Glycolysis and Pyruvate Processing Notes
Overview of Glycolysis and Pyruvate Processing
Glycolysis produces energy and pyruvate.
Glucose has 6 carbon atoms.
Pyruvate has 3 carbon atoms.
This results in two pyruvate molecules from one glucose.
Glycolysis also produces NADH and ATP.
Problems to Solve Post-Glycolysis
Key issues after glycolysis include:
Regeneration of NAD+ to continue glycolysis.
Removal of accumulated pyruvate since it is not the end product.
There is still energy stored in pyruvate.
Pathways Post-Glycolysis
After glycolysis, there are two main pathways for pyruvate:
Pyruvate Oxidation (if oxygen is available)
Fermentation (if oxygen is limiting)
Conditions for Pathways
Eukaryotic or prokaryotic organisms' decisions depend on environmental conditions regarding oxygen availability.
Under low oxygen (hypoxic conditions), organisms opt for fermentation.
Example in humans: Intense exercise leads to anaerobic conditions, triggering fermentation.
If oxygen is present, pyruvate enters the oxidation pathway.
Fermentation Processes
Fermentation pathways include lactic acid fermentation and alcoholic fermentation.
Lactic Acid Fermentation
Occurs in rapidly contracting muscle cells.
Key reactions:
Pyruvate is converted to lactate.
Coupled reaction: NADH is oxidized to regenerate NAD+.
Reduction: Gain of electrons (hydrogen atoms added).
Structure changes:
Pyruvate (C=C=O) converts to lactate (C-C(OH)).
Purpose: Replenishes NAD+ so glycolysis can continue, yielding 2 ATP per glycolytic cycle.
Alcoholic Fermentation
Primarily takes place in yeast cells.
Key reactions:
Pyruvate is decarboxylated (removal of CO2) to form acetaldehyde (2 carbons).
Acetaldehyde is reduced to ethanol.
Coupling: Oxidation of NADH is again processed to regenerate NAD+.
Alcoholic fermentation products:
Ethanol and carbon dioxide (byproduct).
This process does not occur in muscle cells during intense exercise.
In lab settings, yeast fermentation produces visible CO2 accumulation as a product.
Transport of Pyruvate for Cellular Respiration
Condition for Oxidation: If oxygen is available, the pyruvate undergoes oxidation to carbon dioxide.
Location: These processes occur in mitochondria.
Mitochondrial Structure
Mitochondria have:
Outer mitochondrial membrane (OMM).
Inner mitochondrial membrane (IMM).
Intermembrane space (IMS) between the two membranes.
Matrix: The innermost compartment where pyruvate oxidation occurs.
Transport Mechanism
Pyruvate is transported across the two mitochondrial membranes via active transport.
Requires energy due to concentration gradients.
Type: Secondary active transport, using protons moving down their gradient to pull pyruvate against its gradient.
Bridge Reaction
Link between Glycolysis and Krebs Cycle.
Input: Pyruvate, NAD+, Coenzyme A.
Output: Acetyl-CoA (2 carbons), NADH, CO2.
Coenzyme A carries 2-carbon acetyl groups, facilitating further reactions.
No ATP is consumed in this step.
Citric Acid Cycle (Krebs Cycle)
Acetyl-CoA combines with oxaloacetate (4 carbons).
Produces citrate (6 carbons) as a starting molecule of the cycle.
Key outcomes of the cycle:
Release of two CO2 molecules.
Results in production of:
3 NADH
1 FADH2
1 ATP (or GTP)
The cycle creates energy carriers that will be further used in the electron transport chain.
Overall oxidation of carbon from glucose (6 carbons total from glucose) down to fully oxidized carbon dioxide.
Summary of Key Takeaways
Glycolysis leads to the production of pyruvate and ATP.
Pyruvate can undergo fermentation or oxidation depending on oxygen availability.
Fermentation results in lactate or ethanol, regenerating NAD+.
If oxygen is present, pyruvate enters mitochondrial processes leading to complete oxidation of carbon atoms in the Krebs cycle.
Key focus areas: inputs and outputs of glycolysis, pyruvate oxidation, and Krebs cycle are crucial for understanding cellular respiration in depth.
Low Oxygen Conditions and Fermentation
Overview of Fermentation
Occurs when oxygen levels are very low.
Pathway involved: Fermentation.
Process of Fermentation
Pyruvate is reduced to form:
Lactate (in animals)
Ethanol and Carbon Dioxide (in yeast)
Purpose of Fermentation:
To regenerate NAD+ from NADH.
This allows glycolysis to continue functioning.
Key Reaction: NADH + H+ ⇌ NAD+ + Lactic acid (or Ethanol + CO2)
Aerobic Conditions and Mitochondrial Processes
Aerobic Conditions
When oxygen is present, pyruvate is transported into the mitochondria.
Conversion of Pyruvate
Pyruvate (3 carbons) is oxidized to form Acetyl CoA (2 carbons).
The missing carbon from pyruvate is released as Carbon Dioxide (CO2).
NADH is also produced during this oxidation.
This step is referred to as the Bridge Reaction.
Bridge Reaction: Pyruvate + Coenzyme A → Acetyl CoA + CO2 + NADH
The Krebs Cycle (Citric Acid Cycle)
Entry of Acetyl CoA
Acetyl CoA combines with Oxaloacetate (OAA) (4 carbons) to form Citrate (6 carbons).
Process of the Krebs Cycle
As the cycle progresses, acetyl CoA is oxidized.
CO2 is released at various steps in the cycle.
Production of energy carriers:
NADH produced at several steps.
FADH2 produced at a specific step.
One ATP produced in one turn of the cycle.
Stoichiometry:
Two pyruvate molecules (from one glucose) yield:
2 Acetyl CoA
Therefore, outputs related to glucose should be multiplied by two for accurate results.
Carbon Accounting and Energy Yield
Carbon Balancing
Starting Material:
Glucose: 6 Carbons
Pyruvate: 2 x 3 Carbons = 6 Carbons
Bridge Reaction: Releases 2 CO2 (2 Carbons lost)
Krebs Cycle: Produces 4 CO2 from 2 Acetyl CoA (4 Carbons lost total).
Total CO2 Released: 6 Carbons from glucose converted to 6 CO2.
Energy Production
Total ATP produced from 1 glucose molecule:
4 ATP total (2 from glycolysis + 2 from Krebs cycle).
Total NADH produced:
Glycolysis: 2
Bridge Reaction: 2
Krebs Cycle: 6 (3 from each turn for 2 turns)
Total NADH: 10
Total FADH2 produced:
2 (one per turn in Krebs cycle).
Summary of Key Outputs per Glucose Molecule
Waste products:
Carbon Dioxide: 6
Energy Carriers:
ATP: 4
NADH: 10
FADH2: 2
Energy Utilization via the Electron Transport Chain
Future discussions will involve how the NADH and FADH2 created in these processes will be leveraged in the electron transport chain to synthesize more ATP.
Concept Review
The process during pyruvate oxidation resulting in the release of carbon dioxide is called Decarboxylation.