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1.
J Proteomics ; 169: 202-214, 2017 10 03.
Artigo em Inglês | MEDLINE | ID: mdl-28232208

RESUMO

Bacterial blight, caused by Xanthomonas oryzae pv. oryzae (Xoo), is one of the most devastating diseases resulting in a huge loss of the total rice productivity. The initial interaction between rice and Xoo takes place in the host apoplast and is mediated primarily by secretion of various proteins from both partners. Yet, such secretory proteins remain to be largely identified and characterized. This study employed a label-free quantitative proteomics approach and identified 404 and 323 Xoo-secreted proteins from in vitro suspension-cultured cells and in planta systems, respectively. Gene Ontology analysis showed their involvement primarily in catalytic, transporter, and ATPase activities. Of a particular interest was a Xoo cysteine protease (XoCP), which showed dramatic increase in its protein abundance in planta upon Xoo interaction with a susceptible rice cultivar. Knock-out mutants of XoCP showed reduced pathogenicity on rice, highlighting its potential involvement in Xoo virulence. Besides, a parallel analysis of in planta rice-secreted proteins resulted in identification of 186 secretory proteins mainly associated with the catalytic, antioxidant, and electron carrier activities. Identified secretory proteins were exploited to shed light on their possible role in the rice-Xoo interaction, and that further deepen our understanding of such interaction. BIOLOGICAL SIGNIFICANCE: Xanthomonas oryzae pv. oryzae (Xoo), causative agent of bacterial blight disease, results in a huge loss of the total rice productivity. Using a label-free quantitative proteomics approach, we identified 727 Xoo- and 186 rice-secreted proteins. Functional annotation showed Xoo secreted proteins were mainly associated with the catalytic, transporter, and ATPase activities while the rice secreted proteins were mainly associated with the catalytic, antioxidant, and electron carrier activities. A novel Xoo cysteine protease (XoCP) was identified, showing dramatic increase in its protein abundance in planta upon Xoo interaction with a susceptible rice cultivar. Knock-out mutants of XoCP showed reduced pathogenicity on rice, highlighting its potential involvement in Xoo virulence.


Assuntos
Cisteína Proteases/fisiologia , Oryza/microbiologia , Xanthomonas/metabolismo , Proteínas de Bactérias/análise , Proteínas de Bactérias/metabolismo , Cisteína Proteases/toxicidade , Doenças das Plantas/microbiologia , Proteínas de Plantas/análise , Proteínas de Plantas/metabolismo , Proteômica/métodos , Virulência , Xanthomonas/enzimologia , Xanthomonas/patogenicidade
2.
J Basic Microbiol ; 51(2): 220-9, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21630504

RESUMO

An extracellular lethal toxin produced by Aeromonas hydrophila strain RT860715K originally isolated from diseased rainbow trout (Oncorhynchus mykiss) was purified by using Fast Protein Liquid Chromatography system with hydrophobic interaction chromatography and anion exchange columns. The toxin was a cysteine protease, inhibited by L-cysteine, iodoacetic acid, N-ethylamleimide, P-chloromercuibenzene-sulfonic acid and N-α-p-tosyl-1-lysine-chloromethyl ketone (TLCK), and showed maximal activity at pH 6.0. The molecular weight of the purified enzyme proved to be 94 kDa as estimated by SDS-PAGE. In addition, the toxin was also completely inhibited by HgCl2 but partially inhibited by ethylenediamine tetraacetic acid (EDTA) and CuCl2. Both the extracellular products of Aeromonas hydrophila RT860715K and the purified protease were lethal to rainbow trout (weighing 18 g) with LD50 values of 2.87 and 0.93 µg protein g-1 fish body weight, respectively. The addition of L-cysteine completely inhibited the lethal toxicity of the purified protease, indicating that this cysteine protease was a lethal toxin produced by the bacterium.


Assuntos
Aeromonas hydrophila/enzimologia , Toxinas Bacterianas/isolamento & purificação , Cisteína Proteases/isolamento & purificação , Doenças dos Peixes/microbiologia , Infecções por Bactérias Gram-Negativas/veterinária , Oncorhynchus mykiss , Aeromonas hydrophila/metabolismo , Animais , Toxinas Bacterianas/metabolismo , Toxinas Bacterianas/toxicidade , Cromatografia em Agarose/veterinária , Cromatografia por Troca Iônica/veterinária , Cisteína Proteases/metabolismo , Cisteína Proteases/toxicidade , Eletroforese em Gel de Poliacrilamida , Inibidores Enzimáticos/farmacologia , Infecções por Bactérias Gram-Negativas/microbiologia , Concentração de Íons de Hidrogênio , Dose Letal Mediana , Peso Molecular
3.
J Basic Microbiol ; 50(6): 538-47, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20806257

RESUMO

An extracellular lethal toxin produced by Aeromonas hydrophila strain RT860715K originally isolated from diseased rainbow trout (Oncorhynchus mykiss) was purified by using Fast Protein Liquid Chromatography system with hydrophobic interaction chromatography and anion exchange columns. The toxin was a cysteine protease, inhibited by L -cysteine, iodoacetic acid, N -ethylamleimide, P-chloromercuibenzene-sulfonic acid and N-α-p-tosyl-1-lysine-chloromethyl ketone (TLCK), and showed maximal activity at pH 6.0. The molecular weight of the purified enzyme proved to be 94 kDa as estimated by SDS-PAGE. In addition, the toxin was also completely inhibited by HgCl(2) but partially inhibited by ethylenediamine tetraacetic acid (EDTA) and CuCl2. Both the extracellular products of Aeromonas hydrophila RT860715K and the purified protease were lethal to rainbow trout (weighing 18 g) with LD50 values of 2.87 and 0.93 µg protein g⁻¹ fish body weight, respectively. The addition of L-cysteine completely inhibited the lethal toxicity of the purified protease, indicating that this cysteine protease was a lethal toxin produced by the bacterium.


Assuntos
Aeromonas hydrophila/enzimologia , Cisteína Proteases/isolamento & purificação , Cisteína Proteases/metabolismo , Oncorhynchus mykiss/microbiologia , Aeromonas hydrophila/isolamento & purificação , Animais , Toxinas Bacterianas/química , Toxinas Bacterianas/isolamento & purificação , Toxinas Bacterianas/metabolismo , Toxinas Bacterianas/toxicidade , Cromatografia Líquida/métodos , Cisteína Proteases/química , Cisteína Proteases/toxicidade , Inibidores de Cisteína Proteinase/metabolismo , Eletroforese em Gel de Poliacrilamida , Estabilidade Enzimática , Doenças dos Peixes/microbiologia , Infecções por Bactérias Gram-Negativas/microbiologia , Infecções por Bactérias Gram-Negativas/veterinária , Concentração de Íons de Hidrogênio , Dose Letal Mediana , Peso Molecular , Análise de Sobrevida
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