Utilisateur
It converts 1 glucose → 2 pyruvate, producing 2 net ATP and 2 NADH directly.
It is an anaerobic ATP-generating pathway that functions in almost all cells and predates oxygen-based metabolism.
It occurs in the cytosol and includes 10 enzyme-catalyzed reactions.
Energy investment: ATP is consumed to activate glucose.
Energy payout: ATP and NADH are produced from triose intermediates.
Consume ATP: Steps 1 & 3 (hexokinase, PFK-1).
Generate ATP: Steps 7 & 10 (phosphoglycerate kinase, pyruvate kinase)
Steps 7 (1,3-BPG → 3-PG) and 10 (PEP → pyruvate).
Step 6 (GAPDH), producing NADH.
Steps 1 (hexokinase), 3 (PFK-1), and 10 (pyruvate kinase).
Phosphofructokinase-1 (PFK-1).
Irreversible, exergonic (ΔG ≪ 0), ATP-coupled phosphate transfer, inhibited by G6P (product inhibition).
It converts an aldohexose → ketohexose, shifting the carbonyl between C1 and C2.
Irreversible, ATP-dependent phosphorylation, rate-limiting, highly regulated allosterically.
GAP and DHAP, which are structural isomers
Only GAP continues down the payoff phase, so DHAP is isomerized to maintain two triose molecules.
Two, and all downstream reactions occur twice per glucose.
It contains an acyl phosphate, whose hydrolysis yields highly stabilized resonance products.
Step 6: NADH generated; Step 7: ATP generated.
A dehydration reaction (2-PG → PEP).
Conversion from enolpyruvate → pyruvate is highly favorable (ΔG ≪ 0).
2 ATP per glucose (one per PEP).
2 net ATP. (4 generated − 2 consumed).
Substrate availability, enzyme activity regulation, enzyme amount, compartmentation.
Hexokinase, PFK-1, pyruvate kinase.
G6P (product inhibition).
AMP/ADP activate PFK-1; high PEP inhibits via feedback inhibition.
Activated by F-1,6-BP (feed-forward) and inhibited by ATP.
To maintain steady-state concentrations of intermediates and prevent futile flux.
Steps 1 & 3
Step 8: isomerization (3-PG ⇌ 2-PG).
Step 9: dehydration (2-PG → PEP).
Because G-1-P → G-6-P requires no ATP, saving one ATP compared to glucose entry.
To regenerate NAD⁺ so glycolysis can continue without oxidative phosphorylation.
Lactate (muscle, RBCs) and ethanol (yeast)
Lactate exists as a deprotonated anion, and it is exported via a specific membrane transporter.
It removes accumulated H⁺ from ATP hydrolysis, preventing acid damage to muscle fibers.
It is converted to pyruvate → acetyl-CoA → CAC for oxidation.
PDH occurs in the mitochondrial matrix, requiring pyruvate translocase co-transporting H⁺
Oxidation, decarboxylation, and transacetylation
Pyruvate + CoA + NAD⁺ → Acetyl-CoA + NADH + CO₂.
Because acetyl-CoA cannot be converted back to glucose in mammals.
Enzymes: E1, E2, E3 (decarboxylation, transfer, oxidation).
Cofactors: NAD⁺, FAD, CoA (plus two more: TPP and lipoamide).
It speeds reactions and limits side reactions, allowing coordinated control.
NADH (inhibits), acetyl-CoA (inhibits), NAD⁺/HS-CoA (activate)
Kinase phosphorylates and inactivates PDH; phosphatase dephosphorylates and activates it
Ca²⁺ activates PDH phosphatase, turning PDH on during muscle contraction
