秘鲁鱿鱼皮明胶抗氧化肽的制备及其分子质量分布  被引量:9

Preparation and Molecular Weight Distribution of Gelatin Antioxidant Peptides from Jumbo Flying Squid (Dosidicus Gigas) Skin

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作  者:茅宇虹[1] 杨文鸽[1] 徐大伦[1] 谢果凰[1] 张进杰[1] 

机构地区:[1]宁波大学海洋学院,浙江宁波315211

出  处:《中国食品学报》2014年第9期48-55,共8页Journal of Chinese Institute Of Food Science and Technology

基  金:海洋公益性行业科研专项(201305013);宁波市重大农业科研攻关项目(2012C10001)

摘  要:目的:基于鱿鱼皮明胶肽的抗氧化活性,优化制备工艺,探究其分子质量分布。方法:分别使用4种蛋白酶水解鱿鱼皮明胶,通过测定体外抗氧化活性来确定最适水解用酶。以DPPH自由基清除率为指标,利用单因素及响应面法优化明胶抗氧化肽的制备工艺,通过Tricine-SDS-PAGE及Sephadex G-25凝胶过滤层析测定明胶肽的分子质量分布。结果:碱性蛋白酶为最适水解用酶,最适水解温度55℃,酶添加量7 000 u/g(E/S),时间109 min,底物明胶质量分数6%,pH 6.66。此条件下明胶肽的DPPH自由基清除率达93.18%。90%明胶肽的分子质量介于1.4~10 ku之间。Objective: The hydrolysate of gelatin from squid skin shows antioxidant activity. This study aims to opti- mize the preparation process and explore the molecular weight distribution. Methods: Four different kinds of protease were used to hydrolyze gelatin, and the antioxidant activity of gelatin peptide were measured respectively. Using the scavenging ability on the 1,1-diphenyl-2-picryl-hydrazyl (DPPH) radical, the hydrolysis conditions for preparating the antioxidant peptides from gelatin were optimized by single-factor experiments and response surface methodology, and its molecular weight distribution was explored by Tricine-SDS-PAGE and Sephadex G-25 gel chromatography. Results: The optimal enzyme was alkaline protease, and the optimal hydrolysis conditions were as followers: temperature 55 ℃, enzyme concentration 7 000 U/g (E/S), time 109min, substrate concentration 6% and pH 6.66, respectively. Under these conditions, the scavenging ability on the DPPH radical of gelatin peptide was up to 93.18%. In addition, the molecular weight of 90% gelatin peptides were distributed from 1.4ku to 10ku.

关 键 词:鱿鱼皮 明胶肽 响应面 抗氧化活性 分子质量 

分 类 号:TS254.9[轻工技术与工程—水产品加工及贮藏工程]

 

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