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A novel protocol for bacterial ghosts’ preparation using tween 80

机译:使用补间80制备细菌鬼魂的新方案

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Bacterial ghosts (BGs) can be prepared by both genetic and chemical means. Genetic method include using lysis gene E . Chemical method include incubation with numerous agents for a short time at their minimum inhibitory or minimum growth concentrations (MIC or MGC). The aim of this study is to prepare the BGs with a new protocol via exposing the bacterial cells to tween 80 for an extended period of time followed by sudden reduction of the surrounding pH. Salmonella enterica serovar typhimurium ATCC 13311 was used for this purpose. The cells were incubated in 7% v/v tween 80 solution in Muller-Hinton broth for 24?h at 37 °C then pH was decreased to 3.6 by adding lactic acid for one hour. The bacterial pellets were separated by high speed centrifugation, and then washed three times by half normal saline solution. High quality BGs were visualized by scanning electron microscopy (SEM) revealing punctured cells with intact outer shells and at least one intramembranous tunnel. The absence of vital cells was confirmed by subculturing. The release of respective amounts of proteins and DNA is another evidence of ghost’s production. In addition, the integrity of cells was proved by visualization of Gram-stained cells using light microscopy. In conclusion, this new protocol is simple, economic and feasible for BGs preparation.
机译:细菌鬼(BG)可以通过遗传和化学手段制备。遗传方法包括使用裂解基因E。化学方法包括与多种试剂在其最小抑制浓度或最小生长浓度(MIC或MGC)下短时间孵育。这项研究的目的是通过将细菌细胞暴露于吐温80一段较长的时间,然后突然降低周围的pH值,以一种新的方法制备BG。为此,使用沙门氏菌血清型鼠伤寒沙门氏菌ATCC 13311。将细胞在37%的Muller-Hinton肉汤中的7%v / v吐温80溶液中孵育24?h,然后通过添加乳酸1小时将pH降至3.6。通过高速离心分离细菌沉淀,然后用一半的生理盐水溶液洗涤3次。高质量的BG通过扫描电子显微镜(SEM)可视化,发现带有完整外壳和至少一个膜内通道的穿刺细胞。通过传代培养确认不存在活细胞。释放相应数量的蛋白质和DNA是鬼魂产生的另一个证据。另外,通过使用光学显微镜可视化革兰氏染色的细胞来证明细胞的完整性。总之,此新协议对于BG的准备简单,经济且可行。

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