首页> 美国卫生研究院文献>Sensors (Basel Switzerland) >Colonization of Potato Rhizosphere by GFP-Tagged Bacillus subtilis MB73/2 Pseudomonas sp. P482 and Ochrobactrum sp. A44 Shown on Large Sections of Roots Using Enrichment Sample Preparation and Confocal Laser Scanning Microscopy
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Colonization of Potato Rhizosphere by GFP-Tagged Bacillus subtilis MB73/2 Pseudomonas sp. P482 and Ochrobactrum sp. A44 Shown on Large Sections of Roots Using Enrichment Sample Preparation and Confocal Laser Scanning Microscopy

机译:GFP标记的枯草芽孢杆菌MB73 / 2假单胞菌属菌种对马铃薯根际的定殖。 P482和O骨属sp。使用富集样品制备和共聚焦激光扫描显微镜在大根部显示A44

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摘要

The ability to colonize the host plants’ rhizospheres is a crucial feature to study in the case of Plant Growth Promoting Rhizobacteria (PGPRs) with potential agricultural applications. In this work, we have created GFP-tagged derivatives of three candidate PGPRs: Bacillus subtilis MB73/2, Pseudomonas sp. P482 and Ochrobactrum sp. A44. The presence of these strains in the rhizosphere of soil-grown potato (Solanum tuberosum L.) was detected with a classical fluorescence microscope and a confocal laser scanning microscope (CLSM). In this work, we have used a broad-field-of-view CLMS device, dedicated to in vivo analysis of macroscopic objects, equipped with an automated optical zoom system and tunable excitation and detection spectra. We show that features of this type of CLSM microscopes make them particularly well suited to study root colonization by microorganisms. To facilitate the detection of small and scattered bacterial populations, we have developed a fast and user-friendly enrichment method for root sample preparation. The described method, thanks to the in situ formation of mini-colonies, enables visualization of bacterial colonization sites on large root fragments. This approach can be easily modified to study colonization patterns of other fluorescently tagged strains. Additionally, dilution plating of the root extracts was performed to estimate the cell number of MB73/2, P482 and A44 in the rhizosphere of the inoculated plants.
机译:在具有潜在农业应用的植物生长促进根际细菌(PGPR)的情况下,对宿主植物根际的定殖能力是一项至关重要的功能。在这项工作中,我们创建了三个候选PGPR的GFP标签衍生物:枯草芽孢杆菌MB73 / 2,假单胞菌sp。 P482和O骨属sp。 A44。用经典的荧光显微镜和共聚焦激光扫描显微镜(CLSM)检测土壤土壤马铃薯(Solanum tuberosum L.)的根际中是否存在这些菌株。在这项工作中,我们使用了宽视野CLMS设备,该设备专用于对宏观物体进行体内分析,并配备了自动光学变焦系统以及可调的激发和检测光谱。我们显示这种类型的CLSM显微镜的功能使其特别适合研究微生物对根的定植。为了便于检测散落的小细菌种群,我们开发了一种快速且用户友好的根样品制备富集方法。由于微型菌落的原位形成,所描述的方法使可视化大根碎片上的细菌定殖位点成为可能。可以轻松修改此方法以研究其他荧光标记菌株的定殖模式。另外,对根提取物进行稀释平板接种以估计接种植物的根际中MB73 / 2,P482和A44的细胞数。

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