Enzymatic Enantioselective Hydrolysis of 2‑(3-Chlorophenyl) Propionic Acid Ester Enhanced by PEG: Experiment and Optimization
Enzymatic Enantioselective Hydrolysis of 2‑(3-Chlorophenyl) Propionic Acid Ester Enhanced by PEG: Experiment and Optimization
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PEG 增强的 2-(3-氯苯基) 丙酸酯酶促对映选择性水解:实验与优化
DOI:
10.1021/acs.iecr.8b02377
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发表时间:
2018
影响因子:
4.2
通讯作者:
唐课文
中科院分区:
文献类型:
--
作者:
张盼良;成晴;许卫风;唐课文
Chiral resolution of 2-(3-chlorophenyl) propionic acid (CPA) via the hydrolysis of CPA ester catalyzed by lipase PS fromPseudomonas cepaciais reported. With polyethylene glycol (PEG 400) as a cosolvent, the substrate conversion is increased by 88% with high enantioselectivity. Important factors including lipase type, substrate structure, cosolvent, temperature, pH, enzyme loading, PEG 400 and substrate concentrations, and reaction time were investigated, and the optimal conditions including 15 mg mL–1lipase PS, 20 mmol L–1substrate, 30% (m/m) PEG 400, reaction for 36 h at 70 °C and pH 6.5 were obtained, where the enantiomeric excess and overall conversion rate could reach up to 99.02% and 42.09%, respectively. An uncompetitive inhibition kinetic model was applied to simulate the reaction process, and the model predictions are in good agreement with the experimental data, which is important for a deep understanding of the reaction mechanism, and then for process design and operation.