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Purification and characterization of a putative virulence factor,serine protease,from Vibrio parahaemolyticus
Authors:Lee Chia-Yin  Cheng Min-Fu  Yu Mei-Shiuan  Pan Ming-Jeng
Affiliation:Centro de Referencia para Lactobacilos (CERELA, CONICET), Tucmán, Argentina. glorca@cerela.org.ar
Abstract:Binding of immobilized collagen-I (Cn-I) and fibronectin (Fn) by Lactobacillus acidophilus CRL 639 depends on cell-surface proteins. Capsule formation during the stationary growth phase has a negative effect on adherence of Cn-I and Fn. However, cells from the exponential growth phase, which produce no capsule, exhibit maximal binding. Binding is sensitive to trypsin, proteinase K, pronase E, and heat. Gelatin and soluble Cn-I partially inhibit binding of Cn-I although various proteins, sugars and amino acids do not affect binding to Fn. These results indicate that protein-protein interactions mediate adhesion to extracellular matrix proteins. SDS-PAGE and Western blot analyses of surface proteins revealed that several proteins including the major 43-kDa protein of the S-layer are expressed. Monoclonal antibodies showed that Fn binds to a 15-kDa protein, while Cn-I binds to proteins of 45 and 58 kDa.
Keywords:Lactobacillus    Collagen binding    Fibronectin binding    Polysaccharide    Immunoblot    Protein–protein interaction
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