茶渣硒蛋白的分离纯化及其性质研究
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(1. 安康学院现代农业与生物科技学院,陕西 安康 725000;2. 陕西省富硒食品工程实验室,陕西 安康 725000)

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杨旭(1989—),女,安康学院讲师,硕士。E-mail: yangxuq@hotmail.com

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安康市林业局横向项目(编号:2017AYHX020);安康学院培育项目(编号:2016AYPYZX10);大学生创新创业训练计划项目(编号:2016sxjy029)


Isolation, purification and characterization of selenium-proteinfrom selenium-enriched tea residue
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(1. College of Modern Agriculture and Biotechnology, Ankang University, Ankang, Shaanxi 725000, China;2. Shanxi Engineering Labs of Se-enriched Food, Ankang, Shaanxi 725000, China)

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    摘要:

    通过脱色、沉淀对茶渣硒蛋白提取物进行初步的分离纯化,并测定其硒有机化程度、氨基酸组成、功能特性及抗氧化活性。结果表明,最适脱色剂双氧水的脱色率可达(93.78±0.84)%;在最适沉淀点pH 3.5下制备硒蛋白样品,其中硒有机化程度为79.37%;经初步分离纯化后的硒蛋白提取物含有7种必需氨基酸其中6种含量高于WHO/FAO推荐值;溶解度最高达(52.99±1.59)%,乳化性、乳化稳定性、起泡性和泡沫稳定性分别为(60.16±1.61)%,(96.12±2.55)%,(17.56±1.90)%,(57.45±2.57)%;对DPPH、ABTS、羟基自由基均表现出不同程度的清除能力。

    Abstract:

    The preliminary separation and purification of selenium-protein extracts from selenium-enriched tea residue were carried out by decolorization and precipitation, and the ratio of organic selenium, amino acid composition, functional properties and antioxidant activities were determined. The results indicated that the decolorization rate was (93.78±0.84)% when the optimum decolorizer was hydrogen peroxide. The selenium-protein sample was prepared at pH 3.5, which was the optimal precipitation point. The ratio of organic selenium in sample was 79.37%. Six of the contained seven essential amino acids were higher than the WHO/FAO recommendations. The maximum solubility of selenium-protein sample was only (52.99±159)%, and its emulsibility, emulsifying stability, foamability and foaming stability were (60.16±1.61)%, (96.12±2.55)%, (17.56±1.90)%, (57.45±2.57)%, respectively. The selenium-protein sample also exhibited the different levels of scavenging activities for DPPH, ABTS and hydroxyl radicals.

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杨旭,谢盈.茶渣硒蛋白的分离纯化及其性质研究[J].食品与机械,2018,34(11):146-150.
YANGXu, XIEYing. Isolation, purification and characterization of selenium-proteinfrom selenium-enriched tea residue[J]. Food & Machinery,2018,34(11):146-150.

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  • 收稿日期:2018-07-30
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  • 在线发布日期: 2023-03-17
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