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1.
Fish Shellfish Immunol ; 106: 685-690, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32822860

RESUMO

An l-amino acid oxidase (LAO) is an amino acid metabolism enzyme that also performs a variety of biological activities. Recently, LAOs have been discovered to be deeply involved in innate immunity in fish because of their antibacterial and antiparasitic activity. The determinant of potent antibacterial/antiparasitic activity is the H2O2 byproduct of LAO enzymatic activity that utilizes the l-amino acid as a substrate. In addition, fish LAOs are upregulated by pathogenic bacteria or parasite infection. Furthermore, some fish LAOs show that the target specificity depends on the virulence of the bacteria. All results reflect that LAOs are new innate immune molecules. This review also describes the potential of the immunomodulatory functions of fish LAOs, not only the innate immune function by a direct oxidation attack of H2O2.


Assuntos
Peixes/imunologia , L-Aminoácido Oxidase/imunologia , Animais , Peixes/genética , Brânquias/imunologia , Imunomodulação , Intestinos/imunologia , L-Aminoácido Oxidase/sangue , L-Aminoácido Oxidase/genética , Pele/imunologia
2.
Artigo em Inglês | MEDLINE | ID: mdl-20728563

RESUMO

Fish have a complex innate defense mechanism against microbial invasion. In particular, epidermal mucus and serum in fish play important roles in innate immunity and contain a variety of bioactive substances such as complements, lectins and lysozymes, involved in host defense. Recently, L-amino acid oxidases (LAOs) with antibacterial activity were isolated from the skin and/or gill mucous secretions of rockfish, great sculpin and flounder, and were identified to be a novel type of antibacterial protein in the integument of fish. In the present study, we found LAO activity in the serum of rockfish Sebastes schlegeli. The LAO was isolated from the serum by sequential column chromatography of Con-A lectin affinity chromatography, anion exchange HPLC, hydroxyapatite HPLC and gel filtration HPLC, and characterized. The LAO (a molecular mass of 160 kDa) comprised subunits with a molecular mass of 53 kDa and showed strict substrate specificity, catalyzing only L-lysine with Km 0.37 mM and kcat 57.1s(-1). The serum LAO exhibited a broad antibacterial activity against Gram positive and negative bacteria, most potently against Aeromonas hydrophila and Aeromonas salmonicida with a minimum inhibitory concentration of 0.078 µg/mL. This is the first report of LAO in the serum of fish and its involvement in innate immunity in the rockfish body.


Assuntos
Antibacterianos/sangue , Proteínas de Peixes/sangue , Peixes/imunologia , L-Aminoácido Oxidase/sangue , Sequência de Aminoácidos , Animais , Antibacterianos/farmacologia , Proteínas de Peixes/química , Proteínas de Peixes/isolamento & purificação , Peixes/sangue , Imunidade Inata , L-Aminoácido Oxidase/química , L-Aminoácido Oxidase/isolamento & purificação , Dados de Sequência Molecular
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