Difficulty: Medium
Correct Answer: Because no such phosphate donor exists in oxidative phosphorylation
Explanation:
Introduction / Context:
ATP can be produced by substrate-level phosphorylation (for example, from 1,3-bisphosphoglycerate in glycolysis) or by oxidative phosphorylation in mitochondria. This question probes why an analogous small-molecule “high-energy phosphate donor” has never been isolated from mitochondria.
Given Data / Assumptions:
Concept / Approach:
Peter Mitchell’s chemiosmotic theory explains that electron transport chains pump protons, building a gradient (Δp). ATP synthase harnesses this gradient to synthesize ATP. There is no requirement for a soluble “high-energy phosphate” intermediate analogous to glycolytic donors.
Step-by-Step Solution:
Contrast mechanisms: substrate-level phosphorylation uses a high-energy intermediate; oxidative phosphorylation uses a transmembrane gradient.
Identify mitochondrial catalyst: F1F0-ATP synthase converts electrochemical energy directly into the phosphoanhydride bond.
Therefore, no isolatable small-molecule phosphate donor exists in mitochondria.
Select the option stating nonexistence rather than technical failure.
Verification / Alternative check:
Reconstitution experiments show ATP synthesis when purified ATP synthase is embedded in liposomes with a proton gradient, confirming the gradient is the “donor.”
Why Other Options Are Wrong:
Technique limitations (a) are not the reason; “too short-lived” (c) misstates the mechanism; (d) is false—mitochondria make most ATP aerobically; (e) has no support.
Common Pitfalls:
Assuming every ATP synthesis pathway requires a discrete phosphorylated metabolite.
Final Answer:
Because no such phosphate donor exists in oxidative phosphorylation.
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