Caracterização físico-química e efeito sobre bactérias orais de uma lectina de sementes de Andira surinamensis (Bondt) Splitg. ex Amshoff.

• Ano de defesa: 2012
• Autor(a) principal: Nobre, Camila Bezerra
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• Idioma: por
• Palavras-chave em Português: Bioquímica; Lectina; Lectinas de plantas; Purificação; Biofilme; Uso terapêutico; Leguminosa; Lectinas; Agentes antibacterianos
• Link de acesso: http://www.repositorio.ufc.br/handle/riufc/10466

Andira surinamensis (Bondt) Splitg. ex Amshoff seeds, a species belonging to the Leguminosae family, Papilionoideae subfamily, Dalbergieae tribe, have a glucose/mannose specific lectin rabbit erythrocytes that agglutinate native or treated with proteolytic enzymes. The lectin from Andira surinamensis seeds was purified by affinity chromatography on Mannose-Sepharose matrix followed by ion exchange chromatography on DEAE-Sephacel matrix. This procedure resulted in a purified lectin, named ASL. ASL purification process was monitored by specific hemagglutinating activity and SDS-PAGE, where it was observed that this lectin is composed of six protein bands, a higher molecular weight of approximately 20 kDa and five other bands of lower apparent molecular weight between 15 and 12 kDa.The intact molecular mass of the purified lectin was determined by mass spectrometry with electrospray ionization (ESI). The analysis of the intact mass spectrum showed the presence of two majority ions of molecular mass 12.220+ 2 and 13.258 + 2 Da. ASL also had its primary structure partially sequenced by mass spectrometry sequence. This lectin is a glycoprotein and shows high stability, being able to maintain their hemagglutinating activity in a wide pH range and after exposure to temperatures up to 80 °C for 1 hour. After dialysis against the chelating agent EDTA, ASL had its hemagglutinating activity decreased, but recovered its activity after the addition of metals, being dependent on divalent metal cations. We also evaluate the effect of ASL on planktonic bacterial growth and biofilm formation and found that it interfered with the growth of two different planktonic gram-positive bacterial strains (Streptococcus mitis and Streptococcus salivarius) and biofilm formation by Stafilococcus aureus e Streptococcus salivarius.