食品科学 ›› 2009, Vol. 30 ›› Issue (4): 52-56.doi: 10.7506/spkx1002-6630-200904005

• 工艺技术 • 上一篇    下一篇

花生多肽的制备及纯化的研究

刘丽娜1,段家玉2,何东平3,张声华1 ,*   

  1. 1.华中农业大学 2.临沂大学 3.武汉工业学院  
  • 收稿日期:2008-01-11 修回日期:2008-05-07 出版日期:2009-02-15 发布日期:2010-12-29
  • 通讯作者: 何东平 E-mail:hedp123456@163.com

Study on Preparation and Purification of Peanut Polypeptides

LIU Li-na3,DUAN Jia-yu2,HE Dong-ping3,ZHANG Sheng-hua1,*   

  1. (1. Huazhong Agricultural University, Wuhan 430070, China;2. Linyi Normal University, Linyi 276005, China;
    3. Wuhan Polytechnic University, Wuhan 430023, China)
  • Received:2008-01-11 Revised:2008-05-07 Online:2009-02-15 Published:2010-12-29
  • Contact: HE Dong-ping3 E-mail:hedp123456@163.com

摘要:

用AS1.398 中性蛋白酶水解花生蛋白得到花生多肽粗品,对影响花生蛋白水解的各种影响因素,如酶制剂的筛选,酶解工艺参数等进行了系统研究,得到最佳工艺条件为:pH6.7、反应温度50℃、酶解时间2.5h、加酶量为6500U/g 底物。超滤截取相对分子量小于5kD 和3kD 以下的两部分,冷冻干燥后用Sephadex G-25 柱层析分别得到两个和一个活性峰。在三甲基甘氨酸SDS- 聚丙烯酰胺凝胶电泳上显示单一条带的纯品。相对分子量分别在6.5kD 和 2kD 左右。

关键词: 花生多肽, 制备, 分离, 纯化

Abstract:

Neutral protease AS1.398 was used to hydrolyze peanut protein to produce polypeptides. The effects of pH, enzyme dosage, hydrolysis time and temperature on degree of hydrolysis were investigated through single factor tests respectively, and these factors were optimized through response surface methodology (RSM) that was designed based on Box-Behnken central combination. The optimum hydrolysis conditions are as follows: pH 6.7, enzyme dosage (ratio of enzyme to substrate) 6500 U/g, hydrolysis temperature 50 ℃ and time 2.5 h. The hydrolysates of peanut were ultrafiltrated with 5-kD or 3-kD hollow fiber ultrafiltration membrane, and the retentates of 5-kD and 3-kD hollow fiber ultrafiltration membrane was collected respectively and then purified through Sephadex G-25 column chromatography with 10% ethanol solution as eluent. Chromatogram showed that the retentate of 5-kD hollow fiber ultrafiltration membrane is composed of two fractions, whose molecular weights are about 6.5 kD and 2 kD determined using SDS-PAGE method, respectively.

Key words: peanut polypeptides, preparation, isolation, purification

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