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作 者:陈洲[1] 贾会勇[2] 闫巧娟[1] 杨绍青[2] 滕超[2] 江正强[2]
机构地区:[1]中国农业大学工学院,北京100083 [2]中国农业大学食品科学与营养工程学院,北京100083
出 处:《微生物学通报》2013年第2期212-219,共8页Microbiology China
基 金:农业科技成果转化资金项目(No.2010GB23600652)
摘 要:【目的】嗜热拟青霉β-木糖苷酶基因在大肠杆菌中高效分泌表达重组β-木糖苷酶摇瓶发酵条件优化,及5 L发酵罐放大培养。【方法】通过单因素试验对诱导剂种类及其添加量、诱导起始OD600、培养温度、培养时间进行优化研究。【结果】摇瓶优化结果表明:2%乳糖为诱导剂、培养温度为33°C、OD600控制在0.8?0.9时诱导为最佳产酶条件,在此条件下培养48 h后胞外酶活达到103.9 U/mL,胞外分泌的比例高达99%以上。进行5 L发酵罐放大培养,发酵48 h胞外酶活达到最高值392.5 U/mL,蛋白含量为10.1 g/L。【结论】该重组大肠杆菌高效分泌β-木糖苷酶,具有较好的工业化生产前景。[Objective] The fermentation conditions for production of recombinant β-xylosidase from Paecilomyces thermophila expressed in E. coli were optimized and produced in a 5 L fermentor. [Methods] Single factor experiments were used to investigate the effect of different inducers and their concentrations, initial cell density, cultivation temperature and time on the expression of recombinant β-xylosidase. [Results] The results showed that the β-xylosidase could be induced by IPTG and lactose, lactose was better than that of IPTG. Under the optimal conditions by adding 2% lactose at a initiated 006oo of 0.8-0.9 and incubation for 48 h at 33 ℃ the ratio of extracellular enzyme reached over 99% and enzyme activity was 103.9 U/mL. Further optimization of the culture conditions were performed in 5 L fermentor, the highest β-xylosidase activity of 392.5 U/mL and extracellular protein concentration of 10.1 g/L were obtained after 48 h. [Conclusion] The recombinant β-xylosidase with high level production will be useful in various industrial applications.
分 类 号:TQ925[轻工技术与工程—发酵工程]
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