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Overview of Cellular Respiration Pathways
Mar 16, 2025
Summary of Glycolysis, Link Reaction, and Krebs Cycle
Introduction
Overview of breaking down glucose through glycolysis, link reaction, and Krebs cycle.
Aim: Understand the transformation of the six-carbon glucose molecule into carbon dioxide and its role in cellular respiration.
Glycolysis
Location:
Cytoplasm
Initial Step:
Glucose is phosphorylated by 2 ATP.
Phosphorylation adds phosphate groups to glucose, creating fructose 1,6-bisphosphate.
Makes glucose more reactive.
Breakdown:
Fructose 1,6-bisphosphate splits into two triose phosphate molecules.
Triose phosphates yield 4 ATP through substrate-level phosphorylation.
Undergoes dehydrogenation, releasing hydrogen.
Hydrogen accepted by NAD, forming 2 reduced NADs.
End Product:
Pyruvate
Link Reaction
Location:
Mitochondrial Matrix
Pyruvate Conversion:
Pyruvate undergoes decarboxylation, releasing CO2.
Forms a two-carbon molecule, which undergoes further dehydrogenation.
Hydrogen accepted by NAD, forming 2 reduced NADs.
Produces acetyl group, which combines with coenzyme A to form acetyl CoA.
End Product:
Acetyl CoA
Krebs Cycle (Citric Acid Cycle)
Location:
Mitochondrial Matrix
Initial Step:
Acetyl CoA combines with oxaloacetate (4-carbon) to form citrate (6-carbon).
Coenzyme A is released and can transport other acetyl groups.
Cycle Progression:
Citrate undergoes decarboxylation and dehydrogenation.
Produces CO2 and 2 reduced NADs.
Converts to a 5-carbon molecule.
Further decarboxylation and dehydrogenation of the 5-carbon molecule.
Produces CO2, 2 reduced NADs.
Results in a 4-carbon molecule.
4-carbon molecule undergoes substrate-level phosphorylation.
Produces 2 ATP.
Further dehydrogenation forms 2 reduced FADs and 2 reduced NADs.
Oxaloacetate is regenerated.
Conclusion
Glucose Breakdown:
Complete breakdown of glucose (6-carbon) into CO2.
Six molecules of CO2 are produced.
Energy Production:
Total from the glucose breakdown: 6 ATP, 10 reduced NADs, and 2 reduced FADs.
Future Topics:
Discussion on the role of reduced NADs and FADs in chemiosmosis and ATP synthesis.
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