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Conversion to glucose

Early applications of crystalline fructose focused on foods for special dietary applications, primarily calorie reduction and diabetes control. The latter application sought to capitalize on a signiftcandy lower serum glucose level and insulin response in subjects with noninsulin-dependent diabetes melUtus (21,22) and insulin-dependent diabetes (23). However, because fmctose is a nutritive sweetener and because dietary fmctose conversion to glucose in the hver requires insulin in the same way as dietary glucose or sucrose, recommendations for its use are the same as for other nutritive sugars (24). Review of the health effects of dietary fmctose is available (25). [Pg.45]

These short-chain fatty acids are acetic, butyric, lactic and propionic acids, also known as volatile fatty acids, VFA. They are produced from fermentation of carbohydrate by microorganisms in the colon and oxidised by colonocytes or hepatocytes (see above and Chapter 4). Butyric acid is activated to produce butyryl-CoA, which is then degraded to acetyl-CoA by P-oxidation acetic acid is converted to acetyl-CoA for complete oxidation. Propionic acid is activated to form propionyl-CoA, which is then converted to succinate (Chapter 8). The fate of the latter is either oxidation or, conversion to glucose, via glu-coneogenesis in the liver. [Pg.138]

Figure 8.13 The central role of transdeamination in metabolism of amino adds and further metabolism of the oxoacids in the liver. The box contains the reactions for conversion of the amino acids to their respective oxoacids. Processes are as follows (1) digestion of protein in the intestine and absorption of resultant amino acids, (2) degradation of endogenous protein to amino acids (primarily but not exclusively muscle protein), (3) protein synthesis, (4) conversion of amino acid to other nitrogen-containing compounds (see Table 8.4), (5) oxidation to CO2, (6) conversion to glucose via gluconeogenesis, (7) conversion to fat. Figure 8.13 The central role of transdeamination in metabolism of amino adds and further metabolism of the oxoacids in the liver. The box contains the reactions for conversion of the amino acids to their respective oxoacids. Processes are as follows (1) digestion of protein in the intestine and absorption of resultant amino acids, (2) degradation of endogenous protein to amino acids (primarily but not exclusively muscle protein), (3) protein synthesis, (4) conversion of amino acid to other nitrogen-containing compounds (see Table 8.4), (5) oxidation to CO2, (6) conversion to glucose via gluconeogenesis, (7) conversion to fat.
The composition of poplar wood was usedasamodel for the feedstock composition however, as used in this simulation, the poplar is modeled as consisting of only cellulose, xylan, and lignin, with compositions of 49.47, 27.26, and 23.27%, respectively. Laboratory results for carbonic acid pretreatment are relatively scarce, so for the purpose of this comparative study, stoichiometry of pretreatment reactions was assumed to be equal to those used in the comparison model (3) cellulose conversion to glucose 6.5% xylan conversion to xylose 75 and lignins solubilized 5%. Thus, economic comparisons made with this model assess different equipment and operating costs but not product yields. For the successful convergence of the carbonic acid model, the simulation required initial specification of several variables. These variables included initial estimates for stream variables and inputs for the unit operation blocks. [Pg.1091]

Answer In maize, C02 is fixed by the C4 pathway elucidated by Hatch and Slack. Phospho-enolpyruvate is rapidly carboxylated to oxaloacetate, some of which undergoes transamination to aspartate but most of which is reduced to malate in the mesophyll cells. Only after subsequent decarboxylation of labeled malate does 14C02 enter the Calvin cycle for conversion to glucose. The rate of entry into the cycle is limited by the rate of the rubisco-catalyzed reaction. [Pg.228]

Use of acetyl groups for gluconeogenesis results, in effect, in withdrawal of intermediates from the Krebs cycle. If continued, this withdrawal would result in cessation of the cycle. The total quantities of these intermediates present in the liver are relatively small, compared with the amount of protein in the body available for breakdown and conversion to glucose. Hence, it would make little sense to deplete the intermediates in the liver for use in gluconeogenesis. [Pg.232]


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See also in sourсe #XX -- [ Pg.200 ]




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Glucose conversion to 2-oxo-l-gulonate

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