Describe the features of adenosine‑triphosphate (ATP) that make it a universal energy currency in living cells, explain how ATP is synthesised, and relate its role to the energy requirements of cellular processes (Cambridge AS & A Level Biology 9700, 2025‑27).
1. Structure of ATP
Adenine – nitrogenous base.
Ribose – five‑carbon sugar.
Three phosphate groups (α, β, γ) linked by phosphoanhydride bonds (P–O–P).
Suggested diagram: schematic of ATP showing adenine, ribose, and the three phosphate groups (α, β, γ).
A “high‑energy phosphate bond” is a phosphoanhydride bond whose hydrolysis releases a large amount of free energy because:
Electrostatic repulsion: each phosphate carries a –2 charge; the close proximity creates strong repulsive forces that destabilise the bond.
Resonance stabilisation of the products: after hydrolysis the inorganic phosphate (Pi) and ADP are resonance‑stabilised, lowering the energy of the products.
Increase in entropy: one molecule is converted into two, increasing disorder and favouring the reaction.
Standard free‑energy change (ΔG°′) ≈ –30.5 kJ mol⁻¹ under standard conditions.
In the cellular environment (high [ATP], low [ADP] and [Pi]) the actual ΔG is more negative, ≈ –50 kJ mol⁻¹, providing a larger usable energy pool.
Hydrolysis of the terminal (γ) phosphate releases the greatest amount of energy; a second hydrolysis (ADP → AMP) can supply additional energy when required.
4. ATP Turnover in the Cell
Typical cellular concentration: 2–5 mM (≈10⁹ molecules per cell).
Turnover rate: a cell can hydrose and regenerate its ATP pool every <10–30 s, i.e. 10⁴–10⁶ ATP molecules are turned over each second.
5. Synthesis of ATP – Syllabus Pathways (AO2)
5.1 Substrate‑level phosphorylation
Direct transfer of a phosphate group from a high‑energy metabolic intermediate to ADP.
Key syllabus reactions:
Phosphoglycerate kinase (glycolysis) – produces 1 ATP per glucose.
Succinyl‑CoA synthetase (citric‑acid cycle) – produces 1 GTP ≈ 1 ATP per turn of the cycle.
Energy from electron transport creates a proton motive force (PMF) across a membrane.
ATP synthase uses the flow of protons back across the membrane to drive synthesis of ATP from ADP + Pi.
Exact syllabus references:
ATP synthase in the mitochondrial inner membrane – oxidative phosphorylation.
ATP synthase in the chloroplast thylakoid membrane – photophosphorylation.
6. Linking ATP Turnover to Cellular Energy Demands (exam‑style examples)
ATP provides the immediate energy needed for three exemplar processes listed in the syllabus:
Active transport – e.g. Na⁺/K⁺‑ATPase pumps ions against their gradients.
Mechanical work – e.g. myosin‑ATPase in muscle contraction; flagellar rotation.
Anabolic reactions – e.g. DNA polymerase, ribosomal protein synthesis, and biosynthesis of macromolecules.
In each case the exergonic hydrolysis of ATP is coupled to an endergonic process, allowing the overall reaction to proceed spontaneously.
7. Energy Yield from the Three Macronutrients
Macronutrient
Typical oxidation (kJ mol⁻¹)
Approx. ATP produced per gram
Comments
Carbohydrate (glucose)
~2 800 kJ mol⁻¹
≈ 3.6 mol ATP g⁻¹
Complete oxidation via glycolysis, TCA cycle and oxidative phosphorylation.
Lipid (palmitate, C₁₆:₀)
~9 800 kJ mol⁻¹
≈ 9.6 mol ATP g⁻¹
β‑oxidation yields many acetyl‑CoA units; highest ATP per gram.
Protein (average amino‑acid mixture)
~4 200 kJ mol⁻¹
≈ 4.5 mol ATP g⁻¹
Deamination and entry of carbon skeletons into the TCA cycle.
These values explain why lipids are the most energy‑dense food source, while carbohydrates provide a rapid supply of ATP.
8. Features that Make ATP a Universal Energy Currency (ordered as in the syllabus)
Small, water‑soluble molecule – diffuses easily throughout the cytosol and organelles.
Rapid turnover and high cellular concentration – guarantees an immediate supply of energy.
Standardised energy unit – the ΔG of hydrolysis (≈ –30 kJ mol⁻¹) provides a common reference for comparing the energy demands of different reactions.
Reversible interconversion – ATP ↔ ADP + Pi can be driven forward or backward depending on cellular needs.
Universal presence – the same molecule is used by bacteria, archaea and eukaryotes, making it a true “currency”.
Specific binding sites on enzymes – conserved ATP‑binding motifs in kinases, ATPases and motor proteins ensure precise energy transfer.
9. Comparison with Other Energy Carriers (within the context of an energy currency)
Carrier
Advantages as an energy source
Why it is not the universal currency
GTP (guanosine‑triphosphate)
Similar high‑energy phosphoanhydride bonds; used in protein synthesis and signalling.
Lower cellular concentration and specialised roles rather than a general energy pool.
Creatine phosphate (muscle)
Very rapid release of phosphate to regenerate ATP.
Limited stores, tissue‑specific, not present in all cell types.
Proton motive force (PMF)
Directly drives ATP synthase; stores large amounts of free energy.
Membrane‑bound, not a soluble molecule; must be converted to ATP for most cellular work.
10. Summary
ATP’s simple yet versatile structure, the high‑energy phosphoanhydride bonds, rapid synthesis through substrate‑level and chemiosmotic phosphorylation, and its ubiquitous presence across all domains of life make it the ideal universal energy currency. By providing a standard, readily interchangeable source of free energy, ATP links the catabolic breakdown of carbohydrates, lipids and proteins to the diverse endergonic processes that sustain life.
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