Gluconeogenesis

spinqualitylabelsall models Human phosphoglycerate kinase complex with phosphoglyceric acid, ADP (stick model) AlF4-, Cl- and Mg+2 ions (green) (PDB code 2y3i) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Under development! Gluconeogenesis ([1]) is a metabolic pathway that results in the generation of glucose from certain non-carbohydrate carbon substrates. In humans the main gluconeogenic precursors are lactate, glycerol (which is a part of the triglyceride molecule), alanine and glutamine. Other glucogenic amino acids and all Citric Acid Cycle intermediates (through conversion to oxaloacetate) can also function as substrates for gluconeogenesis. Lactate is transported back to the liver where it is converted into pyruvate by the Cori cycle using the enzyme lactate dehydrogenase. Interconversion of pyruvate and lactate acid. Pyruvate, the first designated substrate of the gluconeogenic pathway, can then be used to generate glucose. Phosphoglycerate kinase is an enzyme that catalyzes the reversible transfer of a phosphate group from 1,3-bisphosphoglycerate (1,3-BPG) to ADP producing 3-phosphoglycerate (3-PG) and ATP: 1,3-bisphosphoglycerate + ADP ⇌ glycerate 3-phosphate + ATP Like all kinases it is a transferase. PGK is a major enzyme used in glycolysis, in the first ATP-generating step of the glycolytic pathway. In gluconeogenesis, the reaction catalyzed by PGK proceeds in the opposite direction, generating ADP and 3-phosphoglycerate (3-PG). Catabolism of amino acids, Citric Acid Cycle and Gluconeogenesis 1) Alanine, cysteine, glycine, serine, tryptophan, threonine => pyruvate 2) Tryptophan, threonine, phenylalanine, tyrosine, isoleucine, leucine, lysine => Acetyl-CoA 3) Arginine, histidine, glutamine, proline => glutamate => α-Ketoglutarate 4) Threonine, methionine, isoleucine, valine => Succinyl-CoA 4C chain (CoA excluded) 5) Tyrosine, phenylalanine, aspartate => Fumarate 6) Aspartate, asparagine => Oxaloacetate => [by Phosphoenolpyruvate carboxykinase] phosphoenolpyruvate (PEP) => ... => Glucose The location of the enzyme that links these two parts of gluconeogenesis by converting oxaloacetate to PEP – PEP carboxykinase (PEPCK) – is variable by species: it can be found entirely within the mitochondria, entirely within the cytosol, or dispersed evenly between the two, as it is in humans. E. coli GTP-driven PEPCK active site is located in a pocket at the enzyme surface. Water molecules are shown as red spheres. Fatty acids Odd-chain fatty acids can be oxidized to yield Acetyl-CoA and Propionyl-CoA, the latter serving as a precursor to Succinyl-CoA, which can be converted to pyruvate and enter into gluconeogenesis. In contrast, even-chain fatty acids are oxidized to yield only acetyl-CoA, whose entry into gluconeogenesis requires the presence of a glyoxylate cycle (also known as glyoxylate shunt) to produce four-carbon dicarboxylic acid precursors. Pathway 1) Gluconeogenesis begins in the mitochondria with the formation of oxaloacetate by the carboxylation of pyruvate. This reaction also requires one molecule of ATP, and is catalyzed by pyruvate carboxylase. This enzyme is stimulated by high levels of acetyl-CoA (produced in β-oxidation in the liver) and inhibited by high levels of ADP and glucose. Pyruvate carboxylase: Pyruvate => Oxaloacetate 2) Oxaloacetate is reduced to malate using NADH, a step required for its transportation out of the mitochondria. 3) Malate is oxidized to oxaloacetate using NAD+ in the cytosol, where the remaining steps of gluconeogenesis take place. 4) Oxaloacetate is decarboxylated and then phosphorylated to form phosphoenolpyruvate using the enzyme PEPCK. A molecule of GTP is hydrolyzed to GDP during this reaction. The next steps in the reaction are the same as reversed glycolysis. However, fructose 1,6-bisphosphatase converts fructose 1,6-bisphosphate to fructose 6-phosphate, using one water molecule and releasing one phosphate (in glycolysis, phosphofructokinase 1 converts F6P and ATP to F1,6BP and ADP). This is also the rate-limiting step of gluconeogenesis.

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Alexander Berchansky