Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Coenzyme nucleotide

The nucleotide coenzymes are structurally related to the mononucleotides. Typical nucleotide coenzymes are adenosine triphosphate (ATP), flavin-adenine-dinucleotide (FAD) and numerous other phosphate esters of complex structure, containing adenosine, guanosine, cytidine or uridine. Five coenzymes are known for example, which are derived from cytidine diphosphate (CDP) CDP-choline, CDP-ethanolamine, CDP-diglyceride, CDP-glycerol and CDP-ribitol. [Pg.788]


Silver ions will oxidatively desulphurize nucleoside and other phos-phorothioates to generate a phosphorylating agent. This reaction has been utilized for the preparation of nucleotide coenzymes and has the advantage that it can be carried out on a large scale without the formation of contaminating symmetrical pyrophosphates. [Pg.133]

Synthesis of nucleotides and nucleosides, nucleotide coenzymes, polynucleotides, and histidine... [Pg.184]

Mechanism of Hydrogen Transfer by Pyridine Nucleotide Coenzymes 239... [Pg.252]

The natural substrates which are most frequently used are the nucleotide coenzymes NAD+ and NADP+, which are reversibly reduced by many enzymes ... [Pg.287]

Fluorimetric methods are useful for monitoring reactions involving the nucleotide coenzymes. The natural fluorescence of the reduced forms in the region of 460 nm can be used in kinetic assays. However, this fluorescence is destroyed at pH values below 2.0, whereas any oxidized forms of the coenzymes present are stable. If the pH of the solution is then raised above 10.5 and heated, the oxidized forms are themselves converted to fluorescent derivatives. This latter procedure lends itself to fixed time assays such as is illustrated in Procedure 8.6. [Pg.290]

What can enzyme-catalysed reactions that involve the nucleotide coenzyme NAD be monitored by ... [Pg.294]

Enzyme reactions involving the nucleotide coenzymes can often be followed fluorimetrically... [Pg.294]

J. London and M. Knight, Concentrations of nicotinamide nucleotide coenzymes in micro-organisms, J. Gen. Microbiol. 44, 241-254 (1966). [Pg.445]

The pyridine nucleotides NAD and NADP always function in unbound form. The oxidized forms contain an aromatic nicotinamide ring in which the positive charge is delocalized. The right-hand example of the two resonance structures shown contains an electron-poor, positively charged C atom at the para position to nitrogen. If a hydride ion is added at this point (see above), the reduced forms NADH or NADPH arise. No radical intermediate steps occur. Because a proton is released at the same time, the reduced pyridine nucleotide coenzymes are correctly expressed as NAD(P)H+HT... [Pg.32]

The best-known aldopentose (1), D-ribose, is a component of RNA and of nucleotide coenzymes and is widely distributed. In these compounds, ribose always exists in the fura-nose form (see p. 34). Like ribose, D-xylose and L-arabinose are rarely found in free form. However, large amounts of both sugars are found as constituents of polysaccharides in the walls of plant cells (see p.42). [Pg.38]

We conclude this chapter by describing some chemical features of nucleotide coenzymes and some of the enzymes (dehydrogenases and flavoproteins) that use them. The oxidation-reduction chemistry of quinones, iron-sulfur proteins, and cytochromes is discussed in Chapter 19. [Pg.512]

TABLE 13-9 Some Enzymes (Flavoproteins) That Employ Ravin Nucleotide Coenzymes... [Pg.515]

Dolphin, D., Avramovic, O., Poulson, R (eds) (1987) Pyridine Nucleotide Coenzymes Chemical, Biochemical, and Medical Aspects, John Wiley Sons, Inc., New ork. [Pg.518]

NADPH formed in the oxidative phase is used to reduce glutathione, GSSG (see Box 14-3) and to support reductive biosynthesis. The other product of the oxidative phase is ribose 5-phosphate, which serves as precursor for nucleotides, coenzymes, and nucleic acids. In cells that are not using ribose 5-phosphate for biosynthesis, the nonoxidative phase recycles six molecules of the pentose into five molecules of the hexose glucose 6-phosphate, allowing continued production of NADPH and converting glucose 6-phosphate (in six cycles) to C02. [Pg.550]

Alexander R. Todd Chemistry Work on nucleotides coenzymes... [Pg.83]

Phosphorus -31. NMR spectroscopy using 31P, the ordinary isotope of phosphorus, also has many uses.466 Application of 31P NMR to living tissues has been extraordinarily informative467 and is dealt with in Chapter 6. The many phosphorus nuclei in nucleotides, coenzymes, and phosphorylated metabolites and proteins are all suitable objects of investigation by NMR techniques. [Pg.140]

The oxidation-reduction potential of a pyridine nucleotide coenzyme system is determined by the standard redox potential for the free coenzyme (Table 6-8) together with the ratio of concentrations of oxidized to reduced coenzyme ([NAD+] / [NADH], Eq. 6-64). If these concentrations are known, a redox... [Pg.766]

Three facts account for the need of cells for both the flavin and pyridine nucleotide coenzymes (1) Flavins are usually stronger oxidizing agents than is NAD+. This property fits them for a role in the electron transport chains of mitochondria where a sequence of increasingly more powerful oxidants is needed and makes them ideal oxidants in a variety of other dehydrogenations. (2) Flavins can be reduced either by one- or two-electron processes. This enables them to participate in oxidation reactions involving free radicals and in reactions with metal ions. (3) Reduced flavins... [Pg.781]

Eklund, H., and Branden, C.-I. (1987) in Pyridine Nucleotide Coenzyme Chemical, Biochemical and Medical Aspects, Vol. 2,... [Pg.828]


See other pages where Coenzyme nucleotide is mentioned: [Pg.25]    [Pg.307]    [Pg.96]    [Pg.185]    [Pg.298]    [Pg.48]    [Pg.110]    [Pg.47]    [Pg.106]    [Pg.588]    [Pg.122]    [Pg.656]    [Pg.44]    [Pg.119]    [Pg.23]    [Pg.24]    [Pg.521]    [Pg.550]    [Pg.764]    [Pg.767]    [Pg.767]    [Pg.769]    [Pg.769]    [Pg.771]    [Pg.773]    [Pg.775]    [Pg.777]    [Pg.779]    [Pg.828]    [Pg.829]    [Pg.829]    [Pg.829]   


SEARCH



Coenzymes nucleotide derivatives

Coenzymes nucleotide triphosphate

Diphosphopyridine nucleotide Coenzyme

Group-Transfer Reactions of Nucleotide Coenzymes

Niacin pyridine nucleotide coenzymes

Nucleotide coenzymes functions

Nucleotide coenzymes group transfer reactions

Nucleotide coenzymes metabolism

Nucleotide coenzymes synthesis

Nucleotide handles of coenzymes

Nucleotides and Nucleotide-Coenzymes

Nucleotides as coenzymes

Pyridine nucleotide coenzymes

Pyridine nucleotide coenzymes, complexes

Synthesis of the Nicotinamide Nucleotide Coenzymes

Triphosphopyridine nucleotide coenzyme

Vitamin pyridine nucleotide coenzymes

© 2024 chempedia.info