芬顿氧化体系处理对牦牛乳蛋白结构的影响及蛋白质组学分析OA
Effects of Reactive Oxygen Species-Induced Oxidation on Yak Milk Protein Structure and Proteomic Analysis
为实现对牦牛乳蛋白结构的可控性修饰,精准调控其营养功能,从而改善牦牛乳加工过程中营养品质下降的问题,本研究以不同浓度H2O2(0,0.5,1,3,5,10 mmol·L⁻¹)氧化的牦牛乳蛋白为研究对象,进行羰基、游离巯基、总巯基等氧化指标及蛋白质组学测定,明确氧化处理过程中牦牛乳蛋白的氧化规律及蛋白功能的变化.结果发现,随着H2O2浓度的增加,羰基含量增加,游离巯基、总巯基、二硫键含量下降,溶解度先增加后降低,表面疏水性增加,粒径增大,Zeta电位绝对值增加,二聚酪氨酸含量降低.蛋白质组学分析鉴定到1 351种蛋白,其中5 mmol·L⁻¹ H₂O₂组蛋白功能差异最显著,有183种蛋白下调,276种蛋白上调;1 mmol·L⁻¹ H₂O₂组蛋白功能差异最小,有237种蛋白下调,292种蛋白上调.与对照组相比,0.5 mmol·L⁻¹ H2O2组上调8种通路,下调17种通路;1 mmol·L⁻¹ H2O2组上调22种通路,下调10种通路;3 mmol·L⁻¹ H2O2组上调11种通路,下调16种通路;5 mmol·L⁻¹ H2O2组上调10种通路,下调9种通路;10 mmol·L⁻¹ H2O2组上调10种通路,下调14种通路.本研究为牦牛乳的绿色加工及相关产品的质量控制提供理论依据.
To achieve the controllable structural modification of yak milk protein and precisely regulate its nutritional functions,thereby mitigating the decline in nutritional quality during yak milk processing,this study used yak milk protein oxidized by different concentrations of H2O2(0,0.5,1,3,5,10 mmol·L⁻¹)as the research object.Oxidation indicators,including carbonyl content,free sulfhydryl groups,total sulfhydryl groups,and proteomic analysis,were determined to clarify the oxidation rules and functional changes of yak milk protein during oxidative treatment.The results showed that with increasing H2O2 concentration,carbonyl content increased,while free sulfhydryl groups,total sulfhydryl groups,and disulfide bonds decreased.Solubility first increased and then decreased,surface hydrophobicity increased,particle size,and the absolute value of Zeta potential increased,and dityrosine content decreased.A total of 1351 proteins were identified by proteomic analysis.The 5 mmol·L⁻¹ H₂O₂treatment group showed the most significant alterations in protein function,with 183 proteins downregulated and 276 proteins upregulated.In comparison,the 1 mmol·L⁻¹ H₂O₂ group displayed the least distinct changes in protein function,where 237 proteins were downregulated and 292 proteins upregulated.Compared with the control group,the 0.5 mmol·L-¹ H2O2 group had 8 upregulated pathways and 17 downregulated pathways;the 1 mmol·L-¹ H2O2 group had 22 upregulated pathways and 10 downregulated pathways;the 3 mmol·L-¹ H2O2 group had 11 upregulated pathways and 16 downregulated pathways;the 5 mmol·L-¹ H2O2 group had 10 upregulated pathways and 9 downregulated pathways;and the 10 mmol·L-¹ H2O2 group had 10 upregulated pathways and 14 downregulated pathways.This study provides a theoretical basis for the green processing of yak milk and the quality control of related products.
刘振东;张仁艳;杨杰;舒森彪;赵小龙;李梁
西藏农牧大学 食品科学学院,西藏 林芝 860000||西藏自治区特色农畜产品精深加工与高值化利用重点实验室,西藏 林芝 860000西藏农牧大学 食品科学学院,西藏 林芝 860000||西藏自治区特色农畜产品精深加工与高值化利用重点实验室,西藏 林芝 860000西藏农牧大学 食品科学学院,西藏 林芝 860000||西藏自治区特色农畜产品精深加工与高值化利用重点实验室,西藏 林芝 860000西藏农牧大学 食品科学学院,西藏 林芝 860000||西藏自治区特色农畜产品精深加工与高值化利用重点实验室,西藏 林芝 860000昌都市畜牧总站,西藏 昌都 854000西藏农牧大学 食品科学学院,西藏 林芝 860000||西藏自治区特色农畜产品精深加工与高值化利用重点实验室,西藏 林芝 860000
轻工纺织
牦牛乳蛋白氧化修饰氧化规律蛋白质组学
Yak milk proteinoxidative modificationoxidation patternproteomics
《高原农业》 2026 (2)
137-155,19
中国农业大学支援西藏农牧学院专项资金项目(2024CT083)国家自然科学基金项目(32160561).
评论