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首页> 外文期刊>Antonie van Leeuwenhoek: Journal of Microbiology and serology >Is Urografin density gradient centrifugation suitable to separate nonculturable cells from Escherichia coli populations?
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Is Urografin density gradient centrifugation suitable to separate nonculturable cells from Escherichia coli populations?

机译:Urografin密度梯度离心法是否适合于从大肠杆菌群体中分离出不可培养的细胞?

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摘要

The ability of Urografin or Percoll density gradient centrifugations to separate nonculturable subpopulations from heterogeneous Escherichia coli populations was analysed. Bacterial counts (total, active and culturable cells) and flow cytometric analyses were carried out in all recovered bands. After Urografin centrifugation, and despite the different origin of E. coli populations, a common pattern was obtained. High-density bands were formed mainly by nonculturable cells. However, the increase in cell density would not be common to all nonculturable cells, since part of this subpopulations banded in low-density zones, mixed with culturable cells. Bands obtained after Percoll centrifugation were heterogeneous and culturable and nonculturable cells were recovered along the gradient. Thus, fractionation in Urografin cannot be only attributed to changes in buoyant densities during the transition from culturable to nonculturable state. Urografin density gradients allow us to obtain enriched fractions in nonculturable subpopulations from a heterogeneous population, but working conditions should be carefully chosen to avoid Urografin toxicity.
机译:分析了尿移植素或Percoll密度梯度离心法从异质大肠杆菌群体中分离出不可培养亚群的能力。在所有回收带中进行细菌计数(总细胞,活跃细胞和可培养细胞)和流式细胞仪分析。尿移植蛋白离心后,尽管大肠杆菌种群起源不同,但仍获得了相同的模式。高密度带主要由不可培养的细胞形成。但是,细胞密度的增加并非对所有不可培养的细胞都是普遍的,因为部分亚群聚集在低密度区域,与可培养细胞混合。 Percoll离心后获得的条带是异质的,可培养,不可培养的细胞沿梯度回收。因此,在从可培养状态到不可培养状态的转变过程中,尿移植素的分级不能仅归因于浮力密度的变化。尿移植素的密度梯度使我们能够从异质群体中获得不可培养亚群的富集级分,但应谨慎选择工作条件,以避免尿移植素的毒性。

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