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Nucleotide synthesis and

Reisner M, Carmeli S, Werman M, Sukenik A (2004) The cyanobacterial toxin cylindrospermopsin inhibits pyrimidine nucleotide synthesis and alters cholesterol distribution in mice. [Pg.118]

The selective protection of hydroxyl groups is obviously most frequent in carbohydrate synthesis and, in fact, photosensitive protecting groups have been used to this effect in oligosaccharide synthesis, nucleotide synthesis, and saccharide modification. Here, as well as in other Sections, special attention will be devoted to 2-nitrobenzyl derivatives, whose re-... [Pg.180]

Nitrobenzyl phosphoric esters, which are photolyzed to the free acids (compare Scheme 3), are used in nucleotide synthesis and are very efficiently cleaved (90-98%) at >320 nm in the presence of a polymeric carbonyl reagent ((P)-N(CH3)-CONHNH2) to remove the aromatic photoproducts an example is given in Scheme 30. [Pg.203]

Turowski, M., Kaliszan, R., Lullmann, C., Genieser, H. G., and Jastorff, B., New stationary phases for the high performance liquid chromatographic separation of nucleosides and cyclic nucleotides. Synthesis and chemometric analysis of retention data, /. Chromatogr. A, 728, 201-211, 1996. [Pg.182]

Three major feedback mechanisms cooperate in regulating the overall rate of de novo purine nucleotide synthesis and the relative rates of formation of the two end products, adenylate and guanylate (Fig. 22-35). The first mechanism is exerted on the first reaction that is unique to purine synthesis—transfer of an amino group to PRPP to form 5-phosphoribosylamine. This reaction is catalyzed by the allosteric enzyme glutamine-PRPP amidotransferase, which is inhibited by the end products IMP, AMP, and GMP. AMP and GMP act synergisti-cally in this concerted inhibition. Thus, whenever either AMP or GMP accumulates to excess, the first step in its biosynthesis from PRPP is partially inhibited. [Pg.866]

The equilibria in these phosphoribosyltransferase reactions favor nucleotide synthesis, and since the inorganic pyrophosphate released is rapidly hydrolyzed by inorganic pyrophosphatase, the coupling of these reactions makes the synthesis of nucleotide irreversible. However, the efficiency of salvage is heavily dependent on the intracellular concentration of PRPP. [Pg.548]

Phosphate Facilitates energy storage and release, nucleotide synthesis, and maintenance of acid-base balance in body fluids Men women 700 mg/d... [Pg.613]

Two activities of the immunosuppressive metabolite of Leflimomide, A77 1 726. Inhibition of pyrimidine nucleotide synthesis and protein tyrosine phosphorylation. Biochem. Pharmacol. 52,... [Pg.208]

Folic acid (Mr = 441, Fig. 1) is a vitamin essential for de novo nucleotide synthesis and one-carbon metabolism. The ability to acquire folate, therefore, is important to the viability of proliferating cells. [Pg.69]

Synthetic biology uses the DNA sequence information of a virus to resynthesize the viral molecule via throughput technology of nucleotide synthesis and robotics. Using these technologies, it is possible, for example, to spread the small pox virus, and cause mass chaos which has been already eliminated from the earth. Thus, the power of synthetic biology has to be protected from terrorists just like the nuclear bombs falling in their hands. [Pg.159]

The pentose phosphate pathway is an alternative pathway for glucose degradation that is particularly abundant in the liver and adipose tissue. It provides the cell with a source of NADPH to serve as a reducing agent for bios)mthetic reactions. It also provides ribose-5-phosphate for nucleotide synthesis and erythrose-4-phosphate for bios)mthesis of the amino acids tryptophan, t)rrosine, and phenylalanine. [Pg.655]

The pentose phosphate pathway is an important pathway for generating NADPH (for biosynthetic reactions) and pentose sugars (for nucleotide biosynthesis). It operates exclusively in the cytosol. Be aware that in contrast to pathways, such as glycolysis (with a linear sequence of reactions) or the citric acid cycle (with a circular sequence of reactions), the pentose phosphate pathway has several possible "branches" that can be taken to allow it to supply the cell with different products as needed. The primary products of the pathway include NADPH (from the oxidative reactions), pentoses (used in nucleotide synthesis), and miscellaneous other sugar phosphates. [Pg.42]

The synthesis of deoxyuridine, cytidine, deoxycytidine and thymidine nucleotides from UMP (Fig. 6.13) involves three reactions CTP synthetase, ribonucleotide reductase, and thymidylate synthase (80). The first enzyme converts UTP into CTP and the second catalyzes the conversion of CDP, UDP, ADP and GDP into their respective deoxyribonucleotides. The last enzyme, thymidylate synthase, catalyzes the reductive methylation of deoxyUMP at the C-5 position giving deoxyTMP. The human enzyme has been extensively studied as it is a target enzyme in cancer chemotherapy. Besides these three enzymes, two other enzymes are involved in pyrimidine nucleotide synthesis and interconversion. DeoxyCMP deaminase converts deoxyCMP into deoxyUMP and deoxyUTP triphosphatase converts deoxyUTP into deoxyUMP. Giardia lamblia, and Trichomonas vaginalis lack both ribonucleotide reductase and thymidylate synthase and... [Pg.105]

The previous section 3.3 on the use of tervalent phosphorus acid derivatives for synthesis of compounds of biological relevance has this year been divided into two parts, 3.3 use for nucleotide synthesis, and 3.4 use for sugar phosphate, phospholipid, or phosphopeptide synthesis. [Pg.81]

Meeker, R.B. and Harden, T.K. (1983). Muscarinic cholinergic receptor-mediated control of cyclic AMP metabolism agonist-induced changes in nucleotide synthesis and degradation. Mol. Pharmacol, 23, 384-392... [Pg.246]

The basic concepts that are applied to the synthesis of polynucleotides are similar to those of polypeptide synthesis. The chain is built up by successive addition of nucleoside units or small oligonucleotides. In practice, the problems involved in such operations have proved to be quite difficult, and the techniques for nucleotide synthesis and polymerization are not so highly developed as in peptide chemistry. Nevertheless, it is an important area in macromolecular synthesis, and some of the reactions that are the basis of present procedures in this area are therefore discussed in the succeeding paragraphs. [Pg.483]

The aim of present work was to study how nucleotide synthesis and their metabolism is affected by hormones taking part in activation of mammary gland. [Pg.488]

S-substituted mercaptoethanols can serve as phosphate protective groups in nucleotide synthesis,and l-oxopyrldin-2-yldlazomethane has... [Pg.263]


See other pages where Nucleotide synthesis and is mentioned: [Pg.267]    [Pg.537]    [Pg.334]    [Pg.61]    [Pg.980]    [Pg.226]    [Pg.14]    [Pg.164]    [Pg.635]    [Pg.265]    [Pg.1628]    [Pg.414]    [Pg.416]    [Pg.70]    [Pg.226]    [Pg.106]    [Pg.889]    [Pg.851]    [Pg.271]    [Pg.300]    [Pg.121]    [Pg.335]    [Pg.297]    [Pg.366]    [Pg.369]    [Pg.180]    [Pg.334]    [Pg.3]   


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