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X-ray micrography and imaging of Escherichia coli cell shape using laser plasma pulsed point x-ray sources.

机译:使用激光等离子体脉冲点X射线源进行X射线显微照相和大肠杆菌细胞形状成像。

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摘要

High-resolution x-ray microscopy is a relatively new technique and is performed mostly at a few large synchrotron x-ray sources that use exposure times of seconds. We utilized a bench-top source of single-shot laser (ns) plasma to generate x-rays similar to synchrotron facilities. A 5 microlitres suspension of Escherichia coli ATCC 25922 in 0.9% phosphate buffered saline was placed on polymethylmethyacrylate coated photoresist, covered with a thin (100 nm) SiN window and positioned in a vacuum chamber close to the x-ray source. The emission spectrum was tuned for optimal absorption by carbon-rich material. Atomic force microscope scans provided a surface and topographical image of differential x-ray absorption corresponding to specimen properties. By using this technique we observed a distinct layer around whole cells, possibly representing the Gram-negative envelope, darker stained areas inside the cell corresponding to chromosomal DNA as seen by thin section electron microscopy, and dent(s) midway through one cell, and 1/3- and 2/3-lengths in another cell, possibly representing one or more division septa. This quick and high resolution with depth-of-field microscopy technique is unmatched to image live hydrated ultrastructure, and has much potential for application in the study of fragile biological specimens.
机译:高分辨率X射线显微镜技术是一种相对较新的技术,主要在使用几秒钟曝光时间的几个大型同步加速器X射线源上进行。我们利用台式单发激光(ns)等离子体源产生类似于同步加速器设施的X射线。将大肠杆菌ATCC 25922在0.9%磷酸盐缓冲盐水中的5微升悬浮液置于涂覆有聚甲基丙烯酸甲酯的光致抗蚀剂上,用薄的(100 nm)SiN窗口覆盖,并放置在靠近X射线源的真空室中。调整了发射光谱,以使富含碳的材料获得最佳吸收。原子力显微镜扫描提供了与样品特性相对应的X射线吸收差异的表面和地形图。通过使用这项技术,我们在整个细胞周围观察到一个独特的层,可能代表革兰氏阴性包膜,通过薄层电子显微镜观察到,细胞内部较暗的染色区域对应于染色体DNA,并且在一个细胞的中途出现了凹痕,另一个单元格中的1/3和2/3长度,可能表示一个或多个分隔间隔。这种具有景深显微镜技术的快速而高分辨率的图像无法与水合活的超微结构图像相媲美,并且在研究脆弱的生物标本方面具有巨大的潜力。

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