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作 者:曾凡逵[1] 赵鑫[1] 周添红[1] 高祥虎[1] 耿庆芬[1] 刘刚[1]
机构地区:[1]中国科学院兰州化学物理研究所环境材料与生态化学发展中心,甘肃兰州730000
出 处:《现代食品科技》2011年第12期1466-1468,1489,共4页Modern Food Science and Technology
基 金:现代农业产业技术体系建设专项资金(nycytx-15)
摘 要:将从新鲜马铃薯中分离出来的淀粉配置成1.33%(m/V)的水溶液,经高压灭菌锅121℃蒸煮180 min后,采用正丁醇螯合直链淀粉。将样品置于泡沫箱中过夜缓慢冷却后,再通过离心(8700 g,30 min)实现直链淀粉与支链淀粉的分离。过量的甲醇(两倍于支链淀粉溶液体积)添加到浓缩的支链淀粉溶液中将支链淀粉沉淀,随后通过离心(8700 g,30 min)获得支链淀粉。直链淀粉和支链淀粉通过进一步分离纯化后分别采用进行光谱测量(与碘试剂结合)和光学显微镜进行分析,结果表明该方法能有效地分离马铃薯直链淀粉和支链淀粉。Starch isolated from fresh potato was dissolved in distilled water to make an aqueous solution (1.33 %, m/V) and n-Butanol was added to chelate the amylose after the sample had been autoclaved at 121 ℃ for 180 minutes on a fluid cycle. The sample were transferred to a styrofoam cooler for slow cooling overnight, then crude amylose and amylopectin was separated by centrifugation (8 300 g, 30 min). Excess methanol (amylopectin solution: methanol, 1:2) was added to the concentrated amylopectin solution to precipitate the amylopectin, and then the amylopectin was obtained by centrifugation (8700 g, 30 min). After a further purification, the amylase and amylopecfm fractions were identified by UV-Vis scans of their complex formed with iodine and optical microscope. The results showed that the obtained potato amylase and amylopectin were purified to apparent homogeneity.
分 类 号:TS235.2[轻工技术与工程—粮食、油脂及植物蛋白工程]
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