Adenosine triphosphate glycolysis

Glycolysis is stimulated to maintain brain adenosine triphosphate levels in moderate hypoxia 595... 

In the past decade, a large number of studies emphasized the heterogeneous scale-free degree distribution of metabolic networks Most substrates participate in only a few reactions, whereas a small number of metabolites ( hubs ) participate in a very large number of reactions [19,45,52]. Not surprisingly, the list of highly connected metabolites is headed by the ubiquitous cofactors, such as adenosine triphosphate (ATP), adenosine diphosphate (ADP), and nicotinamide adenine dinucleotide (NAD) in its various forms, as well as by intermediates of glycolysis and the tricarboxylic acid (TCA) cycle. 

The reaction is essentially irreversible under physiological conditions and is a major regulatory step of glycolysis. PFK-1 is an inducible, highly regulated, allosteric enzyme. In its active form, muscle PFK-1 is a homotetramer (M.W. 320,000) that requires K+ or NH4, the latter of which lowers Km for both substrates. When adenosine triphosphate (ATP) levels are low during very active muscle contraction, PFK activity is modulated positively despite low concentration of fructose-6-phosphate. Allosteric activators of muscle PFK-1 include adenosine monophosphate (AMP), adenosine diphosphate (ADP), fructose-6-phosphate, and inorganic phosphate (Pi) inactivators are citrate, fatty acids, and ATP. 

The two major metabolic pathways necessary for normal RBC metabolism are the hexose monophosphate shunt pathway, with its associated enzyme systems, and the Embden-Myerhof pathway of anaerobic glycolysis. The former is responsible primarily for maintaining Hgb in the rednced state and thns preventing the formation of methemoglobin, while the latter metabolizes glucose to lactic acid, which leads to adenosine triphosphate formation. 

Glycolysis The biochemical process by which glucose is converted to pyruvate in the cytosol of the cell. It results in the production of 2 mol of adenosine triphosphate (ATP) and 2 mol of the reduced cofactor nicotinamide adenine dinucleotide (NADH), which transfers its reducing equivalents to the mitochondrion for the production of ATP via oxidative phosphorylation. 

L12. Lichtman, M. A., Miller, D. R., Cohen, J., and Waterhouse, C., Reduced red cell glycolysis, 2, 3-diphosphoglycerate and adenosine triphosphate concentration and increased hemoglobin-oxygen affinity caused by hypophosphatemia. Ann. Intern. Med. 74, 562-568 (1971). 

This is the first reaction in the biochemical pathway called glycolysis. A phosphoryl group is transferred from a donor molecule, adenosine triphosphate, to the recipient molecule, glucose. The products are glucose-6-phosphate and adenosine diphosphate. This enz)rme, called hexokinase, is an example of a transferase. 

The Krebs cycle is a series of enzymatic reactions that catalyzes the aerobic metabolism of fuel molecules to carbon dioxide and water, thereby generating energy for the production of adenosine triphosphate (ATP) molecules. The Krebs cycle is so named because much of its elucidation was the work of the British biochemist Hans Krebs. Many types of fuel molecules can be drawn into and utilized by the cycle, including acetyl coenzyme A (acetyl CoA), derived from glycolysis or fatty acid oxidation. Some amino acids are metabolized via the enzymatic reactions of the Krebs cycle. In eukaryotic cells, all but one of the enzymes catalyzing the reactions of the Krebs cycle are found in the mitochondrial matrixes. 

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