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中国精品科技期刊2020
酶法辅助提取红松种壳多酚的工艺优化研究[J]. 华体会体育, 2013, (04): 184-188. DOI: 10.13386/j.issn1002-0306.2013.04.087
引用本文: 酶法辅助提取红松种壳多酚的工艺优化研究[J]. 华体会体育, 2013, (04): 184-188. DOI: 10.13386/j.issn1002-0306.2013.04.087
Enzymatic assisted extraction of polyphenolics from red pine hull[J]. Science and Technology of Food Industry, 2013, (04): 184-188. DOI: 10.13386/j.issn1002-0306.2013.04.087
Citation: Enzymatic assisted extraction of polyphenolics from red pine hull[J]. Science and Technology of Food Industry, 2013, (04): 184-188. DOI: 10.13386/j.issn1002-0306.2013.04.087

酶法辅助提取红松种壳多酚的工艺优化研究

Enzymatic assisted extraction of polyphenolics from red pine hull

  • 摘要: 利用在乙醇提取红松种壳提取多酚物质工艺中加入纤维素酶酶解工艺,以提高多酚得率。通过单因素实验,研究了乙醇浓度、酶解时间、料液比、酶解温度、加酶量、pH对红松种壳中提取多酚得率的影响。并在单因素实验基础上,设计六因素五水平的Small Composite:Hartley Method中心组合实验及响应面法分析对红松种壳中多酚的提取工艺进行优化,建立了二次多项式回归方程的预测模型,结果表明,提取红松种壳多酚的最佳工艺为:乙醇浓度61%、酶解时间2h、液料比36∶1、酶解温度62℃、加酶量106U/g、pH4.6。在此工艺条件下,红松壳多酚得率可达8.93mg/g。在乙醇提取红松壳多酚工艺中,采用纤维素酶预先进行酶解可以增加多酚得率,增加量为0.97mg/g。 

     

    Abstract: In the present study, the extraction process, based on ethanol extraction of polyphenolics, was modified by adding cellulase in order to increase the extraction rate of polyphenolics from red pine hulls.Ethanol concentration, enzymatic hydrolysis time, materials to water rate, enzymatic hydrolysis temperature, enzyme additive amount, and pH were chosen as six factors, and polyphenolic extraction rate was selected as the response factor.The optimization of polyphenolics extraction rate was performed by employing Small Composite (Hartley Method) and Response Surface Methodology design.The polynomial regression equation was well established.The optimized parameters were as follows:ethanol concentration 61 %, enzymatic hydrolysis time 2h, water to materials rate 36:1, enzymatic hydrolysis temperature 62℃, enzyme additive amount 106U/g, and pH4.6.The extraction rate was 8.93mg/g under optimized conditions.Compared with the nonenzymatic ethanol extraction process, the extraction rate was increased by 0.97mg/g with the assistance of cellulase.

     

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