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Optimization of ultrasound-accelerated synthesis of enzymatic caffeic acid phenethyl ester by response surface methodology

机译:响应面法优化超声加速酶法咖啡酸苯乙酯的合成

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摘要

The ultrasound-accelerated enzymatic synthesis of caffeic acid phenethyl ester (CAPE) from caffeic acid and phenethyl alcohol was investigated in this study. A commercial immobilized lipase from Candida antarctica, called Novozym? 435, was used as the catalyst. A 5-level-4-factor central-composite rotatable design (CCRD) and response surface methodology (RSM) were employed to evaluate the effects of reaction time, substrate molar ratio, enzyme amount, and ultrasonic power on percent molar conversion of CAPE. The results indicated that reaction time, substrate molar ratio, and ultrasonic power significantly affected percent molar conversion, whereas enzyme amount did not. A model for synthesis of CAPE was established. Based on ridge max analysis, the optimum condition for CAPE synthesis was predicted to be reaction time 9.6h, substrate molar ratio 1:71, enzyme amount 2938 PLU, and ultrasonic power 2W/cm~2 with the molar conversion value of 96.03±5.18%. An experiment was performed under this optimal condition and molar conversion of 93.08±0.42% was obtained.
机译:本研究研究了由咖啡酸和苯乙醇超声加速酶法合成咖啡酸苯乙酯(CAPE)的方法。来自南极假丝酵母的商业化固定化脂肪酶,称为Novozym? 435用作催化剂。采用五级四因子中心复合材料可旋转设计(CCRD)和响应表面方法(RSM)来评估反应时间,底物摩尔比,酶量和超声功率对CAPE摩尔转化率的影响。结果表明,反应时间,底物摩尔比和超声功率显着影响摩尔转化率,而酶的量则没有。建立了CAPE的合成模型。基于岭峰分析,预测CAPE合成的最佳条件为反应时间9.6h,底物摩尔比1:71,酶量2938 PLU,超声功率2W / cm〜2,摩尔转化率96.03±5.18。 %。在该最佳条件下进行实验,得到93.08±0.42%的摩尔转化率。

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