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利用富集样本制备和共聚焦激光扫描显微镜,在根的大切片上观察到 GFP 标记的枯草芽孢杆菌 MB73/2、假单胞菌 P482 和食酸寡养单胞菌 A44 在马铃薯根际的定殖。

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.

机构信息

Laboratory of Biological Plant Protection, Intercollegiate Faculty of Biotechnology UG&MUG, University of Gdansk, Kladki 24, 80-822 Gdansk, Poland.

出版信息

Sensors (Basel). 2012 Dec 18;12(12):17608-19. doi: 10.3390/s121217608.

Abstract

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.

摘要

在具有农业应用潜力的植物促生根际细菌(PGPR)的研究中,定殖宿主植物根际的能力是一个关键特征。在这项工作中,我们创建了三个候选 PGPR 的 GFP 标记衍生物:枯草芽孢杆菌 MB73/2、假单胞菌 P482 和食酸寡养单胞菌 A44。使用经典荧光显微镜和共聚焦激光扫描显微镜(CLSM)检测这些菌株在土壤中生长的马铃薯(Solanum tuberosum L.)根际中的存在。在这项工作中,我们使用了一种宽视场 CLSM 设备,专门用于宏观物体的体内分析,该设备配备了自动光学变焦系统和可调激发和检测光谱。我们表明,这种类型的 CLSM 显微镜的特点使它们特别适合研究微生物对根的定殖。为了方便检测小而分散的细菌种群,我们开发了一种用于根样准备的快速且用户友好的富集方法。所描述的方法通过 mini-colonies 的原位形成,能够可视化大根片段上的细菌定殖位点。该方法可以很容易地修改,以研究其他荧光标记菌株的定殖模式。此外,对根提取物进行稀释平板计数,以估计接种植物根际中 MB73/2、P482 和 A44 的细胞数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4911/3571856/060745bac1b8/sensors-12-17608f1.jpg

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