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Frederic L. Holmes, “Hans Krebs: The Formation of a Scientific Life”, 1991. CONTINUED.

 

Here I present: Frederic L. Holmes, “Hans Krebs: Formation of a Scientific Life, 1991. ­CONTINUED.

Let’s go through the Hans Krebs “citrate cycle”, step by step. I’ll give both the cycle overview and the key molecules/energy outputs.


1. Purpose of the TCA Cycle

Central metabolic pathway in aerobic respiration.

Oxidizes acetyl-CoA to CO₂.

Produces reducing equivalents (NADH, FADH₂) for the electron transport chain and GTP (or ATP).



2. Steps of the TCA Cycle

1. Citrate formation

Acetyl-CoA (2C) + Oxaloacetate (4C) → Citrate (6C)

Enzyme: Citrate synthase


2. Isomerization

Citrate → Isocitrate

Enzyme: Aconitase
(via cis-Aconitate intermediate)


3. First oxidative decarboxylation

Isocitrate (6C) → α-Ketoglutarate (5C) + CO₂ + NADH

Enzyme: Isocitrate dehydrogenase


4. Second oxidative decarboxylation

α-Ketoglutarate (5C) → Succinyl-CoA (4C) + CO₂ + NADH

Enzyme: α-Ketoglutarate dehydrogenase


5. Substrate-level phosphorylation

Succinyl-CoA → Succinate

Produces GTP (or ATP)

Enzyme: Succinyl-CoA synthetase


6. Oxidation

Succinate → Fumarate + FADH₂

Enzyme: Succinate dehydrogenase


7. Hydration

Fumarate → Malate

Enzyme: Fumarase


8. Oxidation to regenerate oxaloacetate

Malate → Oxaloacetate + NADH

Enzyme: Malate dehydrogenase



3. Energy Yield per Acetyl-CoA

3 NADH → ~7.5 ATP

1 FADH₂ → ~1.5 ATP

1 GTP (or ATP) → 1 ATP


Total: ~10 ATP per acetyl-CoA


4. Krebs Cycle SMILES’ Notation. The letter A, B, C, D, E, F, G, H refer to the “tree-structure” BELOW this blog post.

A.  Citrate.

C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O

B.  Isocitrate.

C(C(C(C(=O)O)O)C(=O)O)C(=O)O

C.  Alpha-Ketoglutarate.

C(CC(=O[O-])C(=O)C(=O[O-]

D.  Succinyl-Coenzyme-A.

CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)CCC(=O)O)O

E.  Succinate.

C(CC(=O)[O-])C(=O)[O-]

F.  Fumarate.

C(=C/C(=O)[O-])\C(=O)[O-]

G.  Malate.

C(C(C(=O)[O-])O)C(=O)[O-]

H.  Oxaloacetate.

C(C(=O)C(=O)[O-])C(=O)[O-]

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