Pterin-dependent hydroxylase

Dioxygen reduction (oxidase activity) and activation for incorporation into organic substrates are catalysed by a number of mononuclear non-haem iron enzymes. We will first consider the intramolecular dioxygenases, in which both atoms of oxygen are introduced into the substrate, then the monoxygenases (in which we choose to include the pterin-dependent hydroxylases), the large family of a-hetoacid-dependent enzymes, and finally isopenicillin N-synthase. 

The hereditary absence of phenylalanine hydroxylase, which is found principally in the liver, is the cause of the biochemical defect phenylketonuria (Chapter 25, Section B).430 4308 Especially important in the metabolism of the brain are tyrosine hydroxylase, which converts tyrosine to 3,4-dihydroxyphenylalanine, the rate-limiting step in biosynthesis of the catecholamines (Chapter 25), and tryptophan hydroxylase, which catalyzes formation of 5-hydroxytryptophan, the first step in synthesis of the neurotransmitter 5-hydroxytryptamine (Chapter 25). All three of the pterin-dependent hydroxylases are under complex regulatory control.431 432 For example, tyrosine hydroxylase is acted on by at least four kinases with phosphorylation occurring at several sites.431 433 4338 The kinases are responsive to nerve growth factor and epidermal growth factor,434 cAMP,435 Ca2+ + calmodulin, and Ca2+ + phospholipid (protein kinase C).436 The hydroxylase is inhibited by its endproducts, the catecholamines,435 and its activity is also affected by the availability of tetrahydrobiopterin.436... 

Figure 20 Proposed roles of the iron center and the pterin cofactor in the oxygen activation mechanism for pterin-dependent hydroxylases.

The fourth class, the pterin-dependent hydroxylases, includes the aromatic amino acid hydroxylases, which use tetrahydrobiopterin as cofactor for the hydroxylation of Phe, Tyr, and Trp. The latter two hydroxylases catalyse the rate-limiting steps in the biosynthesis of the neurotransmitters/hormones dopamine/noradreanalme/ adrenaline and serotonin, respectively. 

Fe(Tpipr2)(OOPtn)] which is relevant as a model for potential intermediates in pterin-dependent hydroxylases, has been reported and its structure and reactivity investigated.96... 

Tetrahydrobiopterin (BPH4) is the natural cofactor required for the mammalian aromatic amino acid monooxygenases phenylalanine, tyrosine and tryptophan hydroxylase [4,89]. During the course of the reaction catalyzed by these enzymes, a molecule of oxygen is cleaved in order to hydroxylate the respective amino acid substrate. The remaining atom of oxygen is reduced to water at the expense of the cofactor, which is oxidized to the quinonoid form. Despite the many studies on the pterin-dependent hydroxylases, their precise mechanism of action is not well understood. This discussion will focus on mammalian phenylalanine hydroxylase (PAH), which has been favored for investigation due to its relative stability and ease of... 

Figure 20 Transformation carried out by pterin-dependent hydroxylases.

Soluble MMO Pterine-dependent hydroxylases (Phenylalanine, Tyrosine, Tryptophan) Isopenicillin N synthase... 

Scheme 6. Role of tetrahydropterin in pterin-dependent hydroxylases.

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