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Spec Mapping — OCR H420 Module 2.1.1 — Cell structure, content statements requiring the comparison of plant and animal cells and a description of the structures unique to plant cells (cellulose cell wall, large permanent vacuole, plasmodesmata, plastids) (refer to the official OCR H420 specification document for exact wording). This lesson is the structural foundation for the transport-in-plants content in Module 3.1 (xylem, phloem, symplast/apoplast pathways) and recurs synoptically throughout the spec.
In addition to the organelles shared with animal cells, plant cells have features that reflect their sessile, autotrophic lifestyle: the cell wall, the large permanent vacuole, plasmodesmata, and chloroplasts (covered in detail in the previous lesson). This lesson focuses on plant-specific structures and systematically compares plant cells with animal cells.
The historical paradigm of the plant cell as a "walled cell" goes back to Robert Hooke (1665), who chose the word "cell" because the walled compartments he saw in cork reminded him of monks' cells in a monastery — Hooke was observing dead cell walls, not living cytoplasm. The discovery that cells communicate through plasmodesmata is a more recent story, dating from Eduard Tangl (1879) who first showed cytoplasmic threads connecting adjacent cell cytoplasms — overturning the textbook view that cells were sealed off from one another.
The diagram highlights the four uniquely plant features: the rigid cellulose cell wall outside each plasma membrane, the middle lamella of pectin gluing adjacent cells together, the plasmodesmata (purple connections) running through the wall and joining the two cytoplasms into a symplastic continuum, and the large permanent vacuole with its own bounding tonoplast membrane.
The plant cell wall is a rigid layer found outside the plasma membrane. It is secreted by the cell itself, principally by the Golgi apparatus. The primary wall of a growing plant cell is largely composed of cellulose, a polymer of β-glucose, along with hemicelluloses, pectins, and some structural proteins. In tissues that have finished expanding, a secondary cell wall may be laid down inside the primary wall, often containing lignin, which provides additional rigidity and waterproofing.
The middle lamella is a thin layer of calcium and magnesium pectates that cements adjacent plant cells together. It is the first layer deposited between daughter cells after cytokinesis and lies between the primary walls of neighbouring cells.
While animal cells have small, temporary vacuoles, plant cells have a single, large permanent vacuole that can occupy up to 90% of the cell volume in mature cells. The vacuole is bounded by a specialised single membrane called the tonoplast.
Exam Tip: A common question asks why a plant cell bursts in very hypotonic solutions only to a limited extent. Answer: the cell wall resists expansion, so although the cell becomes fully turgid, it does not burst as an animal cell would. The wall provides the pressure that balances the osmotic pull.
Plant cells are connected to their neighbours by cytoplasmic channels called plasmodesmata (singular: plasmodesma). They pass through the cell wall at specific pit fields and link the cytoplasm of adjacent cells.
| Feature | Plant cell | Animal cell |
|---|---|---|
| Cell wall | Present (cellulose) | Absent |
| Plasma membrane | Present | Present |
| Nucleus | Present | Present |
| Mitochondria | Present | Present |
| RER and SER | Present | Present |
| Golgi apparatus | Present | Present |
| Ribosomes (80S) | Present | Present |
| Lysosomes | Usually absent (vacuole performs similar roles) | Present |
| Chloroplasts | Present (in photosynthetic tissues) | Absent |
| Large permanent vacuole | Present | Absent (small temporary vacuoles only) |
| Tonoplast | Present | Absent |
| Centrioles | Absent (in higher plants) | Present |
| Plasmodesmata | Present | Absent |
| Storage carbohydrate | Starch in amyloplasts | Glycogen granules |
| Cell shape | Usually fixed, polygonal | Usually variable, often rounded |
Exam Tip: When writing about plant vs animal cells, go beyond a bullet list. Explain why each unique feature exists in terms of the plant lifestyle: cellulose wall and turgor for support without a skeleton; chloroplasts for autotrophic nutrition; large vacuole for solute storage and turgor; plasmodesmata for intercellular communication in an immobile body.
Water and dissolved substances can move through plant tissue by two routes — a directly synoptic link to Module 3.1 (transport in plants).
The existence of plasmodesmata is therefore not a curiosity — it is what makes the symplast pathway possible and gives plant cells the option of intercellular communication and bulk-solute movement without exporting and re-importing across membranes.
A summary table at quantitative depth distinguishes A* candidates from A:
| Feature | Plant cell | Animal cell |
|---|---|---|
| Typical size | 10–100 µm | 10–30 µm |
| Cell wall | Cellulose (10 nm microfibrils, multiple lamellae) | Absent |
| Plasma membrane | Phospholipid bilayer + proteins; no cholesterol | Phospholipid bilayer + proteins + cholesterol (~20 mol% of lipids) |
| Vacuole | Single, large, permanent (up to 90% of cell volume) | Small, temporary, multiple |
| Chloroplasts | Present in photosynthetic cells (20–100 per mesophyll cell) | Absent |
| Plasmodesmata | Present (~10⁶ per cm² of cell wall) | Absent (but gap junctions provide a functional analogue) |
| Centrioles | Absent in higher plants | Present (pair at the centrosome) |
| Storage carbohydrate | Starch in amyloplasts | Glycogen granules in cytoplasm / liver |
| Cell shape | Usually fixed, polygonal | Usually variable, often rounded; held by cytoskeleton |
| Cytokinesis | Cell plate forms in the middle (vesicles fuse) | Contractile ring of actin-myosin pinches inwards |
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