Journal
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 76, Issue 21, Pages 7292-7298Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.00324-10
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Funding
- U.S. Department of Energy [DE-FG02-05ER63949, DE-FG02-06ER64250]
- U.S. Environmental Protection Agency (EPA) [R831712, R833323]
- U.S. EPA and National Science Foundation [EF0830117]
- UC TSR TP
- Altair Nanotechnologies, Inc.
- Deutsche Forschungsgemeinschaft (DFG
- German Research Foundation) [MA 3333/1-1]
- Otis Williams Postdoctoral Fellowship
- NSF [DMR05-20415]
- Direct For Biological Sciences [0830117] Funding Source: National Science Foundation
- Div Of Biological Infrastructure [0830117] Funding Source: National Science Foundation
- EPA [R831712, 909011, R833323, 909236] Funding Source: Federal RePORTER
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Engineered nanoparticles are increasingly incorporated into consumer products and are emerging as potential environmental contaminants. Upon environmental release, nanoparticles could inhibit bacterial processes, as evidenced by laboratory studies. Less is known regarding bacterial alteration of nanoparticles, including whether bacteria affect physical agglomeration states controlling nanoparticle settling and bioavailability. Here, the effects of an environmental strain of Pseudomonas aeruginosa on TiO2 nanoparticle agglomerates formed in aqueous media are described. Environmental scanning electron microscopy and cryogenic scanning electron microscopy visually demonstrated bacterial dispersion of large agglomerates formed in cell culture medium and in marsh water. For experiments in cell culture medium, quantitative image analysis verified that the degrees of conversion of large agglomerates into small nanoparticle-cell combinations were similar for 12-h-growth and short-term cell contact experiments. Dispersion in cell growth medium was further characterized by size fractionation: for agglomerated TiO2 suspensions in the absence of cells, 81% by mass was retained on a 5-mu m-pore-size filter, compared to only 24% retained for biotic treatments. Filtrate cell and agglomerate sizes were characterized by dynamic light scattering, revealing that the average bacterial cell size increased from 1.4 mu m to 1.9 mu m because of nano-TiO2 biosorption. High-magnification scanning electron micrographs showed that P. aeruginosa dispersed TiO2 agglomerates by preferential biosorption of nanoparticles onto cell surfaces. These results suggest a novel role for bacteria in the environmental transport of engineered nanoparticles, i.e., growth-independent, bacterially mediated size and mass alterations of TiO2 nanoparticle agglomerates.
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