Activity of Debaryomyces hansenii UFV-1 a-galactosidases against a-D-galactopyranoside derivatives

α-d-Galactopyranosides were synthesized and their inhibitory activities toward the Debaryomyces hansenii UFV-1 extracellular and intracellular α-galactosidases were evaluated. Methyl α-d-galactopyranoside was the most potent inhibitor compared to the others tested, with values of 0.82 and 1.12 mmol...

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Detalles Bibliográficos
Autores: Rezende, Sebastião T. de, Viana, Pollyanna A., Alves, Arianne de A., Manfrini, Rozângela M., Alves, Ricardo J., Bemquerer, Marcelo P., Santoro, Marcelo M., Guimarães, Valéria M.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:Brasil
Institución:Universidade Federal de Viçosa (UFV)
Repositorio:LOCUS Repositório Institucional da UFV
Idioma:inglés
OAI Identifier:oai:locus.ufv.br:123456789/19851
Acceso en línea:https://doi.org/10.1016/j.carres.2011.01.024
http://www.locus.ufv.br/handle/123456789/19851
Access Level:acceso abierto
Palabra clave:α-Galactosidases
Debaryomyces hansenii UFV-1
α-d-Galactopyranoside derivatives
Inhibition
Descripción
Sumario:α-d-Galactopyranosides were synthesized and their inhibitory activities toward the Debaryomyces hansenii UFV-1 extracellular and intracellular α-galactosidases were evaluated. Methyl α-d-galactopyranoside was the most potent inhibitor compared to the others tested, with values of 0.82 and 1.12 mmol L−1, for extracellular and intracellular enzymes, respectively. These results indicate that the presence of a hydroxyl group in the C-6 position of α-d-galactopyranoside derivatives is important for the recognition by D. hansenii UFV-1 α-galactosidases.