When a certain trisaccharide is completely methylated (i.e. all of the free OH groups have been converted to OCH3 groups) and then hydrolyzed (i.e. all of the glycosidic linkages have been broken) equal molar amounts of 2,3,4,6-tetra-O-methyl-D-galactose, 2,3,4-tri-O-methyl-D- mannose, and 1,2,4,6-tetra-O-methyl-D-glucose are obtained. When this same trisaccaride is treated with beta-galactosidase ( an enzyme that hydrolyzes the indicated glycosidic bond indicted by it's name) it yields D- galactose and a disaccharide. Treatment of the resulting disaccharride with alpha- mannosidase yields D-mannose and D-glucose. Draw the structure of the beta anomer of the original trisaccharide.

Biochemistry
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Chapter1: Biochemistry: An Evolving Science
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When a certain trisaccharide is completely methylated (i.e. all of the free OH groups have been converted to OCH3 groups) and then hydrolyzed (i.e. all of the glycosidic linkages have been broken) equal molar amounts of 2,3,4,6-tetra-O-methyl-D-galactose, 2,3,4-tri-O-methyl-D- mannose, and 1,2,4,6-tetra-O-methyl-D-glucose are obtained. When this same trisaccaride is treated with beta-galactosidase ( an enzyme that hydrolyzes the indicated glycosidic bond indicted by it's name) it yields D- galactose and a disaccharide. Treatment of the resulting disaccharride with alpha- mannosidase yields D-mannose and D-glucose. Draw the structure of the beta anomer of the original trisaccharide. 

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Trisaccharide is a sugar compound which is made up of three monosaccharide when attached together. It is a large molecule. They are connected by two glycosidic bonds.

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