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Appl. Environ. Microbiol., Oct 1996, 3722-3726, Vol 62, No. 10
C Du and KW Nickerson
Spores from Cry(sup+) strains of Bacillus thuringiensis bound fluorescein
isothiocyanate-labeled antibodies specific for the 65-kDa activated Cry 1Ac
toxin, whereas spores from Bacillus cereus and Cry(sup-) strains of B.
thuringiensis did not. The Cry(sup+) spores could be activated for
germination by alkaline conditions (pH 10.3), whereas Cry(sup-) spores
could not. Once the surrounding exosporia had been removed or
permeabilized, Cry(sup+) spores were able to bind the toxin receptor(s)
from insect gut brush border membrane vesicle preparations, and their
germination rates were increased ca. threefold in the presence of brush
border membrane vesicles. A model is presented whereby in the soil the Cry
toxins on the spore surface are protected by the exosporium while in the
gut they are exposed and available for binding to the insect receptors.
This model explains why the disulfide-rich C terminus of the cry genes is
so highly conserved even though it is removed during the processing of the
protoxin to the activated toxin. It also highlights the trade-off resulting
from having Cry toxins located on the spore surface, i.e., decreased spore
resistance versus enhanced insect pathogenesis.
Copyright © 1996, American Society for Microbiology
Bacillus thuringiensis HD-73 Spores Have Surface-Localized Cry1Ac Toxin: Physiological and Pathogenic Consequences
School of Biological Sciences, University of Nebraska, Lincoln, Nebraska 68588-0666
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