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作 者:包海生[1] 高秀峰[1] 郑雪妮[1] 李永生[2]
机构地区:[1]四川大学华西基础医学与法医学院,四川成都610041 [2]四川大学化学工程学院,四川成都610065
出 处:《酿酒科技》2012年第2期27-29,共3页Liquor-Making Science & Technology
基 金:四川大学"214"振兴计划科研启动基金(NO.0082204127092)
摘 要:以壳聚糖为载体,甲醛为预交联剂,戊二醛为交联剂,用环氧氯丙烷法进行载体活化,乙二胺为螯合配基,制备了壳聚糖Zn2+固定化亲和层析填料。利用该填料对重组ALDH粗酶液进行了纯化,经分段盐析和亲和层析,纯化倍数达到9.23,回收率达到29%。结果表明,制备的壳聚糖Zn2+固定化亲和层析填料,能够用于带有组氨酸标签重组蛋白的快速分离与纯化。该方法对重组ALDH的纯化倍数和回收率均高于目前的其他分离纯化方法。The immobilized metal affinity chromatography(IMAC) matrixes were successfully prepared with chitosan as support,formaldehyde as precrosslinking agent,glutaraldehyde as crosslinking agent,3-Chloro-1,2-epoxypropane as activated agent,ethylenediamine as chelating ligand and Zn2+ as center ions.Then it was used to separate and purify aldehyde dehydrogenase(ALDH) tagged with 6×His.The yield of ALDH was 29.0 % and the purification fold reached 9.23 times by ammonium sulfate precipitation and immobilized metal affinity chromatography.It proved that the prepared high-efficiency immobilized metal affinity chromatography matrixes could be used to rapidly separate and purify the His-tagged recombinant protein and the purification fold and recovery rate purified by chitosan Zn2+ immobilized affinity chromatography were higher than any other methods reported currently.
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