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作 者:赵金金[1] 徐志辉[1] 胡磊[1] 罗文雅[1] 胡威[1] 尤红娟[1] 李向阳[1] 颜超[1] 郑葵阳[1] 汤仁仙[1]
机构地区:[1]徐州医学院病原生物学与免疫学教研室,江苏徐州221004
出 处:《徐州医学院学报》2014年第5期302-305,共4页Acta Academiae Medicinae Xuzhou
基 金:基金项目:江苏省普通高校研究生科研创新计划(CXZZ12-0986);徐州市科技计划项目(XZZD1331)
摘 要:目的:优化人可溶性TRAIL蛋白生产菌发酵及纯化条件,从而提高TRAIL的产量及活性。方法①探索6种不同培养液、培养液pH值、异丙基硫代半乳糖苷( IPTG)诱导浓度及时间,选择最佳发酵条件;②联合镍离子亲和层析及超滤法纯化人可溶性TRAIL蛋白。结果①人可溶性TRAIL的最佳发酵条件为pH7.4的YPD培养液,所用IPTG的最佳浓度为0.2 mmol/L,最佳诱导时间为6 h;②经镍离子亲和层析和超滤联合作用可得纯度极高的蛋白。结论成功完成了人可溶性TRAIL发酵及纯化条件的优化,为今后大量提取TRAIL蛋白奠定了基础。Objective To optimize the production and purification conditions of human soluble TNF -related apop-tosis inducing ligand ( TRAIL) , thereby increasing the productivity and activity of TRAIL .Methods ①6 different me-dium, pH, the induced concentration and time of isopropyl β-D-1-thiogalactopyranoside ( IPTG) were investigated and the optimum fermentation conditions were selected .②Better human soluble TRAIL protein was obtained through the combination of nickel ion affinity chromatography and ultrafiltration .Results ①The optimum fermentation conditions for human soluble TRAIL was YPD medium at pH 7.4.The optimum concentration of IPTG used was 0.2 mmol/L, the best time was 6 hours.②Through nickel ion affinity chromatography and ultrafiltration combination , higher effects and more purity protein could be obtained .Conclusion The fermentation conditions for human soluble TRAIL are successfully op-timized, which lays foundation for future extraction of large amount of TRAIL protein .
分 类 号:R373.2[医药卫生—病原生物学]
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