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Suppressing glucose uptake and acetic acid production increases membrane protein overexpression in Escherichia coli

机译:抑制葡萄糖摄取和乙酸产生会增加大肠杆菌中膜蛋白的过表达

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Background The production of integral membrane spanning proteins (IMP's) constitutes a bottleneck in pharmaceutical development. It was long considered that the state-of-the-art was to produce the proteins as inclusion bodies using a powerful induction system. However, the quality of the protein was compromised and the production of a soluble protein that is incorporated into the membrane from which it is extracted is now considered to be a better method. Earlier research has indicated that a slower rate of protein synthesis might overcome the tendency to form inclusion bodies. We here suggest the use of a set of E. coli mutants characterized by a slower rate of growth and protein synthesis as a tool for increasing the amount of soluble protein in high- throughput protein production processes. Results A set of five IMP's was chosen which were expressed in three mutants and the corresponding WT cell (control). The mutations led to three different substrate uptake rates, two of which were considerably slower than that of the wild type. Using the mutants, we were able to express three out of the five membrane proteins. Most successful was the mutant growing at 50% of the wild type growth rate. A further effect of a low growth rate is a low acetic acid formation, and we believe that this is a possible reason for the better production. This hypothesis was further supported by expression from the BL21(DE3) strain, using the same plasmid. This strain grows at a high growth rate but nevertheless yields only small amounts of acetic acid. This strain was also able to express three out of the five IMP's, although at lower quantities. Conclusions The use of mutants that reduce the specific substrate uptake rate seems to be a versatile tool for overcoming some of the difficulties in the production of integral membrane spanning proteins. A set of strains with mutations in the glucose uptake system and with a lower acetic acid formation were able to produce three out of five membrane proteins that it was not possible to produce with the corresponding wild type.
机译:背景技术完整的跨膜蛋白(IMP's)的生产构成了药物开发的瓶颈。长期以来,人们一直认为,最先进的技术是使用功能强大的诱导系统将蛋白质制成包涵体。但是,蛋白质的质量受到了损害,现在人们认为,将可溶性蛋白质掺入提取膜的过程中是一种更好的方法。较早的研究表明,较慢的蛋白质合成速度可能会克服形成包涵体的趋势。我们在这里建议使用以生长和蛋白质合成速度较慢为特征的一组大肠杆菌突变体作为增加高通量蛋白质生产过程中可溶性蛋白质数量的工具。结果选择了一组五个IMP,它们在三个突变体和相应的WT细胞(对照)中表达。突变导致三种不同的底物吸收率,其中两种比野生型慢得多。使用突变体,我们能够表达五种膜蛋白中的三种。最成功的是突变体以野生型生长速率的50%生长。低生长速率的另一个影响是乙酸形成量低,我们认为这是提高产量的可能原因。使用相同质粒从BL21(DE3)菌株表达进一步支持了该假设。该菌株以高生长速率生长,但是仅产生少量乙酸。该菌株还能够表达五个IMP中的三个,尽管数量较少。结论使用降低特定底物摄取率的突变体似乎是克服生产跨膜完整蛋白过程中某些困难的通用工具。一组在葡萄糖摄取系统中具有突变且乙酸形成较低的菌株能够产生五种膜蛋白中的三种,而相应的野生型则无法产生。

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