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Peter G. Stroot

Researcher at University of South Florida

Publications -  40
Citations -  494

Peter G. Stroot is an academic researcher from University of South Florida. The author has contributed to research in topics: Nitrifying bacteria & Nitrification. The author has an hindex of 9, co-authored 40 publications receiving 476 citations. Previous affiliations of Peter G. Stroot include University of Cincinnati.

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Use of 16S rRNA Gene Terminal Restriction Fragment Analysis To Assess the Impact of Solids Retention Time on the Bacterial Diversity of Activated Sludge

TL;DR: Terminal restriction fragment length polymorphism analysis of 16S rRNA genes was used to investigate the reproducibility and stability in the bacterial community structure of laboratory-scale sequencing batch bioreactors and to assess the impact of solids retention time (SRT) on bacterial diversity.
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Swelling-induced instabilities in microscale, surface-confined poly(N-isopropylacryamide) hydrogels

TL;DR: In this paper, the authors employ confocal microscopy for the in situ, three-dimensional study of micron-scale hydrogels that are pinned to a solid substrate and find four general modes of swelling-induced deformation: lateral differential swelling, local sinusoidal edge buckling, bulk sinusoid buckling and surface creasing.
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Size-Exclusion “Capture and Release” Separations Using Surface-Patterned Poly(N-isopropylacrylamide) Hydrogels

TL;DR: The potential use of the hydrogel monoliths as size-selective "catch and release" structures was demonstrated with a mixture of 6 and 20 microm polystyrene microspheres, where the 6 microm diameter particles were selectively concentrated and separated from the larger particles.
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Removal of Sediment and Bacteria from Water Using Green Chemistry

TL;DR: Two fractions of mucilage gum were extracted from the Opuntia ficus-indica cactus and tested as flocculation agents against sediment and bacterial contamination and showed water purification abilities.
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Monitoring biosensor capture efficiencies: development of a model using GFP-expressing Escherichia coli O157:H7.

TL;DR: Green fluorescent protein (GFP) transformed E. coli O157:H7 was used to develop a novel method for directly and easily measuring the cell capture efficiency of any given biosensor platform, and can facilitate the development and optimization of new biosensor design configurations and sample processing strategies.