期刊文献+

富硒糙米抗氧化肽酶法制备工艺优化 被引量:4

Optimization of Antioxidant Peptides from Se-enriched Brown Rice Proteins by Enzymolysis
下载PDF
导出
摘要 以富硒糙米蛋白为原料,优化富硒糙米蛋白抗氧化肽酶法制备工艺。以酶解产物抗氧化能力指数(oxygen radical absorbance capacity,ORAC)和水解度为评价指标,考察酶种类、酶解时间、pH值、底物浓度、加酶量及酶解温度对酶解产物抗氧化活性的影响。在单因素试验基础上,采用三因素三水平响应面法确定富硒糙米抗氧化肽的制备工艺。结果表明:中性蛋白酶较适宜制备富硒糙米抗氧化肽,其最佳酶解工艺条件为:pH 8.0,底物浓度3%,酶解时间69 min,酶解温度55℃,加酶量12 000 U/g。在此条件下,富硒糙米蛋白酶解产物的抗氧化能力为(1 232.57±62.34)μmol TE/g,显著高于同等条件下非富硒糙米蛋白酶解物的抗氧化能力。 The preparation process of antioxidant peptides from selenium-enriched brown rice(Se-BR)protein hydrolysates were optimized in this study.Effects of six factors including enzymes,hydrolysis time,pH,substrate concentration,enzyme dosage and temperature on the oxygen radical absorbance capacity(ORAC)and degree of hydrolysis(DH)were evaluated.Based on the single factor experiments,a procedure optimized using the response surface analysis with three factors(hydrolysis time,temperature and enzyme dosage)was conducted in order to obtain the optimal enzymolysis conditions.The results showed that neutral protease was suitable for producing antioxidant peptides from Se-BR protein.The optimal enzymolysis conditions were as follows:pH value of 8.0,substrate concentration of 3%,enzymolysis time of 69 min,enzymolysis temperature of 55℃and enzyme dosage of 12 000 U/g protein.Under the conditions,the antioxidant capacity of the Se-BR proteolysis product was(1 232.57±62.34)μmol TE/g,which was significantly higher than that of the non-Se-BR protein under the same conditions.
作者 杜润峰 赵爽 刘昆仑 陈复生 DU Runfeng;ZHAO Shuang;LIU Kun-lun;CHEN Fu-sheng(College of Food Science and Technology,Henan University of Technology,Zhengzhou 450001,Henan,China)
出处 《食品研究与开发》 CAS 北大核心 2019年第1期70-75,共6页 Food Research and Development
基金 国家自然科学基金项目(31601417) 河南省高等学校青年骨干教师培养计划项目(2016GGJS-071) 河南省高等学校重点科研项目计划基础研究专项(19zx013) 河南工业大学科学研究基金项目(2018RCJH05)
关键词 富硒糙米 酶解 抗氧化肽 制备工艺 响应面 Se-enriched brown rice enzymolysis antioxidantpeptides preparation process response surface
  • 相关文献

参考文献7

二级参考文献150

共引文献187

同被引文献36

引证文献4

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部