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首页> 外文期刊>Molecules >Glutaraldehyde Cross-Linking of Immobilized Thermophilic Esterase on Hydrophobic Macroporous Resin for Application in Poly(ε-caprolactone) Synthesis
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Glutaraldehyde Cross-Linking of Immobilized Thermophilic Esterase on Hydrophobic Macroporous Resin for Application in Poly(ε-caprolactone) Synthesis

机译:固定化高温酯酶在疏水性大孔树脂上的戊二醛交联,用于聚(ε-己内酯)的合成

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摘要

The immobilized thermophilic esterase from Archaeoglobus fulgidus was successfully constructed through the glutaraldehyde-mediated covalent coupling after its physical adsorption on a hydrophobic macroporous resin, Sepabeads EC-OD. Through 0.05% glutaraldehyde treatment, the prevention of enzyme leaching and the maintenance of catalytic activity could be simultaneously realized. Using the enzymatic ring-opening polymerization of ε-caprolactone as a model, effects of organic solvents and reaction temperature on the monomer conversion and product molecular weight were systematically investigated. After the optimization of reaction conditions, products were obtained with 100% monomer conversion and Mn values lower than 1010 g/mol. Furthermore, the cross‑linked immobilized thermophilic esterase exhibited an excellent operational stability, with monomer conversion values exceeding 90% over the course of 12 batch reactions, still more than 80% after 16 batch reactions.
机译:通过将戊二醛介导的共价偶联物物理吸附在疏水性大孔树脂Sepabeads EC-OD上,成功地构建了由戊二醛介导的共价偶联物,从而成功地构建了固定的嗜热古菌酯酶。通过0.05%的戊二醛处理,可以同时实现酶浸出的预防和催化活性的维持。以ε-己内酯的酶促开环聚合为模型,系统地研究了有机溶剂和反应温度对单体转化率和产物分子量的影响。优化反应条件后,获得的产物的单体转化率为100%,Mn n 值低于1010 g / mol。此外,交联的固定化嗜热酯酶表现出出色的操作稳定性,在12批反应过程中,单体转化率超过90%,16批反应后仍超过80%。

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