[3.5.2] Respiration Flashcards

1
Q

Why is respiration important?

A
  • Respiration produces ATP (to release energy).
  • For active transport, protein synthesis etc.
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2
Q

Summarise the stages of aerobic and anaerobic respiration.

A

Aerobic Respiration

  1. Glycolysis - cytoplasm (anaerobic).
  2. Link reaction - mitochondrial matrix.
  3. Krebs cycle - mitochondrial matrix.
  4. Oxidation phosphorylation - inner mitochondrial matrix.

Anaerobic Respiration

  1. Glycolysis - cytoplasm.
  2. NAD regeneration- cytoplasm.
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3
Q

Describe the process of glycolysis.

A
  1. Glucose phosphorylated to glucose phosphate.
    • Using inorganic phosphates from 2 ATP.
  2. Hydrolysed to 2x triose phosphate.
  3. Oxidised to 2x pyruvate.
    • 2 NAD reduced.
    • 4 ATP regenerated (net gain of 2).
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4
Q

Explain what happens after glycolysis if respiration is anaerobic.

A
  1. Pyruvate converted to lactate (animals & some bacteria) or ethanol (plants & yeast).
  2. Oxidising reduced NAD -> NAD regenerated.
  3. So glycolysis can continue (which needs NAD) allowing continued production of ATP.
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5
Q

Suggest why anaerobic respiration produces less ATP per molecule of glucose than aerobic respiration.

A
  • Only glycolysis invovled which produces little ATP (2 molecules).
  • No oxidative phosphorlyation which forms majority of ATP (around 34 molecules).
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6
Q

What happens after glycolysis if respiration is aerobic?

A
  • Pyruvate is actively transported into the mitochondrial matrix.
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7
Q

Describe the link reaction.

A
  1. Pyruvate oxidised (and decarboxylated) to acetate.
    • CO₂ produced.
    • Reduced NAD produced (picks up H).
  2. Acetate combined with coenzyme A, forming Acetyl Coenzyme A.
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8
Q

Describe the Krebs cycle.

A
  1. Acetyl coenzyme A reacts with a 4C molecule.
    • Releasing coenzyme A
    • Producing a 6C molecule that enters the Krebs cycle.
  2. In a series of oxidation-reduction reactions, the 4C molecule is regenerated and:
    • 2x CO₂ lost.
    • Coenzymes NAD & FAD reduced.
    • Substrate level phosphorylation (direct transfer of Pi from intermediate compound to ADP) which produces ATP.
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9
Q

Describe the process of oxidative phosphorylation.

A
  1. Reduced NAD/FAD oxidised to release H atoms -> split into protons (H⁺) and electrons (e⁻).
  2. Electrons transferred down electron transfer chain (chain of carriers at decreasing energy levels).
    • By redox reactions.
  3. Energy released by electrons used in the production of ATP from ADP + Pi (chemiosmotic theory):
    • Energy used by electron carriers to actively pump protons from matrix -> intermembrane space.
    • Protons diffuse into matrix down an electrochemical gradient, via ATP synthase (embedded).
    • Releasing energy to synthesise ATP from ADP + Pi.
  4. In matrix at the end of electron transfer chain, oxygen is the final electron acceptor (electrons can’t pass along otherwise).
    • So protons, electrons and oxygen combine to form water.
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10
Q

Give examples of other respiratory substrates.

A
  • Breakdown of products of lipids and amino acids, which enter the Krebs cycle. For example:
    • Fatty acids from hydrolysis of lipids -> converted to Acetyl Coenzyme A.
    • Amino acids from hydrolysis of proteins -> converted to intermediates in Krebs cycle.
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