Big Chemical Encyclopedia

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

Articles Figures Tables About

Adenosine diphosphate phosphate complex

Ill these simultaneous reactions, die energy released when the complex molecule AB is broken down is immediately used to build a molecule of adenosine triphosphate (ATP) from a molecule of adenosine diphosphate (ADP) and an inorganic phosphate (P,). ATP is a high energy compound. It is called the energy currency of the body because once it is formed, it provides energy that the body can spend later to drive vital reactions in cells (Figure 1). [Pg.168]

ADP (adenosine diphosphate) and ATP (adenosine triphosphate) are complex organic molecules (Fig. 17.9) that, in essence, differ only hy the presence of an extra phosphate group in ATP. In the coupled reaction with glucose, about 38 mol of ATP are synthesized for every mole of glucose consumed. This gives an overall free energy change for the coupled reaction of... [Pg.469]

The nucleotide anhydride, adenosine 5 -triphosphate (24), when digested with aqueous barium hydroxide, gives a complex mixture containing such products as adenine, adenosine, adenosine 2 -, 3 -, and 5 -phosphates, adenosine 5 -pyrophosphate, and adenosine 2 (or 3 ),5 -diphosphate. - In addition, a nucleotide was foimd in this digest whose structure proved - to be that of adenosine 3 5 -cyclic phosphate (25). This component did not consume metaperiodate, and was degraded enzymically to adenosine 5 -phosphate (26) and adenosine 3 -phosphate (27), without the formation of adenosine 2 -phosphate. Hydrolysis of (25) with an acidic ion-exchange resin did, however, produce the 2 - and 3 -phosphates of adenosine. Compound (25) possessed only one phosphoryl dissociation, and showed a ratio of nucleoside to phosphate of 1 1, which, along with a molecular-... [Pg.319]

The free energy gained from the quinol oxidation inthe cytochrome-6c, complex allows further proton transfer from the cytoplasm to the periplasm. The 6c,-complex also mediates ET to the periplasmic side. There, soluble cytochromes accept the electrons and transport them back to the RC to reduce D+. The electron transfer is cycUc and therefore does not cause transmembrane potential. This potential is generated by the electrogenic proton translocation in the cytochrome-6c, complex. The electrochemical proton gradient is utilized by the ATP-synthase to form adenosine triphosphate from adenosine diphosphate and phosphate. [Pg.103]

Irradiation of water leads to formation of (HO) . By contrast, in the brain, strong water-soluble electron donors (DH) such as nicotinamide adenine dinucleotide phosphate (NADPH), catechin, hydroquinone, ascorbic acid or glutathione (L-y-glutamyl-L-cysteinyl-glycine GSH) can promote formation of (HO) from H2O2 in the presence of Cu+ or some iron complexes (e.g. Fe -adenosine diphosphate complexes) according to Eqs. (15) and (16) (Florence, 1984 Kadiiska et al., 1992). [Pg.441]

The nature of DCC implies that typically only the library composition at thermodynamic equilibrium is of interest and the library distribution is performed only after analysis has confirmed that equilibrium is reached. However, Sev-erin et al. showed that much additional information can be obtained from the kinetic profile, leading toward the final composition. They demonstrated that a simple mixture of commercially available dyes and a rhodium complex can be used to time the addition of adenosine diphosphate (ADP) and adenosine triphosphate (ATP) to the mixture. The phosphates ADP and ATP compete with the dyes for complexa-tion with rhodium and consequently induce changes in the UV-vis spectrum. Importantly, the presence of the analytes also changes the kinetic profile of equilibration process to an extent that depends on the time at which the analytes were added to the mixture. Consequently, from a simple UV-vis measurement after a defined time interval (15 min)... [Pg.3037]

Figure 5. Liposome Glucose Efflux Experiment. G = glucose, B = boronic acid, BG = glucose-boronate complex, Ei = hexokinase, E2 = glucose-6-phosphate dehydrogenase, 6-PG = 6-phosphogluconate, NADP = nicotinamide adenine dinucleotide phosphate, NADPH = reduced form of nicotinamide adenine dinucleotide phosphate, ADP = adenosine diphosphate, ATP = adenosine triphosphate. Figure 5. Liposome Glucose Efflux Experiment. G = glucose, B = boronic acid, BG = glucose-boronate complex, Ei = hexokinase, E2 = glucose-6-phosphate dehydrogenase, 6-PG = 6-phosphogluconate, NADP = nicotinamide adenine dinucleotide phosphate, NADPH = reduced form of nicotinamide adenine dinucleotide phosphate, ADP = adenosine diphosphate, ATP = adenosine triphosphate.
Fig. 1. Energy metabolism in the normal myocardium (ATP adenosine-5 -triphosphate, ADP adenosine-5 -diphosphate, P phosphate, PDH pyruvate dehydrogenase complex, acetyl-CoA acetyl-coenzyme A, NADH and NAD" nicotinamide adenine dinucleotide (reduced and oxidized), FADH2 and FAD flavin adenine dinucleotide (reduced and oxidized). Fig. 1. Energy metabolism in the normal myocardium (ATP adenosine-5 -triphosphate, ADP adenosine-5 -diphosphate, P phosphate, PDH pyruvate dehydrogenase complex, acetyl-CoA acetyl-coenzyme A, NADH and NAD" nicotinamide adenine dinucleotide (reduced and oxidized), FADH2 and FAD flavin adenine dinucleotide (reduced and oxidized).

See other pages where Adenosine diphosphate phosphate complex is mentioned: [Pg.1027]    [Pg.12]    [Pg.86]    [Pg.385]    [Pg.197]    [Pg.336]    [Pg.223]    [Pg.69]    [Pg.1297]    [Pg.305]    [Pg.85]    [Pg.396]    [Pg.45]    [Pg.527]    [Pg.138]    [Pg.51]    [Pg.433]    [Pg.162]    [Pg.7177]    [Pg.1274]    [Pg.3428]    [Pg.497]    [Pg.195]    [Pg.3501]    [Pg.198]    [Pg.210]    [Pg.866]    [Pg.256]    [Pg.503]    [Pg.612]    [Pg.202]    [Pg.165]    [Pg.172]    [Pg.1646]    [Pg.135]    [Pg.123]    [Pg.202]    [Pg.1055]    [Pg.3105]    [Pg.103]   
See also in sourсe #XX -- [ Pg.317 ]




SEARCH



Adenosine 5 diphosphate

Adenosine phosphate complexes

Adenosine, complexes

Adenosine-5’-phosphat

Phosphate Complexes

© 2024 chempedia.info