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作 者:边疆[1] 陶好霞[1] 薛冲[1] 巩新[1] 马清钧[1]
机构地区:[1]北京军事医学科学院生物工程研究所
出 处:《生物工程进展》1995年第6期33-35,20,共4页Progress in Biotechnology
摘 要:我们采用本院基础医学研究所组建的IL—6工程菌E.coilDH5a(pBV—hlL-6),在选定的培养基及pH值下,采用30升发酵罐进一步观察了工程菌的生长和rIL-6的表达,确定了发酵工艺条件。在此条件下连续进行了三批次的培养试验。结果表明,工程首的生长密度达到2.51±0.02g[干重]/L[发酵液],rIL—6产率为182.4±2.0mg/g[干重]。rIL—6以包涵体形式表达于大肠杆菌细胞中,破菌后选用非离子型去垢剂或尿素等变性剂提取包涵体中的杂蛋白,可使rIL—6的纯度达到70.1±1.3%,收率为71.9±1.9%。洗涤后的包涵体,经过凝胶柱纯化和复性,rIL—6纯度达到95%以上,柱纯化的收率为72.3±0.9%;采用依赖IL—6,小鼠杂交瘤细胞系7TD1及MTT比色法测定生物活性,rIL—6比活性达2×108U/mg。We have adopted recombinant IL - 6 (rIL - 6 ) producing E. coli DH5a (pBV - hIL) and observed the growth and expression of rIl-6 in 30 liters fermentor under the selected composition of medium and pH value. The fermentative technological conditions were determined. The results of three batches of experiment under the conditions showed that the cell density of recombiant bacteria was 2. 51 ±0. 02g [dry weight]/L[fermcnted liquor]and the yield of rIL-6 was 182. 4±2. 0mg/g [dry weight]. rIL-6 is expressed in form of inclusion bodies in cells. Impurified proteins in inclusion bodies were extracted by nonion-detergent or urea or the other denaturant and the purity of rIL-6 can reach 70. 1± 1. 3% and the yield is 71. 9± 1. 9% The washed inclusion bodies were purified through gel filtration chromatography and renatured. The purity of rIL-6reached above 95 % and the yield was 72. 3±0. 9%. The specific activity of rIL-6 was 2 × 108U/mg which detected by using the IL-6-dependent mouse - mouse hybrid Cell line 7TD1 and MTT colorimetric assay.
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