Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, Jiangsu, China.
Appl Biochem Biotechnol. 2021 Sep;193(9):2742-2758. doi: 10.1007/s12010-021-03561-5. Epub 2021 Apr 7.
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.
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%。