麦芽提取物、α-淀粉酶和葡萄糖淀粉酶水解木薯淀粉的工艺优化

F. Aderibigbe, A. Anozie, L. Adejumo, R. Owolabi
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引用次数: 2

摘要

以麦芽提取物、α -淀粉酶和葡萄糖淀粉酶为主要原料,研究了木薯淀粉的水解。研究并优化了温度、pH和时间对木薯粉水解成葡萄糖浆的影响。本研究采用了三个层次的过程变量。三个层次的工艺变量分别是:温度(60、67和74℃)、时间(1.5、2.0和2.5 h)和pH(4.5、5和5.5)。利用实验数据建立了多项式回归模型。结果表明,还原糖的产量受麦芽提取物、α淀粉酶和木薯淀粉葡萄糖淀粉酶水解的变量变化的强烈影响。模型的拟合用决定系数R2表示,R2为0.987,表明该模型可以解释98.7%的响应变异。该值还表明,只有1.3%的总变化不能被模型解释。这表明,方程(2)是一个合适的模型来描述有关还原糖生产的实验响应。采用f检验进行方差分析(p≤0.05),验证模型的统计学意义。麦芽提取物、α -淀粉酶和葡萄糖淀粉酶水解的最佳温度、时间和pH为74℃;最佳条件下的最大还原糖产量为268 g/l,转化率为76.57%或76.57葡萄糖当量(DE)。
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Optimization of Cassava Starch Hydrolysis by Malt Extract, α-Amylase and Glucoamylase
Cassava starch hydrolysis was investigated in this study using malt extract, alpha amylase and glucoamylase. The effects of process variables, namely: temperature, pH and time were studied and optimized for hydrolysis of cassava (Manihot esculenta) flour to glucose syrup. Three levels of process variables were used for the study. The three levels of process variables were: temperature (60, 67 and 74 oC), time (1.5, 2.0 and 2.5 h) and pH (4.5, 5 and 5.5). A polynomial regression model was developed using the experimental data. The results showed that production of reducing sugar was strongly affected by the variation of variables on malt extract, alpha amylase and glucoamylase hydrolysis of cassava starch. The fit of the model was expressed by the coefficient of determination R2 which was found to be 0.987 indicating that 98.7 % of the variability in the response can be explained by the model. The value also indicates that only 1.3% of the total variation is not explained by the model. This shows that equation (2) is a suitable model to describe the response of the experiment pertaining to reducing sugar production. The statistical significance of the model was validated by F-test for analysis of variance (p ≤ 0.05). For malt extract, alpha amylase and glucoamylase hydrolysis, the optimum value of temperature, time and pH were found to be 74 oC; pH 5.5 and time 1.5 h. The maximum reducing sugar production at optimum condition was 268 g/l representing 76.57 % conversion or 76.57 dextrose equivalent (DE)
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