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Terrance J. Leighton

Researcher at Children's Hospital Oakland Research Institute

Publications -  28
Citations -  1183

Terrance J. Leighton is an academic researcher from Children's Hospital Oakland Research Institute. The author has contributed to research in topics: Endospore & Exosporium. The author has an hindex of 18, co-authored 28 publications receiving 1134 citations.

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Kinetics of size changes of individual Bacillus thuringiensis spores in response to changes in relative humidity.

TL;DR: It is found that individual dormant spores of Bacillus thuringiensis grow and shrink in response to increasing and decreasing relative humidity, and shrink to near their original size on reexposure to dry air.
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In vitro high-resolution structural dynamics of single germinating bacterial spores

TL;DR: Atomic force microscopy is used to probe the high-resolution structural dynamics of single Bacillus atrophaeus spores germinating under native conditions and shows that AFM can reveal previously unrecognized germination-induced alterations in spore coat architecture and topology as well as the disassembly of outer spore Coat rodlet structures.
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The High-Resolution Architecture and Structural Dynamics of Bacillus Spores

TL;DR: In this paper, high-resolution native structures of bacterial endospores, including the exosporium and spore coats of four Bacillus species in air and water environments, were directly visualized using in vitro atomic force microscopy.
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Imaging and 3D Elemental Characterization of Intact Bacterial Spores by High-Resolution Secondary Ion Mass Spectrometry

TL;DR: This work uses depth profile analysis to access the 3D compositional information of an intact spore without the additional sample preparation steps typically used to access substructural information in biological samples.
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Architecture and high-resolution structure of Bacillus thuringiensis and Bacillus cereus spore coat surfaces.

TL;DR: The results demonstrate that variations in storage and preparation procedures result in architectural changes in individual spore surfaces, which establish AFM as a useful tool for evaluation of preparation and processing "fingerprints" of bacterial spores.