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响应面法优化葛根蛋白酶解工艺及其体外抗氧化特性分析
引用本文:庞会娜,董红影,肖凤琴,张红印,韩荣欣,王海东,严铭铭,邵帅.响应面法优化葛根蛋白酶解工艺及其体外抗氧化特性分析[J].食品工业科技,2022,43(24):197-204.
作者姓名:庞会娜  董红影  肖凤琴  张红印  韩荣欣  王海东  严铭铭  邵帅
作者单位:1.长春中医药大学,吉林长春 1301172.吉林省中药保健食品科技创新中心,吉林长春 130117
基金项目:吉林省科技发展计划项目(20180623041TC);吉林省教育厅科学技术研究项目(JJKH20210970KJ);长春中医药大学2021年大学生创新创业训练计划项目。
摘    要:目的:优化葛根蛋白酶解工艺并研究其抗氧化特性。方法:以DPPH自由基清除能力、水解度(DH)为评价指标,结合SDS-PAGE电泳结果,筛选最佳水解蛋白酶;在单因素实验基础上,利用Box-Behnken响应面法优化葛根蛋白酶解工艺,并对最佳葛根蛋白酶解物进行抗氧化特性研究。结果:葛根蛋白酶解最佳工艺条件为:酶解温度55 ℃、pH9、酶底比2%,该条件下制备的葛根蛋白酶解物清除DPPH自由基、ABTS+自由基、OH自由基的IC50值分别为0.15、0.38、1.41 mg/mL,还原能力为0.553。结论:该条件下制备的葛根蛋白酶解物具有较好的抗氧化特性。

关 键 词:葛根蛋白    Box-Behnken响应面法    酶解工艺    抗氧化特性
收稿时间:2021-10-18

Optimization of Enzymatic Hydrolysis Process of Pueraria Protein by Response Surface Methodology and Its Antioxidant Properties in Vitro
PANG Huina,DONG Hongying,XIAO Fengqin,ZHANG Hongyin,HAN Rongxin,WANG Haidong,YAN Mingming,SHAO Shuai.Optimization of Enzymatic Hydrolysis Process of Pueraria Protein by Response Surface Methodology and Its Antioxidant Properties in Vitro[J].Science and Technology of Food Industry,2022,43(24):197-204.
Authors:PANG Huina  DONG Hongying  XIAO Fengqin  ZHANG Hongyin  HAN Rongxin  WANG Haidong  YAN Mingming  SHAO Shuai
Affiliation:1.Changchun University of Traditional Chinese Medicine, Changchun 130117, China2.Jilin Province Traditional Chinese Medicine Health Food Science and Technology Innovation Center, Changchun 130117, China
Abstract:Objective: To optimize the enzymatic hydrolysis process of Pueraria protein and study its antioxidant properties. Methods: DPPH radical scavenging ability and DH were used as the index to screen the best hydrolytic protease. Base on the single factor experiments, the Box-Behnken response surface design was used to optimize the enzymatic hydrolysis process of Pueraria protein, and the antioxidant properties of the optimum hydrolysate in vitro was analyzed. Results: The optimal hydrolysis conditions for alkaline protease were as follows: Temperature 55 ℃, pH9 and enzyme substrate ratio 2%. Under these conditions, the IC50 of DPPH·, ABTS+·, and ·OH radicals were 0.15, 0.38, 1.41 mg/mL and a reduction capacity of 0.553. Conclusion: Under these conditions, Pueraria protein hydrolysate had remarkable antioxidant properties.
Keywords:
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