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Heterologous expression of codon optimized Trichoderma reesei Ce16A in Pichia pastoris

机译:密码子优化的里氏木霉Ce16A在毕赤酵母中的异源表达

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The Cel6A deficiency has become one of the limiting factors for cellulose saccharification in biochemical conversion of cellulosic biomass to fuels and chemicals. The work attempted to use codon optimization to enhance Trichoderma reesei Cel6A expression in Pichia pastoris. Two recombinants P. pastoris GS115 containing AOX1 and GAP promotors were successfully constructed, respectively. The optimal temperatures and pHs of the expressed Cel6A from two recombinants were consistent with each other, were also in the extremely similar range to that reported on the native Cel6A from T. reesei. Based on the shake flask fermentation, AOX1 promotor enabled the recombinant to produce 265 U/L and 300 mg/L of the Ce16A enzyme, and the GAP promotor resulted in 145 U/L and 200 mg/L. High cell density fed batch (HCDFB) fermentation significantly improved the enzyme titer (1100 UAL) and protein yield (2.0 g/L) for the recombinant with AOX1 promotor. Results have showed that the AOX1 promotor is more suitable than the GAP for the Cel6A expression in P. pastoris. And the HCDFB cultivation is a favorable way to express the Ce16A highly in the methanol inducible yeast. (C) 2016 Published by Elsevier Inc.
机译:Cel6A缺乏症已成为纤维素生物质向燃料和化学物质的生化转化中纤维素糖化的限制因素之一。这项工作试图使用密码子优化来增强里氏木霉Cel6A在毕赤酵母中的表达。分别成功构建了两个含有AOX1和GAP启动子的重组毕赤酵母GS115。来自两个重组体的表达的Cel6A的最佳温度和pH彼此一致,也与里氏木霉天然Cel6A报道的温度和pH极为相似。基于摇瓶发酵,AOX1启动子使重组体产生265 U / L和300 mg / L的Ce16A酶,而GAP启动子导致145 U / L和200 mg / L。高细胞密度补料分批(HCDFB)发酵显着提高了带有AOX1启动子的重组体的酶滴度(1100 UAL)和蛋白质产量(2.0 g / L)。结果表明,AOX1启动子比GAP更适合于巴斯德毕赤酵母中Cel6A表达。 HCDFB培养是在甲醇可诱导酵母中高表达Ce16A的有利方法。 (C)2016由Elsevier Inc.发布

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