Affiliation:
1. Unité des Bactéries Entomopathogènes, Institut Pasteur, 75724 Paris Cedex 15, France1 and
2. CIB Biological Control Unit, Medellin, Columbia2
Abstract
ABSTRACT
The fragment containing the gene encoding the cytolytic Cyt1Ab1 protein from
Bacillus thuringiensis
subsp.
medellin
and its flanking sequences (I. Thiery, A. Delécluse, M. C. Tamayo, and S. Orduz, Appl. Environ. Microbiol. 63:468–473, 1997) was introduced into
Bacillus sphaericus
toxic strains 2362, 2297, and Iab872 by electroporation with the shuttle vector pMK3. Only small amounts of the protein were produced in recombinant strains 2362 and Iab872. The protein was detected in these strains only by Western blotting and immunodetection with antibody raised against Cyt1Ab1 protein. Large amounts of Cyt1Ab1 protein were produced in
B. sphaericus
recombinant strain 2297, and there was an additional crystal, other than that of the binary toxin, within the exosporium. The production of the Cyt1Ab1 protein in addition to the binary toxin did not increase the larvicidal activity of the
B. sphaericus
recombinant strain against susceptible mosquito populations of
Culex pipiens
or
Aedes aegypti
. However, it partially restored (10 to 20 times) susceptibility of the resistant mosquito populations of
C. pipiens
(SPHAE) and
Culex quinquefasciatus
(GeoR) to the binary toxin. The Cyt1Ab1 protein produced in recombinant
B. thuringiensis
SPL407(p
cyt1Ab1
) was synthesized in two types of crystal—one round and with various dense areas, surrounded by an envelope, and the other a regular cuboid crystal, very similar to that found in the
B. sphaericus
recombinant strain.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
27 articles.
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