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Sustainable synthesis of N-acetyllactosamine using an immobilized beta-galactosidase on a tailor made porous polymer

机译:使用固定化的β-半乳糖苷酶在裁缝制作多孔聚合物上使用固定化β-半乳糖苷酶的可持续合成

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Porous polymer particles containing surface epoxy groups were synthesized for immobilizing beta-galactosidase from Bacillus circulans. Enzyme immobilization was achieved by covalent attachment to a custom made porous polymer and the biocatalyst was characterized in terms of optimal pH and thermal stability, and its catalytic efficiency evaluated for synthesizing N-acetyllactosamine (Gal-beta-(1 -> 4)-GlcNAc) in different solvents and using a 1 : 5 molar ratio of donor (pNP-beta-Gal) : acceptor (GlcNAc). The reaction proceeded with high conversion rates and regioselectivity. Yields up to 60% of beta-(1 -> 4) with biosolvent 3 were found. Reusability assays were performed with the same reaction conditions finding that the immobilized enzyme retains about 85% of its activity after twenty batches with conversion yields above 60%. Furthermore, reaction scale up, biosolvent recovery and recycling are achieved retaining catalytic activity.
机译:合成含有表面环氧基的多孔聚合物颗粒以将β-半乳糖苷酶从芽孢杆菌中加固。 通过与定制的多孔聚合物共价连接来实现酶固定,并且在最佳pH和热稳定性方面表征生物催化剂,并评估了合成N-乙酰萘胺(GAL-BETA-(1-> 4)-GLCNAC的催化效率 )在不同的溶剂和使用1:5的供体(PNP-BETA-GAL):受体(GLCNAc)。 反应以高转化率和区域选择性进行。 发现高达β-(1 - > 4)的β-(1 - > 4)的β-(1-> 4)。 通过相同的反应条件进行可重用性测定,发现固定化酶在20%后20%的转化率后保持约85%的活性。 此外,实现了反应规模,生物溶剂回收率和再循环,以保持催化活性。

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