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Glycogen, III

Myrback, Karl, Products of the Enzymic Degradation of Starch and Glycogen, III, 251-310... [Pg.458]

Dahlia tubers, inulin from, II, 254 Dambonitol, III, 46 Damson gum, I, 343 IV, 246, 247 structure of, IV, 253 blood group activity of, IV, 50, 52 Deamination, mechanism of, II, 62 Degradation, of acylated nitriles of al-donic acids, IV, 119-151 of aldonic acids, III, 149 of aldose sugars, I, 254 enzymatic, of starch and glycogen, III, 251-310... [Pg.340]

Deuterium-labelled glycogen, III, 246 Dextran, 2,3-dimethyl-D-gIucose from methylated, V, 161 Dextran acetate, II, 218 Dextran beers, IV, 333 Dextran esters, II, 218 Dextran ethers, II, 218 Dextran triacetate, II, 210, 212 Dextran tribenzoate, II, 210, 212 Dextrans... [Pg.340]

Fig. 2.—Absorption Spectra of Polysaccharide-Iodine Complexes. (I) Mytiltis edulis glycogen, (II) rabbit liver glycogen, (III) waxy-maize starch (amylopectin). [Solutions contained 0.01% of polysaccharide and 0.02% of iodine in 0.2% of potassium iodide, and were read against an iodine—potassium iodide reference solution.]... Fig. 2.—Absorption Spectra of Polysaccharide-Iodine Complexes. (I) Mytiltis edulis glycogen, (II) rabbit liver glycogen, (III) waxy-maize starch (amylopectin). [Solutions contained 0.01% of polysaccharide and 0.02% of iodine in 0.2% of potassium iodide, and were read against an iodine—potassium iodide reference solution.]...
III Cori Glycogen debranching enzyme Mild hypoglycemia, liver enlargement Short outer branches Single glucose residue at outer branch... [Pg.195]

Galvin-Parton P, Hommes FA (1996) Abnormal oligosaccharide pattern in glycogen storage disease type III. J Inherit Metab Dis 19 383-384... [Pg.332]

In glycogenosis type III, the outer chain length of glycogen is reduced in glycogenosis type IV, it is increased. [Pg.440]

Chen YT, He JK, Ding JH, Brown BI (1987) Glycogen debranching enzyme purification, antibody characterization, and immunoblot analysis of type III glycogen storage disease. Am J Hum Genet 41 1002-1015... [Pg.469]

Relationships in glycolysis and gluconeogenesis. Points at which ATP is produced or consumed are indicated. Compounds in the same metabolic pools are indicated by purple boxes. Three small pseudocycles (la, II, III) in the paired sequences occur between glycogen and pyruvate, or between glycogen and glucose (lb, II, III). Only enzymes that are unique to either glycolysis or gluconeogenesis are indicated (screened in blue). [Pg.262]

We will focus our discussion on the well-understood regulatory enzymes that modulate the flux between glycogen and the hexose monophosphate pool (pseudocycle la), and between fructose-6-phosphate and fructose-1,6-bisphosphate (pseudocycle II). Some aspects of the regulation between the 3-carbon pool and pyruvate (pseudocycle III) are discussed in the next chapter. [Pg.267]

Other investigators have also differentiated the two activities. The apparent absence of transferase but not glucosidase activity has been proposed as a subclass of type III glycogen storage disease (37). Exposure of the enzyme to guanidine inhibited glucosidase activity on "fast B5" to a greater extent than the combined activity on "63-a-maltotriosylmaltotetraose"... [Pg.141]

III. Enzyme-catalyzed Reactions of Starch Synthesis in Plants and Algae and Glycogen 85... [Pg.85]

Caproic acid, as glycogenic agent, II, 134 labelled with isotopic C, III, 231 —, deuterio-, metabolism of, II, 152 Caprylic acid, as glycogenic agent, II, 134 labelled with isotopic C, III, 231 metabolism of, II, 152 Carbamic acid, N-phenyl. See Carba-nilic acid. [Pg.334]


See other pages where Glycogen, III is mentioned: [Pg.461]    [Pg.327]    [Pg.344]    [Pg.361]    [Pg.461]    [Pg.327]    [Pg.344]    [Pg.361]    [Pg.1215]    [Pg.299]    [Pg.206]    [Pg.462]    [Pg.697]    [Pg.145]    [Pg.78]    [Pg.113]    [Pg.337]    [Pg.330]    [Pg.440]    [Pg.450]    [Pg.456]    [Pg.36]    [Pg.230]    [Pg.124]    [Pg.439]    [Pg.249]    [Pg.119]    [Pg.120]    [Pg.240]    [Pg.303]    [Pg.327]    [Pg.327]   
See also in sourсe #XX -- [ Pg.3 , Pg.11 , Pg.34 , Pg.35 , Pg.36 , Pg.37 , Pg.50 , Pg.51 , Pg.52 , Pg.53 ]




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Type III glycogen storage disease

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