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Engineering Escherichia coli for Increased Productivity of Serine-Rich Proteins Based on Proteome Profiling

机译:基于蛋白质组图谱分析工程大肠杆菌以提高富含丝氨酸的蛋白质的生产力

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Variations in proteome profiles of Escherichia coli in response to the overproduction of human leptin, a serine-rich (11.6% of total amino acids) protein, were examined by two-dimensional gel electrophoresis. The levels of heat shock proteins increased, while those of protein elongation factors, 30S ribosomal protein, and some enzymes involved in amino acid biosynthesis decreased, after leptin overproduction. Most notably, the levels of enzymes involved in the biosynthesis of serine family amino acids significantly decreased. Based on this information, we designed a strategy to enhance the leptin productivity by manipulating the cysK gene, encoding cysteine synthase A. By coexpression of the cysK gene, we were able to increase the cell growth rate by approximately twofold. Also, the specific leptin productivity could be increased by fourfold. In addition, we found that cysK coexpression can improve the production of another serine-rich protein, interleukin-12 β chain, suggesting that this strategy may be useful for the production of other serine-rich proteins as well. The approach taken in this study should be useful in designing a strategy for improving recombinant protein production.
机译:通过二维凝胶电泳检查了人瘦素(一种富含丝氨酸的氨基酸(占总氨基酸的11.6%))过量生产后,大肠杆菌蛋白质组谱的变化。瘦素过量生产后,热休克蛋白的水平增加,而蛋白延伸因子,30S核糖体蛋白和一些参与氨基酸生物合成的酶的水平降低。最值得注意的是,参与丝氨酸家族氨基酸生物合成的酶水平显着降低。基于此信息,我们设计了一种策略,通过操纵编码半胱氨酸合酶A的 cysK 基因来提高瘦蛋白的产量。通过共表达 cysK 基因,我们能够使细胞生长速度提高大约两倍。而且,瘦蛋白的单位生产率可以提高四倍。此外,我们发现 cysK 共表达可以改善另一种富含丝氨酸的蛋白白介素12β链的产生,这表明该策略也可能对其他富含丝氨酸的蛋白的产生也有用。 。本研究中采用的方法在设计改善重组蛋白生产的策略中应该是有用的。

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