Results Glossary Entry Canonical life Glycolysis is the τ-categorical entry-loop of metabolic circulation: a ten-step open chain (glucose → 2 pyruvate) that injects free energy into the cellular Loop_L by net-producing 2 ATP and 2 NADH per glucose. As a morphism it is the unive…
Results · Life Glossary · Process LG-P03-glycolysis γ_Gly Canonical Lean · planned

Glycolysis

Glycolysis is the τ-categorical entry-loop of metabolic circulation: a ten-step open chain (glucose → 2 pyruvate) that injects free energy into the cellular Loop_L by net-producing 2 ATP and 2 NADH per glucose. As a morphism it is the universal feeder into the Krebs/respiratory loop, instantiating VI.D31 (Metabolic Circulation) at the substrate-level phosphorylation tier.

Life Glossary Primary: VI.D31 process metabolic circulation feeder morphism substrate level phosphorylation

τ-Definition

Glycolysis is the τ-categorical entry-loop of metabolic circulation: a ten-step open chain (glucose → 2 pyruvate) that injects free energy into the cellular Loop_L by net-producing 2 ATP and 2 NADH per glucose. As a morphism it is the universal feeder into the Krebs/respiratory loop, instantiating VI.D31 (Metabolic Circulation) at the substrate-level phosphorylation tier.

Categorical invariant. Glycolysis = source-side feeder morphism into Loop_L: a non-closed γ-chain whose composition with mitochondrial loops yields the full metabolic circulation orbit guaranteed by VI.D31.

Primary registry anchor: VI.D31

Supporting items: VI.T05, VI.T09, VI.D32, VI.P11

τ-Derivation Chain

  1. I.K0 — Universe Postulate
  2. VI.D15 — Life Sector
  3. VI.D31 — Metabolic Circulation — substrate-level phosphorylation as feeder morphism
  4. VI.T05 — Metabolic Fiber Theorem — open chain composes with closed loop
  5. VI.D32 — ATP/ADP oscillation realised at the glycolytic gate

Empirical Correlate

Biomarker: Glucose, glucose-6-phosphate, fructose-1,6-bisphosphate, dihydroxyacetone-phosphate, glyceraldehyde-3-phosphate, 1,3-BPG, 3-PG, 2-PG, PEP, pyruvate; net yield 2 ATP + 2 NADH + 2 pyruvate per glucose.

Measurable range: Erythrocyte flux ~2 mmol·L⁻¹·h⁻¹; tumour cells (Warburg phenotype) ~10-100× resting somatic rate; PFK-1 flux control coefficient typically dominant (0.3-0.7).

Observation method: Lactate/pyruvate ratio assay; ¹³C-glucose isotope tracing; ²H₂O labelling for hexose flux; extracellular acidification rate (ECAR) on Seahorse analyzer; ³¹P-NMR for phosphorylated intermediates.

Calibration anchor: LG-Y02-kinetic-pseudoscalar-channel

Anchor chain:

  1. VI.L18 chirality channel
  2. D-glucose stereospecificity preserved through all ten enzymatic steps
  3. L-lactate (not D-lactate) as anaerobic terminal product

Manuscript reference: manuscript-sources/book-06/part03/ch19-metabolism.tex

Lean Coverage

Status: Planned

Save or share this page for inspection

Download a portable dossier, copy a reviewer note, or send this page to someone who can inspect it.

Email to expert