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Applied and Environmental Microbiology, October 1998, p. 3932-3938, Vol. 64, No. 10
Department of
Entomology1 and
Interdepartmental
Graduate Program in Genetics,2 University of
California, Riverside, California 92521, and
USDA Forest
Service, North Central Forest Experiment Station, Michigan State
University, East Lansing, Michigan 488233
Received 2 March 1998/Accepted 22 June 1998
The insecticidal activity of Bacillus thuringiensis
strains toxic to coleopterous insects is due to Cry3 proteins assembled into small rectangular crystals. Toxin synthesis in these strains is
dependent primarily upon a promoter that is active in the stationary phase and a STAB-SD sequence that stabilizes the cry3
transcript-ribosome complex. Here we show that significantly higher
yields of Cry3A can be obtained by using dual sporulation-dependent
cyt1Aa promoters to drive the expression of
cry3Aa when the STAB-SD sequence is included in the
construct. The Cry3A yield per unit of culture medium obtained with
this expression system was 12.7-fold greater than that produced by DSM
2803, the wild-type strain of B. thuringiensis from which Cry3Aa was originally
described, and 1.4-fold greater than that produced by NB176, a mutant
of the same strain containing two or three copies of
cry3Aa, which is the active ingredient of the commercial
product Novodor, used for control of beetle pests. The toxicities of
Cry3A produced with this construct or the wild-type strain were similar
when assayed against larvae of the cottonwood leaf beetle,
Chrysomela scripta. The volume of Cry3A crystals produced
with cyt1Aa promoters and the STAB-SD sequence was 1.3-fold
that of typical bipyramidal Cry1 crystals toxic to lepidopterous
insects. The dual-promoter/STAB-SD system offers an additional method
for potentially improving the efficacy of insecticides based on
B. thuringiensis.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Optimization of Cry3A Yields in Bacillus
thuringiensis by Use of Sporulation-Dependent Promoters in
Combination with the STAB-SD mRNA Sequence
*
Corresponding author. Mailing address: Department of
Entomology, University of California, Riverside, CA 92521. Phone: (909) 787-5006. Fax: (909) 787-3086. E-mail:
brian.federici{at}ucr.edu.
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