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Proteomic Profiling of Recombinant Escherichia coli in High-Cell- Density Fermentations for Improved Production of an Antibody Fragment Biopharmaceutical

机译:高细胞密度发酵中重组大肠杆菌的蛋白质组学分析可提高抗体片段生物制药的生产

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摘要

By using two-dimensional polyacrylamide gel electrophoresis, a proteomic analysis over time was conducted with high-cell-density, industrial, phosphate-limited Escherichia coli fermentations at the 10-liter scale. During production, a recombinant, humanized antibody fragment was secreted and assembled in a soluble form in the periplasm. E. coli protein changes associated with culture conditions were distinguished from protein changes associated with heterologous protein expression. Protein spots were monitored quantitatively and qualitatively. Differentially expressed proteins were quantitatively assessed by using a t-test method with a 1% false discovery rate as a significance criterion. As determined by this criterion, 81 protein spots changed significantly between 14 and 72 h (final time) of the control fermentations (vector only). Qualitative (on-off) comparisons indicated that 20 more protein spots were present only at 14 or 72 h in the control fermentations. These changes reflected physiological responses to the culture conditions. In control and production fermentations at 72 h, 25 protein spots were significantly differentially expressed. In addition, 19 protein spots were present only in control or production fermentations at this time. The quantitative and qualitative changes were attributable to overexpression of recombinant protein. The physiological changes observed during the fermentations included the up-regulation of phosphate starvation proteins and the down-regulation of ribosomal proteins and nucleotide biosynthesis proteins. Synthesis of the stress protein phage shock protein A (PspA) was strongly correlated with synthesis of a recombinant product. This suggested that manipulation of PspA levels might improve the soluble recombinant protein yield in the periplasm for this bioprocess. Indeed, controlled coexpression of PspA during production led to a moderate, but statistically significant, improvement in the yield.
机译:通过使用二维聚丙烯酰胺凝胶电泳,使用10升规模的高细胞密度,磷酸盐限制的工业化大肠埃希氏菌进行长时间的蛋白质组分析。在生产过程中,重组人源化抗体片段被分泌并以可溶形式组装在周质中。与培养条件有关的大肠杆菌蛋白质变化与与异源蛋白质表达有关的蛋白质变化区别开来。对蛋白质斑点进行定量和定性监测。通过t检验方法以1%的错误发现率作为显着性标准,定量评估差异表达的蛋白质。根据此标准确定,在对照发酵的14至72小时(最终时间)(仅载体)之间,有81个蛋白斑点发生了明显变化。定性(开-关)比较表明,在对照发酵中仅在14或72小时出现了20个蛋白斑点。这些变化反映了对培养条件的生理反应。在72小时的对照发酵和生产发酵中,有25个蛋白点显着差异表达。另外,此时仅在对照或生产发酵中存在19个蛋白斑点。数量和质量的变化归因于重组蛋白的过表达。发酵过程中观察到的生理变化包括磷酸饥饿蛋白的上调,核糖体蛋白和核苷酸生物合成蛋白的下调。应激蛋白噬菌体休克蛋白A(PspA)的合成与重组产物的合成密切相关。这表明操纵PspA水平可能会提高该生物过程在周质中的可溶性重组蛋白产量。实际上,在生产过程中受控的PspA共表达可导致产量适度提高,但具有统计学意义。

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