首页 | 本学科首页   官方微博 | 高级检索  
     

响应面法优化磷酸化改性花生分离蛋白-多肽膜的制备工艺
引用本文:于丽娜,杜德红,彭娅萍,杨伟强,李勇,顾博,孙杰,张初署,毕洁,王明清. 响应面法优化磷酸化改性花生分离蛋白-多肽膜的制备工艺[J]. 中国油料作物学报, 2019, 41(1): 130. DOI: 10.7505/j.issn.1007-9084.2019.01.018
作者姓名:于丽娜  杜德红  彭娅萍  杨伟强  李勇  顾博  孙杰  张初署  毕洁  王明清
作者单位:1.山东省花生研究所,山东青岛,266100;2.青岛农业大学,山东青岛,266109; 3.西海岸现代农业示范区管委会,山东青岛,266000
基金项目:山东省自然科学基金(ZR2016CM43,ZR2016YL021,ZR2017MC060,ZR2017MC062);山东省重点研发计划(2015GGX108006);山东省农业科学院重大科技成果培育计划(2016CGPY10);山东省农业科学院青年科研基金(2016YQN18)
摘    要:    为了优化磷酸化改性花生分离蛋白-多肽膜制备工艺条件,在单因素基础上,通过响应面Box-Benhnken进行实验设计。结果表明,最优工艺参数:蛋白浓度8%、pH值8.2、甘油百分含量(占蛋白)13.4%、黄原胶百分含量(占蛋白)1%、时间60min、温度69℃、超声波功率270W、超声波频率28kHz、多肽溶液的浓度61mg/mL;此工艺条件下,膜厚度、吸水率和透光率理论预测值分别为86μm、41.9%和53.6%,验证实验值分别为88±2μm、43.1±1.2%和52.4±1.5%,两者的差值分别为2.33%、2.86%和2.24%,说明响应面二次模型的拟合良好;磷酸化改性花生分离蛋白-多肽膜的抗拉强度9.62MPa、断裂延伸率101.68%、溶解性47.69%、水蒸气透过率6.95 g•m-2· h-1等功能性质和DPPH自由基清除活性IC50值7.70 mg·mL-1、羟自由基清除活性IC50值5.98 mg·mL-1、超氧阴离子自由基清除活性IC50值4.20 mg·mL-1、铁离子螯合力活性IC50值3.79 mg·mL-1、铜离子螯合力活性IC50值13.61 mg·mL-1、脂质过氧化抑制活性IC50值8.62 mg·mL-1、铁还原力IC50值13.93mg·mL-1、钼还原力IC50值5.49mg·mL-1等抗氧化活性较磷酸化改性花生分离蛋白膜有所改善。本研究结果为磷酸化改性花生分离蛋白在蛋白膜方面的应用提供一种新途径。

关 键 词:磷酸化改性花生分离蛋白-多肽膜  制备工艺  响应面法  抗氧化活性  

Optimization of phosphorelated peanut protein isolate – polypeptide films preparation by response surface methodology #br#
YU Li-na,DU De-hong,PENG Ya-ping,YANG Wei-qiang,LI Yong,GU Bo,SUN Jie,ZHANG Chu-shu,BI Jie,WANG Ming-qing. Optimization of phosphorelated peanut protein isolate – polypeptide films preparation by response surface methodology #br#[J]. Chinese Journal of Oil Crop Sciences, 2019, 41(1): 130. DOI: 10.7505/j.issn.1007-9084.2019.01.018
Authors:YU Li-na  DU De-hong  PENG Ya-ping  YANG Wei-qiang  LI Yong  GU Bo  SUN Jie  ZHANG Chu-shu  BI Jie  WANG Ming-qing
Affiliation:1. Shandong Peanut Research Institute, 266100, China; 2. Qingdao Agricultural University, 266109, China; 3. Management Committee of West Coast Modern Agricultural Demonstration Area, Qingdao 266000, China
Abstract:     order to optimize the preparation process conditions of phosphorelated peanut protein isolate - polypeptide films, experiment was carried out with the response surface Box-Benhnken experiment, on the basis of single factor experiments. The results showed that the optimum conditions obtained were protein concentration, pH value, glycerol percentage content of protein, xanthan gum percentage content of protein, time, temperature, ultrasonic power, ultrasonic frequency, polypeptide concentration of 8%, 8.2, 13.4%, 1%, 60min, 69℃, 270w, 28kHz, 61mg/mL, respectively. Under the optimum conditions, the theoretical predictive values of film thickness, water absorption and light transmittance were 86μm, 41.9% and 53.6%, respectively. The results of verification experiment showed that film thickness, water absorption rate and light transmittance rate could reach 88±2μm, 43.1±1.2% and 52.4±1.5%, respectively. The differences between experimental and theoretical values were 2.33%, 2.86% and 2.24%, respectively. This suggested the response surface quadratic model fitted well. The functional properties were better than those of phosphorelated modified peanut protein isolate films, and these functional properties included tensile strength of 9.62 MPa, elongation of 101.68 %, solubility of 47.69 %, water vapor permeability of 6.95 g•(m2·h)-1 and antioxidant activities including DPPH free radical scavenging activity of IC50 7.70 mg·mL-1, hydroxy free radical scavenging activity of IC50 5.98 mg·mL-1, superoxide anion free radical scavenging activity of IC50 4.20 mg·mL-1, iron ion chelating activity of IC50 3.79 mg·mL-1, copper ion chelating activity of IC50 13.61 mg·mL-1, lipid peroxidation inhibition activity of IC50 8.62 mg·mL-1, iron reducing power of IC50 13.93 mg·mL-1, molybdenum reducing power of IC50 5.49 mg·mL-1 of phosphorelated peanut protein isolate - polypeptide films. The results of this study provided a new way for the application of phosphorelated peanut protein isolate.
Keywords: phosphorelated modified peanut protein isolate - polypeptide films  preparation process  response surface methodology  antioxidant activities   
本文献已被 CNKI 等数据库收录!
点击此处可从《中国油料作物学报》浏览原始摘要信息
点击此处可从《中国油料作物学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号