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The Citric Acid Cycle

The Citric Acid Cycle. Dr. Sooad Al-Daihan Biochemistry department. Introduction. Also called citric acid cycle or the Krebs cycle (after its discoverer, Hans Krebs).

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The Citric Acid Cycle

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  1. The Citric Acid Cycle Dr. Sooad Al-Daihan Biochemistry department

  2. Introduction • Also called citric acid cycle or the Krebs cycle (after its discoverer, Hans Krebs). • TCA cycle is a series of reactions catalyzed by different enzymes in which acetyl CoA is oxidized into CO2, H2O and energy. • It occurs in the mitochondrial matrix aerobically. • The enzymes involved in the TCA cycle are present in the mitochondrial matrix either free or attached to the inner surface of the mitochondrial membrane.

  3. Continue.. • The citric acid cycle is the final common pathway for the oxidation of fuel molecules: • amino acids, fatty acids and carbohydrates. • Most fuel molecules enter the cycle as acetyl coenzyme A. • The function of the citric acid cycle is the harvesting of high-energy electrons from carbon fuels.

  4. Continue.. • The citric acid cycle itself neither generates a large amount of ATP nor includes oxygen as a reactant. • Instead, the citric acid cycle removes electrons from acetyl CoA and uses these electrons to form NADH and FADH2. • The citric acid cycle includes a series of oxidation-reduction reactions that result in the oxidation of an acetyl group to two molecules of carbon dioxide. The citric acid cycle oxidizes two-carbon units, producing two molecules of CO2, one molecule of GTP, and high-energy electrons in the form of NADH and FADH2.

  5. The amphibolic nature of TCA cycle • The citric acid cycle is the gateway to the aerobic metabolism of any molecule that can be transformed into an acetyl group. • The cycle is also an important source of precursors, not only for the storage forms of fuels, but also for the building blocks of many other molecules such as amino acids, nucleotide bases, cholesterol, and porphyrin. This pathway is utilized for both catabolic reactions to generate energy & anabolic reactions to generate metabolic intermediates for biosynthesis.

  6. Metabolic pathway • In oxidative phosphorylation, electrons released in the reoxidation of NADH and FADH2 flow through a series of membrane proteins to generate a proton gradient across the membrane. • The citric acid cycle, in conjunction with oxidative phosphorylation, provides the vast majority of energy used by aerobic cells in human beings, greater than 95%. • In TCA, the removal of high-energy electrons from carbon fuels. • These electrons reduce O2 to generate a proton gradient . • Which is used to synthesize ATP .

  7. The TCA Cycle Has Eight Steps

  8. Continue.. • Step 1:Formation of Citrate - An irreversible reaction catalyzed by citrate synthase. -Inhibited by: ATP , NADH, Citrate. • Step 2:Formation of Isocitrate -A reversible reaction catalyzed by aconitase . • Step 3: Oxidative decarboxylation of isocitrate -The enzyme isocitrate dehydrogenase catalyzes the irreversible oxidative decarboxylation of isocitrate to form α-ketoglutarate and CO2. -Stimulated by: isocitrate, NAD+, Mn2+, ADP, Ca2+. -Inhibited by: NADH and ATP.

  9. Continue.. • Step 4:Oxidative decarboxylation of α-ketoglutarate -In this irreversible reaction, α-ketoglutarate is converted to succinyl-CoAand CO2 by the action of the α-ketoglutarate dehydrogenase complex . -α-ketoglutarate dehydrogenase complex closely resembles the PDH complex in both structure and function. -NAD+ serves as electron acceptor and CoA as the carrier of the succinyl group. - Inhibited by: NADH, ATP, Succinyl-CoA - Stimulated by: Ca2+

  10. Continue. • Step 5:Conversion of succinyl-CoA to succinate -Reversible reaction catayzed by succinyl-CoA synthetase (succinate thiokinase) -Results in the formation of GTP and CoA-SH -Nucleoside diphosphate kinaseinterconverts GTP and ATP by a readily reversible phosphoryl transfer reaction: GTP + ADP GDP + ATP

  11. Continue.. • Step 6: Oxidation of Succinate to Fumarate. • Succinate is oxidized to fumarateby the flavoproteinsuccinate dehydrogenase • Only TCA cycle enzyme contained within the mitochondrial membrane. • Results in the formation of FADH2

  12. Continue.. • Step 7:Hydration of fumarate to malate -The reversible hydration of fumarate to L-malate is catalyzed by fumarase . • Step 8:Oxidation of malate to oxaloacetate -In the last reaction of the citric acid cycle, NAD-linked L-malate dehydrogenase catalyzes the oxidation of L-malate to oxaloacetate.

  13. Enzyme Control of the TCA Cycle

  14. Inhibitors of TCA Cycle • Fluoroacetyl CoA: -It inhibits aconitase enzyme -It combines with oxaloacetate giving rise to fluorocitrate . • Malonic acid: -Inhibits succinate dehydrogenase (competitive inhibition) • Arsenate and Mercury : -Inhibit Pyruvate dehydrogenase and α-ketoglutarate dehydrogenase complexs. - By reacting with sulphydral group of lipoic acid leading to accumulation of pyruvic lactic acid and α- ketoglutarate.

  15. Products of Kreb’s Cycle • 2 CO2 • 3 NADH • 1 ATP Per 1 Acetyl CoA (double for 1 glucose) • 1 FADH2 • ATP Yield: • Each NADH yields 3 ATP • Each FADH2yields 2 ATP

  16. Summary of total energy yield of complete oxidation of 1 glucose molecule

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