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Construction of Monophosphoryl Lipid A Producing Escherichia coli Mutants and Comparison of Immuno-Stimulatory Activities of Their Lipopolysaccharides

机译:产生大肠杆菌的单磷酰基脂质A突变体的构建及其脂多糖的免疫刺激活性比较

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The lipid A moiety of Escherichia coli lipopolysaccharide is a hexaacylated disaccharide of glucosamine phosphorylated at the 1- and 4′-positions. It can be recognized by the TLR4/MD-2 complex of mammalian immune cells, leading to release of proinflammatory cytokines. The toxicity of lipid A depends on its structure. In this study, two E. coli mutants, HW001 and HW002, were constructed by deleting or integrating key genes related to lipid A biosynthesis in the chromosome of E. coli W3110. HW001 was constructed by deleting lacI and replacing lacZ with the Francisella novicida lpxE gene in the chromosome and only synthesizes monophosphoryl lipid A. HW002 was constructed by deleting lpxM in HW001 and synthesizes only the pentaacylated monophosphoryl lipid A. The structures of lipid A made in HW001 and HW002 were confirmed by thin layer chromatography and electrospray ionization mass spectrometry. HW001 and HW002 grew as well as the wild-type W3110. LPS purified from HW001 or HW002 was used to stimulate murine macrophage RAW264.7 cells, and less TNF-α were released. This study provides a feasible way to produce interesting lipid A species in E. coli.
机译:大肠杆菌脂多糖的脂质A部分是在1-和4'-位磷酸化的葡糖胺的六酰化二糖。它可以被哺乳动物免疫细胞的TLR4 / MD-2复合物识别,从而导致促炎性细胞因子的释放。脂质A的毒性取决于其结构。在这项研究中,通过删除或整合与大肠杆菌W3110染色体中的脂质A生物合成相关的关键基因,构建了两个大肠杆菌突变体HW001和HW002。通过删除lacI并用染色体上的新弗朗西斯菌新的lpxE基因取代lacZ来构建HW001,并且仅合成单磷酰基脂质A。通过删除HW001中的lpxM来构建HW002,并且仅合成五酰基化的单磷酰基脂质A。通过薄层色谱和电喷雾电离质谱法确认了HW002和HW002。 HW001和HW002与野生型W3110一样生长。从HW001或HW002纯化的LPS用于刺激鼠巨噬细胞RAW264.7细胞,并释放较少的TNF-α。这项研究提供了一种在大肠杆菌中生产有趣的脂质A物种的可行方法。

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