食品科学 ›› 2026, Vol. 47 ›› Issue (3): 120-130.doi: 10.7506/spkx1002-6630-20250815-117

• 生物工程 • 上一篇    下一篇

米糠蛋白抗氧化肽的分离鉴定及其构效关系

董晓兵,刘晓兰,李冠龙,郑成鑫,汲广习,郑喜群   

  1. (1.齐齐哈尔大学食品与生物工程学院,黑龙江 齐齐哈尔 161006;2.黑龙江省玉米深加工理论与技术重点实验室,黑龙江 齐齐哈尔 161006;3.齐齐哈尔龙江阜丰生物科技有限公司,黑龙江 齐齐哈尔 161006;4.黑龙江八一农垦大学食品学院,黑龙江 大庆 163319)
  • 出版日期:2026-02-01 发布日期:2026-03-16
  • 基金资助:
    “十四五”国家重点研发计划重点专项(2021YFD2100902;2021YFD2100904); 黑龙江省“双一流”建设学科协同创新成果建设项目(LJGXCG2023-104); 中央引导地方科技发展专项(ZY23QY06);新时代龙江优秀博士论文资助项目(LJYXL-2023023); 黑龙江省省属本科高校优秀青年教师基础研究支持计划项目(YQJH2024271)

Isolation, Identification, and Structure-Activity Relationship of Antioxidant Peptides from Rice Bran Protein

DONG Xiaobing, LIU Xiaolan, LI Guanlong, ZHENG Chengxin, JI Guangxi, ZHENG Xiqun   

  1. (1. College of Food and Bioengineering, Qiqihar University, Qiqihar 161006, China; 2. Heilongjiang Key Laboratory of Corn Deep Processing Theory and Technology, Qiqihar 161006, China; 3. Qiqihar Longjiang Fufeng Biotechnology Co. Ltd., Qiqihar 161006, China; 4. College of Food Science, Heilongjiang Bayi Agricultural University, Daqing 163319, China)
  • Online:2026-02-01 Published:2026-03-16

摘要: 从米糠蛋白抗氧化肽混合物中分离鉴定获得新的抗氧化活性单肽,并揭示其潜在抗氧化机制。以课题组前期制备的米糠蛋白抗氧化肽混合物为研究对象,以1,1-二苯基-2-三硝基苯肼、2,2’-联氮-二(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除能力为靶向跟踪指标,顺次采用超滤、凝胶色谱、离子交换色谱、反相-高效液相色谱技术手段分离纯化。采用液相色谱-串联质谱联用技术鉴定活性组分中的多肽序列。通过计算机辅助筛选结合分子对接技术揭示鉴定肽的潜在抗氧化机制。结果表明,从反相高效液相色谱分离后获得的高抗氧化活性组分R-2中鉴定出183 条肽段,最终筛选出5 条具有抗氧化潜力的米糠蛋白活性肽,分别为WCY、YFC、HWC、AHWC、QGYY。其中WCY、YFC、HWC、AHWC表现出良好的体外抗氧化活性。分子对接结果表明这4 条肽段与Kelch样环氧氯丙烷相关蛋白-1(Kelch-like ECH-associated protein-1,Keap1)的结合能均低于-7 kcal/mol,其相互作用力主要为氢键和疏水相互作用,表明其可通过抑制Keap1/核因子E2相关因子2信号通路起到抗氧化作用。综上,本研究筛选出的米糠蛋白抗氧化肽具有作为天然抗氧化剂的潜力,可在为米糠蛋白活性肽在食品与医药领域的开发应用提供理论基础。

关键词: 米糠蛋白;抗氧化肽;分子对接;构效关系;功能活性

Abstract: This study isolated and identified novel antioxidant peptides from an enzymatic hydrolysate of rice bran protein and elucidated their potential mechanisms of action. Based on the scavenging capacity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) cation radical, bioactivity-guided fractionation was employed to obtain the antioxidant peptides through sequential ultrafiltration, gel filtration chromatography, ion-exchange chromatography, and reversed-phase high-performance liquid chromatography (RP-HPLC). The peptide sequences were identified using liquid chromatography-mass spectrometry (LC-MS). Computer-aided screening combined with molecular docking technology was utilized to reveal the antioxidant mechanisms of the identified peptides. The results showed that 183 peptide segments were identified from fraction R-2 with high antioxidant activity, obtained after RP-HPLC separation. Finally, five antioxidant peptides were selected: WCY, YFC, HWC, AHWC, and QGYY. Among these, WCY, YFC, HWC, and AHWC exhibited potent in vitro antioxidant activity. Molecular docking results indicated that the binding energies of these four peptides to Kelch-like ECH-associated protein-1 (Keap1) were all below −7 kcal/mol, with hydrogen bonding and hydrophobic interactions as the primary intermolecular forces. This suggests their antioxidant mechanism might be through inhibiting the Keap1/nuclear factor E2-related factor 2 (Nrf2) signaling pathway. In conclusion, the antioxidant peptides derived from rice bran protein possess potential as natural antioxidants. This study provides a theoretical foundation for the development and application of bioactive peptides from rice bran protein in the food and medicinal industries.

Key words: rice bran protein; antioxidant peptides; molecular docking; structure-activity relationship; functional activity

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