五倍子多糖的纤维素酶提取工艺优化及其抗氧化活性分析

    Optimization of Cellulase Extraction Process of Polysaccharide from Galla chinensis and Determination of Its Antioxidant Activity

    • 摘要: 为优化纤维素酶提取五倍子多糖工艺,并研究其体外抗氧化活性。在单因素试验结果基础上,以酶添加量、酶解温度、液料比及酶解时间为自变量,多糖得率为响应值,利用Box-Behnken响应面法进行工艺优化,进一步以DPPH自由基和羟自由基清除率大小为指标考察五倍子多糖的体外抗氧化活性。结果表明:纤维素酶提取五倍子多糖最佳工艺为酶添加量1.3%、酶解温度49℃、液料比13∶1、酶解时间1.6 h、酶解pH4.8,此条件下五倍子多糖得率为4.27%,与回归模型的理论预测值4.32%误差小于5%。五倍子多糖对DPPH自由基和羟自由基的半数抑制浓度分别为0.785、1.173 mg·mL−1,表明其对两种自由基具有较强的清除作用。纤维素酶法可显著提高五倍子多糖得率,工艺简便可行,获得的五倍子多糖具有体外抗氧化活性。

       

      Abstract: The study aimed to optimize the cellulase extraction process of polysaccharide from Galla chinensis and study its antioxidant activity in vitro. On the basis of single factor test results, Box-Behnken response surface methodology was used to optimize the extraction process of polysaccharide from Galla chinensis with the amount of enzyme, enzymolysis temperature, liquid-to-material ratio and enzymolysis time as independent variables, and the yield of polysaccharide as response value. DPPH radical and hydroxyl radical scavenging rates were used to investigate the antioxidant activities of polysaccharides from Galla chinensis in vitro. The results showed that the optimal extraction conditions of polysaccharide from Galla chinensis by cellulase were as follows: enzyme dosage was 1.3%, enzymolysis temperature was 49℃, liquid-to-material ratio was 13∶1, enzymolysis time was 1.6 h and enzymolysis pH was 4.8. Under these conditions, the yield of polysaccharide from Galla chinensis was 4.27%, and the theoretical prediction value of regression model was 4.32%, and the error between the two conditions was less than 5%. Polysaccharide from Galla chinensis had strong scavenging effects on DPPH free radical and hydroxyl free radical, with median inhibitory concentrations of 0.785 mg·mL−1, 1.173 mg·mL−1, respectively. Cellulase enzymatic method can significantly improve the yield of polysaccharide from Galla chinensis, the process is simple and feasible, and the polysaccharide obtained from Galla chinensis has antioxidant activity in vitro.

       

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