Enzymes phosphate-metabolizing inhibition

The enzyme has been partially purified (70-fold) from 38,000 X 9 supernatant fluid from sheep brain homogenates by Ipata (55-58). Thq enzyme (MW 140,000) is reported to be specific for 5 -AMP and 5 -IMP although the substrate specificity does not appear to have been examined closely. 2 - and 3 -AMP are not hydrolyzed (56). Unlike the enzyme from many sources the brain enzyme does not require divalent cations and indeed Co2+, which stimulates several other 5 -nucleotidases, was inhibitory at 5 mM. The enzyme is strongly inhibited by very low concentrations of ATP, UTP, and CTP (50% inhibition by 0.3 pM ATP) but not by GTP. 2 -AMP, 3 -AMP, and a variety of other nucleoside monophosphates, nucleosides, and sugar phosphates do not inhibit. A kinetic examination of ATP, UTP, and CTP inhibition (56-58) revealed that inhibition curves were sigmoidal, indicating cooperativity between inhibitor molecules and an allosteric type of interaction between inhibitor and protein. The metabolic significance of ATP inhibition is... 

Inhibition of Phosphate-Metabolizing Enzymes by Vanadium Compounds... 

Figure 9-1 Sites of feedback inhibition in carbamyl phosphate metabolism of E. coli. Note that aspartate trascarbamylase is the first enzyme on the unique pathway to pyrimidine compounds.

AT-Acetyl-D-glucosamine 6-phosphate is metabolized to the D-fructose ester more slowly (by preparations of kidney enzyme) than is D-glucosamine 6-phosphate/ Acetate inhibits the disappearance of AT-acetyl-n-glucos-amine 6-phosphate, but does not affect the disappearance of D-glucosamine 6-phosphate. A possible sequence of reactions for these transformations is as follows. ... 

Many enzymes are dependent on dissociable metal ions for their activity, and the operation of most of the important metabolic systems thus requires the presence of these cofactors. For example, the list of enzymes requiring Mg is a long one and includes the oxidases and decarboxylases for the keto acids, most of the enzymes involved in phosphate metabolism, some dehydrogenases, some peptidases, phosphoglucomutase and enolase. These enzymes may be inhibited with inhibitors forming stable complexes with Mg ions. For example, malonate and other dicarboxylic compounds are able to chelate effectively with Mg" and other metal ions, and their inhibition may result from the reduction of metal ion concentration in the medium or the removal of the metal ions from the enzyme [3] ... 

In addition to acting as an inhibitor of dynein and (Na, K)-ATPase, vanadium is also a potent inhibitor of RNase (57) and alkaline and acid phosphatases (58.59). This suggests that vanadium generally tends to inhibit enzymes of phosphate metabolism. However, according to Gibbons et al. (53), the mechanism of Inhibition is not the same in each enzyme. The Inhibition of RNase and alkaline phosphatase is greater by oxyvanadium (IV) than by vanadium (V). 

Histamine is synthesised by decarboxylation of histidine, its amino-acid precursor, by the specific enzyme histidine decarboxylase, which like glutaminic acid decarboxylase requires pyridoxal phosphate as co-factor. Histidine is a poor substrate for the L-amino-acid decarboxylase responsible for DA and NA synthesis. The synthesis of histamine in the brain can be increased by the administration of histidine, so its decarboxylase is presumably not saturated normally, but it can be inhibited by a fluoromethylhistidine. No high-affinity neuronal uptake has been demonstrated for histamine although after initial metabolism by histamine A-methyl transferase to 3-methylhistamine, it is deaminated by intraneuronal MAOb to 3-methylimidazole acetic acid (Fig. 13.4). A Ca +-dependent KCl-induced release of histamine has been demonstrated by microdialysis in the rat hypothalamus (Russell et al. 1990) but its overflow in some areas, such as the striatum, is neither increased by KCl nor reduced by tetradotoxin and probably comes from mast cells. 

The high toxicity of AOA is due to its very high efficiency as a transaminase inhibitor (K =0.45 pM) as compared to its efficacy as a PAL inhibitor (K. = 120 pM) (48), making it impossible to effectively inhibit PAL iti vivo without also greatly inhibiting amino acid metabolism. Other pyridoxyl phosphate-requiring enzymes, such as ACC synthase (an enzyme involved in ethylene production) (49), are also more sensitive to AOA than to AOPP. 

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