RESUMEN
The mosquitocidal toxin 1 (mtx1) gene from genomic DNA of B. sphaericus strain 2297 was cloned and expressed in E. coli. DNA sequencing analysis of the cloned gene revealed a single open reading frame encoding an 870-amino acid polypeptide. Expression level of the full-length gene in E. coli was very low even though strong promoter was used or the gene was expressed as a fusion protein. Expression level was highly improved after the putative leader sequence was deleted, and the truncated gene was expressed as a fusion protein with glutathione S-transferase (GST-tMtx1). E. coli cells expressing GST-tMtx1 was highly toxic to Culex quinquefasciatus larvae and showed lower toxicity against Anopheles dirus and Aedes aegypti larvae. Enterobacter amnigenus An11, a mosquito larval gut colonizable bacteria, transformed with the cloned gene exhibited mosquito larvicidal activity. Result suggested that there is a potential to develop this protein to be used as an alternative mosquito control agent.
Asunto(s)
Bacillus/genética , Bacillus/metabolismo , Proteínas Bacterianas/genética , Proteínas Bacterianas/farmacología , Toxinas Bacterianas/genética , Toxinas Bacterianas/farmacología , Clonación Molecular , Culicidae/efectos de los fármacos , Animales , ADN Bacteriano/química , ADN Bacteriano/aislamiento & purificación , Enterobacter/genética , Enterobacter/metabolismo , Escherichia coli/genética , Escherichia coli/metabolismo , Regulación Bacteriana de la Expresión Génica , Glutatión Transferasa/genética , Glutatión Transferasa/metabolismo , Insecticidas/farmacología , Larva/efectos de los fármacos , Datos de Secuencia Molecular , Sistemas de Lectura Abierta , Regiones Promotoras Genéticas , Señales de Clasificación de Proteína/genética , Señales de Clasificación de Proteína/fisiología , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Análisis de Secuencia de ADNRESUMEN
Cyt2Aa2 is a cytolytic and mosquito larvicidal toxin produced by Bacillus thuringiensis subsp. darmstadiensis. The toxin contains 3 tryptophan residues at positions 132, 154, and 157. To study the role of tryptophan on protein structure and functions, each tryptophan residue was substituted by phenylalanine and other different amino acids. Expression test in Escherichia coli showed that all mutant proteins were highly produced as inclusion bodies similar to that of the wild type. The mutant W157F showed haemolytic and mosquito larvicidal activities comparable to the wild type but the mutant W157V and all other mutants at positions 132 and 154 have completely lost these activities. Solubilization and proteinase K activation tests indicated that aromatic residue is required at position 157 and tryptophan residues at positions 132 and 154 are critical residues playing important role to maintain structure and functions of the protein and cannot be changed to any other amino acid.
Asunto(s)
Bacillus thuringiensis/química , Proteínas Bacterianas/toxicidad , Toxinas Bacterianas , Endotoxinas/toxicidad , Pliegue de Proteína , Triptófano/fisiología , Toxinas de Bacillus thuringiensis , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Secuencia de Bases , Dicroismo Circular , Cartilla de ADN , Endotoxinas/química , Endotoxinas/genética , Proteínas Hemolisinas , Mutagénesis Sitio-DirigidaRESUMEN
The binary toxin gene encoding BinA (42 kDa) and BinB (51 kDa) from Bacillus sphaericus strain 2297 was cloned and expressed in E. coli. Low expression level was found when both proteins were expressed from a single operon. High expression was observed when the gene encoding an individual protein was placed downstream of the T7 promoter. The expression level of BinB was not different when expressed alone (non-fusion) or as a fusion form with T7 peptide (T7-BinB). Both forms of BinB were equally stable. Unlike BinB, the non-fusion form of BinA was less stable than T7-BinA. The mosquito larvicidal test showed that BinA or BinB alone was not toxic to mosquito larvae, but high toxicity was found when both BinA and BinB were applied. The results suggest that a short peptide of T7 linked to the N-terminus of either BinA or BinB does not affect their toxicity, but may make the toxin, especially BinA, more stable.
Asunto(s)
Toxinas Bacterianas/biosíntesis , Toxinas Bacterianas/genética , Culex/efectos de los fármacos , Culex/crecimiento & desarrollo , Escherichia coli/enzimología , Escherichia coli/genética , Animales , Toxinas Bacterianas/toxicidad , Clonación Molecular , Expresión Génica , Immunoblotting/métodos , Insecticidas/metabolismo , Insecticidas/toxicidad , Larva/crecimiento & desarrollo , Operón , Control Biológico de Vectores/métodos , Subunidades de Proteína/biosíntesis , Subunidades de Proteína/genética , Proteínas Recombinantes de Fusión/biosíntesis , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/toxicidad , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/toxicidad , Transformación BacterianaRESUMEN
A recombinant plasmid harboring cry4A, cry4B and cry11A from Bacillus thuringiensis subsp. israelensis and binary toxin genes from Bacillus sphaericus has been constructed. The three cry genes were placed under the control of the cry4B promoter whereas the binary toxin gene was controlled by its native promoter. The expression of toxins in Escherichia coli harboring the resulting plasmid, p4BDA-5142, was investigated. Cry4B expression was highest compared to other toxins. Although the level of toxin expression was low compared with E. coli expressing single toxins, the recombinant E. coli strain harboring p4BDA-5142 exhibited broad range mosquito-larvicidal activity against all Aedes, Culex and Anopheles larvae. This work has shown that the development of the recombinant plasmid can be used to broaden the host range spectrum of the appropriate bacterial host for mosquito control.
Asunto(s)
Bacillus/genética , Proteínas Bacterianas/genética , Toxinas Bacterianas/genética , Culicidae , Endotoxinas/genética , Insecticidas , Plásmidos/genética , Aedes/crecimiento & desarrollo , Animales , Anopheles/crecimiento & desarrollo , Bacillus thuringiensis/genética , Toxinas de Bacillus thuringiensis , Proteínas Bacterianas/toxicidad , Toxinas Bacterianas/toxicidad , Clonación Molecular , Culex/crecimiento & desarrollo , Culicidae/crecimiento & desarrollo , Endotoxinas/toxicidad , Escherichia coli/genética , Escherichia coli/metabolismo , Expresión Génica , Genes Bacterianos , Proteínas Hemolisinas , Larva/crecimiento & desarrollo , Operón , Control Biológico de Vectores/métodos , Regiones Promotoras Genéticas , Proteínas Recombinantes/biosíntesis , Transformación BacterianaRESUMEN
The cytolytic delta-endotoxin gene from Bacillus thuringiensis subsp. darmstadiensis was amplified from genomic DNA by PCR by using primers designed from the sequence of cyt2Aa1 gene of B. thuringiensis subsp. kyushuensis. DNA sequence analysis revealed an open reading frame translating to a 259-amino acid sequence. The cloned gene was designated cyt2Aa2. This gene was highly expressed in Escherichia coli as inclusion bodies that could be solubilized in 50 m M Na(2)CO(3), pH 10.5. Activation of the solubilized protoxin by proteinase K (1% wt/wt, proteinase K/protoxin) yielded the active fragment of about 23 kDa. Cyt2Aa2 showed high hemolytic activity against sheep erythrocytes (hemolytic end- point 0.25 microgram/ml) and was toxic to Culex quinquefasciatus and Aedes aegypti larvae (LC(50) 0.5-1.0 microgram/ml).