首页 | 官方网站   微博 | 高级检索  
     

响应面优化碱性蛋白酶法提取藜麦淀粉工艺
引用本文:孔露,孔茂竹,余佳熹,吕远平.响应面优化碱性蛋白酶法提取藜麦淀粉工艺[J].食品研究与开发,2020,41(2):100-106.
作者姓名:孔露  孔茂竹  余佳熹  吕远平
作者单位:四川大学轻纺与食品学院,四川成都610065
摘    要:采用青海高原藜麦作为原料,碱性蛋白酶作为酶解剂,研究藜麦淀粉的提取工艺。在单因素试验的基础上,以藜麦淀粉提取率作为评价指标,利用响应面法优化提取藜麦淀粉的工艺条件。结果表明:最佳工艺条件为酶添加量为0.598%,pH值为9.09,酶解时间为122 min,酶解温度为40.60℃,在此条件下藜麦淀粉提取率的预测值为89.26%。以最佳工艺条件对藜麦淀粉进行提取,验证试验中藜麦淀粉的提取率为(89.09±0.15)%,蛋白质残留率为(1.02±0.46)%。藜麦淀粉提取率的预测值与实测值的相对误差为0.19%,与所建立的模型预测值接近,表明此模型优化藜麦淀粉提取工艺具有可行性与科学性。

关 键 词:藜麦  淀粉  提取  碱性蛋白酶  响应面法
收稿时间:2019/1/31 0:00:00

Optimization of Alkaline Protease Extraction of Chenopodium quinoa Starch by Response Surface Methodology
Affiliation:(College of Light Industry,Textile and Food Engineering,Sichuan University,Chengdu 610065,Sichuan,China)
Abstract:Using Qinghai plateau Chenopodium quinoa as raw material and alkaline protease as enzymatic agent to study the extraction process of Chenopodium quinoa starch.On the basis of single factor experiment,the extraction rate of Chenopodium quinoa starch was used as the evaluation index,and the response surface method was used to optimize the process conditions for extracting Chenopodium quinoa starch.The results indicated that the optimal conditions were enzyme dose added at 0.598%,under the condition of pH 9.09,hydrolysis for 122 min and enzymatic hydrolysis temperature at 40.60℃.Under this condition,the predicted extraction rate of Chenopodium quinoa starch was 89.26%.Extraction of Chenopodium quinoa starch was under optimal processing conditions.The starch extraction rate was(89.09±0.15)%,and the protein residual rate was (1.02±0.46) %. The relative error between the predicted value and the measured value was 0.19 %, which was close to the predicted value of the established model. It indicated that this model was feasible and scientific to optimize the extraction technology of Chenopodium quinoa starch.
Keywords:Chenopodium quinoa  starch  extraction  alkaline protease  response surface methodology
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《食品研究与开发》浏览原始摘要信息
点击此处可从《食品研究与开发》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号