Skip to topic
    ← Back to course topics

    Structure of eukaryotic cells — AQA A-Level Biology

    Verified courseTeaching note checked against the official specification.

    Eukaryotic cells are complex, membrane-bound cellular units characterised by a distinct nucleus and membrane-bound organelles such as mitochondria, chloroplasts, and the Golgi apparatus. Mastery of their ultrastructure and specialised functions is essential for understanding cellular compartmentalisation and metabolic processes in AQA A-Level Biology.

    Structure of eukaryotic cells explained

    Structure of eukaryotic cells covers 4 specification points, including Cell-surface membrane nucleus (containing… and In complex multicellular organisms, eukaryotic….

    Read the full explanation

    Open a point below for its explanation and revision guidance.

    The structure of eukaryotic cells, restricted to the structure and function of: cell-surface membrane nucleus (containing chromosomes, consisting of protein- bound, linear DNA, and one or more nucleoli) mitochondria chloroplasts (in plants and algae) Golgi apparatus and Golgi vesicles lysosomes (a membrane-bound organelle that releases hydrolytic enzymes) ribosomes rough endoplasmic reticulum and smooth endoplasmic reticulum cell wall (in plants, algae and fungi) cell vacuole (in plants).

    Eukaryotic cells contain membrane-bound organelles. The cell-surface membrane is a phospholipid bilayer controlling exchange. The nucleus has a double-membrane envelope with pores, containing linear DNA bound to histones, and nucleoli. Mitochondria have a folded inner membrane (cristae) and matrix, releasing ATP. Chloroplasts, found in plants and algae, contain thylakoids stacked into grana and stroma for photosynthesis. The Golgi apparatus modifies, packages and transports proteins and lipids, forming vesicles and lysosomes (containing hydrolytic enzymes). Ribosomes synthesise proteins. Rough ER has ribosomes and transports proteins; smooth ER synthesises lipids. Plant, algal and fungal cell walls provide support. Plant cell vacuoles maintain turgor.

    In complex multicellular organisms, eukaryotic cells become specialised for specific functions.

    Most somatic cells in a multicellular organism contain identical genomes. Specialisation occurs because transcription factors activate only specific genes, altering the cell's shape and organelle proportions to suit its function. For example, a pancreatic acinar cell contains extensive rough endoplasmic reticulum and Golgi apparatus to synthesise and secrete digestive enzymes. A neutrophil possesses numerous lysosomes with hydrolytic enzymes to digest engulfed pathogens. A sperm cell features a mid-piece packed with mitochondria to supply ATP for its flagellum. Some highly specialised cells even lose their DNA entirely; mature mammalian red blood cells lack a nucleus to maximise space for haemoglobin.

    Specialised cells are organised into tissues, tissues into organs and organs into systems.

    A tissue is a group of similar cells working together to carry out one function: squamous epithelium lining the alveoli, ciliated epithelium lining the trachea, cardiac muscle in the heart wall, xylem and phloem in a plant. An organ is made of several different tissues working together to perform an overall function; the stomach combines glandular epithelium that secretes enzymes, smooth muscle that churns, connective tissue and blood vessels, and a leaf combines palisade mesophyll, spongy mesophyll, epidermis and vascular tissue. An organ system is a set of organs working together, such as the digestive system of mouth, oesophagus, stomach, ileum, pancreas and liver, or the gas exchange and circulatory systems. This hierarchy allows large organisms to overcome the limits of diffusion, since a small surface area to volume ratio means diffusion alone cannot supply all cells.

    Students should be able to apply their knowledge of these features in explaining adaptations of eukaryotic cells.

    Application questions give you an unfamiliar cell, as an electron micrograph, a table of organelle counts or a short description, and expect you to link a named feature to the job that cell does, in that order. The moves are always the same. Many mitochondria means more ATP released in aerobic respiration, for active transport or for movement. Many ribosomes, or extensive rough endoplasmic reticulum, means rapid synthesis of protein, often for export. A large Golgi apparatus with many vesicles means modification, packaging and secretion of proteins and lipids. Many lysosomes means hydrolysis of engulfed pathogens. Microvilli, or a folded membrane, mean a large surface area for absorption; many carrier proteins mean rapid active transport, co-transport or facilitated diffusion, while channel proteins allow facilitated diffusion; many chloroplasts mean more light absorbed.

    Your focus

    1. Name one structure in a micrograph or diagram of an unfamiliar cell that shows it is a eukaryote, choosing from mitochondrion, nuclear envelope, rough endoplasmic reticulum, vesicle or lysosome, and give one function of that structure.
    2. Describe two functions of the Golgi apparatus and state the structures it forms.
    3. Explain how one structural feature of each of the chloroplast, the cell wall, the permanent vacuole and the smooth endoplasmic reticulum lets it do its job, and state which three of the four are absent from an animal cell.
    Show all 13 objectives
    1. State that chloroplasts are found in plants and algae.
    2. Explain how differential gene expression allows cells to develop into specialised types.
    3. Relate specific structural features and organelle proportions of a named specialised cell to its function.
    4. Deduce the specialised function of an unfamiliar cell from data regarding its organelle distribution.
    5. Define tissue, organ and organ system, and place a named example at each level.
    6. Identify, from a description of a structure, whether it is a tissue or an organ, and justify the decision.
    7. Explain why multicellular organisms of large size require organ systems rather than relying on diffusion.
    8. Explain how three features of an epithelial cell in the proximal convoluted tubule allow rapid reabsorption of glucose.
    9. Interpret an electron micrograph of an unfamiliar cell to suggest its function, citing two organelles as evidence.
    10. Justify why the number of an organelle, rather than its presence, is what makes a cell adapted to its role.

    Which command word is this?

    Give a factual account of the structure or sequence without needing to explain reasons why. For example, describing the appearance of the Golgi apparatus as a series of flattened, curved cisternae with vesicles.

    Structure of eukaryotic cells exam tips

    Topic Overview

    The ultrastructure of eukaryotic cells encompasses the specialised organelle networks that enable compartmentalised biochemical reactions in animals, plants, algae, and fungi. Understanding the distinct architectural roles of the nucleus, endomembrane system, mitochondria, and chloroplasts is fundamental to explaining how complex cells maintain metabolic efficiency.

    This topic forms the core foundation for subsequent AQA units including cellular transport, immunology, bioenergetics (photosynthesis and respiration), and protein synthesis. A strong command of organelle structure and organelle isolation techniques such as cell fractionation enables students to link micro-scale structures with macro-scale biological functions.

    Key Concepts
    • →Compartmentalisation: Membrane-bound organelles provide isolated microenvironments with specialised enzymes and pH conditions, preventing interfering metabolic reactions.
    • →The Endomembrane System: The continuous trafficking network involving the nuclear envelope, rough and smooth endoplasmic reticulum, transport vesicles, Golgi apparatus, and lysosomes.
    • →Energy Transducing Organelles: Mitochondria and chloroplasts contain double membranes, internal fluid matrices, and folded internal membranes (cristae and thylakoids) designed to maximise surface area for ATP synthesis.
    • →Structural Diversity Across Taxa: Plant and algal cells contain cellulose or glycoprotein walls, vacuoles, and chloroplasts; fungal cells feature chitin cell walls and lack chloroplasts; animal cells lack cell walls and large permanent vacuoles.
    Marking Points
    • identifying a membrane-bound organelle as evidence that a cell is eukaryotic, such as a mitochondrion, nucleus, endoplasmic reticulum, Golgi apparatus, lysosome or vesicle
    • describing the nucleus as having a double membrane or nuclear envelope with pores, and containing chromosomes of DNA bound to histones plus a nucleolus
    • stating the Golgi apparatus modifies, packages or transports proteins or lipids, or forms vesicles and lysosomes
    • identifying that lysosomes contain hydrolytic enzymes that are released to digest material
    • linking mitochondria to the release of ATP and ribosomes to the production of protein
    • stating that chloroplasts are found in plants and algae
    • Describe how differential gene expression leads to specialisation by altering cell shape and organelle proportions without changing the genome of somatic cells.
    • Identify the specific organelle that is abundant or modified in a named specialised cell, such as extensive rough endoplasmic reticulum in pancreatic cells.
    • Link the abundance of a specific organelle directly to the cell's function, for example, mitochondria releasing ATP for active transport or movement.
    • Explain structural losses as functional adaptations, such as the absence of a nucleus in a mature red blood cell to accommodate more haemoglobin.
    • Award credit for defining a tissue as a group of similar or specialised cells with a shared function.
    • Award credit for defining an organ as different tissues working together to perform a particular function.
    • Award credit for defining an organ system as a group of organs working together.
    • Award credit for a correct worked example running through all the levels, such as epithelial cell, epithelium, ileum, digestive system.
    • Award credit for linking the level of organisation to body size and a small surface area to volume ratio, so that diffusion alone is insufficient.
    • one mark for naming the feature seen in the cell rather than restating the data given
    • one mark for saying there are many of the organelle, or that the membrane is folded, where number or surface area is the adaptation
    • one mark for the process the feature carries out, such as mitochondria releasing ATP in aerobic respiration
    • one mark for linking that process to the overall function of the cell, such as the co-transport of glucose into the cell from the lumen
    • one mark for a second, genuinely different adaptation where the question asks for more than one
    Examiner Tips
    • 💡Answer structure and function in matched pairs; a list of organelle names without functions rarely provides a complete explanation.
    • 💡Read exclusions carefully, as in 'other than the Golgi apparatus, name one structure', because an excluded answer cannot be credited.
    • 💡When identifying chloroplasts, state their occurrence in plants and algae to match the specification clause.
    • 💡When describing cellular adaptations, explicitly link the structural feature to the process it performs and its ultimate function for the cell.
    • 💡If presented with an unfamiliar cell in a table or micrograph, identify which organelles are unusually abundant to deduce the cell's primary function.
    • 💡Give one worked example at every level in the same answer; examiners credit the chain, not the definitions alone.
    • 💡Use plant examples as readily as animal ones, since leaf and root questions are common alongside gut questions.
    • 💡If asked why large organisms need organ systems, bring in surface area to volume ratio explicitly.
    • 💡Count the marks and give that many separate feature-and-function pairs; three marks means three distinct adaptations.
    • 💡Where transport proteins are involved, say which kind of transport they carry out, since channel, carrier and co-transport proteins function differently.
    • 💡Answer 'describe and explain' in two halves for every point: what the feature is, then why it helps.
    • 💡Always specify 80S ribosomes when discussing eukaryotic cytoplasm, and 70S ribosomes when describing the interior of mitochondria or chloroplasts.
    • 💡When asked to describe organelle adaptations, explicitly link structure to function: do not just state 'folded cristae', specify 'folded cristae provide a large surface area for enzymes and electron transport chain proteins involved in ATP synthesis'.
    • 💡Ensure units match before calculating magnification: always convert measurements into the units required by the question (e.g. mm to um) before dividing by magnification.
    Common Mistakes
    • naming the nucleolus or the cell-surface membrane as evidence that a cell is eukaryotic; prokaryotes also have a cell-surface membrane, and the nucleolus is a region inside the nucleus rather than a membrane-bound organelle
    • writing 'mitochondria for ATP' without specifying that they release ATP, or stating that they 'produce energy'
    • saying the Golgi apparatus makes proteins, when it modifies, packages and transports them
    • describing ribosomes as membrane-bound structures, whereas they lack a membrane
    • stating that chloroplasts are found in all eukaryotic cells; correct by specifying that they occur in plants and algae
    • Stating that all cells in a multicellular organism contain identical DNA; correct by noting that mature mammalian red blood cells lack a nucleus and DNA, while gametes are haploid.
    • Writing that sperm cells or muscle cells 'produce energy'; correct by specifying that their abundant mitochondria release ATP during aerobic respiration.
    • Claiming a red blood cell 'has no organelles' when asked about a specific missing structure; correct by explicitly naming the absent structure, such as the nucleus.
    • Confusing differentiation with mutation; correct by explaining that specialisation usually involves changes in gene expression via transcription factors, not changes to the DNA base sequence.
    • Calling blood, or xylem, an organ when each is a tissue.
    • Defining a tissue as 'lots of cells' without saying that they are similar and share a function.
    • Assigning organs to only one system, for example placing the pancreas in the endocrine system alone when it is also a digestive organ.
    • Stating that an organ is made of one type of tissue.
    • Mixing plant and animal examples within the same chain, so the hierarchy no longer holds together.
    • listing the organelles visible in a figure without linking any of them to the function of the cell
    • omitting 'many', since it is the number rather than the presence of an organelle that is being credited
    • writing that mitochondria 'give energy' rather than release ATP in aerobic respiration
    • giving two versions of the same adaptation, such as microvilli and folded membrane, when two different features are required
    • conflating channel proteins, which only perform facilitated diffusion, with carrier proteins that can also perform active transport and co-transport
    • Believing plant cells contain chloroplasts instead of mitochondria. In reality, plant cells possess both; mitochondria are vital for ATP production in darkness and non-photosynthetic tissues such as roots.
    • Confusing the function of smooth endoplasmic reticulum (SER) with rough endoplasmic reticulum (RER). SER synthesises, stores, and transports lipids and carbohydrates, whereas RER processes proteins synthesised by surface-bound 80S ribosomes.
    • Assuming that eukaryotic cell walls act as selective barriers to solutes. Cell walls are fully permeable to small dissolved substances; the underlying phospholipid bilayer of the cell surface membrane regulates permeability.
    Revision Plan
    1. 1Day 1-2: Review and sketch the ultrastructure of animal, plant, fungal, and algal cells, labelling all organelles and noting structural differences.
    2. 2Day 3-4: Construct a detailed flow diagram tracking the pathway of protein synthesis, post-translational modification, and secretion through the endomembrane system.
    3. 3Day 5: Practice magnification and scale calculations using the formula A = I / M, converting accurately between mm, um, and nm.
    4. 4Day 6-7: Complete past exam questions focused on cell fractionation, organelle identification from electron micrographs, and comparison tables of eukaryotic taxa.
    Exam Question Types
    • 📋Organelle Identification and Function: Label diagrams or identify organelles from transmission electron micrographs and state their specific functions.
    • 📋Magnification and Unit Conversion Calculations: Calculate actual size, image size, or magnification level from micrographs, requiring unit conversions.
    • 📋Comparative Essay and 6-Mark Questions: Compare the ultrastructure of different eukaryotic kingdoms or explain the coordinated journey of a secreted protein.
    Command Word Expectations (AQA)
    Describe

    Give a factual account of the structure or sequence without needing to explain reasons why. For example, describing the appearance of the Golgi apparatus as a series of flattened, curved cisternae with vesicles.

    Explain

    Give biological reasons for a feature or process. You must connect cause and effect, such as explaining how folded mitochondrial cristae increase surface area for oxidative phosphorylation to yield ATP.

    Compare

    Identify both similarities and differences between two structures or cell types. Using comparative conjunctions (e.g. 'whereas', 'both') is required to gain marks.

    How Students Lose Marks (Examiner Pitfalls)
    Pitfall: Confusing the precise roles of the rough endoplasmic reticulum (RER) and the Golgi apparatus during protein modification and transport.
    ❌ Weak Answer (Loses Marks):The rough ER makes proteins and then sends them out of the cell, while the Golgi also modifies them.
    Example improved answer:Ribosomes on the rough endoplasmic reticulum synthesise polypeptide chains, which fold inside the lumen and are packaged into transport vesicles. These vesicles fuse with the cis-face of the Golgi apparatus, where proteins are post-translationally modified (e.g. via glycosylation) and sorted into secretory vesicles that fuse with the cell surface membrane for exocytosis.
    Examiner Tip: Explicitly state that the rough endoplasmic reticulum synthesises and folds polypeptides into transport vesicles, whereas the Golgi apparatus chemically modifies (e.g. adds carbohydrates to form glycoproteins), packages, and sorts them.
    Pitfall: Stating that mitochondria 'produce' or 'create' energy rather than generating ATP via aerobic cellular respiration.
    ❌ Weak Answer (Loses Marks):Mitochondria are the powerhouse of the cell because they make energy for cell reactions.
    Example improved answer:Mitochondria are the site of aerobic respiration where adenosine triphosphate (ATP) is produced via oxidative phosphorylation across the folded inner cristae membrane.
    Examiner Tip: Never use the phrase 'produces energy'. Always specify that mitochondria 'synthesise ATP' through 'aerobic respiration'.
    Step-by-Step Worked Solutions

    Question: A transmission electron micrograph shows a mitochondrion with a measured image length of 48 mm. The magnification of the image is x25000. Calculate the actual length of the mitochondrion in micrometres (um). Show your working.

    1. 1.Step 1: State the magnification formula rearranged for actual size: Actual size (A) = Image size (I) / Magnification (M).
    2. 2.Step 2: Convert the image size from millimetres (mm) to micrometres (um) by multiplying by 1000: 48 mm x 1000 = 48000 um.
    3. 3.Step 3: Divide the converted image size by the magnification: 48000 um / 25000 = 1.92 um.
    Final Answer: Actual length = 1.92 um

    Question: Describe the pathway taken by an amino acid from its uptake at the cell surface membrane to its secretion as an extracellular enzyme. [6 marks]

    1. 1.Step 1: Uptake - The amino acid enters the cell across the plasma membrane via active transport or facilitated diffusion involving specific carrier proteins.
    2. 2.Step 2: Translation - The amino acid is transferred to ribosomes on the rough endoplasmic reticulum (RER) and incorporated into a polypeptide chain during translation.
    3. 3.Step 3: Folding and transport - The polypeptide enters the lumen of the RER, folds into its tertiary structure, and is pinched off into transport vesicles.
    4. 4.Step 4: Golgi processing - Transport vesicles fuse with the cis-face of the Golgi apparatus, where the protein is modified (e.g. addition of carbohydrate groups to form a glycoprotein).
    5. 5.Step 5: Packaging - The processed enzyme is packaged into Golgi secretory vesicles.
    6. 6.Step 6: Exocytosis - The secretory vesicle moves along the cytoskeleton, fuses with the cell surface membrane, and releases the enzyme outside the cell via exocytosis (requiring ATP).
    Final Answer: The amino acid is imported across the membrane, assembled into a polypeptide on RER ribosomes, folded and transported in vesicles to the Golgi apparatus for modification, and finally packed into secretory vesicles for release via exocytosis.
    Active Recall Memory Test
    What is the structural composition of the eukaryotic nucleus envelope, and what is the role of nuclear pores?
    Key Fact: The nuclear envelope is a double membrane continuous with the rough ER; nuclear pores allow the selective exit of mRNA and ribosomes and the entry of nucleotides and steroid hormones.
    Name two organelles other than the nucleus that contain their own DNA and 70S ribosomes.
    Key Fact: Mitochondria and chloroplasts.
    Which organelle contains hydrolytic enzymes such as lysozymes to digest worn-out cellular components?
    Key Fact: Lysosomes.
    What is the functional difference between rough endoplasmic reticulum and smooth endoplasmic reticulum?
    Key Fact: The rough ER possesses ribosomes and folds/packages synthesised polypeptides; the smooth ER lacks ribosomes and synthesises, stores, and transports lipids and carbohydrates.
    Frequently Asked Questions
    What is the difference between cristae and thylakoids?
    Cristae are folds of the inner mitochondrial membrane that provide a large surface area for enzymes and electron carriers in aerobic respiration. Thylakoids are flattened, disc-shaped membranous sacs found within chloroplasts that contain chlorophyll and accessory pigments for the light-dependent reactions of photosynthesis. Cristae are specific to mitochondria, while thylakoids are arranged in stacks called grana inside chloroplasts.
    Why do mitochondria and chloroplasts have their own circular DNA and 70S ribosomes?
    Mitochondria and chloroplasts possess circular DNA and 70S ribosomes because of their evolutionary origin via endosymbiosis. Early ancestral eukaryotic cells engulfed aerobic and photosynthetic prokaryotes that established a symbiotic relationship rather than being digested. Having their own genetic material and ribosomes allows these organelles to synthesise some of their own proteins independently of the nuclear genome.
    How do lysosomes differ from regular transport vesicles?
    Transport vesicles are short-lived, transient membrane-bound spheres responsible for carrying proteins and lipids between organelles, such as from the rough ER to the Golgi. Lysosomes are specialised, permanent organelles containing concentrated hydrolytic enzymes, such as proteases, lipases, and lysozymes, maintained at an acidic pH. Their primary function is cellular digestion, including breaking down phagocytosed pathogens, damaged organelles, or autolysing the entire cell.
    Do all eukaryotic cells have a cell wall?
    No, animal cells completely lack a cell wall and are bounded solely by the cell surface membrane. However, plant cells (cellulose), algal cells (cellulose and glycoproteins), and fungal cells (chitin) all possess rigid cell walls. These cell walls provide structural support, resist osmotic lysis, and determine cell shape.