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中国精品科技期刊2020
翟娅菲,王宇浩,汤国新,等. 介质阻挡放电等离子体辅助糖基化对β-乳球蛋白抗氧化活性的影响及构效关系研究J. 食品工业科技,2025,46(19):75−84. doi: 10.13386/j.issn1002-0306.2024090294.
引用本文: 翟娅菲,王宇浩,汤国新,等. 介质阻挡放电等离子体辅助糖基化对β-乳球蛋白抗氧化活性的影响及构效关系研究J. 食品工业科技,2025,46(19):75−84. doi: 10.13386/j.issn1002-0306.2024090294.
ZHAI Yafei, WANG Yuhao, TANG Guoxin, et al. Effect of Dielectric Barrier Discharge Plasma-assisted Glycation on the Antioxidant Activity of β-Lactoglobulin and Its Structure-Activity RelationshipJ. Science and Technology of Food Industry, 2025, 46(19): 75−84. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090294.
Citation: ZHAI Yafei, WANG Yuhao, TANG Guoxin, et al. Effect of Dielectric Barrier Discharge Plasma-assisted Glycation on the Antioxidant Activity of β-Lactoglobulin and Its Structure-Activity RelationshipJ. Science and Technology of Food Industry, 2025, 46(19): 75−84. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090294.

介质阻挡放电等离子体辅助糖基化对β-乳球蛋白抗氧化活性的影响及构效关系研究

Effect of Dielectric Barrier Discharge Plasma-assisted Glycation on the Antioxidant Activity of β-Lactoglobulin and Its Structure-Activity Relationship

  • 摘要: 本文研究了介质阻挡放电(dielectric barrier discharge,DBD)等离子体辅助糖基化处理对β-乳球蛋白(β-lactoglobulin,β-LG)及其水解产物抗氧化能力的影响;通过测定其内源荧光、紫外吸收光谱、巯基含量、表面疏水性、平均粒径以及二级结构等,分析β-LG结构变化与抗氧化活性之间的关系。结果表明,经DBD等离子体辅助糖基化处理5 min后,糖基化β-LG的DPPH·清除能力达到129.8 μmol trolox equivalent(TE)/g,铁还原能力达到75.1 μmol Fe2+/g;经水解后,糖基化β-LG的DPPH·清除能力和铁还原力分别进一步提高到193.5 μmol TE/g和95.5 μmol Fe2+/g。DBD等离子体辅助糖基化处理5 min时β-LG的内源荧光和紫外吸收强度降低,巯基含量和表面疏水性显著降低(P<0.05),平均粒径增大,α-螺旋相对含量降低而β-折叠相对含量增多。综上,DBD等离子体辅助糖基化处理可以通过改变β-LG蛋白的结构,显著增强其抗氧化活性。

     

    Abstract: This study examined the antioxidant activity of β-lactoglobulin (β-LG) and its hydrolysate after the treatment of dielectric barrier discharge (DBD) plasma-assisted glycation. The relationship between the structure and antioxidant activity of β-LG was analyzed by measuring the internal fluorescence, ultraviolet absorption spectrum, sulfhydryl content, surface hydrophobicity, average particle size, and secondary structure of treated β-LG. The results showed that after DBD plasma-assisted glycation for 5 min, the DPPH radical scavenging capacity of β-LG reached 129.8 μmol trolox equivalent (TE)/g, and the iron reduction capacity was increased to 75.1 μmol Fe2+/g. The hydrolysate exhibited further enhancement in both DPPH radical scavenging capacity and iron reduction capacity, reaching 193.5 μmol TE/g and 95.5 μmol Fe2+/g, respectively. After DBD plasma-assisted glycation for 5 min, the endogenous fluorescence, ultraviolet absorption intensity, the relative content of α-helix, sulfhydryl group content and surface hydrophobicity (P<0.05) of β-LG significantly decreased, whereas the average particle size and the relative content of β-fold increased. In conclusion, DBD plasma-assisted glycation can effectively improve the antioxidant activity of β-LG by changing its structure.

     

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