食品科学 ›› 2011, Vol. 32 ›› Issue (13): 32-36.doi: 10.7506/spkx1002-6630-201113008

• 基础研究 • 上一篇    下一篇

抗氧化活性花生肽的氨基酸组成及质谱分析

范远景1,高海成1,孟凡莉2   

  1. 1.合肥工业大学生物与食品工程学院 2.南京百汇食品有限公司
  • 出版日期:2011-07-15 发布日期:2011-07-02
  • 基金资助:
    安徽省2008 科技攻关计划重大科技专项(0801032091);合肥市科技项目(2008-1025)

Preparation, Amino Acid Composition and UPLC-TOF-MS Analysis of Peanut-derived Antioxidant Peptide Fractions

FAN Yuan-jing1,GAO Hai-cheng1,MENG Fan-li2   

  1. 1.School of Biology and Food Technology, Hefei University of Technology, Hefei 230009, China; 2. Baihui Food Co. Ltd., Nanjing, Nanjing 211225, China
  • Online:2011-07-15 Published:2011-07-02

摘要: 目的:研究具有抗氧化活性花生肽的氨基酸组成及分子质量。方法:采用葡聚糖凝胶G-25、G-15对花生蛋白酶解液进行分离纯化,得到具有抗氧化活性花生肽组分J22和F22,通过氨基酸分析仪和液相色谱-飞行时间质谱联用仪进一步分析氨基酸组成及分子质量关系。结果:与在花生蛋白中的含量相比,J22组分中Ile从3.75%上升至13.34%,Met从0.79%上升至5.18%,Tyr由3.44%上升到45.84%,His由2.68%上升到12.53%;F22组分中Ile从3.75%上升至6.12%,Met从0.79%上升至3.78%,Tyr由3.44%上升到11.53%,His由2.68%上升到51.13%。J22组分主要是由分子质量为291.9D和391.3D的短肽组成的混合物,F22组分主要是由分子质量为205D和391.3D的短肽组成的混合物。结论:花生肽组分J22和F22中Tyr、His含量较高,分子质量小,易于吸收,且有一定分子质量及氨基酸残基决定的结构,是花生肽抗氧化活性较高的重要原因。

关键词: 花生肽, 抗氧化活性, 氨基酸分析, 液相色谱-飞行时间质谱仪

Abstract: Objective: To prepare peanut-derived antioxidant peptides and analyze their amino acid composition and molecular weights. Methods: Defatted cold-pressed soybean cake was hydrolyzed by alcalase or flavourzyme and the hydrolysates were preliminarily separated to collect peptides having a molecular weight of less than 1 kD. The obtained peptides were further separated by sequential chromatographies on Sephadex G-25 and Sephadex G-15 columns to obtain two peptide fractions with higher hydroxyl free radical scavenging activity named as J22 (from alcalase hydrolysis) and F22 (from flavourzyme hydrolysis). The amino acid composition of the two fractions was analyzed using an amino acid analyzer. Meanwhile, Waters Acquity UPLC -LCT premier time-of-flight mass spectrometer (UPLC-TOF-MS) was used to analyze their molecular weight distribution. Results: Compared with peanut protein, Ile, Met, Tyr and His contents in the fraction J22 were increased to 13.34%, 5.18%, 45.84% from 3.75%, 0.79%, 3.44%, respectively; similarly, Ile, Met, Tyr and His contents in the fraction F22 were increased to 6.12%, 3.78%, 11.53% and 51.13% from 3.75%, 0.79%, 3.44%, respectively. Two short-chain peptides were found in each of the two fractions with respective molecular weights of 291.9 D and 391.3 D for the fraction J22 and of 205 D and 391.3 D for F22. Conclusion: J22 and F22 are both rich in tyrosine and histidine. Both fractions with small molecular weights are characteristics of fast absorption. A certain molecular weight and amino acid residues offer them with higher antioxidant activity.

Key words: peanut peptide, antioxidant activity, amino acid assay, liquid-chromatography-time of flight mass spectrometry(LC-TOF-MS)

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