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L-赖氨酸与D-核糖的模式美拉德反应及其产物抗氧化性能研究 被引量:30

Study on Model Maillard Reaction of L-lysine and D-ribose and Antioxidant Activity of Its Products
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摘要 研究L-赖氨酸与D-核糖的模式美拉德反应(L-赖氨酸的氨基与D-核糖的羰基的物质量之比分别为1:1、1:2和2:1),考察了三个体系反应过程中产物pH值、吸光度的变化,并以金属螯合能力、超氧阴离子自由基(O-2·)清除能力、二苯代苦味酰自由基(DPPH·)清除能力以及还原能力为指标,评价了美拉德反应产物(MRPs)的抗氧化效果。结果表明:美拉德反应是个酸度和褐变不断增强的反应;MRPs的最大吸收波长在460nm左右;达到相同褐变程度,即吸光度(A)为2.2时,1:2的体系最快,其次是1:1的体系,2:1的体系相对最慢。MRPs有较好的金属螯合能力,可有效清除O-2·和DPPH·自由基,但反应终产物几乎没有还原能力。 The Maillard reaction products(MRPs) were prepared using L-lysine and D-ribose(the molar ratio of - NH2 and - C=O is 1:1, 1:2, 2:1, respectively) by model Maillard reaction. The pH value and absorbance of the Maillard reaction products (MRPs) were determined. In this research, the antioxidative activities of MRPs, including iron-chelation activity, scavenging effect on superoxide anion radical and DPPH · radical, and reducing power were studied. The results showed that browning and acidity increased with the heating time; the wavelength of maximal absorbance was about 460 nm; While reaching the same browing degree, namely absorbance 2.2, their reaction speeds were shown as follows: 1:2〉 1:1 〉2:1. Three kinds of MRPs with different proportions of amido and carbonyl exhibited good iron-chelation activities and scavenging activities against superoxide anion radical and DPPH · radical, but they almost did not have reducing powers.
出处 《食品科学》 EI CAS CSCD 北大核心 2008年第5期112-115,共4页 Food Science
基金 上海市重点学科建设项目专项基金(T1102) 上海市教育委员会科研项目(07zz134)
关键词 美拉德反应 金属螯合 O-2· DPPH· 还原能力 抗氧化能力 Maillard reaction iron-chelation superoxide anion 1,1-diphenyl-2-picrylhydrazyl(DPPH·) reduc-ing power antioxidant activity
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  • 1赖祥林,唐冰.葛根的实验研究与临床应用新进展[J].中国中药杂志,1989,14(5):52-55. 被引量:72
  • 2郭建平,孙其荣,周全,赵彤英,高玉田.葛根总黄酮不同提取工艺的探讨[J].中草药,1995,26(10):522-522. 被引量:99
  • 3郑学钦,胡春.用化学发光法检测芦丁等物质清除超氧阴离子自由基的作用[J].中国药学杂志,1997,32(3):140-142. 被引量:31
  • 4方起程 林茂 等.葛根黄酮的研究[J].中华医学杂志,1974,54(5):271-271.
  • 5Nicoli M C, Ancse M, et al. Loss and /or formation of antioxidants during food processing and storage [R]. Cancer Lett,1997.
  • 6Branen A L. Toicology and biochemistry of butylated hydroxyanisole and butylated hydroxytoluene [J]. J Am Oil Chem Soc, 1975, 52:59.
  • 7Lingnert H, Hall G. Formation of antioxidative Maillard reaction products during food processing, amino-carbonyl reactions in food and biological ystems [M]. Tokyo: Elsevier, 1986,273.
  • 8Franzke C, Iwainsky H. Antioxidant capacity of melanoidin[J]. Dtsch Lebensm. Rundsch, 1954, 50: 251-254.
  • 9Lee K G, Shibamoto T. Toxicology and antioxidant activities of non-enzymatic browning reaction products: review [J]. Food Reviews international, 2002, 18: 151.
  • 10Elizalde B E, Dalla R M, Lerici C R. Effect of Maillard reaction volatile products on lipid oxidation [J]. J Am Oil Chem Soc, 1991.68:758.

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