首页 | 本学科首页   官方微博 | 高级检索  
     检索      

鲍鱼性腺小肽的制备及抗氧化活性的初步研究
引用本文:欧柳舒,沈建东,翁凌,陶志鹏,张凌晶,曹敏杰.鲍鱼性腺小肽的制备及抗氧化活性的初步研究[J].厦门水产学院学报,2014(1):13-19.
作者姓名:欧柳舒  沈建东  翁凌  陶志鹏  张凌晶  曹敏杰
作者单位:[1]集美大学生物工程学院,福建厦门361021 [2]福建省水产品深加工工程研究中心,福建厦门361021
基金项目:国家海洋局海洋公益性项目(201305015);十二五国家科技支撑计划资助项目(2012BAD38B09)
摘    要:以雄性皱纹盘鲍性腺为原料,建立了蛋白酶酶解制备抗氧化活性蛋白肽的工艺条件.分别对木瓜蛋白酶和中性蛋白酶进行单因素研究,并以二者的复合酶为工具酶进行响应面分析.结果显示,雄性鲍鱼性腺的最优酶解条件为木瓜蛋白酶与中性蛋白酶的比例为1:4、pH=6.6、酶解温度为53.7℃、酶解时间为70.4min.高效液相色谱(HPLC)分析结果表明,酶解液中多肽的分子质量主要分布在1ku以下.制备的酶解液具有较强的清除自由基效果,清除1,1-二苯基-2-三硝基苯肼(DPPH)的EC50值为6.8mg/mL,还原力的AC0.5值为12.87mg/mL.

关 键 词:鲍鱼  性腺  酶解条件  抗氧化活性肽  蛋白酶

Antioxidant Activity of Enzymatic Hydrolysates Prepared from Pacific Abalone (Haliotis discus hannai) Gonads
Authors:OU Liu-shu  SHEN Jian-dong  WENG Ling  TAO Zhi-peng  ZHANG Ling-jing  CAO Min-jie
Institution:1. College of Biological Engineering, Xiamen 361021, China; 2. Engineering Research Center for Aquatic Products Processing of Fujian Province, Jimei University, Xiamen 361021, China)
Abstract:Using male abalone gonads as raw material, the present study optimized the proteinase hydrolyzing conditions to produce antioxidant peptides. Single-factor experiments using papain and neutral proteinase were adopted respectively and the combination of both enzymes was performed. The results showed that the optimal hydrolyzing conditions for preparation of active antioxidant peptides from male abalone gonads were using the proportion of papain to neutral proteinase at 1 : 4, at pH = 6. 6 and 53.7 ℃, with hydrolyzing duration of 70. 4 min. High performance liquid chromatography (HPLC) analysis showed that the molecular mass of peptides in the hydrolysate was mostly below 1 ku. The hydrolysate thus obtained from male abalone gonads revealed a significant effect in scavenging free radicals. The half scavenging effect (EC50) of DPPH radical was 6. 8 mg/mL and the half absorbanee effect (AC0.5) of reducing power was 12. 87 mg/mL.
Keywords:abalone  gonads  hydrolyzing conditions  antioxidant active peptides  proteinase
本文献已被 维普 等数据库收录!
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