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Glycogen, a polymer of glucose, is an energy-storage molecule in animals.
When there is adequate ATP present, excess glucose is shunted into glycogen for storage.
Glycogen is made and stored in both the liver and muscles.
The glycogen is hydrolyzed into the glucose monomer, glucose-1-phosphate (G-1-P), if blood sugar levels drop.
The presence of glycogen as a source of glucose allows ATP to be produced for a longer period of time during exercise.
Glycogen is broken down into G-1-P and converted into glucose-6-phosphate (G-6-P) in both muscle and liver cells; this product enters the glycolytic pathway.
Galactose is the sugar in milk.
Infants have an enzyme in the small intestine that metabolizes lactose to galactose and glucose.
In areas where milk products are regularly consumed, adults have also evolved this enzyme.
Galactose is converted in the liver to G-6-P and, thus, can enter the glycolytic pathway.
Fructose is one of the three dietary monosaccharides, along with glucose and galactose, which are absorbed directly into the bloodstream during digestion.
Fructose is absorbed from the small intestine and passes to the liver where it is metabolized, primarily to glycogen .
The catabolism of both fructose and galactose produces the same number of ATP molecules as glucose.
Sucrose is a disaccharide with a molecule of glucose and a molecule of fructose bonded together with a glycosidic linkage.
The catabolism of sucrose breaks it down to monomers of glucose and fructose.
The glucose can directly enter the glycolytic pathway while fructose must first be converted to glycogen, which can be broken down to G-1-P and enter the glycolytic pathway as described above.
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