Abstract
1) Treatment with Lea enzyme preparation from Bac. cereus Lea destroys Lea activity of O Le(a+b-) erythrocytes and glycolipid, and liberates fucose and galactose as monosaccharides.
2) The enzymatic treatment of O Le(a-b+) erythrocytes and glycolipid results the liberation of galactose which is unrelated to the end unit of the blood group determinant.
3) On the basis of the number of moleculs of the fucose, Lea combining sites on each O Le(a+b-) red cell are estimated to be 955, 000.