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Catabolism
Metabolic pathways
Energy production
Glucoregulation
References
External links
Catabolism
Oligosaccharides and/or polysaccharides are typically cleaved into smaller monosaccharides by enzymes called glycoside hydrolases. The
monosaccharide units then enter monosaccharide catabolism. Organisms vary in the range of monosaccharides they can absorb and use and
they can also vary in the range of more complex carbohydrates they are capable of disassembling.
Metabolic pathways
Carbon fixation, or photosynthesis, in which CO2 is reduced to carbohydrate.
Glycolysis - the oxidation metabolism of glucose molecules to obtain ATP and pyruvate
Pyruvate from glycolysis enters the Krebs cycle, also known as the citric acid cycle, in aerobic organisms after moving through pyruvate
dehydrogenase complex.
The pentose phosphate pathway, which acts in the conversion of hexoses into pentoses and in NADPH regeneration. NADPH is an essential
antioxidant in cells which prevents oxidative damage and acts as precursor for production of many biomolecules.
Glycogenesis - the conversion of excess glucose into glycogen as a cellular storage mechanism; this prevents excessive osmotic pressure
buildup inside the cell
Glycogenolysis - the breakdown of glycogen into glucose, which provides a glucose supply for glucose-dependent tissues.
Gluconeogenesis - de novo synthesis of glucose molecules from simple organic compounds. An example in humans is the conversion of a
few amino acids in cellular protein to glucose.
Metabolic use of glucose is highly important as an energy source for muscle cells and in the brain, and red blood cells.
Energy production
Typically, a breakdown of one molecule of glucose by aerobic respiration (i.e. involving both glycolysis and Krebs cycle) is about 33-35 ATP
This is categorized as:
Anaerobic breakdown by glycolysis - yielding 8-10 ATP
Aerobic respiration by Krebs cycle - yielding 25 ATP
Glucoregulation
Glucoregulation is the maintenance of steady levels of glucose in the body; it is part of homeostasis, and so keeps a constant internal
environment around cells in the body.
The hormone insulin is the primary regulatory signal in animals, suggesting that the basic mechanism is very old and very central to animal
life. When present, it causes many tissue cells to take up glucose from the circulation, causes some cells to store glucose internally in the
form of glycogen, causes some cells to take in and hold lipids, and in many cases controls cellular electrolyte balances and amino acid uptake
as well. Its absence turns off glucose uptake into cells, reverses electrolyte adjustments, begins glycogen breakdown and glucose release into
the circulation by some cells, begins lipid release from lipid storage cells, etc. The level of circulatory glucose (known informally as "blood
sugar") is the most important signal to the insulin-producing cells. Because the level of circulatory glucose is largely determined by the
intake of dietary carbohydrates, diet controls major aspects of metabolism via insulin. In humans, insulin is made by beta cells in the
pancreas, fat is stored in adipose tissue cells, and glycogen is both stored and released as needed by liver cells. Regardless of insulin levels,
no glucose is released to the blood from internal glycogen stores from muscle cells.
The hormone glucagon, on the other hand, has an effect opposite to that of insulin, forcing the conversion of glycogen in liver cells to
glucose, which is then released into the blood. Muscle cells, however, lack the ability to export glucose into the blood. The release of
glucagon is precipitated by low levels of blood glucose. Other hormones, notably growth hormone, cortisol, and certain catecholamines (such
as epinepherine) have glucoregulatory actions similar to glucagon.
Human diseases of carbohydrate metabolism
Diabetes mellitus
Lactose intolerance
Fructose intolerance
Galactosemia
Glycogen storage disease