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1.
Bioresour Technol ; 101(6): 1871-6, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19880313

RESUMO

A total of 75 Bacillus thuringiensis strains, among them 62 of Taiwan's microbiota, were screened for their enterotoxin genes, hemolysin BL activity and cytotoxicity. All the strains harbored enterotoxin genes and were cytotoxic to the cultivated Chinese hamster ovary (CHO) cells. The hemolysin BL and cytotoxicity titers of the B. thuringiensis culture in casitone yeast sucrose (CYS) broth were lower than those in brain heart infusion (BHI) broth, and when the B. thuringiensis strains were cultivated in CYS broth for 5 days, no cytotoxicity was detected. The spores and crystal toxins collected from 40 isolates showed high levels of insecticidal activity against Plutella xylostella. All strains exhibiting low cytotoxicity also had low pesticidal activity. Our study demonstrated that it is difficult to find B. thuringiensis strains that are both effective against insect targets and do not produce enterotoxins or cytotoxic effects in CHO cells. However, it is possible to avoid or reduce unwanted properties, but not the insecticidal activity, of some B. thuringiensis preparations by alteration of culture media and conditions.


Assuntos
Bacillus thuringiensis/metabolismo , Fermentação , Controle Biológico de Vetores/métodos , Animais , Células CHO , Caseínas/farmacologia , Cricetinae , Cricetulus , Proteínas Hemolisinas/química , Insetos , Inseticidas/química , Reação em Cadeia da Polimerase , Especificidade da Espécie , Sacarose/farmacologia , Taiwan
2.
J Invertebr Pathol ; 95(1): 71-6, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17266983

RESUMO

In this study, a new microsporidian, PX2, was isolated from the diamondback moth, Plutella xylostella, and then compared with another isolate (PX1), and with Nosema spodopterae and N. bombycis. Sequence data showed that the rRNA gene organizations of PX1 and PX2 exhibited a typical Nosema-specific organization: 5'-LSUrRNA (large subunit ribosomal RNA)-ITS (internal transcribed spacer)-SSUrRNA-IGS (intergenic spacer)-5S-3'. Phylogenetic analysis (maximum likelihood, neighbor joining, maximum parsimony, and Bayesian analysis) of the LSUrRNA and SSUrRNA gene sequences, and the sequences of the alpha-tubulin, beta-tubulin, and RPB1 (DNA dependent RNA polymerase II largest subunit) genes found that PX1 was closer to N. bombycis and N. spodopterae than to PX2. Comparison of the identities of the rRNA domains and of the other three genes showed a high divergence in the sequences of the rRNA spacer regions (ITS and IGS). This is consistent with the hypothesis that PX2, if not PX1, might represent a new Nosema species.


Assuntos
Lepidópteros/microbiologia , Nosema/genética , Nosema/patogenicidade , Filogenia , Animais , Brassicaceae , DNA Fúngico/genética , Microsporidiose/genética , Nosema/classificação , RNA Fúngico/genética , Taiwan
3.
Curr Microbiol ; 47(4): 295-9, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-14629010

RESUMO

A new cry gene (cry1Ca9) was cloned and sequenced from a Bacillus thuringiensis isolate native to Taiwan (G10-01A). The cry1C-type gene, designated cry1Ca9, consisted of an open reading frame of 3,567 bp, encoding a protein of 1,189 amino acid residues. The polypeptide has the deduced amino acid sequences predicting molecular masses of 134.7 kDa. The gene sequence was compared against the GenBank nucleotide sequence data base. It was found that the cry1Ca9 gene coded for a 134.7-kDa protoxin which had greater than 99.8% homology with the previously reported cry1Ca1 gene, as only three mismatches were found between the two amino acid sequences. When the Cry1Ca9 toxin was expressed in a crystal-negative strain of B. thuringiensis (cryB-), elliptical crystals were produced. Cell extracts from this recombinant strain appear to have high insecticidal activity against lepidopteran larvae (Plutella xylostella).


Assuntos
Bacillus thuringiensis/genética , Proteínas de Bactérias/genética , Toxinas Bacterianas/genética , Endotoxinas/genética , Sequência de Aminoácidos , Animais , Bacillus thuringiensis/metabolismo , Toxinas de Bacillus thuringiensis , Proteínas de Bactérias/química , Proteínas de Bactérias/toxicidade , Toxinas Bacterianas/toxicidade , Sequência de Bases , Clonagem Molecular , DNA Bacteriano/química , DNA Bacteriano/isolamento & purificação , Endotoxinas/química , Endotoxinas/toxicidade , Expressão Gênica , Genes Bacterianos/genética , Proteínas Hemolisinas , Insetos/efeitos dos fármacos , Insetos/crescimento & desenvolvimento , Larva/efeitos dos fármacos , Larva/crescimento & desenvolvimento , Dados de Sequência Molecular , Peso Molecular , Controle Biológico de Vetores , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/genética , Proteínas Recombinantes/toxicidade , Alinhamento de Sequência , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Homologia de Sequência do Ácido Nucleico
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