Optimization of enzymatic synthesis of ethyl hexanoate in a solvent free system using response surface methodology (RSM)

Sarita D. Gawas, N. Lokanath, V. Rathod
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引用次数: 15

Abstract

Abstract The present paper demonstrates application of biocatalysis to the synthesis of ethyl hexanoate, i.e. pineapple flavour ester, in a solvent free system. In order to evaluate the effect of various process parameters on reaction conversion, response surface methodology (RSM) complemented by central composite design (CCD) was employed. A maximum conversion of 88.57% was obtained while changing one factor at a time, at optimum conditions of temperature (50 °C), enzyme dose (2%), molar ratio acid to alcohol (1:3), speed of agitation 250 rpm and reaction time of 120 min. Based on this RSM study, the optimum predicted conditions were: 1:3.39 alcohol to acid ratio, 2.35% enzyme loading and 48.83 oC, for a predicted conversion of 90.99%. The activation energy for the enzymatic esterification was determined and calculated to be 25.76 kJ/mol. The positive values of Gibbs-free energy (ΔG), enthalpy (ΔH) and negative value of entropy (ΔS) revealed that the esterification reaction was non-spontaneous and an endothermic reaction. The reaction seems to follow bi-substrate Ping Pong Bi Bi mechanism with inhibition by both substrates.
响应面法优化无溶剂体系中酶促合成己酸乙酯的工艺
摘要:本文介绍了生物催化在无溶剂体系中合成己酸乙酯即菠萝风味酯的应用。为了评价不同工艺参数对反应转化的影响,采用响应面法(RSM)和中心复合设计(CCD)相结合的方法。在温度(50℃)、酶量(2%)、酸醇摩尔比(1:3)、搅拌速度250 rpm、反应时间120 min的条件下,每次改变1个因素,最大转化率为88.57%。基于RSM研究,最佳预测条件为:醇酸比1:3.39、酶量2.35%、温度48.83℃,预测转化率为90.99%。测定并计算了酶促酯化反应的活化能为25.76 kJ/mol。吉布斯自由能(ΔG)为正值,焓(ΔH)为负值,熵(ΔS)为负值,表明酯化反应是非自发反应,为吸热反应。该反应似乎遵循双底物乒乓乒乓机制,两种底物均有抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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