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中国精品科技期刊2020
许美玉, 王希希, 黄群, 林超, 宋洪波, 王艺伟, 滕慧. 酶法改善卵白蛋白乳化性研究[J]. 食品工业科技, 2017, (08): 150-155. DOI: 10.13386/j.issn1002-0306.2017.08.021
引用本文: 许美玉, 王希希, 黄群, 林超, 宋洪波, 王艺伟, 滕慧. 酶法改善卵白蛋白乳化性研究[J]. 食品工业科技, 2017, (08): 150-155. DOI: 10.13386/j.issn1002-0306.2017.08.021
XU Mei-yu, WANG Xi-xi, HUANG Qun, LIN Chao, SONG Hong-bo, WANG Yi-wei, TENG Hui. Improving emulsifying property of ovalbumin with enzymatic modification[J]. Science and Technology of Food Industry, 2017, (08): 150-155. DOI: 10.13386/j.issn1002-0306.2017.08.021
Citation: XU Mei-yu, WANG Xi-xi, HUANG Qun, LIN Chao, SONG Hong-bo, WANG Yi-wei, TENG Hui. Improving emulsifying property of ovalbumin with enzymatic modification[J]. Science and Technology of Food Industry, 2017, (08): 150-155. DOI: 10.13386/j.issn1002-0306.2017.08.021

酶法改善卵白蛋白乳化性研究

Improving emulsifying property of ovalbumin with enzymatic modification

  • 摘要: 采用碱性蛋白酶通过酶法改性以改善卵白蛋白乳化性。在单因素实验的基础上,以乳化活性为响应值,选取酶解时间、pH、酶解温度为考察因素,根据Box-Behnken中心组合设计原理建立数学模型,进行响应面分析。获得卵白蛋白乳化性的酶法改性最佳工艺为:底物浓度1.0%、酶用量30000 U/g、酶解时间195 min、p H9.0、酶解温度38℃。在此条件下改性卵白蛋白乳化活性为0.967±0.031,乳化活性相比未改性提高89.61%,说明碱性蛋白酶改性改善卵白蛋白乳化性效果理想。 

     

    Abstract: The emulsifying activity and emulsion stability of ovalbumin were improved by enzymatic modification with Alcalase.On the basis of single factor experiments, and the emulsifying activity as response value, enzymatic hydrolysis duration, p H value and enzymatic hydrolysis temperature were chosen as impact factors. The Box-Behnken center-united experimental design principle was used to design the experiments and the response surface analysis was adopted. The optimal enzymatic modification conditions by the response surface analysis were showed as follows: enzymatic hydrolysis duration 195 min, p H value 9.0, enzymatic hydrolysis temperature 38 ℃, substrate concentration 1.0% and Alcalase usage 30000 U/g. Under the optimal conditions, the emulsifying activity of ovalbumin was 0.967 ± 0.031 increasing with 89.61%, indicating that the effect of improving the emulsification of ovalbumin with alkaline protease modification was ideal.

     

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