AQA GCSE Biology

Cell Biology

A cell is tiny enough to hide in a full stop, yet organised enough to build a whale.

Meet the structures that keep cells working, watch chromosomes copy and divide, then track substances across membranes. The exam habit throughout is simple: name the structure, state the mechanism, explain the consequence.

  • Compare eukaryotic and prokaryotic cells
  • Turn microscope images into real sizes
  • Choose diffusion, osmosis or active transport
  • 6 illustrated pages
  • Free to read
  • Combined & Separate
  • Foundation & Higher

Your revision route

What you’ll learn

  • Compare eukaryotic and prokaryotic cells and relate sub-cellular structures to their functions.
  • Explain how specialised cells and differentiation support functions in multicellular organisms.
  • Compare light and electron microscopes and calculate magnification, image size and real size.
  • Describe the cell cycle, mitosis, chromosomes and the importance of identical daughter cells.
  • Evaluate medical and plant uses of stem cells, including therapeutic cloning, risks and ethical issues.
  • Explain diffusion, osmosis and active transport using concentration gradients and energy requirements.
  • Relate surface area to volume ratio and exchange-surface adaptations to transport needs.
  • Plan and evaluate microscopy and osmosis practicals safely.
  • For separate Biology, explain microbial culturing, aseptic technique and bacterial-population calculations.

Build the big picture

Key ideas

Two cell plans, one enormous scale gap

A eukaryotic cell stores DNA inside a nucleus; a much smaller prokaryotic cell keeps its DNA loose in the cytoplasm.

  • Animal, plant, algal, fungal and protist cells are eukaryotic: they have a cell membrane, cytoplasm and genetic material enclosed in a nucleus.
  • A bacterial cell is prokaryotic: it has cytoplasm and a membrane inside a cell wall, but no nucleus.
  • Bacterial DNA forms one main loop, and plasmids are smaller DNA rings that may carry extra genes.
  • Typical eukaryotic cells are about 10–100 µm across; a bacterium is roughly 1 µm, so compare sizes with ratios, orders of magnitude and standard form.

The punchline: Classify the cell by where its DNA sits, then compare its size numerically.

A cell is a workshop, not a bag of jelly

Each sub-cellular structure handles a particular piece of the cell's work, from controlling entry to building proteins.

  • The nucleus contains DNA and controls activities; cytoplasm hosts most chemical reactions; the cell membrane controls movement into and out of the cell.
  • Mitochondria are the main site of aerobic respiration, while ribosomes make proteins.
  • Plant cells often also have chloroplasts for photosynthesis, a cellulose wall for strength and a permanent vacuole of cell sap for support.
  • Algal cells are eukaryotic and also have a cellulose cell wall; estimate relative sizes or areas when an exact measurement is unavailable.

The punchline: For every structure, write its precise function—not merely its name.

Specialised cells wear the right equipment

A cell's shape and sub-cellular structures are tuned to the job it performs in a tissue, organ or whole organism.

  • Sperm cells have a tail for swimming, many mitochondria for respiration and an acrosome containing enzymes that help penetrate the egg.
  • Nerve cells have a long fibre and branched endings for rapid connections; muscle cells contain contractile fibres and many mitochondria.
  • Root hair cells have a long extension for absorption; xylem cells form hollow lignified tubes, while phloem cells form living transport tubes.
  • An adaptation earns the mark only when you link structure → mechanism → function.

The punchline: Do not list features: explain how each feature improves the cell's job.

Differentiation turns options into expertise

Cells begin less specialised, then develop different structures so a multicellular organism can divide up its work.

  • As organisms develop, cells differentiate and acquire the sub-cellular structures needed for particular functions.
  • Most animal cells differentiate early; in mature animals, cell division is mainly used for repair and replacement.
  • Many plant cells keep the ability to differentiate throughout life, especially cells in meristems.

The punchline: Differentiation changes cell structure and therefore changes cell function.

Three cells, two fundamental plans

Start with the DNA, then inspect the equipment. Eukaryotic cells use a nucleus; a much smaller bacterium does not.

  • Animal cellEukaryotic: nucleus, cytoplasm, membrane, mitochondria and ribosomes; no cellulose wall or chloroplasts.
  • Plant or algal cellEukaryotic: the shared cell parts plus a cellulose wall; plant cells often also have chloroplasts and a permanent vacuole.
  • Bacterial cellProkaryotic: no nucleus; one main DNA loop and possible plasmids lie in cytoplasm inside a membrane and cell wall.
Classify by DNA location first. Then link each extra structure to the function it enables.

Magnification makes bigger; resolution reveals more

A microscope can enlarge a cell, but resolving power decides whether two nearby details can be seen separately.

  • Light microscopes reveal cells and larger structures; electron microscopes have much greater magnification and resolving power.
  • Higher resolving power has revealed smaller sub-cellular structures in finer detail, improving cell models over time.
  • Use magnification = image size ÷ real size, convert both sizes into the same units first, and use standard form where appropriate.
  • A biological drawing should use clear single lines, labels and a title, with a scale or calculated magnification.

The punchline: Convert units before calculating, and never attach a unit to magnification.

Separate Biology: grow one microbe, not a mystery crowd

Microbiology depends on aseptic technique: unwanted organisms would spoil the result and may create a hazard.

  • Bacteria reproduce by binary fission, sometimes about every 20 minutes when nutrients and temperature are suitable; grow them in broth or as colonies on agar.
  • Sterilise media and dishes, sterilise the inoculating loop, open the lid briefly, and secure it with tape without sealing all the way around.
  • Incubate school cultures upside down at no more than 25 °C, then keep plates closed; these controls reduce contamination and pathogen risk.
  • Calculate population after whole divisions and clear-zone area with πr²; expressing bacterial populations in standard form is Higher Tier.

The punchline: Separate Biology only: aseptic technique protects both validity and safety.

Chromosomes are organised DNA packages

Inside the nucleus, long DNA molecules are arranged as chromosomes carrying many genes.

  • A gene is a section of DNA, and each chromosome carries many genes.
  • In body cells, chromosomes are normally found in pairs.
  • Before mitosis, the DNA is copied so each new nucleus can receive an identical chromosome set.

The punchline: Keep the hierarchy clear: nucleus contains chromosomes; chromosomes contain genes.

Make the model move

Interactive checkpoint

Touch the science. Change a state, build a route or test a relationship.

Turn the microscope dials

Make magnification respond

Change the image size and real size. Both sliders use micrometres, so the calculation needs no hidden unit conversion.

magnification = image size ÷ real size

1000 µm20000 µm
µm
5 µm100 µm
µm

Magnification600 times

Magnification = image size ÷ real size. The matching micrometre units cancel, so magnification has no unit; write a value such as ×600.

Choose the crossing

Which membrane route fits the evidence?

Explore each cell scenario. Use the substance and gradient—not a memorised cell name—to identify the mechanism.

Diffusion follows the oxygen gradient

When oxygen concentration is higher outside, oxygen diffuses through the membrane into the respiring cell.

1 of 4 states explored

Diffusion and osmosis move down a gradient without energy from respiration. Active transport spends transferred energy to move particles against one.

Cell division begins long before the split

The cell cycle is a preparation-and-division sequence, with mitosis forming only its nuclear-dividing stage.

  • Before division, a cell grows, increases sub-cellular structures such as ribosomes and mitochondria, and replicates its DNA.
  • During mitosis, one set of chromosomes is pulled to each end and the nucleus divides.
  • The cytoplasm and cell membrane then divide, producing two genetically identical daughter cells.
  • Mitosis supports growth and development, plus repair and replacement; identify it wherever identical body cells are being produced.

The punchline: Describe the full cell cycle in order; do not use ‘mitosis’ for every stage.

Stem cells hold biological options open

An undifferentiated stem cell can copy itself and produce cells that later specialise.

  • Embryonic stem cells can form most human cell types; adult bone-marrow stem cells can form several types, including blood cells.
  • Therapeutic cloning can make an embryo genetically matched to a patient, reducing rejection risk when its stem cells are used.
  • Possible treatments for conditions such as diabetes or paralysis must be weighed against viral-infection risk and ethical or religious objections.
  • Meristem stem cells can form any plant cell throughout life, helping clone rare plants or rapidly produce identical disease-resistant crops.

The punchline: Evaluate stem cells by balancing source, potential benefit, evidence, risk and ethics.

Diffusion follows the crowd gradient

Random particle motion produces a net movement from higher concentration to lower concentration.

  • Diffusion moves dissolved particles or gases down a concentration gradient and requires no energy from respiration.
  • Oxygen and carbon dioxide diffuse during gas exchange; urea diffuses from cells into blood plasma for excretion.
  • A steeper concentration gradient, higher temperature and larger membrane surface area usually increase diffusion rate.
  • A thin membrane shortens the diffusion path; an efficient blood supply and ventilation maintain steep gradients in animals.

The punchline: State the substance, direction and concentration gradient in every diffusion answer.

Three routes across a cell membrane

The substance, concentration gradient and energy requirement reveal which transport mechanism is operating.

  • DiffusionDissolved particles or gases move down a concentration gradient; no energy from respiration is required.
  • OsmosisWater diffuses from a dilute solution to a more concentrated one through a partially permeable membrane.
  • Active transportParticles move against their concentration gradient using energy transferred by respiration.
Ask three questions: what moves, which way is the gradient, and is energy from respiration required?

Growth creates a transport problem

As an organism becomes larger, its surface area to volume ratio falls, so its outer surface can no longer supply every cell fast enough.

  • A single-celled organism has a large surface area to volume ratio, so exchange across its surface can meet its needs.
  • Multicellular organisms need specialised exchange surfaces and organ systems because they have longer transport distances and a smaller ratio.
  • Alveoli and small-intestine villi combine large area, thin barriers and rich blood supplies; fish gills also maintain exchange with flowing water.
  • Root hairs enlarge the absorbing surface, while broad, thin leaves and stomata support gas exchange in plants.

The punchline: Calculate the ratio, then connect organism size to the need for specialised exchange.

Osmosis is water's membrane crossing

Water diffuses through a partially permeable membrane from a dilute solution to a more concentrated one.

  • Osmosis is passive: water moves down its water-concentration gradient and no energy from respiration is required.
  • Plant tissue gains mass when net water enters and loses mass when net water leaves.
  • Calculate percentage mass change from the initial mass; a negative answer represents a loss.
  • Analyse water uptake with percentages or a compound measure such as change in mass per unit time, not description alone.

The punchline: A complete definition must name water, a partially permeable membrane and the correct direction.

Active transport climbs uphill

When a cell needs particles to move against their concentration gradient, energy from respiration pays the cost.

  • Active transport moves a substance from a more dilute solution to a more concentrated solution and requires energy from respiration.
  • Root hair cells use it to absorb mineral ions when the soil solution is more dilute than the cell contents.
  • Cells in the small intestine use it to absorb sugar into blood even when the sugar concentration is already higher in the blood.
  • Diffusion and osmosis move down a gradient; active transport is the mechanism that can move against one.

The punchline: Look at the gradient first: movement against it identifies active transport.

Words worth knowing

Key definitions

eukaryotic cell
A cell whose genetic material is enclosed within a nucleus. Animals, plants, algae, fungi and protists are eukaryotes.
prokaryotic cell
A small cell with no nucleus; its main DNA loop lies in the cytoplasm. Bacteria are prokaryotes.
plasmid
A small ring of DNA in a bacterial cell that may carry additional genes.
differentiation
The process by which a cell changes to become specialised for a particular function.
resolution
The ability of a microscope to distinguish two close points as separate details.
magnification
How many times larger an image is than the real object; it is a ratio with no unit.
chromosome
A long DNA molecule carrying many genes; chromosomes are found in the nucleus of eukaryotic cells.
gene
A section of DNA that contains the information for a particular product or characteristic.
mitosis
The stage of the cell cycle in which copied chromosomes separate and the nucleus divides.
stem cell
An undifferentiated cell that can divide to make more cells and can produce certain specialised cell types.
diffusion
The net movement of dissolved particles or gas particles from higher concentration to lower concentration.
osmosis
The diffusion of water from a dilute solution to a more concentrated solution through a partially permeable membrane.
partially permeable membrane
A membrane that allows some particles, such as water molecules, through but blocks others.
active transport
The energy-requiring movement of substances from a more dilute solution to a more concentrated solution.
surface area to volume ratio
The surface area of an object divided by its volume, written as a ratio to compare available exchange surface with internal demand.

Calculate with confidence

Equations

Magnification

magnification = image size / real size

Compares the measured size of an image with the object's actual size.

Symbols used in Magnification
SymbolMeaningUnit
magnificationnumber of times larger the image appearsno unit, often written with ×
image sizemeasured size of the imagemm, µm or nm
real sizeactual size of the objectthe same unit as image size

Exam tip: Convert first: 1 mm = 1000 µm and 1 µm = 1000 nm. Magnification itself has no unit.

Percentage change in mass

percentage change = (final mass − initial mass) / initial mass × 100

Expresses a gain or loss in tissue mass relative to its starting mass.

Symbols used in Percentage change in mass
SymbolMeaningUnit
initial massmass before immersiong
final massmass after immersion and blottingg
percentage changerelative gain or loss in mass%

Exam tip: Divide by the initial mass, not the final mass; keep the sign because a negative value means mass was lost.

Separate Biology: colony or inhibition-zone area

area = πr²

Calculates the cross-sectional area of a circular colony or clear zone from its radius.

Symbols used in Separate Biology: colony or inhibition-zone area
SymbolMeaningUnit
rradius of the colony or clear zonemm or cm
areacross-sectional areamm² or cm²

Exam tip: If given a diameter, divide it by two before squaring; the area unit must also be squared.

Follow it step by step

Processes to remember

How to choose a membrane-transport mechanism

  1. Identify the substance: osmosis applies only to water.
  2. Check whether a partially permeable membrane is involved.
  3. Compare concentrations on the two sides and state the direction of net movement.
  4. Choose diffusion for particles moving down the gradient, osmosis for water down its gradient, or active transport for movement against the gradient.
  5. Mention energy from respiration only for active transport.

Exam tip: Do not decide from the cell type alone; the substance and concentration gradient determine the mechanism.

How to describe the cell cycle in order

  1. The cell grows and increases the number of sub-cellular structures.
  2. Its DNA replicates, making two copies of every chromosome.
  3. During mitosis, one chromosome set moves to each end and the nucleus divides.
  4. The cytoplasm and cell membrane divide to form two genetically identical daughter cells.

Exam tip: Reserve ‘mitosis’ for nuclear division; growth, DNA replication and cytoplasmic division are other stages of the cell cycle.

Separate Biology: calculate bacterial population

  1. Put the total growth time and mean division time in the same units.
  2. Calculate the number of complete divisions: total time / mean division time.
  3. Double the starting population once for each complete division: final population = starting population × 2ⁿ.
  4. Higher Tier: express a very large answer in standard form if requested.

Exam tip: The exponent is the number of divisions, not the number of minutes.

See the thinking

Worked example

Worked example: microscope magnification

A cell image is 48 mm wide. The cell's real width is 80 µm. Calculate the magnification.

  1. Write the equation: magnification = image size / real size.
  2. Convert the image size: 48 mm = 48,000 µm.
  3. Substitute values in matching units: magnification = 48,000 µm / 80 µm.
  4. Calculate and cancel the units: magnification = 600.

Answer: The image has a magnification of ×600.

The sizes must use the same unit before division. The micrometre units cancel, so magnification is a ratio rather than a measurement with a unit.

Protect the marks

Common mistakes

Watch out: Saying every cell has a nucleus.

Do this instead: Bacterial cells are prokaryotic and have no nucleus; their main DNA loop lies in the cytoplasm.

Watch out: Writing that mitochondria make energy.

Do this instead: Mitochondria are the main site of aerobic respiration, which transfers energy from glucose.

Watch out: Treating magnification and resolution as synonyms.

Do this instead: Magnification enlarges an image; resolution determines whether close details can be distinguished.

Watch out: Using mitosis as the process that produces gametes.

Do this instead: At GCSE, mitosis produces genetically identical cells for growth, development, repair and replacement.

Watch out: Defining osmosis as any movement from high to low concentration.

Do this instead: Name water, a partially permeable membrane, and movement from dilute to more concentrated solution.

Watch out: Saying active transport is a type of diffusion.

Do this instead: Active transport uses energy from respiration to move substances against a concentration gradient.

Watch out: Claiming that bigger organisms have a larger surface area to volume ratio.

Do this instead: As similarly shaped organisms grow, volume increases faster than surface area, so the ratio becomes smaller.

Watch out: Promising that stem cells will cure a condition.

Do this instead: Use evidence-based language: treatments may help, but benefits, risks and ethical issues must be evaluated.

Plan it like the exam

Required practicals

Use a light microscope to observe plant and animal cells

Combined Science and separate Biology

Aim: Prepare, observe, draw and label plant and animal cells using a light microscope, including a magnification scale.

Method

  1. Place a thin specimen on a clean slide; add a suitable stain if instructed, then lower a coverslip at an angle to reduce trapped air bubbles.
  2. Put the slide on the stage and begin with the lowest-power objective lens.
  3. Use the coarse focus to find the specimen, then sharpen it with fine focus; use fine focus only at high power.
  4. Centre the specimen before changing to a higher-power objective and adjust the light if needed.
  5. Draw several representative cells using clear single lines, add labels and include a scale or calculated magnification.
  6. Repeat with the other specimen type and compare visible structures.

Variables

Independent
type of prepared cell specimen or magnification being compared
Dependent
structures resolved and measurements made in the microscope image
Controls
  • specimen thickness and preparation method
  • stain identity and amount
  • lighting and focus procedure
  • calibrated scale or the same image-measurement method

Analysis: Label only structures supported by the image. Calculate total magnification from the eyepiece and objective, or use an image scale to estimate real size, stating units and sensible precision.

Safety

  • Wear eye protection when using stains and avoid skin contact; follow the school's reagent guidance.
  • Handle glass slides and coverslips by their edges and report chips or breakages.
  • Carry the microscope with two hands and keep it away from the bench edge.

Improvements

  • Use a thin, flat specimen so light passes through and structures do not overlap.
  • Calibrate the scale for each magnification used.
  • Observe several fields of view rather than choosing one unusually clear cell.

Separate Biology: investigate antibiotics or antiseptics

Separate Biology only

Aim: Use aseptic technique to compare how antibiotics or antiseptics affect bacterial growth on agar by measuring clear zones of inhibition.

Method

  1. Disinfect the bench, wash hands and label the base of a sterile agar plate before inoculation.
  2. Sterilise the inoculating loop in a flame as instructed, let it cool, then use it to spread the bacterial culture evenly across the agar.
  3. Open the lid only slightly and briefly; place sterile treatment discs on the agar with sterile forceps.
  4. Include a control disc carrying only the solvent, then replace the lid promptly.
  5. Tape the lid in a few places without sealing all the way around, invert the plate and incubate at no more than 25 °C.
  6. Keep the incubated plate closed; measure two perpendicular clear-zone diameters and calculate a mean, or calculate area with πr².
  7. Repeat each treatment on separate plates and compare mean clear-zone sizes.

Variables

Independent
identity or concentration of the antibiotic or antiseptic on each disc
Dependent
mean diameter or calculated area of the clear zone around the disc
Controls
  • bacterial strain and starting culture
  • agar depth and plate size
  • disc size and treatment volume
  • incubation temperature and time
  • solvent-only control disc

Analysis: A larger clear zone suggests stronger inhibition under the tested conditions. Compare repeats and the solvent control; zone size does not by itself show that a treatment is safe or effective in a patient.

Safety

  • Use only the school-approved microorganism and follow trained supervision for flame sterilisation.
  • Incubate at no more than 25 °C, tape without fully sealing to avoid anaerobic conditions, store plates upside down and never reopen them.
  • Wear eye protection, disinfect spills as instructed and dispose of cultures through the school's sterilisation procedure.

Improvements

  • Spread the same volume of one well-mixed bacterial culture evenly on every plate.
  • Use discs with equal diameter and equal treatment volume.
  • Repeat treatments and measure zones in two directions to reduce random error.

Investigate osmosis in plant tissue

Combined Science and separate Biology

Aim: Measure how a range of salt or sugar concentrations changes the mass of equal plant-tissue pieces.

Method

  1. Prepare labelled tubes containing equal volumes of a range of salt or sugar concentrations, including distilled water.
  2. Cut plant-tissue cylinders to equal length and diameter, remove any skin, blot them consistently and record each initial mass.
  3. Place one cylinder in each solution for the same time at the same temperature.
  4. Remove each cylinder, blot it in the same way and record its final mass.
  5. Calculate percentage change in mass for every concentration.
  6. Repeat each concentration, calculate a mean and plot mean percentage change against concentration.

Variables

Independent
concentration of the salt or sugar solution
Dependent
percentage change in mass of the plant tissue
Controls
  • plant species and source tissue
  • initial cylinder length and diameter
  • solution volume
  • immersion time and temperature
  • blotting method before each weighing

Analysis: Positive percentage change means net water entry; negative change means net water loss. The graph's zero-change concentration estimates where there was no net movement of water.

Safety

  • Use a tile and cut away from fingers when using a cork borer or scalpel; follow teacher supervision.
  • Wear eye protection if the chosen solutions require it and wipe up spills promptly.

Improvements

  • Use a cork borer and ruler to make cylinders with equal dimensions.
  • Use several concentrations around the zero-change point.
  • Repeat each concentration and calculate a mean after checking anomalies.

Try it before you move on

Quick check

Say your answer first, then open the card to check it.

Where is the main genetic material in a bacterial cell?

Answer: As a loop of DNA free in the cytoplasm, rather than enclosed in a nucleus.

Bacteria are prokaryotes; they may also contain smaller DNA rings called plasmids.

An image is 30 mm wide and the real cell is 50 µm wide. What is the magnification?

Answer: ×600

30 mm = 30,000 µm, then magnification = 30,000 / 50 = 600.

What two preparations happen before mitosis?

Answer: The cell grows and increases sub-cellular structures, and its DNA replicates.

Mitosis then separates the copied chromosomes as the nucleus divides.

A potato cylinder gains mass in a dilute solution. What caused the gain?

Answer: Net movement of water into its cells by osmosis through partially permeable membranes.

Water moved from the more dilute solution towards the more concentrated cell contents.

Why can root hair cells absorb mineral ions when their concentration is lower in the soil?

Answer: Active transport moves the ions against their concentration gradient using energy from respiration.

Diffusion cannot produce net movement from lower concentration to higher concentration.

Separate Biology: why are school microbial cultures incubated at no more than 25 °C?

Answer: To reduce the likelihood of growing pathogens that are harmful to humans.

Aseptic technique protects the culture from contamination; the temperature limit also reduces biological risk.

Good questions, clear answers

Frequently asked questions

What is the difference between a cell wall and a cell membrane?

A cell membrane controls movement into and out of a cell. A wall lies outside it and provides support; plant and algal cell walls are made of cellulose.

Why are electron microscopes more useful for tiny cell structures?

They have much greater resolving power as well as magnification, so nearby structures can be distinguished and smaller details can be revealed.

Are mitosis and the cell cycle the same thing?

No. The cell cycle includes growth, increasing sub-cellular structures, DNA replication, mitosis and division of the cytoplasm and cell membrane.

Why are stem cells controversial?

They may enable useful treatments, but embryonic sources raise ethical or religious objections and treatments can carry risks such as transfer of viral infection.

How do diffusion, osmosis and active transport differ?

Diffusion moves particles down a concentration gradient. Osmosis is water diffusion through a partially permeable membrane. Active transport uses energy to move against a gradient.

Is culturing microorganisms part of Combined Science?

Not in this AQA scope. Culturing microorganisms and its required practical are separate Biology only; the guide labels that material explicitly.

See the whole topic

Illustrated notes

Use the guide above for searchable explanations, then revise from the visual note sheets below.

GCSE Biology — Cell Biology, page 1: eukaryotes, prokaryotes and cell parts
GCSE Biology — Cell Biology, page 1: eukaryotes, prokaryotes and cell parts
GCSE Biology — Cell Biology, page 2: cell specialisation and differentiation
GCSE Biology — Cell Biology, page 2: cell specialisation and differentiation
GCSE Biology — Cell Biology, page 3: microscopy, magnification and culturing microbes
GCSE Biology — Cell Biology, page 3: microscopy, magnification and culturing microbes
GCSE Biology — Cell Biology, page 4: chromosomes, the cell cycle and mitosis
GCSE Biology — Cell Biology, page 4: chromosomes, the cell cycle and mitosis
GCSE Biology — Cell Biology, page 5: stem cells — sources, uses and issues
GCSE Biology — Cell Biology, page 5: stem cells — sources, uses and issues
GCSE Biology — Cell Biology, page 6: diffusion, osmosis and active transport
GCSE Biology — Cell Biology, page 6: diffusion, osmosis and active transport

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