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1.
Parasitology ; 139(2): 259-63, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22018391

RESUMO

The purpose of this study was to describe an unreported entomopathogenic fungus that naturally infects the cattle tick Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Engorged female ticks, showed symptoms of fungal infection after controlled tick infestation of cattle. Infected ticks developed a distinctive dark colour, a pale mould grew over the cuticle and the ticks eventually died covered with fungal conidiophores. The responsible fungus was isolated and cultured on mycological medium and submitted to microscopic morphology, biochemical phenotyping and 18S rRNA ribotyping analyses, which identified it as aflatoxin-producing Aspergillus flavus. Spores from the cultured fungus were experimentally sprayed over healthy engorged female ticks, obtaining an 80% prevalence of experimental infection of healthy ticks and their egg masses, the larval progeny after incubation under laboratory conditions was also infected. These results demonstrate that A. flavus is the causative agent of the natural fungal disease of the cattle tick R. microplus described here.


Assuntos
Aspergillus flavus/isolamento & purificação , Rhipicephalus/microbiologia , Animais , Bovinos , Feminino , Rhipicephalus/ultraestrutura
2.
Plant Physiol ; 119(4): 1473-82, 1999 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10198107

RESUMO

The accumulation of the disaccharide trehalose in anhydrobiotic organisms allows them to survive severe environmental stress. A plant cDNA, SlTPS1, encoding a 109-kD protein, was isolated from the resurrection plant Selaginella lepidophylla, which accumulates high levels of trehalose. Protein-sequence comparison showed that SlTPS1 shares high similarity to trehalose-6-phosphate synthase genes from prokaryotes and eukaryotes. SlTPS1 mRNA was constitutively expressed in S. lepidophylla. DNA gel-blot analysis indicated that SlTPS1 is present as a single-copy gene. Transformation of a Saccharomyces cerevisiae tps1Delta mutant disrupted in the ScTPS1 gene with S. lepidophylla SlTPS1 restored growth on fermentable sugars and the synthesis of trehalose at high levels. Moreover, the SlTPS1 gene introduced into the tps1Delta mutant was able to complement both deficiencies: sensitivity to sublethal heat treatment at 39 degrees C and induced thermotolerance at 50 degrees C. The osmosensitive phenotype of the yeast tps1Delta mutant grown in NaCl and sorbitol was also restored by the SlTPS1 gene. Thus, SlTPS1 protein is a functional plant homolog capable of sustaining trehalose biosynthesis and could play a major role in stress tolerance in S. lepidophylla.


Assuntos
Glucosiltransferases/genética , Glucosiltransferases/metabolismo , Plantas/enzimologia , Plantas/genética , Saccharomyces cerevisiae/enzimologia , Saccharomyces cerevisiae/genética , Sequência de Aminoácidos , Sequência de Bases , Clonagem Molecular , Primers do DNA/genética , DNA Complementar/genética , DNA de Plantas/genética , Expressão Gênica , Genes Fúngicos , Genes de Plantas , Teste de Complementação Genética , Temperatura Alta , Dados de Sequência Molecular , Mutação , Saccharomyces cerevisiae/crescimento & desenvolvimento , Homologia de Sequência de Aminoácidos , Trealose/biossíntese
3.
Mol Plant Microbe Interact ; 11(10): 979-87, 1998 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9768515

RESUMO

A cosmid from the Rhizobium tropici CIAT899 symbiotic plasmid, containing most of the nodulation genes described in this strain, has been isolated. Although this cosmid does not carry a nodD gene, it confers ability to heterologous Rhizobium spp. to nodulate R. tropici hosts (Phaseolus vulgaris, Macroptilium atropurpureum, and Leucaena leucocephala). The observed phenotype is due to constitutive expression of the nodABCSUIJ operon, which has lost its regulatory region and is expressed from a promoter present in the cloning vector. Thin-layer chromatography (TLC) analysis of the Nod factors produced by this construction shows that it is still capable of synthesizing sulfated compounds, suggesting that the nodHPQ genes are organized as an operon that is transcribed in a nodD-independent manner and is not regulated by flavonoids.


Assuntos
Lipopolissacarídeos/metabolismo , Rhizobium/genética , Rhizobium/metabolismo , Proteínas de Bactérias/genética , Proteínas de Bactérias/metabolismo , Sequência de Bases , Cosmídeos , DNA Bacteriano/genética , Fabaceae/microbiologia , Expressão Gênica , Genes Bacterianos , Dados de Sequência Molecular , Óperon , Fenótipo , Plantas Medicinais , Plasmídeos/genética , Sulfatos/metabolismo
4.
Appl Environ Microbiol ; 64(4): 1400-4, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9546177

RESUMO

In this work we introduce the confluent and various sizes image analysis method (COVASIAM), an automated colony count technique that uses digital imaging technology for detection and separation of confluent microbial colonies and colonies of various sizes growing on petri dishes. The proposed method takes advantage of the optical properties of the surfaces of most microbial colonies. Colonies in the petri dish are epi-illuminated in order to direct the reflection of concentrated light coming from a halogen lamp towards an image-sensing device. In conjunction, a multilevel threshold algorithm is proposed for colony separation and counting. These procedures improved the quantification of colonies showing confluence or differences in size. We tested COVASIAM with a sample set of microorganisms that form colonies with contrasting physical properties: Saccharomyces cerevisiae, Aspergillus nidulans, Escherichia coli, Azotobacter vinelandii, Pseudomonas aeruginosa, and Rhizobium etli. These physical properties range from smooth to hairy, from bright to opaque, and from high to low convexities. COVASIAM estimated an average of 95.47% (sigma = 8.55%) of the manually counted colonies, while an automated method based on a single-threshold segmentation procedure estimated an average of 76% (sigma = 16.27) of the manually counted colonies. This method can be easily transposed to almost every image-processing analyzer since the procedures to compile it are generically standard.


Assuntos
Contagem de Colônia Microbiana/métodos , Processamento de Imagem Assistida por Computador/métodos , Aspergillus nidulans/isolamento & purificação , Azotobacter vinelandii/isolamento & purificação , Contagem de Colônia Microbiana/instrumentação , Escherichia coli/isolamento & purificação , Estudos de Avaliação como Assunto , Processamento de Imagem Assistida por Computador/instrumentação , Pseudomonas aeruginosa/isolamento & purificação , Rhizobium/isolamento & purificação , Saccharomyces cerevisiae/isolamento & purificação
5.
Mol Plant Microbe Interact ; 9(3): 151-63, 1996 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8850086

RESUMO

We have purified and characterized the nodulation factors produced by Rhizobium tropici CIAT899. This strain produces a large variety of nodulation factors, these being a mixture of sulfated or nonsulfated penta- or tetra-chito-oligosaccharides to which any of six different fatty acyl moieties may be attached to nitrogen of the nonreducing terminal residue. In this mixture we have also found methylated or nonmethylated lipo-chitin oligosaccharides. Here we describe a novel lipo-chitin-oligosaccharide consisting of a linear backbone of 4 N-acetylglucosamine residues and one mannose that is the reducing-terminal residue and bearing a C18:1 fatty acyl moiety on the nonreducing terminal residue. In addition, we have identified, cloned, and sequenced R. tropici nodH and nodPQ genes, generated mutations in the nodH and nodQ genes, and tested the mutant strains for nodulation in Phaseolus and Leucaena plants. Our results indicate that the sulfate group present in wild-type Nod factors plays a major role in nodulation of Leucaena plants by strain CIAT899 of R. tropici.


Assuntos
Proteínas de Bactérias/genética , Genes Bacterianos , Complexos Multienzimáticos , Rhizobium/genética , Sulfato Adenililtransferase , Sulfotransferases/genética , Sequência de Aminoácidos , Proteínas de Bactérias/química , Mapeamento Cromossômico , Clonagem Molecular , Fabaceae/microbiologia , Dados de Sequência Molecular , Estrutura Molecular , Mutação , Fixação de Nitrogênio/genética , Oligossacarídeos/química , Fases de Leitura Aberta , Fenótipo , Plantas Medicinais , Rhizobium/química , Homologia de Sequência de Aminoácidos , Sulfatos/química , Sulfotransferases/química
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