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作 者:辛瑜[1] 仝艳军[1] 杨海麟[1] 张玲[1] 张玉然[1] 陈亦[1] 王武[1]
机构地区:[1]江南大学生物工程学院工业生物技术教育部重点实验室,无锡214122
出 处:《化学学报》2012年第6期803-811,共9页Acta Chimica Sinica
基 金:2010年江苏省科技支撑(No.SBE201077545);2011年江苏省科技支撑(No.SBE201170578);工业微生物重点实验室开放课题(No.KLIB-KF201005);江苏省高校优势学科建设工程资助项目;"111"引智(No.111-2-06)资助项目~~
摘 要:采用分子印迹技术,以谷胱甘肽为模板分子,以丙烯酰胺、甲基丙烯酸为功能单体制备分子印迹聚合物;通过静态吸附试验,探讨了合成分子印迹聚合物时模板分子与功能单体的物质的量比、上样液pH值、吸附平衡时间、上样液浓度对聚合物吸附性能的影响;实验结果表明:以丙烯酰胺、甲基丙烯酸为功能单体制备谷胱甘肽分子印迹聚合物时,谷胱甘肽与丙烯酰胺、甲基丙烯酸的最适摩尔比分别为1∶5和1∶4,以及最适静态吸附条件为:上样液pH值分别为3.0和5.0左右;上样液浓度分别为1.50~2.00 g/L和1.00~1.50 g/L;静态吸附平衡时间为18和20 h左右.同时也探讨了分子印迹聚合物对谷胱甘肽结构类似物的吸附性能,结果表明,所合成的分子印迹聚合物对谷胱甘肽具有良好的选择性吸附能力.同时也研究了分子印迹聚合物对酵母抽提物中谷胱甘肽的吸附性能,以丙烯酰胺和甲基丙烯酸为功能单体制备的分子印迹聚合物对混合体系中谷胱甘肽的一次性提取率分别为41%和77%.分子印迹聚合物均表现出了较好的吸附特性,为分离提纯谷胱甘肽提供一种可选择的途径.Using glutathione (GSH) as template molecule, acrylamide (AM) and methacrylic acid (MAA) as functional monomer, different glutathionemolecularly imprinted polymers (GSHMIPs) were developed and synthesized with molecularly imprinted technique. The effects for adsorption capacity, including molar ratio of template moleculefunctional monomer, pH of loading buffer, adsorption equilibrium time and loading concentration were discussed in detail. The result demonstrated that. the polymers with raw material mole ratios at 1 : 5 for GSH : AM, and 1 : 4 for GSH : MAA showed higher adsorption capacity, the opti mal pH values for the adsorption of GSHMIPAMs and GSH-MIPMAAs to GSH were 3.0 and 5.0, respectively; furthermore, the optimal GSH loading concentrations were 1.50-2.00g/L for GSHMIPAMs, and 1.00- 1.50 g/L for GSHMIPMAAs; additionally, the adsorption equilibrium time was 20 h for GSHMIPAMs and 18 h for GSHMIPMAAs. In addition, the binding of GSH analogues were also applied to the synthesized poly-mers, and the results reflected that GSHMIPs showed low recognition to these analogues. This protocol was further employed for the extraction and separation of GSH from yeast cells samples. The extraction recover ies of GSHMIPAMs and GSHMIPMAAs were 41% and 77%, respectively, it was of great potential in the pu rification of GSH.
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