Bacillus thuringiensis (Bt) Cry toxins from the Cry1A family demonstrate significantly different toxicities against members of the family Noctuidae for unknown reasons. In this study, membrane potential was measured and analyzed in freshly isolated midgut samples from Mythimna separata and Agrotis ipsilon larvae under oral administration and in vitro incubation with Bt toxin Cry1Ab to elucidate the mechanism of action for further control of these pests. Bioassay results showed that the larvae of M. separata achieved a LD50 of 258.84 ng/larva at 24 h after ingestion; M. separata larvae were at least eightfold more sensitive than A. ipsilon larvae to Cry1Ab. Force-feeding showed that the observed midgut apical-membrane potential (Vam) of M. s...
Helicoverpa armigera is a polyphagous pest sensitive to Cry1Ac protein from Bacillus thuringiensis (...
The pore forming activity of Cry1Ab, Cry1Fa and Cry1Ca toxins and their interaction with leucine tra...
The crystal (Cry) toxins from Bacillus thuringiensis (Bt) display high specificity and toxicity agai...
Bacillus thuringiensis (Bt) Cry toxins from the Cry1A family demonstrate significantly different tox...
It is generally accepted that Bacillus thuringiensis Cry toxins insert into the apical membrane of t...
To test the possibility that proteolytic cleavage by midgut juice enzymes could enhance or inhibit t...
Wild type and mutant toxins of Bacillus thuringiensis delta-endotoxins were examined for their bindi...
Binding and competition among Cry1Aa, Cry1Ac, and Cry1Ba toxins were analyzed quantitatively #in vit...
Binding of three Bacillus thuringiensis insecticidal crystal proteins (ICPs) to the midgut epitheliu...
Celangulin V (CV) is the main insecticidal constituent of Celastrus angulatus. The V-ATPase H subuni...
We studied mechanisms of resistance to Bacillus thuringiensis insecticidal crystal protein Cry1C in ...
removed nearly all toxicity for Bombyx mon (>1,000-fold less active than the wild type). The loss...
Helicoverpa armigera is a polyphagous pest sensitive to Cry1Ac protein from Bacillus thuringiensis (...
AbstractThe binding of l-[35S]methionine in vivo labelled CryIC toxin to its receptor in brush borde...
Ligand-blotting experiments on dipteran brush border membrane vesicles (BBMVs) showed binding of Cry...
Helicoverpa armigera is a polyphagous pest sensitive to Cry1Ac protein from Bacillus thuringiensis (...
The pore forming activity of Cry1Ab, Cry1Fa and Cry1Ca toxins and their interaction with leucine tra...
The crystal (Cry) toxins from Bacillus thuringiensis (Bt) display high specificity and toxicity agai...
Bacillus thuringiensis (Bt) Cry toxins from the Cry1A family demonstrate significantly different tox...
It is generally accepted that Bacillus thuringiensis Cry toxins insert into the apical membrane of t...
To test the possibility that proteolytic cleavage by midgut juice enzymes could enhance or inhibit t...
Wild type and mutant toxins of Bacillus thuringiensis delta-endotoxins were examined for their bindi...
Binding and competition among Cry1Aa, Cry1Ac, and Cry1Ba toxins were analyzed quantitatively #in vit...
Binding of three Bacillus thuringiensis insecticidal crystal proteins (ICPs) to the midgut epitheliu...
Celangulin V (CV) is the main insecticidal constituent of Celastrus angulatus. The V-ATPase H subuni...
We studied mechanisms of resistance to Bacillus thuringiensis insecticidal crystal protein Cry1C in ...
removed nearly all toxicity for Bombyx mon (>1,000-fold less active than the wild type). The loss...
Helicoverpa armigera is a polyphagous pest sensitive to Cry1Ac protein from Bacillus thuringiensis (...
AbstractThe binding of l-[35S]methionine in vivo labelled CryIC toxin to its receptor in brush borde...
Ligand-blotting experiments on dipteran brush border membrane vesicles (BBMVs) showed binding of Cry...
Helicoverpa armigera is a polyphagous pest sensitive to Cry1Ac protein from Bacillus thuringiensis (...
The pore forming activity of Cry1Ab, Cry1Fa and Cry1Ca toxins and their interaction with leucine tra...
The crystal (Cry) toxins from Bacillus thuringiensis (Bt) display high specificity and toxicity agai...