ATP as a battery and its synthesis Flashcards

1
Q

Why is ATP often referred to as a ‘battery’ in cells

A

ATP stores energy from catabolism or photosynthesis and releases it to power biosynthetic reactions. It acts like a rechargeable battery—charged by energy-yielding processes and discharged to drive cellular work.

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2
Q

Why is ATP a useful energy carrier in cells

A

ATP → ADP + Pi has a high equilibrium constant (Keq), proceeds spontaneously, and releases significant free energy. This makes it ideal for coupling to thermodynamically unfavorable reactions.

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3
Q

What is the typical [ATP]:[ADP] ratio in cells and why is it important

A

About 3:1. This keeps ATP far from equilibrium, ensuring it remains a high-energy molecule ready to drive cellular processes.

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4
Q

Why is ATP described as thermodynamically unstable but kinetically stable

A

While ATP hydrolysis is energetically favourable, it does not occur spontaneously without enzymes - allowing the cell to tightly regulate when and where energy is released.

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5
Q

What is substrate-level phosphorylation

A

A process where ATP is synthesized by directly transferring a phosphate group from a high-energy intermediate to ADP, often during glycolysis or fermentation.

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6
Q

How does glycolysis contribute to ATP production

A

Glycolysis breaks glucose into pyruvate, forming a doubly phosphorylated sugar that splits and donates phosphate groups to ADP via substrate-level phosphorylation, yielding 2 ATP per glucose.

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7
Q

What role does fermentation play in ATP production

A

In the absence of oxygen, fermentation regenerates NAD⁺, allowing glycolysis to continue producing ATP through substrate-level phosphorylation.

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8
Q

What is oxidative phosphorylation

A

A process where ATP is synthesized using a proton gradient generated by the electron transport chain (ETC), powered by electrons from NADH and FADH₂ produced in the TCA cycle.

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9
Q

How does the TCA cycle support ATP production

A

It oxidizes pyruvate to produce NADH and FADH₂, which donate electrons to the ETC, leading to proton pumping and ATP synthesis via ATP synthase.

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10
Q

What is the role of oxygen in oxidative phosphorylation

A

Oxygen is the terminal electron acceptor in the ETC. It accepts electrons and is reduced to water - preventing toxic accumulation of electrons.

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11
Q

What happens as electrons pass through the ETC

A

Each complex is reduced and oxidized, passing electrons along the chain and using the released energy to pump protons from the cytoplasm to the periplasmic space.

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12
Q

How does Complex I contribute to the proton gradient

A

It transfers electrons from NADH to ubiquinone, releasing free energy that drives conformational changes. This opens proton channels that pump H⁺ across the membrane.

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13
Q

What determines whether a compound is an electron donor or acceptor in the ETC

A

Reduction potential: more negative compounds like NADH donate electrons, while more positive ones like O₂ accept them.

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14
Q

How does the proton gradient drive ATP synthesis

A

Proton flow rotates the ATP synthase complex, causing conformational changes (open, loose, tight states) that bind ADP + Pi and synthesize ATP.

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15
Q

What are the open, loose, and tight states in ATP synthase

A

Open: ADP + Pi bind. Loose: H⁺ flow causes partial closing. Tight: rotation causes spontaneous ATP formation. These states rotate with the rotor’s movement.

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16
Q

Why is oxidative phosphorylation preferred over substrate-level phosphorylation (Reason 1)

A

Flexibility - ETC can extract energy from various sources using universal electron carriers. SLP is limited to specific reactions.

17
Q

Why is oxidative phosphorylation preferred over substrate-level phosphorylation (Reason 2)

A

Efficiency - ETC enables maximal energy extraction from carbon sources and efficient NAD⁺ regeneration, boosting ATP yield.

18
Q

What is the likely evolutionary origin of oxidative phosphorylation

A

Carboxylic acids, such as those in the TCA cycle, were likely among the first metabolic molecules to arise spontaneously from CO₂ and H₂, laying the groundwork for electron transport chains.

19
Q

What is the main function of the electron transport chain (ETC) in ATP synthesis

A

The ETC transfers electrons through a series of protein complexes, releasing energy that pumps protons across the membrane, creating an electrochemical gradient used by ATP synthase.

20
Q

What are the four components of the electron transport chain

A

The ETC consists of Complexes I, II, III, and IV, along with electron carriers like ubiquinone and cytochrome c, embedded in the cell membrane.

21
Q

What is the role of ubiquinone (CoQ) in the ETC

A

Ubiquinone shuttles electrons between Complex I (or II) and Complex III and participates in proton pumping via redox-driven conformational changes.

22
Q

How does Complex I use redox energy to move protons

A

It transfers electrons from NADH to ubiquinone, releasing energy that drives piston-like movements and conformational shifts that pump protons across the membrane.

23
Q

How are protons moved through Complex I during ATP generation

A

Conformational changes open proton channels from the cell interior to a central water-filled ‘river’ in the membrane arm, then eject protons to the outside.

24
Q

What is the relationship between redox potential and electron transfer

A

Compounds with low (negative) redox potential like NADH donate electrons to those with high (positive) redox potential like oxygen, releasing free energy.

25
Q

What is the proton-motive force (PMF)

A

PMF is the electrochemical gradient of protons across the membrane, composed of a pH difference and charge separation, which drives ATP synthesis.

26
Q

What protein complex synthesises ATP from the proton gradient

A

ATP synthase, a rotary motor complex, uses the flow of protons through its base to drive conformational changes in its catalytic head, forming ATP from ADP and Pi.

27
Q

What is the rotational catalysis (binding change) mechanism in ATP synthase

A

As protons enter, the base rotates, causing three active sites in the catalytic head to cycle through Open, Loose, and Tight states, enabling ATP formation.

28
Q

What happens during the ‘Open’ state of ATP synthase

A

ADP and inorganic phosphate (Pi) bind to the enzyme’s active site, preparing for ATP formation.

29
Q

What happens during the ‘Loose’ state of ATP synthase

A

ADP and Pi are held in place within the enzyme, positioned for condensation but not yet reacted.

30
Q

What happens during the ‘Tight’ state of ATP synthase

A

The conformational change forces ADP and Pi to combine, forming ATP, which is then released in the next Open state.

31
Q

How does the ETC ensure the continued flow of electrons

A

Electrons flow downhill in energy from NADH/FADH₂ to oxygen, and each redox step releases energy that powers proton pumping.

32
Q

Why is oxygen an effective terminal electron acceptor

A

Oxygen has a high positive redox potential, readily accepts electrons, and is reduced to non-toxic water.

33
Q

Why is water the final product of oxidative phosphorylation

A

Because oxygen accepts electrons at the end of the ETC and combines with protons to form H₂O, preventing harmful electron buildup.

34
Q

Why is oxidative phosphorylation more efficient than substrate-level phosphorylation (SLP)

A

It extracts more energy from carbon substrates and regenerates NAD⁺ more efficiently, producing many more ATP molecules than SLP.

35
Q

What limits the flexibility of substrate-level phosphorylation

A

SLP is tied to specific metabolic reactions and intermediates, limiting its energy-generating capacity and adaptability.

36
Q

What role did carboxylic acids play in the origin of oxidative phosphorylation

A

Carboxylic acids were likely the first metabolites to arise spontaneously from CO₂ and H₂, forming the basis of early metabolic pathways like the TCA cycle.

37
Q

What connects the TCA cycle and ETC in ATP production

A

The TCA cycle generates NADH and FADH₂, which supply high-energy electrons to the ETC for generating a proton gradient and driving ATP synthesis.

38
Q

What is the energetic benefit of displacing ATP synthesis from equilibrium in the cell

A

Maintaining high ATP relative to ADP ensures energy-releasing hydrolysis reactions remain favorable and capable of driving essential cellular processes.