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Visualizing gene expression in situ

机译:原位可视化基因表达

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Visualizing bacterial cells and describing their responses to the environment are difficult tasks. Their small size is the chief reason for the difficulty, which means that we must often use many millions of cells in a sample in order to determine what the average response of the bacteria is. However, an average response can sometimes mask important events in bacterial physiology, which means that our understanding of these organisms will suffer. We have used a variety of instruments to visualize bacterial cells, all of which tell us something different about the sample. We use a fluorescence activated cell sorter to sort cells based on the fluorescence provided by bioreporter genes, and these can be used to select for particular genetic mutations. Cells can be visualized by epifluorescent microscopy, and sensitive photodetectors can be added that allow us to find a single bacterial cell that is fluorescent or bioluminescent. We have also used standard photomultipliers to examine cell aggregates as field bioreporter microorganisms. Examples of each of these instruments show how our understanding of bacterial physiology has changed with the technology.
机译:可视化细菌细胞并描述它们对环境的反应是困难的任务。它们的体积小是难度的主要原因,这意味着我们必须经常在样品中使用数百万细胞,以确定细菌的平均响应是什么。然而,平均反应有时可以掩盖细菌生理中的重要事件,这意味着我们对这些生物的理解将受到影响。我们使用各种仪器来可视化细菌细胞,所有仪器都告诉我们一些不同的样本的东西。我们使用荧光活性细胞分选仪基于生物功率基因提供的荧光来分类细胞,这些荧光可用于选择特定的遗传突变。细胞可以通过外荧光显微镜观察,并且可以添加敏感光电探测器,使我们能够找到荧光或生物发光的单一细菌细胞。我们还使用标准光电倍增管来检查细胞骨料作为现场生物投资商微生物。这些仪器中的每一个的例子都会显示我们对细菌生理学的理解如何随着该技术而改变。

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