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树脂萃取共固定化醇脱氢酶和葡萄糖脱氢酶连续生产手性二芳基醇。

Co-immobilized Alcohol Dehydrogenase and Glucose Dehydrogenase with Resin Extraction for Continuous Production of Chiral Diaryl Alcohol.

机构信息

Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, Jiangsu, China.

出版信息

Appl Biochem Biotechnol. 2021 Sep;193(9):2742-2758. doi: 10.1007/s12010-021-03561-5. Epub 2021 Apr 7.

Abstract

Ni-functionalized porous ceramic/agarose composite beads (Ni-NTA Cerose) can be used as carrier materials to immobilize enzymes harboring a metal affinity tag. Here, a 6×His-tag fusion alcohol dehydrogenase Mu-S5 and glucose dehydrogenase from Bacillus megaterium (BmGDH) were co-immobilized on Ni-NTA Cerose to construct a packed bed reactor (PBR) for the continuous synthesis of the chiral intermediate (S)-(4-chlorophenyl)-(pyridin-2-yl) methanol ((S)-CPMA) NADPH recycling, and in situ product adsorption was achieved simultaneously by assembling a D101 macroporous resin column after the PBR. Using an optimum enzyme activity ratio of 2:1 (Mu-S5: BmGDH) and hydroxypropyl-β-cyclodextrin as co-solvent, a space-time yield of 1560 g/(L·d) could be achieved in the first three days at a flow rate of 5 mL/min and substrate concentration of 10 mM. With simplified selective adsorption and extraction procedures, (S)-CPMA was obtained in 84% isolated yield.

摘要

Ni-功能化多孔陶瓷/琼脂糖复合珠(Ni-NTA Cerose)可用作固定化酶的载体材料,这些酶带有金属亲和标签。在此,6×His 标签融合的 Mu-S5 醇脱氢酶和来自巨大芽孢杆菌的葡萄糖脱氢酶(BmGDH)被共固定化在 Ni-NTA Cerose 上,构建填充床反应器(PBR)以连续合成手性中间体(S)-(4-氯苯基)-(吡啶-2-基)甲醇((S)-CPMA),同时通过在 PBR 后组装 D101 大孔树脂柱实现原位产物吸附。使用最佳的酶活比 2:1(Mu-S5:BmGDH)和羟丙基-β-环糊精作为共溶剂,在流速为 5 mL/min 和底物浓度为 10 mM 的情况下,在前三天可以达到 1560 g/(L·d)的时空产率。通过简化的选择性吸附和提取程序,(S)-CPMA 的分离收率达到 84%。

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