Biology - Cell Biology
1. Cell Structure
Prokaryotic vs Eukaryotic Cells
| Feature | Prokaryotic Cells | Eukaryotic Cells |
|---|---|---|
| Nucleus | No true nucleus; nucleoid region | True nucleus with nuclear envelope |
| Size | 0.5–5 m | 10–100 m |
| Membrane-bound organelles | Absent | Present (mitochondria, ER, Golgi etc.) |
| DNA | Circular, naked (no histones) | Linear, associated with histones |
| Ribosomes | 70S (smaller) | 80S (larger) |
| Cell wall | Peptidoglycan (bacteria) | Cellulose (plants); none (animals) |
| Examples | Bacteria, archaea | Animals, plants, fungi, protists |
Plant vs Animal Cells
| Feature | Plant Cells | Animal Cells |
|---|---|---|
| Cell wall | Yes (cellulose) | No |
| Chloroplasts | Yes (for photosynthesis) | No |
| Large vacuole | Yes (permanent, central) | Small, temporary (if any) |
| Centrioles | Absent (except in lower plants) | Present |
| Stored carbohydrates | Starch | Glycogen |
2. Organelles
| Organelle | Structure | Function |
|---|---|---|
| Nucleus | Double membrane with nuclear pores | Contains DNA; controls cell activities via gene expression |
| Mitochondria | Double membrane; inner folded into cristae | Site of aerobic respiration (ATP production via Krebs cycle and oxidative phosphorylation) |
| Rough ER | Flattened sacs with ribosomes | Protein synthesis and transport |
| Smooth ER | Flattened sacs without ribosomes | Lipid synthesis; detoxification |
| Golgi apparatus | Stacked, flattened sacs (cisternae) | Modifies, packages, and sorts proteins/lipids for secretion |
| Ribosomes | Small organelles (80S in cytoplasm; 70S in mitochondria/chloroplasts) | Protein synthesis (translation) |
| Lysosomes | Membrane-bound vesicles | Contain digestive enzymes for intracellular digestion |
| Chloroplasts | Double membrane; thylakoids in grana | Site of photosynthesis (light-dependent + light-independent reactions) |
| Cell wall | Rigid layer of cellulose microfibrils | Provides structural support; prevents osmotic lysis |
| Vacuole | Membrane-bound (tonoplast) | Storage; maintains turgor pressure |
| Centrioles | Pair of cylindrical structures | Organise spindle fibres during cell division |
| Cell membrane | Phospholipid bilayer | Controls entry/exit of substances; cell recognition |
3. Microscopy
Light Microscopy
- Uses visible light; magnification up to
- Resolution: — limited by wavelength of light
- Can observe live specimens
- Staining (e.g. iodine for starch, methylene blue for nuclei) increases contrast
Electron Microscopy
- Uses electron beam (shorter wavelength than light)
- Transmission EM (TEM): thin sections; internal detail; up to
- Scanning EM (SEM): 3D surface images
- Resolution: — can see organelles, viruses, large molecules
- Specimens must be fixed, dehydrated, and placed in a vacuum (dead specimens only)
Magnification and Scale
4. Cell Membrane — The Fluid Mosaic Model
Structure
- Phospholipid bilayer: hydrophilic heads face outward, hydrophobic tails face inward
- Proteins: embedded (intrinsic/integral) or attached to surface (extrinsic/peripheral)
- Cholesterol: between phospholipid tails, regulates fluidity
- Glycoproteins/glycolipids: carbohydrate chains on the outer surface for cell recognition
Fluid: phospholipids and proteins can move laterally within the bilayer Mosaic: pattern of different proteins scattered like tiles
Functions of Cell Membrane
- Partially permeable barrier
- Cell-cell recognition (glycoproteins)
- Receptor sites for hormones and neurotransmitters
- Enzyme surfaces (e.g. ATP synthase on inner mitochondrial membrane)
5. Transport Across Membranes
Passive Transport (no ATP required)
| Mechanism | Definition | Direction | Depends On |
|---|---|---|---|
| Simple diffusion | Net movement from high to low concentration | High → low | Concentration gradient |
| Facilitated diffusion | Movement via protein channels or carriers | High → low | Channel/carrier proteins |
| Osmosis | Diffusion of water across a partially permeable membrane | High water potential → low water potential | Water potential gradient |
Water potential ():
- Pure water:
- Solutions: (more negative = more concentrated)
- Water moves from less negative to more negative water potential
Turgor pressure: pressure exerted by cell contents pressing against the cell wall in plant cells.
- Turgid: cell fully swollen with water (normal, healthy state for plants)
- Plasmolysed: cell membrane pulls away from cell wall (in concentrated solution)
Active Transport (ATP required)
- Movement against the concentration gradient (low → high)
- Requires carrier proteins and energy from ATP hydrolysis
- Example: absorption of mineral ions by root hair cells; sodium-potassium pump
Bulk Transport
- Endocytosis: membrane engulfs material to bring it in (phagocytosis for solids, pinocytosis for liquids)
- Exocytosis: vesicles fuse with membrane to release contents (e.g. secretion of hormones, enzymes)
6. Cell Division
Mitosis
Purpose: growth, repair, asexual reproduction; produces 2 genetically identical diploid cells
| Phase | Key Events |
|---|---|
| Interphase (G1, S, G2) | DNA replicates; organelles duplicate; cell grows |
| Prophase | Chromosomes condense; nuclear envelope breaks down; spindle fibres form |
| Metaphase | Chromosomes align at the equator (metaphase plate); attached to spindle |
| Anaphase | Sister chromatids separate; pulled to opposite poles by spindle fibres |
| Telophase | Chromosomes decondense; nuclear envelopes reform; cytokinesis begins |
Result: (diploid → diploid)
Meiosis
Purpose: production of gametes (sex cells); produces 4 genetically unique haploid cells
| Stage | Key Events |
|---|---|
| Meiosis I | Homologous chromosomes pair (bivalents); crossing over occurs (prophase I); homologous chromosomes separate (anaphase I) |
| Meiosis II | Sister chromatids separate (similar to mitosis but starting with half the chromosome number) |
Result: (diploid → haploid)
Significance of Meiosis
Genetic variation through:
- Crossing over (recombination) during prophase I — new combinations of alleles
- Independent assortment — random alignment of homologous chromosomes at metaphase I
- Random fertilisation — fusion of any sperm with any egg
Halving chromosome number so that fertilisation restores the diploid number
Mitosis vs Meiosis
| Feature | Mitosis | Meiosis |
|---|---|---|
| Divisions | 1 | 2 |
| Daughter cells | 2 | 4 |
| Chromosome number | Same (2n) | Halved (n) |
| Genetic variation | No | Yes (crossing over, independent assortment) |
| Function | Growth, repair | Gamete production |
| Where | Somatic cells | Germ cells (gonads) |
Worked Examples
Example 1: Calculating Actual Size from a Micrograph
Problem: A cell in a light micrograph measures 45 mm across. The magnification is . Calculate the actual size of the cell in m. Solution:
Example 2: Distinguishing Mitosis and Meiosis
Problem: A cell has 46 chromosomes and undergoes division. After division, each daughter cell has 23 chromosomes. Was this mitosis or meiosis? Explain. Solution: This was meiosis. Mitosis produces daughter cells with the same chromosome number as the parent (diploid to diploid). The halving from 46 to 23 (diploid to haploid) is characteristic of meiosis, which produces gametes.
Common Pitfalls
- Confusing resolution and magnification: Magnification enlarges the image; resolution determines the clarity of detail. Electron microscopes have higher resolution (not just higher magnification) than light microscopes.
- Mixing up osmosis direction: Water moves from less negative water potential to more negative water potential (high water concentration to low), not the other way around.
- Stating mitosis produces “identical cells” without qualification: Mitosis produces genetically identical cells only in ideal conditions. DNA mutations can introduce variation.
Summary
Cell biology covers the structure and function of prokaryotic and eukaryotic cells, including organelle functions, the fluid mosaic model of cell membranes, transport mechanisms (passive, active, bulk), and cell division (mitosis and meiosis). Microscopy techniques (light and electron) and the ability to calculate actual size from magnification are essential practical skills for the DSE exam.