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The Citric Acid Cycle
AMAL GEORGE
MSc BIOCHEMISTRY
PYRUVATE
Glycogen
Amino Acids
GLUCOSE
GLUCOSE 6
PHOSPHATE
PYRUVATE
ACETYL CoA
Ribose, NADPH
Lactate
Fatty Acids
Ethanol
Synthesis of
glycogen
Degradation
of glycogen
Pentose phosphate
pathway
Glycolysis
Gluconeogenesis
The citric acid
cycle is the final
common pathway
for the oxidation
of fuel molecules
ā€” amino acids,
fatty acids, and
carbohydrates
Most fuel
molecules enter
the cycle as acetyl
coenzyme A
HISTORY
Hans Adolf Krebs. Biochemist; born in Germany. Worked in
Britain. His discovery in 1937 of the ā€˜Krebs cycleā€™ of chemical
reactions was critical to the understanding of cell metabolism
and earned him the 1953 Nobel Prize for Physiology or Medicine.
Location
ļ± In eukaryotes the
reactions of the
citric acid cycle
take place inside
mitochondria
Names:
ļ¶ The Citric Acid Cycle
ļ¶ Tricarboxylic Acid Cycle
ļ¶ Krebs Cycle
An Overview of the Citric Acid Cycle
A four-carbon oxaloacetate condenses with a two-
carbon acetyl unit to yield a six-carbon citrate.
An isomer of citrate is oxidatively decarboxylated and
five-carbon ļ”-ketoglutarate is formed.
ļ”-ketoglutarate is oxidatively decarboxylated to yield a
four-carbon succinate
Oxaloacetate is then regenerated from succinate.
Two carbon atoms (acetyl CoA) enter the cycle and two
carbon atoms leave the cycle in the form of two
molecules of carbon dioxide.
Three hydride ions (six electrons) are transferred to
three molecules of NAD+ ,one pair of hydrogen atoms
(two electrons) is transferred to one molecule of FAD.
The function of the citric acid cycle is the harvesting of high-
energy electrons from acetyl CoA.
1. Citrate Synthase
ā€¢Citrate formed from acetyl CoA and oxaloacetate
ā€¢Only cycle reaction with C-C bond formation
ā€¢Addition of C2 unit (acetyl) to the keto double bond of C4 acid,
oxaloacetate, to produce C6 compound, citrate
citrate synthase
2. Aconitase
ā€¢Elimination of H2O from citrate to form C=C bond of cis-aconitate
ā€¢Stereospecific addition of H2O to cis-aconitate to form isocitrate
aconitase aconitase
3. Isocitrate Dehydrogenase
ā€¢ Oxidative decarboxylation of isocitrate to
a-ketoglutarate (a metabolically irreversible reaction)
ā€¢ One of four oxidation-reduction reactions of the cycle
ā€¢ Hydride ion from the C-2 of isocitrate is transferred to NAD+ to form NADH
ā€¢ Oxalosuccinate is decarboxylated to a-ketoglutarate
isocitrate dehydrogenaseisocitrate dehydrogenase
4. The ļ”-Ketoglutarate Dehydrogenase Complex
ā€¢ Similar to pyruvate dehydrogenase complex
ā€¢ Same coenzymes, identical mechanisms
ā€¢ E1 - a-ketoglutarate dehydrogenase (with TPP)
ā€¢ E2 ā€“ dihydrolipoyl succinyltransferase (with flexible lipoamide prosthetic
group)
ā€¢ E3 - dihydrolipoyl dehydrogenase (with FAD)
ļ”-ketoglutarate
dehydrogenase
5. Succinyl-CoA Synthetase
ā€¢Free energy in thioester bond of succinyl CoA is conserved as GTP or
ATP in higher animals (or ATP in plants, some bacteria)
ā€¢Substrate level phosphorylation reaction
HS-+
GTP + ADP GDP + ATP
Succinyl-CoA
Synthetase
6. The Succinate Dehydrogenase Complex
ā€¢ Complex of several polypeptides, an FAD prosthetic group and iron-sulfur
clusters
ā€¢ Embedded in the inner mitochondrial membrane
ā€¢ Electrons are transferred from succinate to FAD and then to ubiquinone (Q )in
electron transport chain
ā€¢ Dehydrogenation is stereospecific; only the trans isomer is formed
Succinate
Dehydrogenase
7. Fumarase
ā€¢Stereospecific trans addition of water to the double bond of fumarate
to form L-malate
ā€¢Only the L isomer of malate is formed
Fumarase
8. Malate Dehydrogenase
ā€¢ Malate is oxidized to form oxaloacetate.
Malate
Dehydrogenase
Stoichiometry of the Citric Acid Cycle
ļ‚§ Two carbon atoms enter the cycle in the form of acetyl CoA.
ļ‚§ Two carbon atoms leave the cycle in the form of CO2 .
ļ‚§ Four pairs of hydrogen atoms leave the cycle in four
oxidation reactions (three molecules of NAD+ one molecule of
FAD are reduced).
ļ‚§ One molecule of GTP,
is formed.
ļ‚§ Two molecules of water are consumed.
ļ‚§ 9 ATP (2.5 ATP per NADH, and 1.5 ATP per FADH2)
are produced during oxidative phosphorylation.
ļ‚§ 1 ATP is directly formed in the citric acid cycle.
ļ‚§ 1 acetyl CoA generates approximately 10 molecules of
ATP.
Functions of the Citric Acid Cycle
ā€¢ Integration of metabolism. The citric acid cycle is amphibolic
(both catabolic and anabolic).
The cycle is involved in the
aerobic catabolism of
carbohydrates, lipids and
amino acids.
Intermediates of the cycle are
starting points for many
anabolic reactions.
ā€¢ Yields energy in the form of GTP (ATP).
ā€¢ Yields reducing power in the form of NADH2 and
FADH2.
Regulation of the Citric Acid Cycle
ā€¢ Pathway controlled by:
ā€¢ (1) Allosteric modulators
ā€¢ (2) Covalent modification of cycle enzymes
ā€¢ (3) Supply of acetyl CoA (pyruvate dehydrogenase complex)
Three enzymes have regulatory properties
- citrate synthase (is allosterically inhibited by NADH, ATP, succinyl CoA,
citrate ā€“ feedback inhibition)
- isocitrate dehydrogenase (allosteric
effectors: (+) ADP; (-) NADH, ATP. Bacterial ICDH can be covalently modified
by kinase/phosphatase)
-ļ”-ketoglutarate dehydrogenase complex (inhibition by ATP, succinyl CoA
and NADH
Regulation of the citric acid cycle
NADH, ATP, succinyl
CoA, citrate
-
Krebs Cycle is a Source of Biosynthetic
Precursors
THANKYOU
AFAIK. Iā€™m done

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The citric acid cycle

  • 1. The Citric Acid Cycle AMAL GEORGE MSc BIOCHEMISTRY
  • 2. PYRUVATE Glycogen Amino Acids GLUCOSE GLUCOSE 6 PHOSPHATE PYRUVATE ACETYL CoA Ribose, NADPH Lactate Fatty Acids Ethanol Synthesis of glycogen Degradation of glycogen Pentose phosphate pathway Glycolysis Gluconeogenesis
  • 3. The citric acid cycle is the final common pathway for the oxidation of fuel molecules ā€” amino acids, fatty acids, and carbohydrates Most fuel molecules enter the cycle as acetyl coenzyme A
  • 4. HISTORY Hans Adolf Krebs. Biochemist; born in Germany. Worked in Britain. His discovery in 1937 of the ā€˜Krebs cycleā€™ of chemical reactions was critical to the understanding of cell metabolism and earned him the 1953 Nobel Prize for Physiology or Medicine.
  • 5. Location ļ± In eukaryotes the reactions of the citric acid cycle take place inside mitochondria Names: ļ¶ The Citric Acid Cycle ļ¶ Tricarboxylic Acid Cycle ļ¶ Krebs Cycle
  • 6. An Overview of the Citric Acid Cycle A four-carbon oxaloacetate condenses with a two- carbon acetyl unit to yield a six-carbon citrate. An isomer of citrate is oxidatively decarboxylated and five-carbon ļ”-ketoglutarate is formed. ļ”-ketoglutarate is oxidatively decarboxylated to yield a four-carbon succinate Oxaloacetate is then regenerated from succinate. Two carbon atoms (acetyl CoA) enter the cycle and two carbon atoms leave the cycle in the form of two molecules of carbon dioxide. Three hydride ions (six electrons) are transferred to three molecules of NAD+ ,one pair of hydrogen atoms (two electrons) is transferred to one molecule of FAD. The function of the citric acid cycle is the harvesting of high- energy electrons from acetyl CoA.
  • 7. 1. Citrate Synthase ā€¢Citrate formed from acetyl CoA and oxaloacetate ā€¢Only cycle reaction with C-C bond formation ā€¢Addition of C2 unit (acetyl) to the keto double bond of C4 acid, oxaloacetate, to produce C6 compound, citrate citrate synthase
  • 8. 2. Aconitase ā€¢Elimination of H2O from citrate to form C=C bond of cis-aconitate ā€¢Stereospecific addition of H2O to cis-aconitate to form isocitrate aconitase aconitase
  • 9. 3. Isocitrate Dehydrogenase ā€¢ Oxidative decarboxylation of isocitrate to a-ketoglutarate (a metabolically irreversible reaction) ā€¢ One of four oxidation-reduction reactions of the cycle ā€¢ Hydride ion from the C-2 of isocitrate is transferred to NAD+ to form NADH ā€¢ Oxalosuccinate is decarboxylated to a-ketoglutarate isocitrate dehydrogenaseisocitrate dehydrogenase
  • 10. 4. The ļ”-Ketoglutarate Dehydrogenase Complex ā€¢ Similar to pyruvate dehydrogenase complex ā€¢ Same coenzymes, identical mechanisms ā€¢ E1 - a-ketoglutarate dehydrogenase (with TPP) ā€¢ E2 ā€“ dihydrolipoyl succinyltransferase (with flexible lipoamide prosthetic group) ā€¢ E3 - dihydrolipoyl dehydrogenase (with FAD) ļ”-ketoglutarate dehydrogenase
  • 11. 5. Succinyl-CoA Synthetase ā€¢Free energy in thioester bond of succinyl CoA is conserved as GTP or ATP in higher animals (or ATP in plants, some bacteria) ā€¢Substrate level phosphorylation reaction HS-+ GTP + ADP GDP + ATP Succinyl-CoA Synthetase
  • 12. 6. The Succinate Dehydrogenase Complex ā€¢ Complex of several polypeptides, an FAD prosthetic group and iron-sulfur clusters ā€¢ Embedded in the inner mitochondrial membrane ā€¢ Electrons are transferred from succinate to FAD and then to ubiquinone (Q )in electron transport chain ā€¢ Dehydrogenation is stereospecific; only the trans isomer is formed Succinate Dehydrogenase
  • 13. 7. Fumarase ā€¢Stereospecific trans addition of water to the double bond of fumarate to form L-malate ā€¢Only the L isomer of malate is formed Fumarase
  • 14. 8. Malate Dehydrogenase ā€¢ Malate is oxidized to form oxaloacetate. Malate Dehydrogenase
  • 15. Stoichiometry of the Citric Acid Cycle ļ‚§ Two carbon atoms enter the cycle in the form of acetyl CoA. ļ‚§ Two carbon atoms leave the cycle in the form of CO2 . ļ‚§ Four pairs of hydrogen atoms leave the cycle in four oxidation reactions (three molecules of NAD+ one molecule of FAD are reduced). ļ‚§ One molecule of GTP, is formed. ļ‚§ Two molecules of water are consumed. ļ‚§ 9 ATP (2.5 ATP per NADH, and 1.5 ATP per FADH2) are produced during oxidative phosphorylation. ļ‚§ 1 ATP is directly formed in the citric acid cycle. ļ‚§ 1 acetyl CoA generates approximately 10 molecules of ATP.
  • 16. Functions of the Citric Acid Cycle ā€¢ Integration of metabolism. The citric acid cycle is amphibolic (both catabolic and anabolic). The cycle is involved in the aerobic catabolism of carbohydrates, lipids and amino acids. Intermediates of the cycle are starting points for many anabolic reactions. ā€¢ Yields energy in the form of GTP (ATP). ā€¢ Yields reducing power in the form of NADH2 and FADH2.
  • 17. Regulation of the Citric Acid Cycle ā€¢ Pathway controlled by: ā€¢ (1) Allosteric modulators ā€¢ (2) Covalent modification of cycle enzymes ā€¢ (3) Supply of acetyl CoA (pyruvate dehydrogenase complex) Three enzymes have regulatory properties - citrate synthase (is allosterically inhibited by NADH, ATP, succinyl CoA, citrate ā€“ feedback inhibition) - isocitrate dehydrogenase (allosteric effectors: (+) ADP; (-) NADH, ATP. Bacterial ICDH can be covalently modified by kinase/phosphatase) -ļ”-ketoglutarate dehydrogenase complex (inhibition by ATP, succinyl CoA and NADH
  • 18. Regulation of the citric acid cycle NADH, ATP, succinyl CoA, citrate -
  • 19. Krebs Cycle is a Source of Biosynthetic Precursors