首页> 外文期刊>Molecular Microbiology >Tsr-GFP accumulates linearly with time at cell poles, and can be used to differentiate 'old' versus 'new' poles, in Escherichia coli.
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Tsr-GFP accumulates linearly with time at cell poles, and can be used to differentiate 'old' versus 'new' poles, in Escherichia coli.

机译:Tsr-GFP在细胞两极随时间线性累积,可用于区分大肠杆菌中的“旧”极与“新”极。

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SUMMARY: In Escherichia coli, the chemotaxis receptor protein Tsr localizes abundantly to cell poles. The current study, utilizing a Tsr-GFP fusion protein and time-lapse fluorescence microscopy of individual cell lineages, demonstrates that Tsr accumulates approximately linearly with time at the cell poles and that, in consequence, more Tsr is present at the old pole of each cell than at its newborn pole. The rate of pole-localized Tsr accumulation is large enough that old and new poles can always be reliably distinguished, even for cells whose old poles have had only one generation to accumulate signal. Correspondingly, Tsr-GFP can be reliably used to assign new and old poles to any cell without use of information regarding pole heritage, thus providing a useful tool to analyse cells whose prior history is not available. The absolute level of Tsr-GFP at the old pole of a cell also provides a rough estimate of pole (and thus cell) age.
机译:摘要:在大肠杆菌中,趋化性受体蛋白Tsr大量位于细胞极。当前的研究利用Tsr-GFP融合蛋白和单个细胞谱系的延时荧光显微镜观察表明,Tsr在细胞两极几乎随时间线性积累,因此,每个细胞的旧极上存在更多的Tsr。细胞比其新生极。极点本地化的Tsr累积速率足够大,以致始终可以可靠地区分新旧极点,即使对于旧极点只有一代可以累积信号的单元也是如此。相应地,Tsr-GFP可以可靠地用于为任何细胞分配新的和旧的极,而无需使用有关极遗传的信息,从而提供了一个有用的工具来分析先前历史不可用的细胞。 Tsr-GFP在细胞旧极点的绝对水平也提供了一个极点(因此也就是细胞)年龄的粗略估计。

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