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FURTHER STUDIES ON THE CHEMICAL BASIS FOR SEROLOGICAL SPECIFICITY OF GROUP A STREPTOCOCCAL CARBOHYDRATE

Azoproteins prepared with p-aminophenyl-β-N-acetyl-glucosaminide react in precipitin tests with Group A streptococcal antisera. The reaction is nonreciprocal, and antisera to the azoprotein do not react with Group A carbohydrate. Phenyl-N-acetyl-glucosaminides inhibit the reaction of Group A carbohy...

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Detalles Bibliográficos
Autor principal: McCarty, Maclyn
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1958
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136878/
https://www.ncbi.nlm.nih.gov/pubmed/13575668
Descripción
Sumario:Azoproteins prepared with p-aminophenyl-β-N-acetyl-glucosaminide react in precipitin tests with Group A streptococcal antisera. The reaction is nonreciprocal, and antisera to the azoprotein do not react with Group A carbohydrate. Phenyl-N-acetyl-glucosaminides inhibit the reaction of Group A carbohydrate with homologous antisera and with antisera to the azoprotein. The β-anomer is more effective as an inhibitor than the α-anomer. Formation by a soil bacillus of the enzyme which removes N-acetyl-glucosamine from Group A carbohydrate is induced by phenyl-β-N-acetyl-glucosaminide but not by the α-compound. The enzyme, like the glucosaminidase of emulsin, appears to be specific for β-glucosaminides. Neither the induced enzyme nor emulsin effectively remove all of the N-acetyl-glucosamine from the azoprotein antigens. The findings support the view that β-N-acetyl-glucosaminide side chains represent the major antigenic determinant of Group A streptococcal carbohydrate.