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Carbohydrates constants

Phosphorus. Eighty-five percent of the phosphoms, the second most abundant element in the human body, is located in bones and teeth (24,35). Whereas there is constant exchange of calcium and phosphoms between bones and blood, there is very Httle turnover in teeth (25). The Ca P ratio in bones is constant at about 2 1. Every tissue and cell contains phosphoms, generally as a salt or ester of mono-, di-, or tribasic phosphoric acid, as phosphoHpids, or as phosphorylated sugars (24). Phosphoms is involved in a large number and wide variety of metaboHc functions. Examples are carbohydrate metaboHsm (36,37), adenosine triphosphate (ATP) from fatty acid metaboHsm (38), and oxidative phosphorylation (36,39). Common food sources rich in phosphoms are Hsted in Table 5 (see also Phosphorus compounds). [Pg.377]

Application of NMR spectroscopy to heterocyclic chemistry has developed very rapidly during the past 15 years, and the technique is now used almost as routinely as H NMR spectroscopy. There are four main areas of application of interest to the heterocyclic chemist (i) elucidation of structure, where the method can be particularly valuable for complex natural products such as alkaloids and carbohydrate antibiotics (ii) stereochemical studies, especially conformational analysis of saturated heterocyclic systems (iii) the correlation of various theoretical aspects of structure and electronic distribution with chemical shifts, coupling constants and other NMR derived parameters and (iv) the unravelling of biosynthetic pathways to natural products, where, in contrast to related studies with " C-labelled precursors, stepwise degradation of the secondary metabolite is usually unnecessary. [Pg.11]

Table II. Signs of Proton-Proton Constants of Carbohydrate Derivatives... Table II. Signs of Proton-Proton Constants of Carbohydrate Derivatives...
From a study (29) of the relative signs of various H, H coupling constants of carbohydrate derivatives it is evident that the couplings... [Pg.254]

The fact that the absolute magnitudes of these two sets of coupling constants are different is also expected on the basis of the Pople, Bothner-By treatment (48). It would clearly be of some considerable interest if a general study were to be made of the stereospecificity of this geminal dependence since this may lead to another method for determining carbohydrate conformations. [Pg.257]

To maintain constant weight, your daily energy input as calculated from the foods you eat. should be about 700 kJ (170 kcal) greater than output. The difference allows for the fact that about 40 g of protein is required to maintain body tissues and fluids. If the excess of input over output is greater than 700 kJ/day. the unused food (carbohydrate. protein, or fat) is converted to fatty tissue and stored as such in the body. [Pg.218]

Adds of carbohydrate origin which are constantly produced by living systems and are not considered as waste products. [Pg.116]

Commercial A -acetylneuraminic acid aldolase from Clostridium perfringens (NeuAcA EC 4.1.3.3) catalyzes the addition of pyruvate to A-acetyl-D-mannosamine. A number of sialic acid related carbohydrates are obtained with the natural substrate22"24 or via replacement by aldose derivatives containing modifications at positions C-2, -4, or -6 (Table 4)22,23,25 26. Generally, a high level of asymmetric induction is retained, with the exception of D-arabinose (epimeric at C-3) where stereorandom product formation occurs 25 2t The unfavorable equilibrium constant requires that the reaction must be driven forward by using an excess of one of the components in order to achieve satisfactory conversion (preferably 7-10 equivalents of pyruvate, for economic reasons). [Pg.591]

More is known about nitrogen. In a study of modern humans where diet components (protein, lipid and carbohydrate) were measured against the corresponding body components, a shift of between 4.2 and 4.4%o was observed for nitrogen in both plasma protein and hair (Schoeller et al. 1986). This is just outside the usual 3-4%o range. Salmon fishers from coastal British Columbia are enriched by 3%o compared to their diet (Chisholm et al. 1983). Ancient Mexicans have constant 8 N values, as reported by DeNiro and Epstein (1981) 8-10%o, and While and Schwarcz (1989) 9.8 0.8%o. In the latter... [Pg.48]

Without using the formalism of the DIFF, both Ambrose and Norr (1993) and Tieszen and Fagre (1993) have pointed out from their experimental data that the carbonate 5 has a constant spacing from the average diet. Since the conversion of protein, or non-protein, to bioapatite-carbonate is metabolically more complicated than, for example, carbohydrate to protein, a simple physiological explanation may not be obvious. However, the interpretation of the DIFF does becomes clear in the light of a very simple flux model in Section 3. [Pg.221]

Kasaai M.R. 2007. Calculation of Mark-Houwink-Sakurada (MHS) equation viscometric constants for chitosan in any solvent-temperature system using experimental reported viscometric constants data. Carbohydrate Polymers 68, 477-488. [Pg.113]

The binding specificity of d-[ C]glucose by the taste-papillae membranes, compared to that of control membranes isolated from epithelial tissue, has been confirmed in two studies. One inherent problem in the approach is that the stimuli, primarily carbohydrate sweeteners, are not ideal model compounds to use, as they are not active at low concentrations and do not show sufficiently high binding-constants. The use of other stimulus compounds that are at least several hundred times sweeter than sucrose, such as saccharin, dihydrochalcone sweeteners, dipeptide sweeteners, stevioside, perillartine and other sweet oximes, the 2-substituted 5-nitroanilines, and... [Pg.330]

Nolls, P., Parella, T. Spin-edited 2D HSQC-TOCSY experiments for the measurement of homonuclear and heteronuclear coupling constants application to carbohydrates and peptides. /. Magn. Reson. 2005, 176, 15-26. [Pg.249]


See other pages where Carbohydrates constants is mentioned: [Pg.282]    [Pg.282]    [Pg.270]    [Pg.354]    [Pg.94]    [Pg.391]    [Pg.2145]    [Pg.816]    [Pg.236]    [Pg.255]    [Pg.1170]    [Pg.15]    [Pg.17]    [Pg.423]    [Pg.118]    [Pg.422]    [Pg.216]    [Pg.195]    [Pg.172]    [Pg.159]    [Pg.231]    [Pg.126]    [Pg.168]    [Pg.1606]    [Pg.58]    [Pg.519]    [Pg.57]    [Pg.226]    [Pg.282]    [Pg.323]    [Pg.8]    [Pg.25]    [Pg.26]    [Pg.570]    [Pg.16]    [Pg.468]    [Pg.152]    [Pg.150]    [Pg.152]   
See also in sourсe #XX -- [ Pg.33 , Pg.35 , Pg.51 ]




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Carbohydrates bonds, carbon-proton coupling constants

Carbohydrates dielectric constant

Carbohydrates ionization constants

Carbohydrates stability constants

Constants of carbohydrates

Stability constants carbohydrate ligands

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