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作 者:侯付景[1] 苏秀榕[1] 李妍妍[1] 徐彩云[1]
机构地区:[1]宁波大学生命科学与生物工程学院,宁波315211
出 处:《食品科技》2009年第7期181-184,共4页Food Science and Technology
基 金:国家农业科技成果转化资金资助项目(2007GB2C220359);宁波市科技成果转化资金资助项目(2007C100055)
摘 要:目的:通过观察海地瓜体壁的亚显微结构,对它的质地做出合理的解释,选择合理的加工技术;探讨海地瓜的水解产物的体内抗氧化作用。方法:用电镜扫描法观察海地瓜体壁结构;通过正交实验确定复合蛋白酶酶解海地瓜的最适条件。制得海地瓜水解液,灌胃大鼠。56d后,测定大鼠血清和肝脏组织匀浆液中SOD,GSH-Px活力。结果与结论:电镜扫描分析发现海地瓜的肌纤维丝较粗壮,排列凌乱,纤维丝排列紧密。海地瓜肌肉组织的这种排列方式可能是它的肌肉坚韧,难于咀嚼的原因。正交实验确定海地瓜的最佳酶解条件为:2%复合蛋白酶,10%底物,酶解温度55℃,酶解时间70min。水解液稀释一倍,灌胃大鼠。发现灌胃海地瓜水解液的大鼠血液中SOD和GSH-Px的活力和肝脏组织中SOD活力比较空白组具有显著提高,说明海地瓜水解液具有良好的抗氧化活性。Objective: To make a reasonable explaination of body walltexture of Acaudina by observing the ultrastructure. To investigate the antioxidation activity of Acaudina leucoprocta hydrolysate. Method: Acaudina leucoprocta texture was observed by scanning electron microscope; Determine the optimum condition of hydrolysis with the compound protease through the orthogonal experiment. The activity of superoxide dismutase(SOD) and glutathione peroxidase(GSH-Px) in blood serum and liver tissue in mice were analyzed after 56 days of hydrolysate feeding. Result and Conclution: The scanning electron microscope analyses of Acaudina leucoprocta showed that its muscle fiber were thick, in a mess and the fibrils arranged densely. Orthogonal experiment indicated that the rational conditions of enzymatic hydrolysis were: complex protease was 2%, substrate concentration was 10%, the optimal temperature was 55 ℃ and enzymolysis time was 70 min.Then the enzymolysis liquid was diluted with water in the ratio of 1:1. Feeding the mice by gastric perfusion. The results was that the activities of SOD, GSH-Px were enhanced, which showed that this hydrolysate had remarkable antioxidation activity.
分 类 号:TS202.3[轻工技术与工程—食品科学]
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