AQA A-Level Biology Paper 1, June 2024: Question 10

15 marks · Medium difficulty · Extended Answer

Describe and explain cell fractionation and ultracentrifugation for obtaining nuclei, the role of organelles in enzyme production, and the structure and metabolism of ATP.

Practise this question

Question

Three structured questions. Question 10.1 asks to describe and explain how to use cell fractionation and ultracentrifugation to obtain a sample of nuclei from muscle tissue, worth 6 marks. Question 10.2 asks to describe the role of organelles in the production and release of enzymes by animal cells, excluding transcription, worth 5 marks. Question 10.3 asks to describe the structure of ATP and outline how named enzymes break down and resynthesise ATP, worth 4 marks.
Question text

10.1 Describe and explain how you would use cell fractionation and ultracentrifugation to

obtain a sample of nuclei from muscle tissue.

[6 marks]

10.2 Describe the role of organelles in the production and release of enzymes by

animal cells.

Do not include details of transcription in your answer.

[5 marks]

10.3 Describe the structure of ATP.

Outline how named enzymes break down and resynthesise ATP.

[4 marks]

Mark scheme

Show the mark scheme A mark scheme table containing three rows corresponding to questions 10.1, 10.2, and 10.3 with detailed marking guidance, marks, and comments.

Question Marking Guidance Mark Comments

1. Homogenise (tissue) to break open cells 1. Accept blend OR

grind OR chop for

OR

homogenise

Homogenise (tissue) to release

organelles/nuclei;

2. Filter to remove (intact) tissue/cells/debris;

3. Accept ‘slow down’

3. Cold (solution) to prevent enzyme activity;

for prevent

4. (Solution with) equivalent water potential to

4. Accept isotonic for

prevent osmosis

6 ‘equivalent water

10.1 OR potential’

(6 x

(Solution with) equivalent water potential to AO1) 4. Reject if reference

prevent organelles bursting/shrinking; is made to cells

5. Buffered (solution) to stop enzymes/protein

denaturing;

6. Centrifuge/spin at low(er) speed so nuclei in

6. Accept up to 1000

pellet/move to bottom –1

revolutions min OR

OR 1000 × gravity for

Centrifuge at low(er) speed and identified slow spin

– A-LEVEL BIOLOGYspeed– –

supernatant/solution discarded;

1. DNA in nucleus codes for enzyme/protein 1. Accept genetic

(production); material/code OR

gene for DNA

2. Ribosomes/rough endoplasmic reticulum

produce enzyme/protein Accept polypeptide

OR for protein/enzyme

Translation on ribosomes/rough endoplasmic 3. Ignore rER/RER

reticulum; only once

3. Rough endoplasmic reticulum

transports/modifies/processes enzymes/protein;

4. Reject produce

4. Mitochondria produce ATP; energy

5 max

5. Golgi apparatus modify/process/ 5. Accept body for

10.2 package/transport enzymes/protein (5 x

apparatus

AO1)

OR

5 Accept ‘adds

Golgi apparatus make/transport glycoprotein lipid/carbohydrate to’

OR for modify

Golgi apparatus forms/releases vesicles; 5. Accept lipoprotein

for glycoprotein

6. Vesicles move (protein) to cell(-surface)

membrane 5 and 6 Accept

OR lysosome for vesicle

Vesicles fuse with cell(-surface) membrane; 6. Accept exocytosis

– A-LEVEL BIOLOGYfor ‘fuse with–– cell

membrane’

1. Ribose, Adenine and 3 phosphates; 1. Accept a labelled

diagram showing

2. ATP to ADP + Pi by ATP hydrolase in hydrolysis

ribose, adenine and 3

(reaction);

phosphates

3. ADP + Pi to ATP by ATP synthase;

1. Accept adenosine

4. (In) condensation (reaction); and 3 phosphates

1. Reject Adenosine

4 and 3 phosphates if

10.3 (4 x ribose/pentose is also

AO1) mentioned

1. Ignore pentose

sugar

2. Accept ATPase for

ATP hydrolase

2. Accept hydrolayse

3. Accept synthayse

How to answer it

Cell Structure, Organelles & ATP

What this question tests

This exam question evaluates your core knowledge of cell fractionation techniques, intracellular protein/enzyme synthesis pathways involving membrane-bound organelles, and the biochemical structure and cycling of ATP. To secure full marks, you must rigorously combine methodological precision (isotonic, buffered, cold solutions) with accurate physiological processes and named enzymatic reactions.

Part 10.1 (6 Marks)

Cell Fractionation and Ultracentrifugation of Muscle Tissue

✅ Correct Marking Points

  • Homogenisation: Blend/grind the tissue to break open cells and release organelles.
  • Filtration: Filter the homogenate to remove large, unbroken tissue/cells and debris.
  • Cold temperature: Keep the solution ice-cold to slow down enzyme activity and prevent self-digestion of organelles.
  • Isotonic water potential: Ensure the solution has an equivalent water potential to prevent osmosis, which would otherwise cause organelles to shrink or burst.
  • Buffered solution: Add a buffer to maintain constant pH and prevent denaturation of enzymes and proteins.
  • Initial centrifugation: Centrifuge at a slow/low speed so that the heaviest organelle (nuclei) forms a pellet at the bottom.

💡 Key Knowledge

Cell fractionation isolates specific organelles based on density. The sequence of pelleting typically starts with nuclei (densest), followed by mitochondria/chloroplasts, and finally ribosomes/vesicles. Remember the golden trio of solution conditions: Cold, Buffered, Isotonic.

🧠 Exam Technique

Always state why a condition is used, not just what it is. Examiners look for the paired descriptive and explanatory statement (e.g., "cold to prevent enzyme activity"). Saying "isotonic to cells" is penalised because the cells are already broken; phrase it as "isotonic to prevent organelles bursting/shrinking."

❌ Common Errors

  • Stating "cold to kill enzymes" (enzymes are not living organisms; use "slow down enzyme activity").
  • Confusing water potential with concentration terms.
  • Forgetting to mention filtration before ultracentrifugation.
Total: 6 marks (6 × AO1)
Part 10.2 (5 Marks Max)

Production and Release of Enzymes by Animal Cells

✅ Correct Marking Points

  • DNA role: DNA in the nucleus contains the genetic code / base sequence for the enzyme/protein.
  • Ribosomes / RER: Ribosomes or rough endoplasmic reticulum translate the code to produce the protein/enzyme polypeptide chain.
  • RER processing: The rough endoplasmic reticulum transports and modifies/processes the newly synthesized enzymes.
  • Mitochondria: Mitochondria supply ATP required for protein synthesis, transport, and vesicle movement.
  • Golgi apparatus: Golgi apparatus further modifies, packages, and sorts the enzymes into transport vesicles (or forms glycoproteins).
  • Exocytosis: Vesicles fuse with the cell-surface membrane to release the enzymes out of the cell.

💡 Key Knowledge

Trace the secretory pathway sequentially: Nucleus ➔ RER ➔ Golgi ➔ Vesicle ➔ Cell Membrane. Never state that mitochondria "produce energy" (violates conservation of energy rules); instead, state they "produce ATP" or "release energy via aerobic respiration."

🧠 Exam Technique

The question explicitly states: "Do not include details of transcription in your answer." Avoid wasting time writing about mRNA synthesis or RNA polymerase; start directly from the genetic code instructing translation or ribosome function to secure immediate credit.

❌ Common Errors

  • Including detailed transcription steps which gain zero credit and risk contradictions.
  • Writing "RER makes energy" instead of producing proteins.
  • Forgetting the final fusion of vesicles with the cell membrane (exocytosis).
Total: 5 marks max (5 × AO1)
Part 10.3 (4 Marks)

Structure of ATP and Enzymatic Cycling

✅ Correct Marking Points

  • Chemical components: ATP is composed of a ribose sugar, an adenine organic base, and 3 phosphate groups.
  • Breakdown: ATP is broken down into ADP and an inorganic phosphate ( Pi ) via a hydrolysis reaction catalysed by ATP hydrolase (or ATPase).
  • Resynthesis: ADP and an inorganic phosphate ( Pi ) are joined to resynthesise ATP catalysed by ATP synthase .
  • Reaction type: Resynthesis of ATP occurs via a condensation reaction.

💡 Key Knowledge

ATP stands for Adenosine Triphosphate. The bond between the final phosphate groups is unstable and easily broken, releasing a manageable parcel of energy. The enzyme names directly reflect their actions: hydrolase breaks bonds using water, synthase synthesises molecules.

🧠 Exam Technique

When describing ATP structure, make sure to name all three constituent molecules explicitly (ribose, adenine, 3 phosphates). Do not confuse ribose with deoxyribose. Always link breakdown and synthesis to their specific enzymes and reaction types to guarantee full marks.

❌ Common Errors

  • Writing "deoxyribose" instead of "ribose" (DNA vs RNA sugar confusion).
  • Omitting the word "inorganic" when referring to phosphate ( Pi ).
  • Mixing up the enzymes (attributing condensation to ATP hydrolase).
Total: 4 marks (4 × AO1)

Topics

Biology · 3.1 Biological molecules · 3.2 Cells

Question and mark scheme from the AQA A-Level Biology examination, Paper 1, June 2024. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.