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amylic pertaining to amyl.
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amylism poisoning by amylene hydrate.
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amylo-1,6-glucosidase [EC 3.2.1.33] an enzyme of the hydrolase class that catalyzes the cleavage of terminal α-1,6-glucoside linkages, releasing free glucose residues. In mammals, the enzyme also has a transferase activity on the same polypeptide chain (see oligo-1,4-1,4-glucantransferase) and can hydrolyze such linkages occurring at points of branching in glycogen molecules by first transferring to nearby chains those triglucosides adjacent to branch points, thereby exposing the α-1,6-linked branch points to the glucosidase activity. In concert with glycogen phosphorylase, the enzyme can thus degrade glycogen to free glucose and glucose 1-phosphate. It is found in liver and muscle. Deficiency of the enzyme, an autosomal recessive trait, results in glycogen storage disease type III. Called also debranching enzyme (of glycogen).
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amylo-1:4,1:6-transglucosidase 1,4-α-glucan branching enzyme.
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amylodyspepsia Inability to digest starchy foods.
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