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作 者:于张颖[1] 肖发[1] 柳丹丹[1] 翟量[1] 沈立荣[1]
机构地区:[1]浙江大学生物系统工程与食品科学学院,浙江杭州310058
出 处:《食品工业科技》2014年第19期185-188,共4页Science and Technology of Food Industry
基 金:国家自然科学基金项目(31271848);浙江省公益性科技计划项目(2011C22039);杭州市重大科技创新项目(20131812A25)
摘 要:用离心法从鲜王浆中提取蜂王浆主蛋白,进行液料比、pH、抽提时间和离子强度对MRJPs提取率影响的正交实验,并作MRJPs蛋白质量、副产物王浆酸和总糖回收率分析。实验结果表明:影响MRJPs提取率的因素从大到小依次为离子强度〉pH〉抽提时间〉液料比,在最佳提取条件(液料比8mL/g、pH8、抽提8h,离子强度0.5mol/L)下,MRJPs提取率为81.14%。提取的MRJPs蛋白SDS—PAGE电泳和ELISA分析显示,其分子量在42.1~97.4ku,纯度71.7%。副产物分析显示,王浆酸和总糖回收率分别为2.91%和1.26%。该结果为王浆活性蛋白开发和副产物综合利用提供了科学依据。Major Royal Jelly Proteins(MRJPs) was extracted by centrifugation from royal jelly( R J).The orthogonal experiment optimized with four parameters, ratio of solution to royal jelly, pH, extracting time and ionic strength was implemented.The quality of MRJPs,the trans-i0-hydroxy-decenoic and total sugar in by-product were analyzed. Orthogonal experiment showed the factors affecting MRJPs extraction rate in descending order of size were:ionic strength 〉 pH 〉 extracting time 〉 ratio of solution to RJ.81.14% of MRJPs was obtained from RJ under the optimum extraction conditions(the ratio of solution to RJ 8mL/g, pH8, extracting time 8h, ionic strength 0.5mol/L).Analysis of SDS-PAGE and ELISA of extracted MRJPs showed that it possessed molecular weight ranged from 42.1 to 97.4ku, and that its purity reached 71.7%.The by-product contained 2.91% of trans-10-hydroxy-2-decenoic acid and 1.26% of total sugar, respectively.The results provided essential scientific knowledge for development of MRJPs and utilization of its by-products.
分 类 号:TS201.2[轻工技术与工程—食品科学]
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