Search results for "Bacillus thuringiensi"

showing 10 items of 213 documents

Molecular and Insecticidal Characterization of a Cry1I Protein Toxic to Insects of the Families Noctuidae, Tortricidae, Plutellidae, and Chrysomelidae

2006

ABSTRACT The most notable characteristic of Bacillus thuringiensis is its ability to produce insecticidal proteins. More than 300 different proteins have been described with specific activity against insect species. We report the molecular and insecticidal characterization of a novel cry gene encoding a protein of the Cry1I group with toxic activity towards insects of the families Noctuidae, Tortricidae, Plutellidae, and Chrysomelidae. PCR analysis detected a DNA sequence with an open reading frame of 2.2 kb which encodes a protein with a molecular mass of 80.9 kDa. Trypsin digestion of this protein resulted in a fragment of ca. 60 kDa, typical of activated Cry1 proteins. The deduced sequen…

Earias insulanaBacterial ToxinsMolecular Sequence DataBacillus thuringiensisMothsLobesia botranaApplied Microbiology and BiotechnologyHemolysin ProteinsBacterial ProteinsBacillus thuringiensisBotanyInvertebrate MicrobiologyAnimalsAmino Acid SequencePest Control BiologicalBacillus thuringiensis ToxinsEcologybiologyfungiPlutellaSequence Analysis DNAbiology.organism_classificationColeopteraEndotoxinsOpen reading frameCry1AcBiochemistryPlutellidaeLarvaNoctuidaeFood ScienceBiotechnologyApplied and Environmental Microbiology
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Use of Bacillus thuringiensis toxins for control of the cotton pest earias insulana (Boisd.) (Lepidoptera: Noctuidae)

2006

ABSTRACT Thirteen of the most common lepidopteran-specific Cry proteins of Bacillus thuringiensis have been tested for their efficacy against newly hatched larvae of two populations of the spiny bollworm, Earias insulana . At a concentration of 100 μg of toxin per milliliter of artificial diet, six Cry toxins (Cry1Ca, Cry1Ea, Cry1Fa, Cry1Ja, Cry2Aa, and Cry2Ab) were not toxic at all. Cry1Aa, Cry1Ja, and Cry2Aa did not cause mortality but caused significant inhibition of growth. The other Cry toxins (Cry1Ab, Cry1Ac, Cry1Ba, Cry1Da, Cry1Ia, and Cry9Ca) were toxic to E. insulana larvae. The 50% lethal concentration values of these toxins ranged from 0.39 to 21.13 μg/ml (for Cry9Ca and Cry1Ia, …

Earias insulanaBacterial ToxinsPopulationBacillus thuringiensismedicine.disease_causeBinding CompetitiveApplied Microbiology and BiotechnologyMicrobiologyLepidoptera genitaliaHemolysin ProteinsBacterial ProteinsControl of the cotton pest earias insulanaBacillus thuringiensisBotanyInvertebrate MicrobiologymedicineAnimalsToxinsPest Control BiologicaleducationGossypiumeducation.field_of_studyBinding SitesBacillus thuringiensis ToxinsMicrovilliEcologybiologyToxinfungiPlants Genetically Modifiedbiology.organism_classificationEndotoxinsLepidopteraBollwormCry1AcLarvaNoctuidaeBiological AssayFood ScienceBiotechnology
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Critical Domains in the Specific Binding of Radiolabeled Vip3Af Insecticidal Protein to Brush Border Membrane Vesicles from Spodoptera spp. and Cultu…

2021

Vegetative insecticidal proteins (Vip3) from Bacillus thuringiensis have been used, in combination with Cry proteins, to better control insect pests and as a strategy to delay the evolution of resistance to Cry proteins in Bt crops (crops protected from insect attack by the expression of proteins from B. thuringiensis). In this study, we have set up the conditions to analyze the specific binding of 125I-Vip3Af to Spodoptera frugiperda and Spodoptera exigua brush border membrane vesicles (BBMV). Heterologous competition binding experiments revealed that Vip3Aa shares the same binding sites with Vip3Af, but Vip3Ca does not recognize all of them. As expected, Cry1Ac and Cry1F did not compete f…

EcologyBrush borderbiologyChemistryfungiSpodopterabiology.organism_classificationApplied Microbiology and BiotechnologyEpitopeProtein structureCry1AcBiochemistryBacillus thuringiensisBinding siteFood ScienceBiotechnologySf21Applied and Environmental Microbiology
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Structural and functional role of Domain I for the insecticidal activity of the Vip3Aa protein from Bacillus thuringiensis

2022

12 p.-4 fig.-2 tab.

EndotoxinsInsecticidesBacterial ProteinsBacillus thuringiensisAnimalsTrypsinBioengineeringSpodopteraProteïnesBiotecnologiaApplied Microbiology and BiotechnologyBiochemistryBiotechnology
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Activation of Bacillus thuringiensis Cry1I to a 50 kDa stable core impairs its full toxicity to Ostrinia nubilalis

2021

Abstract Bacillus thuringiensis Cry1I insecticidal proteins are structurally similar to other three-domain Cry proteins, although their size, activity spectrum, and expression at the stationary phase are unique among other members of the Cry1 family. The mode of action of Cry1 proteins is not completely understood but the existence of an activation step prior to specific binding is widely accepted. In this study, we attempted to characterize and determine the importance of the activation process in the mode of action of Cry1I, as Cry1Ia protoxin or its partially processed form showed significantly higher toxicity to Ostrinia nubilalis than the fully processed protein either activated with …

EndotoxinsInsecticidesHemolysin ProteinsBacterial ProteinsLarvafungiBacillus thuringiensisAnimalsGeneral MedicineMothsProteïnesApplied Microbiology and BiotechnologyBiotechnologyApplied Microbiology and Biotechnology
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Cross-resistance and mechanism of resistance to Cry1Ab toxin from Bacillus thuringiensis in a field-derived strain of European corn borer, Ostrinia n…

2011

The cross-resistance spectrum and biochemical mechanism of resistance to the Bacillus thuringiensis Cry1Ab toxin was studied in a field-derived strain of Ostrinia nubilalis (Hubner) (Lepidoptera: Crambidae) that was further selected in the laboratory for high levels (>1000-fold) of resistance to Cry1Ab. The resistant strain exhibited high levels of cross-resistance to Cry1Ac and Cry1Aa but only low levels of cross-resistance (<4-fold) to Cry1F. In addition, there was no significant difference between the levels of resistance to full-length and trypsin-activated Cry1Ab protein. No differences in activity of luminal gut proteases or altered proteolytic processing of the toxin were observed in…

European corn borerBt maizeImmunoblottingResistanceDrug ResistanceBacillus thuringiensisOstrinia nubilalisMothsmedicine.disease_causeOstriniaMicrobiologyHemolysin ProteinsCrambidaeBacterial ProteinsBacillus thuringiensismedicineAnimalsEcology Evolution Behavior and SystematicsCross-resistancebiologyStrain (chemistry)Bacillus thuringiensis ToxinsMicrovilliToxinfungifood and beveragesLuminal gut proteasesbiology.organism_classificationToxin bindingEndotoxinsCry1AcBiological Assay
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Insecticidal Genetically Modified Crops and Insect Resistance Management (IRM)

2008

Economically important crops, such as maize and cotton, have been transformed with genes encoding insecticidal proteins from Bacillus thuringiensis (Bt) to confer them protection against the most important insect pests. Of the 114 million hectares globally planted with GM crops in 2007, over one third are insect-resistant Bt crops, and the area keeps increasing every year. The potential for insects to evolve resistance to GM insecticidal plants is considered to be one of the main threats to this technology, since resistance to Bt sprayable products has been demonstrated. Insect resistance management plans for this new class of pesticides are encouraged and became mandatory in the USA. Of th…

European corn borerDiamondback mothbiologyResistance (ecology)business.industryfungifood and beveragesGenetically modified cropsPesticidebiology.organism_classificationBiotechnologyCropAgronomyBt cottonBacillus thuringiensisbusiness
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Analyses of Cry1Ab binding in resistant and susceptible strains of the European corn borer, Ostrinia nubilalis (Hubner) (Lepidoptera: Crambidae).

2006

ABSTRACT Cry1Ab toxin binding analysis was performed to determine whether resistance in laboratory-selected Ostrinia nubilalis strains is associated with target site alteration. Brush border membrane vesicles were prepared using dissected midguts from late instars of susceptible and resistant strains (Europe-R and RSTT) of O. nubilalis . Immunoblot analysis indicated that three different proteins bound to Cry1Ab toxin and were recognized by an anticadherin serum. In a comparison of resistant and susceptible strains, reduced Cry1Ab binding was apparent for all three bands corresponding to cadherin-like proteins in the Europe-R strain, while reduced binding was apparent in only one band for t…

European corn borerInsecticidesBacterial ToxinsBacillus thuringiensisDrug ResistancePlasma protein bindingMothsmedicine.disease_causeApplied Microbiology and BiotechnologyZea maysOstriniaHemolysin ProteinsCrambidaeBacterial ProteinsBacillus thuringiensisBotanymedicineInvertebrate MicrobiologyAnimalsBinding sitePest Control BiologicalEcologybiologyStrain (chemistry)Bacillus thuringiensis ToxinsToxinfungibiology.organism_classificationMolecular biologyEndotoxinsFood ScienceBiotechnologyProtein BindingApplied and environmental microbiology
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Quantitative genetic analysis of Cry1Ab tolerance in Ostrinia nubilalis Spanish populations

2013

30 p.-2 fig.-3 tab.

European corn borerInsecticidesOffspringEuropean corn borerBacillus thuringiensisMothsGenetic analysisOstriniaLepidoptera genitaliaInsecticide ResistanceHeritabilityHemolysin ProteinsBacterial ProteinsBacillus thuringiensisToxicity TestsAnimalsGeneEcology Evolution Behavior and SystematicsGeneticsbiologyBacillus thuringiensis ToxinsfungiPartial resistance allelesfood and beveragesHeritabilitybiology.organism_classificationCadherinsEPIC-PCREndotoxinsSpainCadherinInsect Proteins
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Phage-borne factors and host LexA regulate the lytic switch in phage GIL01.

2011

ABSTRACT The Bacillus thuringiensis temperate phage GIL01 does not integrate into the host chromosome but exists stably as an independent linear replicon within the cell. Similar to that of the lambdoid prophages, the lytic cycle of GIL01 is induced as part of the cellular SOS response to DNA damage. However, no CI-like maintenance repressor has been detected in the phage genome, suggesting that GIL01 uses a novel mechanism to maintain lysogeny. To gain insights into the GIL01 regulatory circuit, we isolated and characterized a set of 17 clear plaque ( cp ) mutants that are unable to lysogenize. Two phage-encoded proteins, gp1 and gp7, are required for stable lysogen formation. Analysis of …

Gene Expression Regulation ViralvirusesBacteriophages Transposons and PlasmidsBacillus thuringiensisBacillus PhagesBiologyMicrobiologyHost-Parasite InteractionsBacteriolysisLysogenBacterial ProteinsLysogenic cycleHost chromosomeSOS responseSOS Response GeneticsMolecular BiologyLysogenyGeneticsBinding SitesSerine Endopeptidasesbiochemical phenomena metabolism and nutritionBacillus PhageTemperatenessLytic cycleDNA ViralbacteriaVirus ActivationRepressor lexAProtein BindingJournal of bacteriology
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