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作 者:张励[1] 叶勤[1] 辛利[2] 杜鹏[2] 甘人宝[2]
机构地区:[1]华东理工大学生物反应器工程国家重点实验室,上海200237 [2]中国科学院生物化学研究所,上海200031
出 处:《微生物学通报》2002年第1期23-26,共4页Microbiology China
基 金:教育部科学技术研究重点项目(No.99166)
摘 要: 本研究采用流加补料培养方式培养重组巴斯德毕赤酵母(Pichia pastoris),表达血管生长抑制素(Angiostatin)。整个培养过程分为以甘油为碳源的生长阶段和以甲醇为碳源的诱导阶段。全过程用氨水调节pH时,诱导阶段菌体生长受到抑制,蛋白的最大表达量为9.08mg/L。进行不同氨离子浓度的摇瓶培养,证实在以甲醇为碳源时,氨离子浓度对菌体的生长有明显的影响。高密度培养中改用 2 mol/L的 KOH溶液调节 pH,诱导阶段菌体有缓慢的生长,蛋白最大表达量增为20mg/L。Fed-batch cultures of recombinant Rchia pastoris were conducted for production of angiostatin. The whole fermentation included a growth phase on glycerol and an expression phase on methanol. When ammonium hydroxide solution was used to adjust pH, the cell growth during the expression phase was inhibited and the highest angiostatin concentration was 9.08 mg/L. Shake-flask cultures were carried out in media containing different quantities of ammonia. The results showed that ammonia had an obvious inhibition effect on the cell growth during the expression phase. Therefore KOH solution was used to adjust pH, and during the expression phase cells were able to grow and the highest angiostatin concentration reached 20 mg/L.
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