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茶渣蛋白的提取及酶解产物抗氧化性质研究 被引量:6

Extraction of Tea Residue Protein and Antioxidant Activity of Enzymatic Hydrolysates
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摘要 我国是茶叶生产消费大国,茶渣中含有丰富的蛋白质,茶渣蛋白具有良好的营养价值和保健功效。以茶渣为原料,以超声波技术为辅助手段,得到茶渣蛋白的最佳提取工艺:料液比为1:70(g/mL)、超声功率150 W、超声波提取时间为70 min、提取温度为90℃、NaOH浓度为0.18mol/L,该条件下茶渣蛋白提取率最大值为(83.17±0.16)%。利用碱提酸沉法得茶渣蛋白,以抗氧化能力为指标利用复合蛋白酶对茶渣蛋白进行酶解得到抗氧化肽,优化得最佳条件:底物浓度1.0%、酶/底物8000 U/g、酶解温度为60℃、pH为8,得茶渣蛋白酶解产物DPPH自由基清除率达到(80.83±0.47)%。在亚油酸体系中,1.0 mg/mL茶渣蛋白酶解产物对亚油酸体系自氧化的抑制能力高于抗坏血酸和VE,略低于人工合成抗氧化剂BHT。 China is a main country in tea production and consumption.There are rich protein in waste tea residue.Tea residue protein has good nutritional value and health care effect.Tea protein was extracted from tea residue assisted by ultrasonic,the optimal extraction condition was determined:solid-liquid ratio was 1:70(g/mL),the ultrasonic power was 150 W,ultrasonic time was 70 min,extraction temperature was 90℃,the NaOH concentration was 0.18 mol/L,the maximum extracting rate of total protein was(83.17±0.16)%.Tea residue protein was extracted by a mixed solution,the optimum index of compound enzymes antioxidant capacity was 1.0%of substrate concentration,8000 U/g of enzyme/substrate,60℃of enzymolysis temperature,pH 8,the DPPH radical scavenging rate of enzymatic achieved(80.83±0.47)%.In LA system,the inhibition of 1.0 mg/mL tea residue protolysate on the autoxidation of linoleic acid system was higher than that of ascorbic acid and VE,slightly lower than that of synthetic antioxidant BHT.
作者 梁杰 汪秀妹 杨艺伟 喻朝阳 张钦华 谢洵 赵晓旭 LIANG Jie;WANG Xiumei;YANG Yiwei;YU Chaoyang;ZHANG Qinhua;XIE Xun;ZHAO Xiaoxu(College of Environmental and Biological Engineering,Fujian Provincial Key Laboratory of Ecology-Toxicological Effects&Control for Emerging Contaminants,Putian University,Putian 351100,China)
出处 《食品科技》 CAS 北大核心 2020年第9期214-220,共7页 Food Science and Technology
基金 国家自然科学基金项目(31801462) 国家级大学生创新创业训练项目(202011498006) 福建省自然科学基金项目(2018J05063) 2018年度福建省高校杰青科研人才培育计划项目 莆田市科技计划项目(2018GP2001) 莆田学院引进人才科研启动项目(2018055)。
关键词 茶渣蛋白 提取 酶解 自由基清除率 抗氧化 tea residue protein extract enzymatic hydrolysis free radical scavenging rate antioxidant
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