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Acetate formation during recombinant protein production in Escherichia coli K-12 with an elevated NAD(H) pool

机译:在大肠杆菌K-12中重组蛋白质产生期间的醋酸酯形成,其中NAD升高(H)池

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Acetate formation is a disadvantage in the use of Escherichia coli for recombinant protein production, and many studies have focused on optimizing fermentation processes or altering metabolism to eliminate acetate accumulation. In this study, E. coli MEC697 (MG1655 nadR nudC mazG) maintained a larger pool of NAD(H) compared to the wild-type control, and also accumulated lower concentrations of acetate when grown in batch culture on glucose. In steady-state cultures, the elevated total NAD(H) found in MEC697 delayed the threshold dilution rate for acetate formation to a growth rate of 0.27 h(-1). Batch and fed-batch processes using MEC697 were examined for the production of beta-galactosidase as a model recombinant protein. Fed-batch culture of MEC697/pTrc99A-lacZ compared to MG1655/pTrc99A-lacZ at a growth rate of 0.22 h(-1) showed only a modest increase of protein formation. However, 1 L batch growth of MEC697/pTrc99A-lacZ resulted in 50% lower acetate formation compared to MG1655/pTrc99A-lacZ and a two-fold increase in recombinant protein production.
机译:醋酸酯形成是使用大肠杆菌用于重组蛋白质产生的缺点,并且许多研究侧重于优化发酵过程或改变代谢以消除醋酸盐的积累。在本研究中,与野生型对照相比,大肠杆菌MEC697(MG1655 NADR NUDC MAZG)与野生型对照相比,将更大的NAD(H)池相比,并且在葡萄糖的分批培养中生长时累积较低浓度的醋酸浓度。在稳态培养物中,MEC697中发现的升高的NAD(H)延迟了醋酸盐地层的阈值稀释率,以0.27h(-1)的生长速率。检查使用MEC697的分批和补料分批方法,用于生产β-半乳糖苷酶作为模型重组蛋白。 MEC697 / PTRC99A-LACZ的氟化批培养物与Mg1655 / ptrc99a-lacz以0.22h(-1)的生长速率相比,仅显示蛋白质形成的适度增加。然而,与Mg1655 / ptrC99A-LacZ相比,MEC697 / PTRC99A-LacZ的1升批量生产为乙酸盐形成50%,重组蛋白质产生的两倍增加。

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