Abstract
The effect of α‐galactosidase, purified from Clostridium sporogenes (Maebashi), was examined on erythrocytes from rats, rabbits and gibbons. The amount of galactose released by α‐galactosidase from Cl. sporogenes and from coffee beans was compared. The amount of sialic acid released by Vibrio cholera sialidase was also determined. Loss of blood group B specificity following treatment with α‐galactosidase was demonstrated with anti‐B lectin. In animal models, removal of all the α‐galactosyl residues with the coffee bean or clostridial α‐galactosidase resulted in no change in the sequestration pattern of the treated erythrocytes overa period of several days. In contrast, erythrocytes treated with sialidase were rapidly sequestered from the circulation.
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