用户名: 密码: 验证码:
Candida antarctica Lipase B Chemically Immobilized on Epoxy-Activated Micro- and Nanobeads: Catalysts for Polyester Synthesis
详细信息    查看全文
文摘
Candida antarctica Lipase B (CALB) was covalently immobilized onto epoxy-activated macroporous poly(methyl methacrylate) Amberzyme beads (235 µm particle size, 220 Å pore size) and nanoparticles (nanoPSG, diameter 68 nm) with a poly(glycidyl methacrylate) outer region. Amberzyme beads allowed CALB loading up to 0.16 g of enzyme per gram of support. IR microspectroscopy generated images of Amberzyme−CALB beads showed CALB is localized within a 50 µm thick loading front. IR microspectroscopy images, recorded prior to and after treatment of Amberzyme−CALB with DMSO/aqueous Triton X-100, are similar, confirming that CALB is largely chemically linked to Amberzyme. The activity of CALB immobilized on Amberzyme, Lewatit (i.e., Novozym 435 catalyst), and nanoPSG was assessed for lactone ring-opening and step-condensation polymerizations. For example, the percent conversion of ε-caprolactone using the same amount of enzyme catalyzed by Amberzym−CALB, Novozym 435, and nanoPSG−CALB for 20 min was 7.0, 16, and 65%, respectively. Differences in CALB reactivity were discussed based on resin physical parameters and availability of active sites determined by active site titrations. Regardless of the matrix used and chemical versus physical immobilization, ε-CL ring-opening polymerizations occur by a chain growth mechanism without chain termination. To test Amberzyme−CALB stability, the catalyst was reused over three reaction cycles for ε-CL ring-opening polymerization (70 °C, 70 min reactions) and glycerol/1,8-octanediol/adipic acid polycondensation reactions (90 °C, 64 h). Amberzyme−CALB was found to have far better stability for reuse relative to Novozym 435 for the polycondensation reaction.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700