ENZYME INHIBITION BY PHENYLALANINE AND ITS METABOLITES

 
        High levels of phenylalanine can cause inhibition of the decarboxylation of 5-hydroxytryptophan, so that little or no serotonin is formed.
 
        Phenylalanine can also inhibit the enzyme tyrosinase.  Tyrosinase  converts tyrosine into 3,4-dihydroxyphenylalanine (DOPA) through an oxidation reaction.
 
 
 

        DOPA can then be used for catecholamine biosynthesis, or in a separate set of reactions it goes on to form the pigment melanin.  The blockage in melanin biosynthesis by the high levels of Phe is responsible for the fair complexions of patients with PKU.

        Phe can also inhibit glutamate decarboxylase, resulting in lower GABA levels in the brain and thus interfering with neurologic function on a level apart from defective catecholamine metabolism.

 

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