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中国精品科技期刊2020
庞会娜,董红影,肖凤琴,等. 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]. 华体会体育,2022,43(24):197−204. doi: 10.13386/j.issn1002-0306.2021100147.
引用本文: 庞会娜,董红影,肖凤琴,等. 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]. 华体会体育,2022,43(24):197−204. doi: 10.13386/j.issn1002-0306.2021100147.
PANG Huina, DONG Hongying, XIAO Fengqin, et al. 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. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021100147.
Citation: PANG Huina, DONG Hongying, XIAO Fengqin, et al. 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. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021100147.

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

Optimization of Enzymatic Hydrolysis Process of Pueraria Protein by Response Surface Methodology and Its Antioxidant Properties in Vitro

  • 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。

     

    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.

     

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