Pyruvate dehydrogenase complex

From WikiMD's Food, Medicine & Wellness Encyclopedia

153-PyruvateDehydrogenaseComplex pyruvatedehydrogenase
E1 Subunit Ecoli
E3 Subunit Putida
PDH schema

Pyruvate dehydrogenase complex (PDC) is a crucial enzyme complex in cellular respiration and metabolism. It plays a pivotal role in the conversion of pyruvate, a product of glycolysis, into acetyl-CoA, which enters the citric acid cycle (also known as the Krebs cycle or TCA cycle). This process is essential for the production of adenosine triphosphate (ATP), the energy currency of the cell. The complex is located in the mitochondria, highlighting its importance in aerobic respiration.

Structure and Function[edit | edit source]

The pyruvate dehydrogenase complex consists of multiple copies of three core enzymes: E1 (pyruvate dehydrogenase), E2 (dihydrolipoyl transacetylase), and E3 (dihydrolipoyl dehydrogenase). These enzymes work in concert to catalyze the decarboxylation of pyruvate, generating acetyl-CoA, NADH, and CO2 as products. The complex is regulated by a specific kinase and phosphatase, which respond to the energy needs of the cell, thereby controlling the activity of PDC.

Regulation[edit | edit source]

The activity of the pyruvate dehydrogenase complex is tightly regulated by its substrates and products, as well as by hormonal signals. High levels of acetyl-CoA and NADH, the products of the reaction, inhibit the complex, a mechanism known as product inhibition. Additionally, the complex is regulated through phosphorylation by pyruvate dehydrogenase kinase, which inactivates the complex, and dephosphorylation by pyruvate dehydrogenase phosphatase, which activates it. This phosphorylation is influenced by the levels of ATP, acetyl-CoA, and NADH, providing a link between the energy status of the cell and the activity of the PDC.

Clinical Significance[edit | edit source]

Mutations in the genes encoding the components of the pyruvate dehydrogenase complex can lead to pyruvate dehydrogenase deficiency, a rare metabolic disorder. This condition is characterized by a buildup of pyruvate and lactate in the blood, leading to lactic acidosis, neurological dysfunction, and, in severe cases, death. Management of the condition involves dietary modifications and supportive care.

Genetic Regulation[edit | edit source]

The genes encoding the components of the pyruvate dehydrogenase complex are located on different chromosomes. The expression of these genes is regulated by various factors, including the availability of substrates and the energy requirements of the cell. This ensures that the production of the complex is matched to the metabolic needs of the cell.

Evolutionary Perspective[edit | edit source]

The pyruvate dehydrogenase complex is highly conserved across different species, indicating its fundamental role in metabolism. The conservation of this complex underscores the importance of efficient energy production and utilization in the evolution of life.


Wiki.png

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD


Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro) available.
Advertise on WikiMD

WikiMD is not a substitute for professional medical advice. See full disclaimer.

Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.


Contributors: Prab R. Tumpati, MD