Cellular respiration is a metabolic process that allows cells to harvest energy from organic molecules to generate ATP.
ENE-1: The highly complex organization of living systems requires constant input of energy and the exchange of macromolecules.
ENE-1.K1: Describe fermentation and cellular respiration processes that allow organisms to convert energy stored in biological macromolecules to produce ATP.
ENE-1.K2: Cellular respiration in eukaryotes involves enzyme-catalyzed reactions that capture energy from biological macromolecules.
ENE-1.K3: The electron transport chain (ETC) transfers energy from electrons in a series of coupled reactions, establishing an electrochemical gradient across membranes.
Electron transport chain reactions occur in chloroplasts, mitochondria, and prokaryotic plasma membranes.
In cellular respiration, electrons from NADH and FADH2 are passed along a chain to the terminal electron acceptor, oxygen.
In photosynthesis, the terminal electron acceptor is NADP+.
Aerobic prokaryotes use oxygen, while anaerobic prokaryotes use alternative molecules.
ENE-1.KC: The transfer of electrons creates a proton gradient across inner mitochondrial membranes or chloroplast membranes.
Protons move from high to low concentration, driving ATP synthesis.
Decoupling of oxidative phosphorylation from electron transport in cellular respiration generates heat for body temperature regulation in endothermic organisms.
ENE-1.L: Cells obtain energy from biological macromolecules via glycolysis which splits glucose to form ATP from ADP, NADH from NAD+, and pyruvate.
Pyruvate is then transported into the mitochondrion for further oxidation.
Krebs cycle produces CO2, ATP, and electron carriers before transferring electrons to ETC in the inner mitochondrial membrane.
During cellular respiration, electrons follow a pathway: glucose -> NADH -> ETC -> oxygen.
The process of breaking down glucose occurs in steps to efficiently harvest energy.
Enzymes (dehydrogenases) take electrons and protons from glucose, reducing NAD+ to NADH while releasing H+ into the solution.
There are three main stages:
Glycolysis
Pyruvate Oxidation and the Citric Acid Cycle
Oxidative Phosphorylation (ETC and Chemiosmosis)
Location: Cytosol
Function: Splits glucose (6C) into 2 pyruvates (3C).
Summary of pathway involves:
Input: Glucose
Outputs: 2 Pyruvates, 2 ATP, 2 NADH.
Energy investment stage: ATP is used to phosphorylate glucose derivatives.
Energy payoff stage: ATP is generated through substrate-level phosphorylation with a net yield of 2 ATP and 2 NADH per glucose.
If oxygen is present, pyruvate enters the mitochondria, where it is oxidized into acetyl CoA, producing CO2 and NADH.
Location: Mitochondrial Matrix.
Converts acetyl CoA into citrate, releasing CO2, synthesizing ATP, and transferring electrons to NADH and FADH2.
Produces:
2 Acetyl CoA -> 2 ATP, 6 NADH, and 4 CO2 per glucose.
Consists of:
Electron Transport Chain (ETC)
Chemiosmosis
ETC in the inner membrane is a collection of proteins that pumps H+ ions, creating a gradient to drive ATP synthesis via ATP synthase.
The final electron acceptor is oxygen, forming water.
Stage | Inputs | Outputs |
---|---|---|
Glycolysis | 1 Glucose | 2 Pyruvate, 2 ATP, 2 NADH |
Pyruvate Oxidation | 2 Pyruvate | 2 Acetyl CoA, 2 CO2, 2 NADH |
Citric Acid Cycle | 2 Acetyl CoA | 4 CO2, 2 ATP, 6 NADH, 2 FADH2 |
Oxidative Phosphorylation | 10 NADH, 2 FADH2 | 26-28 ATP |
Total | 30-32 ATP |
Generates ATP using an ETC without oxygen, utilizing sulfates or nitrates as final electron acceptors.
Extends glycolysis without an ETC; recycles NAD+ in the absence of oxygen, occurring in the cytosol.
Produces:
Alcohol Fermentation: Converts pyruvate to ethanol and CO2.
Lactic Acid Fermentation: Reduces pyruvate to lactate.
Examples include muscle cells performing lactic acid fermentation under strenuous exercise conditions.