Utilisateur
To capture energy from fuel oxidation and use it to make ATP.
Acetyl-CoA condenses with OAA, two carbons oxidized to CO₂, and OAA is regenerated.
3 NADH, 1 FADH₂/QH₂, and 1 GTP.
It occurs in the mitochondrial matrix; it requires O₂ indirectly to reoxidize NADH/FADH₂ via the ETC.
CAC intermediates feed anabolic reactions (amino acids, fats, carbohydrates, nucleotides).
It is irreversible (ΔG ≪ 0), catalyzed by citrate synthase, forms citrate, and is not physiologically regulated.
An isomerization, reversible with ΔG ≈ 0.
Oxidative decarboxylation, irreversible, produces NADH, and is regulated.
Oxidative decarboxylation, irreversible, produces NADH, regulated, and mechanistically similar to PDH
It is a thioester, whose hydrolysis drives substrate-level phosphorylation.
A reversible reaction (ΔG ~ 0), forms GTP, and is a substrate-level phosphorylation.
It is reversible, forms FADH₂/QH₂, and the enzyme is Complex II, an integral membrane protein.
FADH₂ transfers electrons to coenzyme Q (→ QH₂), which then enters the ETC.
A reversible hydration converting fumarate → malate.
A reversible oxidation forming NADH and regenerating OAA.
Because it is cyclic, and flux depends on multiple steps and NAD⁺/NADH balance.
Isocitrate dehydrogenase and α-ketoglutarate dehydrogenase.
Inhibitors: NADH, ATP.
Activators: ADP, Ca²⁺
Because oxidation steps require NAD⁺ as substrate; high NADH inhibits by mass-action.
No — citrate levels are not physiologically relevant to regulate flux.
↓ ADP → ↓ ATP synthase → ↑ H⁺ gradient → ↓ ETC rate → ↓ NADH oxidation → ↓ NAD⁺/NADH → slowed PDH + CAC.
(Flow diagram explicitly from slide.)
↑ ADP → ↑ ATP synthase → ↓ H⁺ gradient → ↑ ETC rate → ↑ NADH oxidation → ↑ NAD⁺/NADH → accelerated PDH + CAC
Ca²⁺ activates regulated enzymes (isocitrate DH, α-KG DH), signaling increased energy demand
It provides precursors for biosynthesis and functions in energy generation.
CAC intermediates are drained for biosynthesis, so they must be replenished.
Amino acid breakdown and pyruvate carboxylase forming oxaloacetate.
Activated by acetyl-CoA, inhibited by ADP.
~10 ATP (7.5 from NADH, 1.5 from FADH₂, 1 from GTP).
Approximately 32 ATP under aerobic conditions
2 net ATP
GTP, which can convert to ATP.
The PDH reaction: pyruvate → acetyl-CoA + CO₂ + NADH.
Isocitrate DH and α-KG DH.
NADH: isocitrate DH, α-KG DH, malate DH.
FADH₂: succinate DH.
GTP: succinyl-CoA synthetase.
Fumarase: fumarate → malate
Succinate dehydrogenase.
Step 7 of glycolysis (PGK) and succinyl-CoA synthetase in the CAC.
Isocitrate DH and α-KG DH (inhibited by NADH/ATP; activated by ADP/Ca²⁺).
Because O₂ allows oxidative phosphorylation, which produces far more ATP, reducing the need for high glycolytic flux (Pasteur effect).
Lactate → pyruvate → acetyl-CoA, then oxidized via the CAC.
