Xanthine oxidase cycle

A Model for Enzymes with [MoOj] Oxidized Centers The Xanthine Oxidase Cycle... 

The chapter consists of nine sections. Sections II through VII deal with the pterin-containing molybdenum enzymes. Biochemical and model studies of molybdopterin, Mo-co, and related species are described in Section II. In Section III, we briefly survey physical and spectroscopic techniques employed in the study of the enzymes, and consider their impact upon the current understanding of the coordination about the molybdenum atom in sulfite oxidase and xanthine oxidase. Model studies are described in Sections IV and V. Section IV concentrates on structural and spectroscopic models, whereas Section V considers aspects of the reactivity of model and enzyme systems. The xanthine oxidase cycle (Section VI) and facets of intramolecular electron transfer in molybdenum enzymes (Section VII) are then treated. Section VIII describes the pterin-containing tungsten enzymes and the evolving model chemistry thereof Future directions are addressed in Section IX. 

Reperfusion of the synovial membrane occurs when exercise is stopped and O2 is subsequently reintroduced to the tissue. O2 is a substrate required for xanthine oxidase activity and O2" is generated. Therefore, repeated cycles of rest-exercise-rest in the inflamed joint may provide a continuous flux of destructive ROM. 

Possible errors due to the competition of cytochrome c reduction with the reversible reduction of quinones by superoxide are frequently neglected. For example, it has been found that quinones (Q), benzoquinone (BQ), and menadione (MD) enhanced the SOD-inhibitable cytochrome c reduction by xanthine oxidase [6]. This seems to be a mystery because only menadione may enhance superoxide production by redox cycling ( °p)"]/ [MD] =-0.20 V against ,0[02 ]/[02] 0.16 V) via Reactions (3) and (4), whereas for... 

Lipoxygenases (LOX), cycloxygenases (COXs), and xanthine oxidase (XO) are metalloen-zymes whose catalytic cycle involves ROS such as lipid peroxyl radicals, superoxide, and hydrogen peroxide. LOXs and COXs catalyze important steps in the biosynthesis of leuco-trienes and prostaglandins from arachidonic acid, which is an important cascade in the development of inflammatory responses. XO catalyzes the ultimate step in purine biosynthesis, the conversion of xanthine into uric acid. XO inhibition is an important issue in the... 

There is, however, more direct evidence for the presence of Mo (IV) in the cycle of xanthine oxidase. This evidence comes from the experiments of Massey and co-workers (24) who used alloxanthine (l) to trap the enzyme in its reduced state. A strong complex is formed between the reduced enzyme and alloxanthine, and excess alloxanthine and reductant can be removed. The enzyme is then reoxidized with Fe(CN)63", and two electrons per molybdenum center are found after the electrons required for the reoxidation of the iron-sulfur and flavin groupings are... 

Kashuba ADM, Bertino JS, Kearns GL et al. (1998) Quantitation of three-month intraindividual variability and influence of sex and menstrual cycle phase on CYP1A2, N-acetyltransferase-2, and xanthine oxidase activity determined with caffeine phenotyping. Clin Pharmacol Ther 63 540-551... 

The postulated catalytic cycles for pterin-containing molybdenum enzymes involve a two-electron change at the molybdenum atom (Mo(VI) Mo(IV)). Microcoulometric titrations of nitrate reductase Chlorella vulgaris) (76), milk xanthine oxidase (77), and sulfite oxidase (78) show that their molybdenum centers are reduced by two electrons. The reduction potentials for the molybdenum center of chicken liver sulfite oxidase are strongly dependent upon pH and upon anion concentration (78). 

Xanthine oxidase and related hydroxylase enzymes exhibit broad substrate specificity and an apparently complex catalytic cycle (109, 237). The important centers identified by EXAFS and EPR studies have... 

Superoxide generated by xanthine oxidase or in the redox cycling of paraquat can cause the reductive release of F3 from ferritin, a process that is dependent on the activity of microsomal NADPH-cytochrome P-450 reductase [119]. Iron appears to be an essential component in the formation of reactive species such as superoxide and hydroxyl radical via redox cycling of cephaloridine. Addition of EDTA or of the specific iron chelator desferrioxamine to an incubation system containing renal cortex microsomes and cephaloridine depressed cephaloridine-induced peroxidation of microsomal lipids significantly EDTA showed a weaker effect than desferrioxamine at equimolar concentrations. By chelating F3 preferentially [120], desferrioxamine reduced the availability of F2 produced by the iron redox cycle and decreased cephaloridine-stimu-lated peroxidation of membrane lipids [36, 37]. 

Uric acid is the chief end product of purine metabolism in primates, birds, lizards, and snakes. An inborn metabolic error in humans results in increased levels of uric acid and its deposition as painful crystals in the joints. This condition (gout) may be treated by the drug allopurinol which is also oxidized by xanthine oxidase to allo-xanthine (dashed line in Eq. 19.29). However, alloxanthine binds so tightly to the molybdenum that the enzyme is inactivated, the catalytic cycle broken, and uric acid formation is inhibited. The extra stability of the alloxanthine complex may be a result of strong N—H --N hydrogen bonding by the nitrogen in the 8-position ... 

Alloxanthine, however, remains tightly bound to the active site of the enzyme by chelation with Mo. Since xanthine oxidase is a molybdenum-dependent enzyme whose catalytic cycle requires the reversible oxidation and reduction of Mo" + to Mo + (Chapter 27), the reoxidation of Mo" + to Mo + in the presence of alloxanthine is very... 

Inhibition of xanthine oxidase by allopurinol, an analogue of hypoxanthine. Nv and Cg of hypoxanthine are reversed in allopurinol. Allopurinol, a suicide enzyme inactivator, is converted to alloxanthine, which binds tightly to the active site of the enzyme via Mo and interrupts the reoxidation of Mo + to Mo " needed to initiate the next catalytic cycle. 

Aerobic organisms produce minor fluxes of superoxide ion during respiration and oxidative metabolism. Thus, up to 15% of the O2 reduced by cytochrome-c oxidase and by xanthine oxidase passes through the HOO /O2 - state.70 The reductase of the latter system is a flavoprotein i that probably reduces O2 to HOOH via a redox cycle similar to that outlined by Eqs. (7-19) - (7-22). Thus, the observed flux of O2 -, which is the carrier of the auto-oxidation cycle, is due to leakage during turnover of xanthine/xanthine oxidase (see Scheme 7-14 for a reasonable mechanistic pathway). 

Administration of allopurinol, an analog of hypoxanthine, is one treatment for gout. The mechanism of action of allopurinol is interesting it acts first as a substrate and then as an inhibitor of xanthine oxidase. The oxidase hydroxylates allopurinol to alloxanthine (oxipurinol), which then remains tightly bound to the active site. The binding of alloxanthine keeps the molybdenum atom of xanthine oxidase in the + 4 oxidation state instead of it returning to the + 6 oxidation state as in a normal catalytic cycle. We see here another example of suicide inhibition. 

Activation of drugs to give toxic products is common. Apart from non-enzymatic activation (e.g., via autoxidation), activation by enzymatic one-electron oxidation or reduction frequently occurs. Several non-specific oxidases and reductases are encountered in mammalian tissues. Enzyme systems that have been studied in detail are peroxidases and microsomal oxidases and reductases. Xanthine oxidase also has received some attention. In many insta .ces the end products of the reaction are critically dependent upon the presence of oxygen in the system. This is because oxygen is an excellent electron acceptor, i.e., it can oxidize donor radicals, forming superoxide in the process. In this way a redox cycle is set up in which the xenobiotic substrate is recovered. The toxic effects of the xenobiotic often can be attributed to the oxidative stress arising from such a cycle. However, it seems that for some substrates, oxidative stress of this kind can be less damaging than anaerobic reduction. Anaerobic reduction can lead to formation of further reduced products with additional toxicity. 

Superoxide generated by xanthine oxidase or in the redox cycling of paraquat can cause the reductive re-... 

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