引发原子转移自由基聚合接枝了聚(甲基丙烯酸缩水甘油酯)。接枝聚合物的环氧基团被修饰成砜基团。通过溶胀研究、FT-IR、SEM 和元素分析对磺化珠粒进行了表征,并将其用于脂肪酶的可逆固定化。在给定的实验条件下,珠粒的吸附蛋白量为 44.7mg/g 珠粒。吸附在珠粒上的脂肪酶保留了其初始活性的 67.4%。固定化脂肪酶在热稳定性和储存稳定性方面均优于游离酶。固定化脂肪酶可以在 pH 值为 8.0 的 1.0 M NaCl 溶液中解吸,并且磺化珠粒在使用后失活时可以用新鲜酶重新充电。