首页> 美国卫生研究院文献>Journal of Bacteriology >Granular Layer in the Periplasmic Space of Gram-Positive Bacteria and Fine Structures of Enterococcus gallinarum and Streptococcus gordonii Septa Revealed by Cryo-Electron Microscopy of Vitreous Sections
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Granular Layer in the Periplasmic Space of Gram-Positive Bacteria and Fine Structures of Enterococcus gallinarum and Streptococcus gordonii Septa Revealed by Cryo-Electron Microscopy of Vitreous Sections

机译:冷冻切片的玻璃体切片显示革兰氏阳性细菌周质空间中的颗粒层和鸡肠球菌和戈登链球菌隔的精细结构

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摘要

High-resolution structural information on optimally preserved bacterial cells can be obtained with cryo-electron microscopy of vitreous sections. With the help of this technique, the existence of a periplasmic space between the plasma membrane and the thick peptidoglycan layer of the gram-positive bacteria Bacillus subtilis and Staphylococcus aureus was recently shown. This raises questions about the mode of polymerization of peptidoglycan. In the present study, we report the structure of the cell envelope of three gram-positive bacteria (B. subtilis, Streptococcus gordonii, and Enterococcus gallinarum). In the three cases, a previously undescribed granular layer adjacent to the plasma membrane is found in the periplasmic space. In order to better understand how nascent peptidoglycan is incorporated into the mature peptidoglycan, we investigated cellular regions known to represent the sites of cell wall production. Each of these sites possesses a specific structure. We propose a hypothetic model of peptidoglycan polymerization that accommodates these differences: peptidoglycan precursors could be exported from the cytoplasm to the periplasmic space, where they could diffuse until they would interact with the interface between the granular layer and the thick peptidoglycan layer. They could then polymerize with mature peptidoglycan. We report cytoplasmic structures at the E. gallinarum septum that could be interpreted as cytoskeletal elements driving cell division (FtsZ ring). Although immunoelectron microscopy and fluorescence microscopy studies have demonstrated the septal and cytoplasmic localization of FtsZ, direct visualization of in situ FtsZ filaments has not been obtained in any electron microscopy study of fixed and dehydrated bacteria.
机译:可以通过玻璃体切片的冷冻电子显微镜获得有关最佳保存细菌细胞的高分辨率结构信息。借助于该技术,最近显示了革兰氏阳性细菌枯草芽孢杆菌和金黄色葡萄球菌的质膜与厚肽聚糖层之间存在周质间隙。这引起了关于肽聚糖的聚合方式的疑问。在本研究中,我们报告了三种革兰氏阳性细菌(枯草芽孢杆菌,戈登链球菌和鸡肠球菌)的细胞包膜结构。在这三种情况下,在周质空间中发现了与质膜相邻的先前未描述的颗粒层。为了更好地了解新生的肽聚糖如何结合到成熟的肽聚糖中,我们研究了已知代表细胞壁产生部位的细胞区域。这些站点均具有特定的结构。我们提出了一种肽聚糖聚合的假想模型,以适应这些差异:肽聚糖前体可以从细胞质输出到周质空间,在那里它们可以扩散直到它们与颗粒层和厚肽聚糖层之间的界面相互作用。然后它们可以与成熟的肽聚糖聚合。我们报告了在大肠埃希菌中隔的胞质结构,可以解释为驱动细胞分裂的细胞骨架元件(FtsZ环)。尽管免疫电子显微镜和荧光显微镜研究已经证明FtsZ在隔膜和细胞质中的定位,但是在固定和脱水细菌的任何电子显微镜研究中都没有获得对FtsZ丝原位的直接观察。

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