期刊文献+

两步法制备菜粕肽及提高蛋白溶解度工艺 被引量:5

A two-step process for preparing rapeseed meal peptides and improving protein solubility
下载PDF
导出
摘要 该实验主要通过固态发酵结合酶解两步法处理菜粕,在此新工艺条件下考察小肽含量及蛋白溶解度的变化.菜粕经黑曲霉固态发酵后小肽质量分数和蛋白溶解度显著提高,分别为7.86%和25.23%,相比于空白对照分别增长了148.08%和174.83%.之后将发酵后的菜粕置于45℃下酶解30 h,小肽质量分数和蛋白溶解度进一步提高,分别为14.12%和44.95%.相比于单步固态发酵和空白对照,小肽含量分别提高了79.64%和393.71%,蛋白溶解度分别提高了78.16%和341.99%.与此同时,酶解结束后,采用Tricine-SDS-PAGE测定菜粕中蛋白质分子质量,电泳结果显示,大分子蛋白质被分解为小分子蛋白质,其分子质量<4.6 kDa.以上结果表明,经发酵、酶解两步法处理菜粕后,相比于传统单步固态发酵,菜粕的营养价值得到进一步提高,可为菜籽粕生物肽制备提供科学依据. The objective of this study was to improve oligo-peptide concentration and protein solubility of rapeseed meal by solid-state fermentation and enzymatic hydrolysis. The peptide content ( w/w ) and protein solubility significantly increased by 148.08% to 7.86% and 174.83% to 25.23% compared to the control,respectively,after solid-state fermentation by Aspergillus niger . The rapeseed meal was then hydrolyzed by enzymes at 45 ℃ for 30 h,the peptide content and protein solubility were further increased to 14.12% and 44.95%,respectively. Compared to single fermentation and the control,the peptide content increased by 79.64% and 393.71%,respectively,and the protein solubility increased by 78.16% and 341.99%,respectively. Moreover,most proteins were broken down to peptides with molecular weight less than 4.6 kDa. The results demonstrated that fermentation and enzymatic hydrolysis together can further increase the value of rapeseed meal and provide a base for preparing rapeseed meal peptides.
作者 帖余 刘军 李丽 王景峰 王国强 赵琦锴 周鹏松 TIE Yu;LIU Jun;LI Li;WANG Jingfeng;WANG Guoqiang;ZHAO Qikai;ZHOU Pengsong(College of Biotechnology Engineering,Sichuan University of Science and Engineering,Zigong 643000,China;Leshan HengFengHuaBang Biotechnology Co.,Ltd,Leshan 614000,China)
出处 《食品与发酵工业》 CAS CSCD 北大核心 2019年第16期143-147,共5页 Food and Fermentation Industries
基金 四川省科技厅重点研发项目(2018FZ0077) 四川省大学生创新创业训练计划项目(201810622078)
关键词 两步法 酶解 菜籽粕 生物肽 蛋白溶解度 two-step method enzymatic hydrolysis rapeseed meal biological peptide protein solubility
  • 相关文献

参考文献8

二级参考文献147

共引文献124

同被引文献76

引证文献5

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