Oxidase xanthine oxidase

Xanthine oxidase Xanthine oxidase Xanthine oxidase Xanthine oxidase (desulfo)... 

Saito et al. (134) found that the cytosolic nitroreductase activity was due to DT-diaphorase, aldehyde oxidase, xanthine oxidase plus other unidentified nitroreductases. As anticipated, the microsomal reduction of 1-nitropyrene was inhibited by 0 and stimulated by FMN which was attributed to this cofactor acting as an electron shuttle between NADPH-cytochrome P-450 reductase and cytochrome P-450. Carbon monoxide and type II cytochrome P-450 inhibitors decreased the rate of nitroreduction which was consistent with the involvement of cytochrome P-450. Induction of cytochromes P-450 increased rates of 1-aminopyrene formation and nitroreduction was demonstrated in a reconstituted cytochrome P-450 system, with isozyme P-448-IId catalyzing the reduction most efficiently. 

O Donnell et al. [70] found that LOX and not cyclooxygenase, cytochrome P-450, NO synthase, NADPH oxidase, xanthine oxidase, ribonucleotide reductase, or mitochondrial respiratory chain is responsible for TNF-a-mediated apoptosis of murine fibrosarcoma cells. 15-LOX activity was found to increase sharply in heart, lung, and vascular tissues of rabbits by hypercholesterolemia [71], Schnurr et al. [72] demonstrated that there is an inverse regulation of 12/15-LOXs and phospholipid hydroperoxide glutathione peroxidases in cells, which balanced the intracellular concentration of oxidized lipids. 

In addition to binding to cytochrome c oxidase, cyanide inhibits catalase, peroxidase, methemoglobin, hydroxocobalamin, phosphatase, tyrosinase, ascorbic acid oxidase, xanthine oxidase, and succinic dehydrogenase activities. These reactions may make contributions to the signs of cyanide toxicity (Ardelt et al. 1989 Rieders 1971). Signs of cyanide intoxication include an initial hyperpnea followed by dyspnea and then convulsions (Rieders 1971 Way 1984). These effects are due to initial stimulation of carotid and aortic bodies and effects on the central nervous system. Death is caused by respiratory collapse resulting from central nervous system toxicity. 

Molybdenum Milk, milk products dried legumes or pulses liver and kidney grains Prosthetic group of enzymes aldehyde oxidase Xanthine oxidase Electron transfer chain enzymes... 

HORSERADISH PEROXIDASE LACTOPEROXIDASE LIGNAN PEROXIDASE LYSYL OXIDASE MANGANESE PEROXIDASE MYELOPEROXIDASE OVOPEROXIDASE PEROXIDASE PYRUVATE OXIDASE XANTHINE OXIDASE Hydrogen selenide,... 

RROLINE DIPEPTIDASE XANTHINE DEHYDROGENASE XANTHINE OXIDASE XANTHINE OXIDASE... 

Coughlan, M. P. 1980. Aldehyde oxidase, xanthine oxidase and xanthine dehydrogenase. Hydroxylases containing molybdenum, iron-sulphur and flavin. In Molybdenum and Molybdenum-Containing Enzymes. M.P. Coughlan (Editor). Pergamon Press, Oxford, pp. 119-185. 

Figure 6.11 Structure of the pterin cofactor, which binds molybdenum in aldehyde oxidase, xanthine oxidase, and sulfite oxidase. [Reproduced by permission from Rajago-palan, KV. Molybdenum, an essential trace element. Nutr. Rev., 45 321-328 (1987).]...

Nitrogenase MoFe protein NADH dehydrogenase Respiratory nitrate reductase Assimilatory nitrate reductase Sulfite oxidase Aldehyde oxidase Xanthine oxidase Xanthine dehydrogenase... 

Molybdenum Hydroxylases (Aldehyde Oxidase, Xanthine Oxidase) Oxidations Purines, pteridine, methrotrexate, quinolones, 6-deoxycyclovir... 

Overproduction of superoxide ( Op has been implicated in the pathogenesis of various cardiovascular diseases. The main sources of human superoxide include the nicotinamide adenine dinucleotide phosphate oxidase (NADPH oxidase) enzyme complex, cyclooxygenase, mitochondrial oxidases, xanthine oxidase, and nitric... 

In summary, a 6-substituted pterin was first identified as a structural component of the molybdenum cofactor from sulfite oxidase, xanthine oxidase and nitrate reductase in 1980 (24). Subsequent studies provided good evidence that these enzymes possessed the same unstable molyb-dopterin (1), and it seemed likely that 1 was a constituent of all of the enzymes of Table I. It now appears that there is a family of closely related 6-substituted pterins that may differ in the oxidation state of the pterin ring, the stereochemistry of the dihydropterin ring, the tautomeric form of the side chain, and the presence and nature of a dinucleotide in the side chain. In some ways the variations that are being discovered for the pterin units of molybdenum enzymes are beginning to parallel the known complexity of naturally occurring porphyrins, which may have several possible side chains, various isomers of such side chains, and a partially reduced porphyrin skeleton (46). 

Sensors have also been constructed from some oxidases directly contacted to electrodes to give bioelectrocatalytic systems. These enzymes utilize molecular oxygen as the electron acceptor for the oxidation of their substrates. Enzymes such as catechol oxidase, amino acid oxidase, glucose oxidase, lactate oxidase, pyruvate oxidase, alcohol oxidase, xanthine oxidase and cholesterol oxidase catalyze the oxidation of their respective substrates with the concomitant reduction of O2 to H2O2 ... 

Long recognized as an essential element for the growth of plants, molybdenum has never been directly demonstrated as a necessary animal nutrient. Nevertheless, it is found in several enzymes of the human body, as well as in 30 or more additional enzymes of bacferia and plants. Aldehyde oxidases, xanthine oxidase of liver and fhe relafed xanthine dehydrogenase, catalyze the reactions of Eqs. 16-58 and 16-59 and contain molybdenum that is essential for catalytic activity. Xanthine oxidase also contains two Pe2S2 clusters and bound FAD. The enzymes can also... 

The phase I reactions are mediated primarily by liver enzymes such as cytochrome P450 (CYP450), FAD-containing mono-oxygenase (FMO), monoamine oxidase (MAO), molybdenum hydroxylase (aldehyde oxidase/xanthine oxidase AO/XO), aldo-ketoreductase (AKR), epoxide hydrolase (EH), and esterase. 

AO/XO Aldehyde oxidase/xanthine oxidase (molybdenum hydroxylases)... 

Besides the monooxygenases discussed above, a number of other oxidoreductases can oxidize xenobiotics. These enzymes are mostly but not exclusively nonmicrosomal, being present in the cytosol or mitochondria of the liver and extrahepatic tissues. The list includes alcohol dehydrogenases, aldehyde dehydrogenases, dihydrodiol dehydrogenases, haemoglobin, monoamine oxidases, xanthine oxidase and aldehyde oxidase. Some of these enzyme systems are discussed below. 

Substrate specificities can be broad and overlapping both among CYP family members and between CYPs and FMOs, and since metabolic transformations are often sequential (e.g. aliphatic hydroxylation being followed by oxidation by alcohol dehydrogenase, further oxidation to the acid, etc.), many enzymes and many metabolites can be involved in processing a single drug. Only a few of the most important enzymes involved in Phase I transformations have been mentioned here. For these and many others (monoamine oxidase, xanthine oxidase, etc.), further information can be found in the previously cited reviews. Bear in mind too that not all Phase I reactions are oxidative enzymes like carbonyl reductases are important in metabolism as well. 

Panoutsopoulos GI, Kouretas D, Beedham C. Contribution of aldehyde oxidase, xanthine oxidase, and aldehyde dehydrogenase on the oxidation of aromatic aldehydes. Chem Res Toxicol 2004 17 1368-1376. 

Hydrogenase Glucose oxidase Xanthine oxidase Aldehyde oxidase Alcohol dehydrogenase... 

J. L. Johnson, B. E. Hainline and K. V. Rajagopalan, Characterization of the molybdenum cofactor of sulfite oxidase, xanthine oxidase, and nitrate reductase. Identification of a pteridine as a structural component,/. Biol. Chem., 1980, 255,1783-1786. 

The initial contribution to this volume provides a detailed overview of how spectroscopy and computations have been used in concert to probe the canonical members of each pyranopterin Mo enzyme family, as well as the pyranopterin dithiolene ligand itself. The discussion focuses on how a combination of enzyme geometric structure, spectroscopy and biochemical data have been used to arrive at an understanding of electronic structure contributions to reactivity in all of the major pyranopterin Mo enzyme families. A unique aspect of this discussion is that spectroscopic studies on relevant small molecule model compounds have been melded with analogous studies on the enzyme systems to arrive at a sophisticated description of active site electronic structure. As the field moves forward, it will become increasingly important to understand the structure, function and reaction mechanisms for the numerous non-canonical [ie. beyond sulfite oxidase, xanthine oxidase, DMSO reductase) pyranopterin Mo enzymes. 

Oxidations are the most common biotransformation reactions that occur with most drugs. There are several classes of enzymes that carry out these reactions cytochrome P450s, flavin monooxygenases, monoamine oxidases, xanthine oxidase, aldehyde oxidases, aldehyde dehydrogenases, and peroxidases. Typical reactions and substrate substructures for each of these classes of enzymes will be described. 

Molybdenum enzymes are aldehyde oxidase, xanthine oxidase/dehydrogenase, sulfite oxidase [15,16],... 

Figure 6.32 Unusual reactions of two oxidases. Xanthine oxidase will also oxidize cinnamaldehyde, showing a preference for the cis-isomer, while galactose oxidase will also oxidize glycerol, which it treats as a pro-chiral substrate...

Molybdenum is considered an ultra-trace element with an approximate amount of 5 mg in the adult human body. It is a cofactor for at least three enzymes in humans (sulfite oxidase, xanthine oxidase, and aldehyde oxidase) and is involved in the catabolism of sulfur-containing amino acids, purine, and pyrimidine. A better understanding of human molybdenum metabolism is needed in order to give evidence-based recommendations regarding optimal nutrition, although molybdenum deficiency and associated pathological symptoms have not yet been observed in humans [74]. 

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