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This lesson completes the detailed tour of eukaryotic organelles by examining chloroplasts (the site of photosynthesis in plants and algae), the plasma membrane, and the centrioles. These structures are vital for energy capture, controlled exchange with the environment, and cell division. You should be able to describe each in precise ultrastructural terms and link structure to function, as required by OCR 2.1.1 (e)(iii).
Chloroplasts are the site of photosynthesis in plants and algae. They are typically 2–10 µm long and shaped like flattened discs (biconvex lenses). A typical plant mesophyll cell contains 20–100 chloroplasts, which move within the cell to optimise light capture.
Embedded in the thylakoid membranes are the photosystems (PS I and PS II), each containing chlorophyll a, chlorophyll b, carotenes, and xanthophylls. Chlorophyll absorbs light energy, which drives the excitation of electrons and ultimately the synthesis of ATP and reduced NADP.
Chloroplasts share several features with mitochondria, both being thought to have originated from prokaryotic endosymbionts:
| Feature | Mitochondria | Chloroplasts |
|---|---|---|
| Number of membranes | Double | Double (plus thylakoid system) |
| Internal folded membrane | Cristae | Thylakoids arranged in grana |
| DNA | Circular, own | Circular, own |
| Ribosomes | 70S | 70S |
| Role | Respiration (ATP production) | Photosynthesis (glucose production) |
| Distribution | Nearly all eukaryotes | Plants, algae, some protists |
Exam Tip: When answering questions about chloroplast structure and photosynthesis, always distinguish between the light-dependent reactions (on thylakoid membranes) and the light-independent reactions / Calvin cycle (in the stroma). Locate each stage precisely in the organelle.
Every eukaryotic cell is bounded by a plasma membrane — a phospholipid bilayer with embedded proteins acting as a selectively permeable boundary. It is 7–10 nm thick and typically appears as a thin line under light microscopy, or as a trilaminar "railway track" structure under TEM.
The accepted model of membrane structure is the fluid mosaic model proposed by Singer and Nicolson in 1972:
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