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作 者:Yue-fei WANG Jie WANG Jing WU Ping XU Yi-qi WANG Jun-jie GAO Danielle HOCHSTETTER
机构地区:[1]Department of Tea Science, Zhejiang University [2]Key Laboratory of Horticultural Plant Growth, Development and Quality Improvement, Ministry of Agriculture [3]College of Pharmacy, Zhejiang Chinese Medical University
出 处:《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》2014年第2期173-180,共8页浙江大学学报(英文版)B辑(生物医学与生物技术)
基 金:supported by the Ministry of Science and Technology of China(No.2012BAD36B06-5)
摘 要:The conditions for extracting polysaccharides from tea (Camellia sinensis L.) fruit peel (TFPPs) were studied. Three parameters (temperature, time, and liquid/solid ratio) affecting the extraction of TFPP were optimized using response surface methodology (RSM). Under the optimized conditions, the yield of TFPP was predicted to be 4.98%. The physicochemical properties, in vitro antioxidant activities, and inhibitory effects on α-glucosidase of frac- tionated TFPPs (TFPP-0, TFPP-20, TFPP-40, and TFPP-60) were investigated. We found that the TFPPs were all acid protein-bound heteropolysaccharides, although with different chemical compositions. They had not only re- markable scavenging activity on 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) and reducing activity, but also excellent inhibitory potential against α-glucosidase in vitro. Our results suggest that tea fruit peel could be treated as a potential bioresource for the development of polysaccharide antioxidants.研究目的:利用响应面优化茶果皮多糖(TFPP)提取条件,用乙醇分级分段得到4个多糖组分(TFPP-0、TFPP-20、TFPP-40和TFPP-60),并研究其理化性质、抗氧化活性和对α-葡萄糖苷酶抑制作用,为综合高效利用茶果皮多糖资源提供理论基础。创新要点:1.首次将茶果皮作为一种潜在生物资源研究;2.首次研究茶果皮多糖这一功能成分;3.将工艺优化、理化性质和生物活性结合研究。研究方法:三因素三水平响应面设计(见表1),傅里叶转换红外光谱法分析茶果皮粗多糖的功能团结构(见图3),高效液相色谱法检测单糖组分(见表2),2,2'-氨基-二(3-乙基-苯并噻唑啉-6-磺酸)二铵盐(ABTS)自由基清除法(见图4a)和铁离子还原能力法(FRAP)(见图4b)分析茶果皮多糖抗氧化活性。重要结论:1.茶果皮多糖是一种水溶性的酸性杂多糖蛋白复合物;2.乙醇分级是一种有效多糖分离手段;3.茶果皮多糖具有出色的生物活性;4.茶果皮资源可以作为一种可再生生物资源进行深度的开发。
关 键 词:POLYSACCHARIDES Tea (Camelfia sinensis L ) fruit peel Physicochemical properties Antioxidant activity α-Glucosidase inhibition
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