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通过电子显微镜、SDS-PAGE和蛋白质免疫印迹法研究单核细胞增生李斯特菌鞭毛的温度依赖性表达。

Temperature-dependent expression of flagella of Listeria monocytogenes studied by electron microscopy, SDS-PAGE and western blotting.

作者信息

Peel M, Donachie W, Shaw A

机构信息

Moredun Research Institute, Edinburgh, UK.

出版信息

J Gen Microbiol. 1988 Aug;134(8):2171-8. doi: 10.1099/00221287-134-8-2171.

Abstract

Washed cells of Listeria monocytogenes serotype 4b, grown in broth culture at 20 degrees C and at 37 degrees C, were examined by electron microscopy for the presence of flagella. Many flagella were seen in cells grown at 20 degrees C, whereas at 37 degrees C very few were expressed. Flagella sheared from the cell surface were partially purified by differential centrifugation. Using SDS-PAGE and Western blotting two distinct protein bands were seen in this preparation, both with an apparent molecular mass of approximately 29 kDa. Further purification of these proteins was achieved by gel filtration and ion-exchange chromatography. Whole organisms grown at 20 degrees C and 37 degrees C were examined in Western blots using an affinity-purified polyclonal antibody, and a monoclonal antibody, both directed against 29 kDa putative flagellin. Bacteria grown at 20 degrees C expressed abundant flagellin, whereas only trace amounts could be detected in organisms grown at 37 degrees C. It is concluded that organisms grown at 20 degrees C both produce and assemble flagellin at the cell surface, and that flagellin production is a less marked feature of organisms grown at 37 degrees C.

摘要

对在20摄氏度和37摄氏度肉汤培养中生长的单核细胞增生李斯特菌4b血清型的洗涤细胞进行电子显微镜检查,以确定是否存在鞭毛。在20摄氏度下生长的细胞中可见许多鞭毛,而在37摄氏度时表达的鞭毛很少。从细胞表面剪切下来的鞭毛通过差速离心进行部分纯化。使用SDS-PAGE和蛋白质印迹法,在该制剂中可见两条不同的蛋白带,两者的表观分子量均约为29 kDa。通过凝胶过滤和离子交换色谱法对这些蛋白质进行了进一步纯化。使用针对29 kDa假定鞭毛蛋白的亲和纯化多克隆抗体和单克隆抗体,对在20摄氏度和37摄氏度下生长的整个生物体进行蛋白质印迹分析。在20摄氏度下生长的细菌表达大量鞭毛蛋白,而在37摄氏度下生长的生物体中只能检测到微量鞭毛蛋白。得出的结论是,在20摄氏度下生长的生物体在细胞表面产生并组装鞭毛蛋白,而鞭毛蛋白的产生在37摄氏度下生长的生物体中不太明显。

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