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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Construction and Application of an Escherichia coli Strain Lacking 62 Genes Responsible for the Biosynthesis of Enterobacterial Common Antigen and Flagella
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Construction and Application of an Escherichia coli Strain Lacking 62 Genes Responsible for the Biosynthesis of Enterobacterial Common Antigen and Flagella

机译:缺乏62个基因的大肠杆菌菌株的构建与应用,负责大肠杆菌常见抗原和鞭毛生物合成的基因

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摘要

The biosynthesis of the enterobacterial common antigen and flagella in Escherichia coli consumes lots of substrates and energy. In this study, 12 genes responsible for the biosynthesis of the enterobacterial common antigen were deleted in E. coli MG1655, resulting in WQM021. WQM021 grew better than MG1655 in both rich LB medium and minimum M9 medium. Compared with MG1655, WQM021 showed higher membrane permeability and higher production efficiency for recombinant proteins, polyhydroxyalkanoate, and L-threonine. Transcriptome analysis revealed that genes relevant to glucose consumption, glycolysis, and flagellar synthesis were significantly upregulated in WQM021. Therefore, 50 genes responsible for flagellar biosynthesis were further deleted in WQM021, resulting in WQM022. WQM022 grew better and could synthesize more polyhydroxyalkanoate and L-threonine than WQM021. The results demonstrate that the productivity of E. coli can be efficiently improved when the enterobacterial common antigen and flagella are eliminated. This strategy has guiding significance in the optimization of other industrial products and microorganisms.
机译:大肠杆菌中肠杆菌共同抗原和鞭毛的生物合成需要消耗大量底物和能量。在这项研究中,在大肠杆菌MG1655中,12个负责肠杆菌共同抗原生物合成的基因被删除,导致WQM021。WQM021在富LB培养基和最低M9培养基中的生长均优于MG1655。与MG1655相比,WQM021对重组蛋白、多羟基烷酸酯和L-苏氨酸具有更高的膜通透性和生产效率。转录组分析显示,与葡萄糖消耗、糖酵解和鞭毛合成相关的基因在WQM021中显著上调。因此,在WQM021中,50个负责鞭毛生物合成的基因被进一步删除,导致WQM022。与WQM021相比,WQM022生长更好,能够合成更多的多羟基烷酸酯和L-苏氨酸。结果表明,去除肠杆菌共同抗原和鞭毛可以有效提高大肠杆菌的生产能力。该策略对其他工业产品和微生物的优化具有指导意义。

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