Cell Structure and Ultrastructure

Master organelles, electron microscopy, prokaryotic vs eukaryotic cells, and cell fractionation for A-Level Biology.

# Cell Structure and Ultrastructure

A-Level Biology requires detailed knowledge of cell organelles, their ultrastructure as revealed by electron microscopy, and techniques for studying cells.


1. Eukaryotic Cell Organelles

Organelle Structure Function
Nucleus Double membrane (nuclear envelope) with pores; contains chromatin/chromosomes Houses DNA; controls cell activity
Nucleolus Dense region within nucleus Produces rRNA and assembles ribosomes
Rough ER Membrane-bound sacs with ribosomes Protein synthesis and transport
Smooth ER Membrane-bound sacs without ribosomes Lipid synthesis; detoxification
Golgi apparatus Stack of flattened membrane sacs Modifies, packages, and secretes proteins
Mitochondria Double membrane; inner membrane folded into cristae; matrix Aerobic respiration; ATP production
Chloroplasts Double membrane; thylakoids (grana); stroma Photosynthesis (plants only)
Lysosomes Membrane-bound vesicles with hydrolytic enzymes Digestion of unwanted material
Ribosomes Two subunits (large + small); 80S (eukaryotic), 70S (prokaryotic) Protein synthesis
Centrioles Cylindrical; made of microtubules Spindle formation during cell division
Cell membrane Phospholipid bilayer with proteins Controls entry/exit of substances

2. Prokaryotic vs Eukaryotic

Feature Prokaryotic Eukaryotic
Size 1-5 μm 10-100 μm
DNA Circular; in nucleoid Linear; in nucleus
Ribosomes 70S 80S
Membrane-bound organelles No Yes
Cell wall Peptidoglycan Cellulose (plants) / chitin (fungi)
Plasmids Yes Rarely

3. Microscopy

Magnification=Image sizeActual size\text{Magnification} = \frac{\text{Image size}}{\text{Actual size}}

Resolution: minimum distance between two distinguishable points.

Microscope Magnification Resolution
Light ×1500 200 nm
TEM ×500,000 0.5 nm
SEM ×100,000 3-10 nm

4. Cell Fractionation

  1. Homogenisation: break cells open in cold, isotonic, buffered solution
  2. Filtration: remove debris
  3. Differential centrifugation: spin at increasing speeds; heaviest organelles sediment first (nuclei → mitochondria → ER → ribosomes)

5. Practice Questions

    1. Describe the structure and function of the Golgi apparatus.
    1. Compare rough and smooth ER.
    1. Why must the homogenisation solution be cold, isotonic, and buffered?
    1. Explain why mitochondria sediment before ribosomes.
    1. Compare prokaryotic and eukaryotic cells.

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Summary

  • Eukaryotic: membrane-bound organelles; 80S ribosomes; linear DNA in nucleus
  • Prokaryotic: no membrane-bound organelles; 70S ribosomes; circular DNA
  • Electron microscopy: higher resolution than light microscopy
  • Cell fractionation: homogenise → filter → differential centrifugation

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