Pyruvate dehydrogenase (cytochrome)

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Pyruvate dehydrogenase (cytochrome)[edit | edit source]

Pyruvate dehydrogenase (cytochrome) is an enzyme complex involved in the metabolism of carbohydrates. It plays a crucial role in the conversion of pyruvate, a product of glycolysis, into acetyl-CoA, which is further utilized in the citric acid cycle for energy production. This enzyme complex is a key regulator of glucose metabolism and is found in the mitochondria of eukaryotic cells.

Structure[edit | edit source]

The pyruvate dehydrogenase (cytochrome) complex consists of multiple subunits, each with a specific function. The core of the complex is formed by three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2), and dihydrolipoamide dehydrogenase (E3). These enzymes work together to catalyze the conversion of pyruvate to acetyl-CoA.

Additionally, the complex contains several regulatory enzymes and cofactors. One of the important regulatory enzymes is pyruvate dehydrogenase kinase, which phosphorylates and inactivates the pyruvate dehydrogenase complex. Pyruvate dehydrogenase phosphatase, on the other hand, dephosphorylates and activates the complex. The cofactors thiamine pyrophosphate (TPP), lipoic acid, and FAD are also essential for the proper functioning of the complex.

Function[edit | edit source]

The main function of the pyruvate dehydrogenase (cytochrome) complex is to convert pyruvate, a three-carbon molecule, into acetyl-CoA, a two-carbon molecule. This reaction occurs in the mitochondria and is a crucial step in the aerobic metabolism of glucose. Acetyl-CoA is further utilized in the citric acid cycle to generate ATP, the energy currency of the cell.

The pyruvate dehydrogenase complex is tightly regulated to ensure proper control of glucose metabolism. The activity of the complex is regulated by phosphorylation and dephosphorylation events mediated by pyruvate dehydrogenase kinase and pyruvate dehydrogenase phosphatase, respectively. This regulation allows the cell to respond to changes in energy demands and nutrient availability.

Role in Disease[edit | edit source]

Malfunctioning of the pyruvate dehydrogenase (cytochrome) complex can lead to various metabolic disorders. Deficiencies in the complex have been associated with pyruvate dehydrogenase complex deficiency (PDCD), a rare genetic disorder characterized by impaired energy production. Symptoms of PDCD can include developmental delays, neurological abnormalities, and lactic acidosis.

See Also[edit | edit source]

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD