뒤로Chapter 7
스터디 가이드 - 스마트 노트
자료에 맞춘 맞춤형 노트, 핵심 정의, 예시, 맥락을 확장해 제공합니다.
Cellular Respiration: Overview and Importance
Introduction to Cellular Respiration
Cellular respiration is a series of metabolic pathways that extract energy from organic molecules, primarily glucose, to produce ATP, the energy currency of the cell. This process is central to the metabolism of all aerobic organisms and is tightly linked to the carbon and energy cycles in ecosystems.
Fermentation: Partial degradation of sugars without oxygen, yielding less ATP.
Aerobic Respiration: Uses oxygen as the final electron acceptor, producing the most ATP.
Anaerobic Respiration: Uses molecules other than oxygen (e.g., sulfate, nitrate) as final electron acceptors.

Additional info: The carbon cycle links photosynthesis and cellular respiration, cycling carbon through ecosystems.
Catabolic Pathways and ATP Production
Energy Flow and the Role of ATP
Living cells require energy, which they obtain from organic molecules. Energy flows into ecosystems as sunlight and leaves as heat. Photosynthesis captures solar energy, producing organic molecules and oxygen, which are then used in cellular respiration to generate ATP.
ATP: Adenosine triphosphate, the main energy carrier in cells.
Exergonic Reactions: Breakdown of organic molecules releases energy.
Equation for Cellular Respiration:

Redox Reactions in Cellular Respiration
Oxidation and Reduction
Redox reactions involve the transfer of electrons between molecules, releasing energy that is used to synthesize ATP. The molecule that loses electrons is oxidized, while the one that gains electrons is reduced.
Reducing Agent: Electron donor.
Oxidizing Agent: Electron acceptor.

Example: In the reaction between methane and oxygen, methane is oxidized and oxygen is reduced.

Cellular Respiration Redox Equation:

Electron Carriers and the Electron Transport Chain (ETC)
NAD+, FAD, and Stepwise Energy Harvest
During cellular respiration, electrons from organic molecules are transferred to electron carriers such as NAD+ and FAD, forming NADH and FADH2. These carriers shuttle electrons to the electron transport chain, where energy is released in controlled steps.
NAD+ (Nicotinamide adenine dinucleotide): Accepts electrons to become NADH.
FAD (Flavin adenine dinucleotide): Accepts electrons to become FADH2.

Additional info: Stepwise energy harvest prevents explosive release of energy, allowing efficient ATP synthesis.

Stages of Cellular Respiration
Overview of the Three Main Stages
Cellular respiration consists of three main stages: glycolysis, pyruvate oxidation and the citric acid cycle, and oxidative phosphorylation. Each stage occurs in a specific cellular location and contributes to the overall production of ATP.
Glycolysis: Occurs in the cytosol; breaks down glucose into pyruvate.
Pyruvate Oxidation & Citric Acid Cycle: Occur in the mitochondrial matrix; complete the oxidation of glucose.
Oxidative Phosphorylation: Occurs in the inner mitochondrial membrane; produces most ATP via the ETC and chemiosmosis.



Glycolysis
Harvesting Chemical Energy from Glucose
Glycolysis is the first step in cellular respiration, occurring in the cytosol and not requiring oxygen. It splits one glucose molecule into two pyruvate molecules, producing a net gain of 2 ATP and 2 NADH per glucose.
Energy Investment Phase: 2 ATP are used.
Energy Payoff Phase: 4 ATP and 2 NADH are produced.
Net Yield: 2 ATP, 2 NADH, 2 pyruvate per glucose.



Pyruvate Oxidation and the Citric Acid Cycle
Completing the Oxidation of Glucose
After glycolysis, pyruvate is transported into the mitochondrion and converted to acetyl-CoA. The citric acid cycle (Krebs cycle) then completes the oxidation of glucose, generating CO2, NADH, FADH2, and ATP.
Pyruvate Oxidation: Produces acetyl-CoA, NADH, and CO2.
Citric Acid Cycle: Each turn produces 3 NADH, 1 FADH2, 1 ATP (or GTP), and 2 CO2 per acetyl-CoA.






Oxidative Phosphorylation and Chemiosmosis
Electron Transport Chain and ATP Synthesis
Oxidative phosphorylation is the final stage of cellular respiration, where most ATP is produced. Electrons from NADH and FADH2 are transferred through the electron transport chain (ETC) to oxygen, forming water. The energy released pumps protons (H+) across the inner mitochondrial membrane, creating a proton gradient. ATP synthase uses this gradient to synthesize ATP in a process called chemiosmosis.
ETC Location: Inner mitochondrial membrane.
ATP Yield: Glycolysis (2 ATP), Citric Acid Cycle (2 ATP), Oxidative Phosphorylation (~26–28 ATP).
Cyanide: Inhibits cytochrome c oxidase, blocking ATP production.






Fermentation and Anaerobic Respiration
ATP Production Without Oxygen
When oxygen is scarce, cells can produce ATP through fermentation or anaerobic respiration. Fermentation regenerates NAD+ for glycolysis, allowing continued ATP production. Two common types are alcoholic fermentation (yeast) and lactic acid fermentation (muscle cells, some bacteria).
Alcoholic Fermentation: Pyruvate is converted to ethanol and CO2.
Lactic Acid Fermentation: Pyruvate is reduced to lactate.
Anaerobic Respiration: Uses alternative electron acceptors (not O2).



Metabolic Pathway Integration and Catabolic Versatility
Connections to Other Metabolic Pathways
Glycolysis and the citric acid cycle are central hubs that connect to the metabolism of proteins, fats, and other carbohydrates. Proteins are deaminated and enter as pyruvate, acetyl-CoA, or cycle intermediates. Fats are broken down into glycerol (glycolysis) and fatty acids (β-oxidation to acetyl-CoA). Intermediates can also be diverted for anabolic pathways to synthesize macromolecules.
Proteins: Deaminated and enter respiration at various points.
Fats: Yield more ATP per gram than carbohydrates.
Anabolic Pathways: Use intermediates to build macromolecules, diverting resources from ATP production.
Summary Table: ATP Yield from Cellular Respiration
Stage | ATP Produced (per glucose) |
|---|---|
Glycolysis | 2 |
Citric Acid Cycle | 2 |
Oxidative Phosphorylation | 26–28 |
Total | 30–32 |
Additional info: The exact ATP yield varies due to differences in shuttle mechanisms and proton leak across the mitochondrial membrane.