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大肠杆菌BL21(DE3)生产β-环状糊精转移酶发酵条件的优化 被引量:1

Optimization of the culture conditions of E.coli BL21(DE3) producing β-cyclodextrin glucanotransferase
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摘要 采用正交试验确定大肠杆菌BL21(DE3)产β-环糊精转移酶的发酵条件。结果表明,生产β-环状糊精转移酶的最适条件为:接种量1%,100mL三角瓶装液量15mL,初始pH值为7.0,Ca2+浓度为1.25mmol/L,Mg2+浓度为2.50mmol/L,温度控制在37℃,转速控制为150r/min。当OD600达到1.4时,加入终浓度5.0g/L的α-乳糖,转速提高至170r/min,37℃诱导12h后过滤,β-CGTase酶活最高可达16.3μ/mL。 The culture condition for producing β-cyclodextrin glucanotransferase by E.coli BL21 (DE3) was primarily established by orthogonal experimental design. The results showed that the optimal fermentation conditions were as follows: the inoculum size was 1%; The load of 100ml-flask was 15ml; initial pH value was 7.0; the concentration of Ca^2+ was 1.25mmol/L, the concentration of Mg^2+ was 2.50mmol/L, incubation temperature was 37~C and the speed was 150r/rain. When the value of OD600 reached 1.4, u-lactose was added so as to the final concentration to 5.0g/L, the speed was increased to 170r/min, and induced 12h at 37℃ then filtered, the β-CGTase activity reached the maximum value as 16.3μ/ml.
出处 《中国酿造》 CAS 2013年第4期52-57,共6页 China Brewing
基金 科技部农业科技成果转化资金项(2010GB2F300436) 国家自然科学基金委员会资助项目(31160229)
关键词 发酵条件 β-环状糊精转移酶 重组大肠杆菌 优化 fermentation conditions β-CGTase recombinant E.coli optimization
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