Energy-Releasing Pathways
Autotrophs: Organisms that produce their own organic molecules through photosynthesis.
Heterotrophs: Organisms that live on organic compounds produced by other organisms.
All organisms utilize cellular respiration to extract energy from organic molecules.
Cellular respiration involves a series of reactions that:
Are oxidations (loss of electrons).
Are dehydrogenations (loss of electrons accompanied by hydrogen).
Result in the loss of a hydrogen atom (1 electron, 1 proton).
In redox reactions, electrons carry energy from one molecule to another.
NAD+ is a key electron carrier:
Accepts 2 electrons and 1 proton to form NADH.
The reaction is reversible.
Aerobic respiration: Final electron receptor is oxygen (O2) and is more common.
Anaerobic respiration: Final electron acceptor is an inorganic molecule (not O2) and is less efficient.
Fermentation: Final electron acceptor is an organic molecule.
During respiration, electrons are transferred through electron carriers to a final electron acceptor with the ultimate goal of producing ATP.
Glycolysis:
Glucose (6 carbons) splits into 2 pyruvate (3 carbons).
Does not require oxygen.
Produces 2 NADH and 2 ATP (net yield).
Pyruvate Oxidation
Krebs Cycle:
Electron Transport Chain & Chemiosmosis.
Splitting of glucose requires an investment of 2 ATP.
Glucose is converted into glucose-6-phosphate, making it more reactive.
Results in a net yield of 2 ATPs and 2 NADH:
Four ATPs and two NADH produced per glucose molecule.
In the presence of oxygen, pyruvate undergoes oxidative decarboxylation to form Acetyl-CoA:
Releases CO2 and transfers electrons to NAD+ to form NADH.
For each glucose, 2 acetyl groups enter the cycle:
Each acetyl group combines with oxaloacetate to form citrate.
NADH and FADH2 are generated.
Total energy captured includes 2 ATP, 6 NADH, and 2 FADH2 per glucose.
A series of membrane-bound electron carriers located in the inner mitochondrial membrane.
Electrons from NADH and FADH2 are transferred through complexes in a series of redox reactions, leading to ATP synthesis via oxidative phosphorylation.
Protons (H+) accumulate in the intermembrane space and create a gradient.
Protons flow back into the mitochondrial matrix through ATP synthase, which uses the gradient to synthesize ATP from ADP and Pi.
Glycolysis: Glucose is converted to pyruvate, producing a net of 2 ATP and 2 NADH.
Formation of Acetyl CoA: Pyruvate is converted to Acetyl CoA with the release of CO2 and production of NADH.
Citric Acid Cycle: Acetyl CoA is oxidized to CO2, yielding ATP, NADH, and FADH2.
Electron Transport and Chemiosmosis: Electron carriers generate a proton gradient, leading to ATP synthesis.
Regulated by feedback inhibition where ATP and citrate inhibit pathways to manage energy production.
Involves the use of inorganic molecules as the final electron acceptor, such as NO3 or SO4.
Organic molecules function as the final electron acceptor, producing byproducts like ethanol or lactic acid without using the electron transport chain.
Aerobic vs. Anaerobic respiration and fermentation differ in electron acceptors and energy yields.
Both pathways allow cells to generate ATP through substrate-level phosphorylation—anaerobic respiration uses a different final electron acceptor compared to aerobic respiration.
Carbohydrates are the main energy source.
Proteins and Lipids can also be broken down into intermediates for use in metabolism.