PS 27-60 - Identifying microbial habitats in soil using quantum dots and x-ray fluorescence tomography

Thursday, August 11, 2016
ESA Exhibit Hall, Ft Lauderdale Convention Center
Sarah L. O'Brien1, Matthew D. Whiteside2, Deirdre Sholto-Douglas3, Alice Dohnalkova4, Daniel M. Durall5, Doga Gursoy3, Melanie D. Jones6, Libor Kovarik4, Barry Lai7, Christian Roehrig3, Shane Sullivan3, Stefan Vogt3 and Kenneth M. Kemner8, (1)Bioscience Division, Argonne National Laboratory, Argonne, IL, (2)Department of Ecological Sciences, Vrije Universiteit, Amsterdam, Netherlands, (3)Argonne National Laboratory, (4)Pacific Northwest National Laboratory, (5)University of British Columbia Okanagan, (6)Biology, University of British Columbia, Okanagan Campus, Kelowna, BC, Canada, (7)X-Ray Science Division, Argonne National Laboratory, Argonne, IL, (8)Biosciences Division, Argonne National Laboratory, Argonne, IL
Background/Question/Methods

The metabolic activities of soil microbes are the primary drivers of biogeochemical processes controlling the terrestrial carbon cycle, nutrient availability to plants, contaminant remediation, water quality, and other ecosystem services. However, we have a limited understanding of microbial metabolic processes such as nutrient uptake rates, substrate preferences, or how microbes and microbial metabolism are distributed throughout the three-dimensional pore network of the soil. Here we use a novel combination of imaging techniques with quantum dots (QDs, engineered semiconductor nanoparticles that produce size or composition-dependent fluorescence) to locate bacteria in the three-dimensional pore network of a soil aggregate.

Results/Conclusions

First, we show using confocal and aberration-corrected transmission electron microscopies that bacteria (Bacillus subtilis, Pseudomonas fluorescens, and Pseudomonas protogens) actively take up and internalize CdSe/ZnS core/shell QDs conjugated to biologically relevant substrates. Next, we show that cells bearing QDs can be identified using fluorescence imaging with hard x-rays at 2ID-D at the Advanced Photon Source (APS). Finally, we demonstrate that the Se constituent to the QDs can be used to label bacteria in three-dimensional tomographic reconstructions of natural soil at sub-μm spatial resolution using hard x-rays at the Advanced Photon Source (APS) and Argonne National Laboratory. This is the first time soil bacteria have been imaged in the intact soil matrix at such high resolution. These results offer a new way to experimentally investigate basic bacterial ecology in situ, revealing constraints on microbial function in soil that will help improve connections between pore-scale and ecosystem-scale processes in models.