Mevalonic acid metabolism

Sandmann, G. and Albrecht, M. (1994) Assays for three enzymes involved in mevalonic acid metabolism. Physiologia Plantarum, 92, 297-301. 

Beck, L. A., Hosick, T. J., Sinensky, M. (1988). Incorporation of a product of mevalonic acid metabolism into proteins of Chinese hamster ovary cell nuclei. J. Cell. Biol. 107, 1307-1316. 

In addition to relatively simple coumarins, a second group of more complex coumarins is known in which the coumarin structure is prenylated (i.e., a five-carbon unit derived from mevalonic acid metabolism is attached). The five-carbon mevalonate-derived unit of these compounds usually is re-... 

Most sexual pheromones of insects appear to be derived from either fatty acid or mevalonic acid metabolism. In a number of instances, modified monoterpenes or sesquiterpenes play roles as aggregation pheromones (Prestwich and Blomquist, 1987). 

Further biosynthetic experiments were performed with the aim to clarify metabolic relationships between polygodial and the esters, as well as to ascertain whether or not polygodial was the precursor of the esters. Two series of experiments [86] were performed injecting labelled [2-14C] mevalonic acid into nine (4.5 pCi) and fourteen (7 pCi) animals, which were sacrificed at various times from 3 to 77 h. The two experiments, performed during the months of March and April, 1984, led to apparently conflicting but not contradictory results. In fact, in the first series of experiments the major specific recovered radioactivity was always associated with polygodial (30). On the other hand, the... 

Plant metabolism can be separated into primary pathways that are found in all cells and deal with manipulating a uniform group of basic compounds, and secondary pathways that occur in specialized cells and produce a wide variety of unique compounds. The primary pathways deal with the metabolism of carbohydrates, lipids, proteins, and nucleic acids and act through the many-step reactions of glycolysis, the tricarboxylic acid cycle, the pentose phosphate shunt, and lipid, protein, and nucleic acid biosynthesis. In contrast, the secondary metabolites (e.g., terpenes, alkaloids, phenylpropanoids, lignin, flavonoids, coumarins, and related compounds) are produced by the shikimic, malonic, and mevalonic acid pathways, and the methylerythritol phosphate pathway (Fig. 3.1). This chapter concentrates on the synthesis and metabolism of phenolic compounds and on how the activities of these pathways and the compounds produced affect product quality. 

It is well established that the iridoids are derived from two units of mevalonic acid (97), which itself is derived from acetyl-CoA. Mevalonate is also known to be a metabolic product of leucine (172), and the latter is a precursor of the monoterpene linalool (173). Wigfield and Wen (174) pursued the incorporation of leucine into the monoterpene unit in both vindoline (3) and catharanthine (4), where levels of 0.07 and 0.02%, respectively, were found, irrespective of the amount of precursor fed. This was important because, although initial results were obtained with [2- C] leucine, the specificity of incorporation was determined with 2- C-la-beled precursor. Two carbons in vindoline (3), C-8 and C-24, were en-... 

Alkaloid biosynthesis needs the substrate. Substrates are derivatives of the secondary metabolism building blocks the acetyl coenzyme A (acetyl-CoA), shikimic acid, mevalonic acid and 1-deoxyxylulose 5-phosphate (Figure 21). The synthesis of alkaloids starts from the acetate, shikimate, mevalonate and deoxyxylulose pathways. The acetyl coenzyme A pathway (acetate pathway) is the source of some alkaloids and their precursors (e.g., piperidine alkaloids or anthraniUc acid as aromatized CoA ester (antraniloyl-CoA)). Shikimic acid is a product of the glycolytic and pentose phosphate pathways, a construction facilitated by parts of phosphoenolpyruvate and erythrose 4-phosphate (Figure 21). The shikimic acid pathway is the source of such alkaloids as quinazoline, quinoline and acridine. 

The terpenoids are secondary metabolites that are found in essential oils, resins, tissues of higher plants and micro-organisms, whilst recently some have also been located in liverworts [5,6]. The terpenoids are formed from linear arrangements of isoprene units, Fig. (1), which are derived from acetate metabolism through mevalonic acid (MVA). This pathway was found to be common to the whole range of natural terpenoid derivatives... 

The biochemical isoprene units may be derived by two pathways, by way of intermediates mevalonic acid (MVA) (Figure 5.4) or 1-deoxy-D-xylulose 5-phosphate (deoxyxylulose phosphate DXP) (Figure 5.6). Mevalonic acid, itself a product of acetate metabolism, had been established as a precursor of the animal sterol cholesterol, and... 

Recently, it has been demonstrated that ecdysteroid accumulation in spinach is inducible by mechanical [50] or insect [51] damage to roots. Evidence was further provided for the involvement of jasmonates in the induction of de novo ecdysteroid synthesis. Also, short- and long-term labelling of 20E from [2-14C]mevalonic acid in spinach demonstrate that ecdysteroids are metabolically stable in this species, which fits much better with a role in plant defence, rather than a phytohormonal role [52], Most recently, it has been demonstrated that root predation by the fungus gnat Bradysia impatiens results in elevated ecdysteroid levels in spinach and a significant reduction in larval establishment of B. impatiens [53],... 

The weight of evidence supports the conclusion that the more expressed inhibition of HMG-CoA reductase by a higher statin blood level reduces the concentrations of other essential products, primarily of isoprenylated proteins and possibly ubiquinone, synthetized downstream from mevalonic acid within the peripheral cells. In parallel, it was also recognized that statins exert pleiotropic effects in various cells far beyond the originally described inhibition of hepatic cholesterol synthesis. All of these effects are considered to be class-specific for the statins. It is important to emphasize that the frequency of untoward side effects observed with the various statins can be related to their potency, the number of metabolic inter-... 

Several metabolic pathways for the biosynthesis of aromatic compounds are now known, (a) The aromatization of alicyclic and isoprenoid compounds derived from mevalonic acid, as in the formation of estrone (I) from testosterone (II). A very common example of this process, which has not yet been experimentally demonstrated, is probably the aromatization of a O OH... 

Taurine is a dietary essential in the cat, which is an obligate carnivore with a limited capacity for taurine synthesis from cysteine. On a taurine-free diet, neither supplementary methionine nor cysteine will maintain normal plasma concentrations of taurine, because cats have an alternative pathway of cysteine metabolism reaction with mevalonic acid to yield felinine (3-hydroxy-1,1-dimethylpropyl-cysteine), which is excreted in the urine. The activity of cysteine sulfinic acid decarboxylase in cat liver is very low. 

Drug metabolism may be influenced by stereochemical factors if the molecule in question possesses one or more chiral centres. Examples of drugs that show stereochemical differences in rates of metabolism include a-methyldopa (where the (S) isomer is decarboxylated more rapidly than the (R) isomer) and the enantiomers of warfarin, which are reduced at different rates. The well-known endogenous compound mevalonic acid (3,5-dihydroxy-3-methylpentanoic acid) is chiral and exists as two enantiomers. When a racemic mixture of mevalonic acid is fed to animals, one optical isomer is absorbed and metabolised, while virtually all of the other isomer is excreted by the kidneys into the urine. 

The first recognized human metabolic defect in the biosynthesis of cholesterol and isoprenoids was mevalonic aciduria [10]. Mevalonic aciduria is an autosomal recessive disorder that is quite rare, with only 30 known patients (D. Haas, 2006). In normal individuals, a small amount of mevalonic acid diffuses from cells into the plasma at levels proportional to the rate of cellular cholesterol formation. Patients with the severe, classical form of mevalonic aciduria excrete 10,000-200,000 times the normal amount of mevalonic acid because they have severely reduced amounts of mevalonate kinase activity. Their clinical features include failure to thrive, anemia, gastroenteropathy, hepatosplenomegaly, psychomotor retardation, hypotonia, ataxia, cataracts, and dysmorphic features [10]. Surprisingly, patients with severe deficiencies in mevalonate kinase show normal plasma cholesterol levels and cultured mevalonic aciduria fibroblasts have a rate of cholesterol synthesis that is half that of normal cells. Close examination of cholesterogenic enzymes in mevalonic aciduria fibroblasts has revealed a 6-fold increase in HMG-CoA reductase activity, which is postulated to compensate for the low mevalonate kinase activity. Thus, mevalonate is overproduced. 

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