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KREBS CYCLE
CITRIC ACID CYCLE
Puranjaya Pancholi
Names:
The Citric Acid
Cycle
Tricarboxylic
Acid Cycle
Krebs Cycle
In
eukaryotes
the reactions
of the citric
acid cycle
take place
inside
mitochondria
Hans Adolf Krebs.
Biochemist; born in
Germany. Worked in
Britain. His discovery in
1937 of the ‘Krebs cycle’ of
chemical reactions was
critical to the
understanding of cell
metabolism and earned
him the 1953 Nobel Prize
for Physiology or Medicine.
• The name of this metabolic pathway is derived from citric acid (a
type of tricarboxylic acid, often called citrate) that is consumed and
then regenerated by this sequence of reactions to complete the
cycle. In addition, the cycle consumes acetate (in the form of
acetyl-CoA) and water, reduces NAD+ to NADH, and produces
carbon dioxide as a waste byproduct. The NADH generated by the
TCA cycle is fed into the oxidative phosphorylation (electron
transport) pathway. The net result of these two closely linked
pathways is the oxidation of nutrients to produce usable chemical
energy in the form of ATP.
• In eukaryotic cells, the citric acid cycle occurs in the matrix of the
mitochondrion. In prokaryotic cells, such as bacteria which lack
mitochondria, the TCA reaction sequence is performed in the
cytosol with the proton gradient for ATP production being across
the cell's surface (plasma membrane) rather than the inner
membrane of the mitochondrion.
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 -
ketoglutarate is formed.
-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
• Citrate formed from acetyl CoA and oxaloacetate
• Only cycle reaction with C-C bond formation
• Addition of C2 unit (acetyl) to the keto double bond
of C4 acid, oxaloacetate, to produce C6 compound,
citrate
citrate synthase
2. Aconitase
• Elimination of H2O from citrate to form C=C bond
of cis-aconitate
• Addition of H2O to cis-aconitate to form isocitrate
aconitase aconitase
3. Isocitrate Dehydrogenase
• Oxidative decarboxylation of isocitrate to
a-ketoglutarate (a metabolically irreversible reaction)
• Hydride ion from the C-2 of isocitrate is transferred to
NAD+ to form NADH
• Oxalosuccinate is decarboxylated to a-ketoglutarate
isocitrate dehydrogenaseisocitrate dehydrogenase
4. The -Ketoglutarate Dehydrogenase Complex
• Similar to pyruvate dehydrogenase complex
• Same coenzymes, identical mechanisms
E1 - a-ketoglutarate dehydrogenase (with TPP)
E2 – dihydrolipoyl succinyltransferase (with flexible
lipoamide prosthetic group)
E3 - dihydrolipoyl dehydrogenase (with FAD)
-ketoglutarate
dehydrogenase
5. Succinyl-CoA Synthetase
• Free energy in thioester bond of succinyl CoA is
conserved as GTP or ATP in higher animals (or ATP
in plants, some bacteria)
HS-+
Succinyl-CoA
Synthetase
• Complex of several polypeptides, an FAD prosthetic group and
iron-sulfur clusters
• Embedded in the inner mitochondrial membrane
• Electrons are transferred from succinate to FAD and then to
ubiquinone (Q) in electron transport chain
• Dehydrogenation is stereospecific; only the trans isomer is
formed
6. The Succinate Dehydrogenase Complex
Succinate
Dehydrogenase
7. Fumarase
• Stereospecific trans addition of water to the
double bond of fumarate to form L-malate
• Only the L isomer of malate is formed
Fumarase
8. Malate Dehydrogenase
Malate
Dehydrogenase
Malate is oxidized to form oxaloacetate.
Krebs cycle
Krebs cycle

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Krebs cycle

  • 1. KREBS CYCLE CITRIC ACID CYCLE Puranjaya Pancholi
  • 2. Names: The Citric Acid Cycle Tricarboxylic Acid Cycle Krebs Cycle In eukaryotes the reactions of the citric acid cycle take place inside mitochondria Hans Adolf Krebs. Biochemist; born in Germany. Worked in Britain. His discovery in 1937 of the ‘Krebs cycle’ of chemical reactions was critical to the understanding of cell metabolism and earned him the 1953 Nobel Prize for Physiology or Medicine.
  • 3. • The name of this metabolic pathway is derived from citric acid (a type of tricarboxylic acid, often called citrate) that is consumed and then regenerated by this sequence of reactions to complete the cycle. In addition, the cycle consumes acetate (in the form of acetyl-CoA) and water, reduces NAD+ to NADH, and produces carbon dioxide as a waste byproduct. The NADH generated by the TCA cycle is fed into the oxidative phosphorylation (electron transport) pathway. The net result of these two closely linked pathways is the oxidation of nutrients to produce usable chemical energy in the form of ATP. • In eukaryotic cells, the citric acid cycle occurs in the matrix of the mitochondrion. In prokaryotic cells, such as bacteria which lack mitochondria, the TCA reaction sequence is performed in the cytosol with the proton gradient for ATP production being across the cell's surface (plasma membrane) rather than the inner membrane of the mitochondrion.
  • 4. 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 - ketoglutarate is formed. -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.
  • 5.
  • 6. 1. Citrate Synthase • Citrate formed from acetyl CoA and oxaloacetate • Only cycle reaction with C-C bond formation • Addition of C2 unit (acetyl) to the keto double bond of C4 acid, oxaloacetate, to produce C6 compound, citrate citrate synthase
  • 7. 2. Aconitase • Elimination of H2O from citrate to form C=C bond of cis-aconitate • Addition of H2O to cis-aconitate to form isocitrate aconitase aconitase
  • 8. 3. Isocitrate Dehydrogenase • Oxidative decarboxylation of isocitrate to a-ketoglutarate (a metabolically irreversible reaction) • Hydride ion from the C-2 of isocitrate is transferred to NAD+ to form NADH • Oxalosuccinate is decarboxylated to a-ketoglutarate isocitrate dehydrogenaseisocitrate dehydrogenase
  • 9. 4. The -Ketoglutarate Dehydrogenase Complex • Similar to pyruvate dehydrogenase complex • Same coenzymes, identical mechanisms E1 - a-ketoglutarate dehydrogenase (with TPP) E2 – dihydrolipoyl succinyltransferase (with flexible lipoamide prosthetic group) E3 - dihydrolipoyl dehydrogenase (with FAD) -ketoglutarate dehydrogenase
  • 10. 5. Succinyl-CoA Synthetase • Free energy in thioester bond of succinyl CoA is conserved as GTP or ATP in higher animals (or ATP in plants, some bacteria) HS-+ Succinyl-CoA Synthetase
  • 11. • Complex of several polypeptides, an FAD prosthetic group and iron-sulfur clusters • Embedded in the inner mitochondrial membrane • Electrons are transferred from succinate to FAD and then to ubiquinone (Q) in electron transport chain • Dehydrogenation is stereospecific; only the trans isomer is formed 6. The Succinate Dehydrogenase Complex Succinate Dehydrogenase
  • 12. 7. Fumarase • Stereospecific trans addition of water to the double bond of fumarate to form L-malate • Only the L isomer of malate is formed Fumarase
  • 13. 8. Malate Dehydrogenase Malate Dehydrogenase Malate is oxidized to form oxaloacetate.