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首页> 外文期刊>Microbial Biotechnology >Glycine significantly enhances bacterial membrane vesicle production: a powerful approach for isolation of LPS‐reduced membrane vesicles of probiotic Escherichia coli
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Glycine significantly enhances bacterial membrane vesicle production: a powerful approach for isolation of LPS‐reduced membrane vesicles of probiotic Escherichia coli

机译:甘氨酸显着增强细菌膜囊泡生产:一种强大的益生菌大肠杆菌液体膜囊泡分离的方法

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Summary Bacterial membrane vesicles (MVs) have attracted strong interest in recent years as novel nanoparticle delivery platforms. Glycine is known to induce morphological changes in the outer layer of bacteria. We report here that glycine dramatically facilitates MV production in a flagella‐deficient mutant of the non‐pathogenic probiotic Escherichia coli strain Nissle 1917. Supplementation of culture medium with 1.0% glycine induced cell deformation at the early exponential phase, eventually followed by quasi‐lysis during the late exponential to stationary phase. Glycine supplementation also significantly increased the number of MVs with enlarged particle size and altered the protein profile with an increase in the inner membrane and cytoplasmic protein contents as compared to non‐induced MVs. Of note, the endotoxin activity of glycine‐induced MVs was approximately eightfold or sixfold lower than that of non‐induced MVs when compared at equal protein or lipid concentrations respectively. Nevertheless, glycine‐induced MVs efficiently induced both immune responses in a mouse macrophage‐like cell line and adjuvanticity in an intranasal vaccine mouse model, comparable to those of non‐induced MVs. We propose that the present method of inducing MV production with glycine can be used for emerging biotechnological applications of MVs that have immunomodulatory activities, while dramatically reducing the presence of endotoxins.
机译:发明细菌膜囊泡(MVS)近年来吸引了强烈的兴趣作为新型纳米颗粒递送平台。已知甘氨酸诱导细菌外层的形态变化。我们在此报告甘氨酸在非致病性益生菌大肠杆菌菌株Nissle 1917的葡萄鞭菌缺失突变体中显着促进了MV产生。在早期指数阶段补充了培养基,最终呈甘氨酸诱导细胞变形,最终用拟裂解在延迟指数到固定阶段。甘氨酸补充剂还显着增加了粒度扩大的MV的数量,并改变了与非诱导的MV的内膜和细胞质蛋白质含量的增加。值得注知的是,在相等的蛋白质或脂质浓度下,甘氨酸诱导的MV的内毒素活性大约比非诱导的MVS低约8倍或六倍。然而,甘氨酸诱导的MVS有效地诱导小鼠巨噬细胞样细胞系和鼻内疫苗小鼠模型中的佐治性的免疫应答,与非诱导的MVs相当。我们提出,用甘氨酸诱导MV生产的本方法可用于新出现具有免疫调节活动的MV的生物技术应用,同时显着降低内毒素的存在。

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