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Oxidative Decarboxylation and Krebs Cycle

This text explains the fates of pyruvate, including oxidative decarboxylation, carboxylation, reduction to lactate or ethanol, and conversion to alanine. It also provides an overview of the Krebs cycle, its regulation, and energy yield.

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Oxidative Decarboxylation and Krebs Cycle

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  1. بسم الله الرحمن الرحيم

  2. Oxidative Decarboxylation and Krebs Cycle By Reem M. Sallam, M.D.; Ph.D. Clinical Biochemistry Unit, Pathology Dept. College of Medicine, King Saud University

  3. Fates of Pyruvate • Oxidative decarboxylation into Acetyl CoA: the enzyme is pyruvate dehydrogenase complex (PDH). It occurs in mitochondria. It is irreversible. Acetyl CoA can enter the Krebs cycle to produce energy, or acts as a building block for fatty acid synthesis. Inhibited by Acetyl CoA and NADH +H. • Carboxylation into oxaloacetate (OAA): the enzyme is pyruvate carboxylase. It occurs in mitochondria. It is irreversible. It needs biotin and ATP. OAA replenishes the Krebs cycle intermediate & provides substrate for gluconeogenesis.

  4. Fates of Pyruvate, continued… • Reduction to lactate: the enzyme is lactate dehydrogenase. (LDH). Important in anaerobic glycolysis. Reversible reaction. • Reduction to ethanol: it occurs in 2 steps: decarboxylation then reduction. Decarboxylation occurs in yeast and some micororganisms and in intestinal bacterial Flora. The enzyme requires thiamine pyrophohsphate (TPP) as a coenzyme. • Conversion to Alanine by alanine aminotransferase (ALT): an amino group is transferred from glutamate to pyruvate, resulting in the formation of alpha ketoglutarate (KG) and alanine. The enzyme requires the coenzyme pyridoxal phosphate (PLP: vit B6 derivative) as a coenzyme. The reaction is reversible.

  5. Oxidative Decarboxylation of Pyruvate The endproduct of aerobic glycolysis (Pyruvate) is transported to mitochondria to be Oxidatively decarboxylated to Acetyl CoA. The enzyme is pyruvate dehydrogenase complex (PDH). PDH is not part of the glycolysis nor of TCA cycle. It occurs in mitochondria. It is irreversible. The endproduct (Acetyl CoA) can enter the Krebs cycle, or used in fatty acid synthesis.

  6. Regulation of PDH Complex: • Allosteric inhibition by Acetyl CoA and NADH • Covalent regulation by a kinase and a phosphatase enzymes (phophorylated form of PDH is inactive, and dephosphorylated form is active) • Insulin activates PDH complex (by stimulating the phosphatase enzyme), and Glucagon inhibits PDH complex (by stimulating the kinase enzyme).

  7. Tricarboxylic Acid Cycle: Krebs Cycle • It is the final common pathway for oxidation of carbohydrates, amino acids, and fatty acids. • It occurs exclusively in mitochondria • It is Aerobic pathway • It is a major source for ATP • It is mainly catabolic with some anabolic features

  8. Tricarboxylic Acid Cycle: Krebs Cycle What are the synthetic reactions related to Krebs cycle (anabolic features)? • Synthesis of Glucose from amino acids • Synthesis of Nonessential amino acids • Synthesis of Fatty acids • Synthesis of Heme

  9. Reactions of Krebs Cycle • Synthesis of citrate (from acetyl CoA + OAA): the enzyme is citrate synthase. Citrate inhibits PFK-1 (The rate limiting step in glycolysis) • Isomerization of citrate to isocitrate by aconitase enzyme. • Oxidation & decarboxylation of Isocitrate to KG by isocitrate dehydrogenase. The reaction releases CO2 and NADH. When NADH is oxidized in the electron transport chain (ETC)  3 ATP molecules, (this is oxidative phosphorylation). • Oxidation & decarboxylation of KG to succinyl CoA by KG dehydrogenase complex. The reaction releases CO2 and NADH. When NADH is oxidized in the ETC  3 ATP molecules, (this is oxidative phosphorylation).

  10. Reactions of Krebs Cycle, continued… • Cleavage of succinyl CoA by succinate thiokinase into succinate. The reaction produces GTP (which can be converted to ATP). This is substrate-level phosphorylation. • Oxidation of succinate to fumarate by succinate dehydrogenase. The reaction produces FADH2, which when oxidized in the ETC  2 ATP (this is oxidative phosphorylation). • Hydration of fumarate by fumarase to malate. • Oxidation of malate to OAA by malate dehydrogenase. The reaction releases NADH, which when oxidized in the ETC  3 ATP (this is oxidative phosphorylation).

  11. Krebs Cycle: Energy Yield The number of ATP molecules produced from the oxidation of one molecule of acetyl CoA using both substrate-level and Oxidative phosphorylation.

  12. Net ATP Production byComplete Glucose Oxidation Aerobic glycolysis: 8 ATP Oxidative decarboxylation: 2 X 3 = 6 ATP Krebs cycle: 2 X 12 = 24 ATP Net: 38 ATP

  13. Take Home Message • Pyruvate is oxidativelydecarboxylated by PDH to acetyl CoA inside the mitochondria • Krebs cycle: • Final common pathway for the oxidation of carbohydrates, fatty acids and amino acids • occurs in the mitochondria • Aerobic • Mainly catabolic, with some anabolic reactions • The complete oxidation of one glucose molecule results in a net production of 38 ATP molecules

  14. Thank you

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