Year 12

AQA A level Biology Cell Structure Notes

Cell Structure

— Biology · AS Level (7402) · Unit 1
★ Exam Tips (from ma'am's lecture):
  • Magnification formulas (M = I/A and I = M × A) appear in MCQs and Paper 2 — units must be the same top and bottom.
  • Exams give a TEM and a SEM micrograph and ask you to tell them apart → TEM = 2D, SEM = 3D.
  • "Function of the nucleus?" → site of transcription (and control centre).
  • NOT in AS syllabus: fungi & protoctista details, peroxisomes (ignore them on diagrams), how LM/EM lenses work (extra knowledge).
  • Remember the 4 extra things a plant cell has vs animal cell (cell wall, chloroplast, large central vacuole, plasmodesmata).
Study tip: make your own mnemonics (they only need to make sense to you) · after class, take a blank paper and "blurt" pointers from memory — no notes!

1. Microscopy & Magnification

Microscopy: a technical field that uses a microscope to view specimens (samples/objects) that are otherwise not visible to the naked eye — the science of investigating small objects and structures. A small object is "magnified" for viewing and analysis.

Why we need it: naked eye sees only 50–100 µm. Body cells are ~5–40 µm, organelles are in nm (ribosome ≈ 25 nm) → invisible without a microscope.

Why can't we see cells? The smallest structure visible to our eye is 50–100 µm. Most cells are only 5–40 µm, so they fall outside our visible range — even skin (the largest organ) shows no cells to the naked eye. Hospital blood/urine tests = microscopy of specimens on slides.

Magnification

Definition: magnification is the ratio of the image size (I) to the actual size (A).

M = Image size (I)Actual size (A)     ⇒    I = M × A
Memory tool "MIA": Magnification = Image / Actual (image comes first, on top — "missing in action").
  • Magnification = enlarging the apparent size, not the physical size (like zooming a photo — the object itself stays the same).
  • It only makes the image bigger, not clearer → clarity is resolution (section 3).
  • No unit for magnification — it is "times" (×). Units in numerator and denominator cancel.
  • Image size and actual size must be in the SAME unit → convert first if they differ (e.g. 5 µm vs 1 mm).
actual = 10 mm, image = 50 mm M = I / A = 50 / 10 M = × 5 units (mm) cancel → just "×5". M is a multiplying factor: 10 mm × 5 = 50 mm (image).

Unit conversions

cmmm µmnm × 10× 1000× 1000 ÷ 10÷ 1000÷ 1000
big → small: multiply · small → big: divide
Unit cm mm µm nm
in metres 10⁻² m 10⁻³ m 10⁻⁶ m 10⁻⁹ m
Trick (order of units): cm & mm are known from O-level. For µm vs nm use the alphabet: M comes before N (L M N O P) → micro is bigger than nano. Similarly C-M-N = centimetre → millimetre → nanometre in "ABC" order.

2. Types of Microscopy

Two types — they differ in the source of radiation (what is projected on the specimen): light or an electron beam.

Microscopy Light microscopy Electron microscopy Scanning (SEM) Transmission (TEM)
image from LM = photomicrograph · image from EM = electron micrograph

3. Light Microscope

Syllabus note: the parts & their jobs are extra (useful for P3 practicals). Must know: source = light, max useful ×1500, features, advantages.

Parts and their jobs

  1. Lamp — source of light.
  2. Diaphragm — controls the amount of light projected onto the slide (may hold a filter).
  3. Condenser lens (convex) — focuses the light rays onto the slide by converging the divergent rays. It does not magnify.
  4. Objective lens — 1st magnifying lens (×4, ×10, ×40; ×100 oil immersion) on a revolving nosepiece.
  5. Eyepiece lens — 2nd magnifying lens (usually ×10).
  6. Coarse adjustment knob — achieves the optimal distance between slide & objective lens.
  7. Fine adjustment knob — achieves optimal sharpness / clarity.

Other labelled parts on the diagram: head (turret), nosepiece, arm, stage (holds slide; stage clips hold it in place), stage stop, illumination, base, light-intensity control.

① lamp② diaphragm③ condenser slide / specimen④ objective (1st)⑤ eyepiece (2nd) eye
light path: lamp → diaphragm → condenser → specimen → objective → eyepiece → eye
Total magnification= magnification of eyepiece × magnification of objective
e.g. ×10 (eyepiece) × ×40 (objective) = ×400

Main features of a light microscope

  1. Source of radiation: light
  2. Maximum useful magnification: ×1500 (beyond this the image is not clearer)
  3. Can view live and dead specimens (does not harm living cells)
  4. Produces coloured images — (a) light is a combination of colours (VIBGYOR); (b) organic dyes are used for staining
  5. Magnifying lenses are made of optical glass
  6. Portable, inexpensive, easy to operate, does not need a skilled professional (even school students use it)

Limit: shows only cell outline and nucleus — organelles like mitochondria are not clearly visible (see cheek-cell picture below).

4. Electron Microscope

Features

  1. Source of radiation: electrons (electron beam from an electron gun)
  2. Max useful magnification: ×250 000
  3. Can ONLY view DEAD specimens
  4. Images are black & white (SEM colours are added by computer)
  5. ★ Metal stains give better contrast (difference between light/dark greys = clarity)
  6. Electromagnetic lenses are used
  7. Expensive, non-portable, needs skilled expertise; large space for set-up
Why vacuum? (exam Q) The whole chamber/column is a vacuum so the electron beam does not collide with air molecules and get scattered. A scattered beam = unclear (unfocused) image. Electrons are extremely tiny (mass ≈ 9.1 × 10⁻³¹ kg), so even air molecules deflect them.
The specimens used in electron microscopy are DEAD and DEHYDRATED !! Water boils in a vacuum — if a hydrated (alive) specimen were placed there, its water content would boil off, rupturing and destroying it (organelles could even lyse). So the specimen is killed and its water removed first.
Light (LM)Transmission (TEM)Scanning (SEM) lampcondenserspecimenobjectiveeyepiece e⁻ sourcecondenserthin specimenprojection lensfluorescent screen e⁻ sourcecondenser3-D specimenmonitor image viewed directlybeam goes THROUGHbeam REFLECTS off surface
whole EM column = vacuum · TEM image on a fluorescent screen · SEM image built on a monitor from reflected electrons
Transmission EM (TEM) Scanning EM (SEM)
e⁻ beam transmits through the specimen reflected from the surface; reflected beams are captured to form the image
image 2D 3D
specimen must be extremely thin does not have to be thin
preparation relatively harder relatively easier
Spot the difference: a TEM micrograph of a mitochondrion looks flat (you see the cristae as lines + 70S ribosomes as dots inside); the SEM micrograph of the same shows 3-D cristae. The coloured SEM pictures are black & white originals coloured by computer.

5. Resolution

Definition: the minimum distance between 2 points before they can be seen as separate points — the ability to distinguish between 2 distinct points.

Paper analogy: two sheets far apart = clearly 2; overlap them = can't tell if 1 or 2. Resolution = how close they can get and still look like 2.
  • Resolution depends on the wavelength (λ) of the radiation (light or e⁻ beam).
  • Shorter wavelength ⇒ higher resolution.
  • Resolution is "generally" half the λ of the radiation.
2 separate pointslooks like 1 blob distance ≥ min. distancedistance < minimum ✗
resolved (high resolution) vs not resolved (low resolution → blurry)
Resolution of a LIGHT microscope Resolution of an ELECTRON microscope
λ of light taken as 400 nm (visible light 400 nm violet – 700 nm red; violet is shortest) λ of the electron beam taken as 1 nm
⇒ resolution = 200 nm (½ × 400) ⇒ resolution = 0.5 nm (½ × 1)
2 points must be ≥ 200 nm apart to be seen as separate; can view specimens as small as ~200 nm 2 points must be ≥ 0.5 nm apart to be seen as separate
Example:
two organelles 100 nm apart under a LM (< 200 nm) → seen as ONE point. Under an EM (0.5 nm limit) → clearly two. That's why an EM shows ribosomes and cristae, LM does not.
Magnification ≠ resolution: magnification = how many times bigger; resolution = how clear / detailed (high-res picture shows 4 distinct cells, low-res looks blurred).
High resolution — sharp edges
Low resolution — blurred

Micrograph examples on the board: cheek cells under a LM (pink outlines + a dark nucleus only) · TEM of a mitochondrion from a liver cell (flat 2D, cristae visible) · mitochondrion under SEM (3-D, coloured by computer).

6. Classification of Living Organisms

5 kingdoms (earlier 3): Prokaryota (bacteria), Protoctista, Fungi, Plantae, Animalia. The big dividing factor is the cell: bacteria = prokaryotes; the other four = eukaryotes.

Classification of living organisms Prokaryotes (bacteria)ProtoctistaFungiPlantaeAnimalia Eukaryotes (4 kingdoms) plants & animals: strictly multicellular
Prokaryotes (bacteria) Eukaryotes
  • strictly unicellular (a colony = many separate cells, not one organism)
  • NO true nucleus
  • NO membrane-bound organelles
  • DNA coiled & concentrated in a region called the nucleoid
  • have a TRUE nucleus
  • often multicellular (plants & animals strictly; yeast is the only unicellular fungus; protoctista = mixed "dumping ground" kingdom)
  • have membrane-bound organelles
Evolution: prokaryotes were the first cells on Earth; eukaryotes evolved from them. Prokaryote = "pro" before + "karyon" nucleus.

Q: What is a "true nucleus"? A nucleus contains genetic material; if it is enclosed by a (double) membrane it is a true nucleus. Genetic material with no membrane around it = naked DNA (still has genetic material — it just has no nucleus).

TRUE nucleus (eukaryote)DNA inside double membrane + pores NO true nucleus (prokaryote)naked DNA in cytoplasm (nucleoid)

7. The Cell — Basic Unit of Life

Cell = basic unit of life. Robert Hooke saw plant cork cells under a microscope; each tiny box had a boundary, so he called it a "cell" (like a jail cell — a small enclosed space).

Cell theory:
  • The cell is the structural and functional unit of all living organisms, made up of "protoplasm" = cell membrane + genetic material + cytoplasm (all three needed to count as a cell).
  • All organisms are composed of one or more cells.
  • New cells arise only by division of pre-existing cells.
  • Structural unit: structure = shape/framework (like a building or phone). Cells → tissue → organ → organ system → organism, so every organism's structure traces back to cells.
  • Functional unit: all vital processes (respiration → ATP, protein synthesis, lipid & enzyme synthesis, DNA replication) happen inside cells (cytoplasm / nucleus). ATP is the only energy form the body can use.
  • A cell can be thought of as a "bag" in which the chemistry of life occurs.
celltissueorganorgan systemORGANISM
"uni" = one → uni-cellular = one cell (bacteria) · multi-cellular = many cells

8. Animal Cell & Plant Cell (cartoon diagrams)

Real cells are never perfect circles — these are cartoon diagrams. Animal cells are irregular (jelly-like, no fixed shape); plant cells have a regular, definite shape because of the cell wall.

Animal cell cell (plasma) membrane → RER (ribosomes on it)continuous w/ nuclear membrane mitochondrion(lysosome = special Golgi vesicle) microtubules / cytoskeleton centrosome = MTOC(2 centrioles at 90°) mitochondrionglycogen granule • cytoskeletonGolgi vesiclesGolgi apparatus nucleus (double membrane + pores)nucleolus SER (smooth, no ribosomes) small temp. vacuole chromatin cytoplasm = internal environment holding all organelles
Animal cell — peroxisome shown on printed diagrams: ignore (not AS)
Plant cell cell wall (fully permeable)+ cell membrane nucleusnucleolus ↗ RERSER chloroplastmitochondrion CENTRAL VACUOLEcell sap: nutrients,waste material Golgi apparatus chloroplast plasmodesma(between cells) tonoplast(vacuole membrane) cytoplasm · ribosomes · cytoskeleton · Golgi vesicles also present
Plant cell — vacuole pushes the nucleus & organelles to the edge. No centrioles in plant cells.
Only in PLANT cells (the 4 differences — memorise!)
cell wall cellulose, outermost, fully permeable (cell membrane = semi-permeable)
chloroplast site of photosynthesis
large permanent central vacuole membrane = tonoplast; contents = cell sap (animal cells: only small temporary vacuoles)
plasmodesmata cytoplasmic channels between neighbouring cells

Common to both: nucleus (+nucleolus, double membrane, pores), RER, SER, Golgi, mitochondria, ribosomes, cytoplasm, cell membrane, cytoskeleton. Animal only: centrioles (in the centrosome / MTOC), lysosomes (a special Golgi vesicle).

9. Structures & Functions of Cellular Organelles

(i) Cell membrane

Cell wall vs membrane: wall = fully permeable (lets anything small enough through); membrane = semi / selectively / partially permeable.
  • Semi-permeable — does not allow all substances to pass through. Letting everything in → cell swells & lyses (or toxins enter); letting everything out → loses vital substances.
  • Made of a phospholipid bilayer = 2 layers (bi = two); each phospholipid = phosphate head + fatty-acid (lipid) tails — 2 different materials joined.
phosphate headsfatty-acid tails (lipid)
phospholipid bilayer — 2 layers

Functions: (i) protects the cytoplasm (and organelles) from harmful/toxic substances; (ii) regulation of material in & out of the cell through its permeability (permeable to a substance → lets it in; impermeable → blocks it). Also separates the cell's internal environment from the external. Full detail: Chapter 4.

Nucleic acids (quick intro)

Nucleic acidsDNAdeoxyribonucleic acid (1 O less) RNAribonucleic acid mRNA (messenger)tRNA (transfer)rRNA (ribosomal)

(ii) Nucleus, nuclear membrane, nucleolus

Remember: DNA never leaves the nucleus. Only DNA's message (mRNA) does — through a nuclear pore.
  • Nucleus = control centre of the cell (like brain / CPU) — contains genetic information as DNA; DNA is made of genes; each gene codes for a polypeptide (amino acids → polypeptide → protein).
  • Each gene = its own specific "passcode" → its own mRNA → its own polypeptide.
  • ① The nucleus is the site of TRANSCRIPTION (DNA → mRNA). Whole chain below = protein synthesis.
DNA (gene) —transcription→ mRNA —translation→ polypeptide   [ = protein synthesis ]

Why a messenger? DNA can't leave the nucleus and amino acids can't enter it → mRNA is the "WhatsApp" courier. Nucleus also holds rRNA (made in the nucleolus). Mitochondria have DNA but no nucleus.

nucleusnucleolusDNA / gene transcriptionmRNA exits via nuclear pore ribosome (80S) in cytoplasmtranslationpolypeptide
transcription in nucleus (mRNA out through pore) → translation on ribosome
  • Nuclear membrane (envelope): a double membrane — a protective boundary controlling what enters/leaves; if everything entered the nucleus it could burst. The membrane itself is impermeable; substances move only through nuclear pores.
  • Nucleolus: a dense body within the nucleus, not membrane-bound, a dense network of RNA and DNA (contains rRNA) — responsible for synthesising ribosomes, which take part in protein synthesis.

(iii) Ribosomes

Link to prokaryotes: ribosomes have no membrane → bacteria (no membrane-bound organelles) do have them.

Definition: small, dense, rounded and granular particles of ribosomal RNA + protein (≈65 % rRNA, 35 % protein — values not required). Made in the nucleolus. Not surrounded by a membrane.

largesmall
2 subunits (no special names)
  • Made of 2 subunits — large + small.
  • 70S (smaller): prokaryotic cells, mitochondria, chloroplasts.
  • 80S (larger): eukaryotic cells — attached to RER and freely suspended in cytoplasm (same type, same job).
  • Only difference at AS level = size (S = Svedberg unit).
  • Ribosome = site of TRANSLATION (mRNA → polypeptide; tRNA brings amino acids — Chapter 6).

(iv) Rough endoplasmic reticulum (RER)

Trick: Ribosomes ↔ Rough ER — ER with ribosomes = rough, ER without = smooth.
  • Usually continuous with the nuclear membrane — mRNA leaving the nuclear pore finds ribosomes faster ("the nearer college" analogy: both colleges offer the same, but the closer is easier).
  • Surface carries 80S ribosomes → rough, grainy look under the microscope.
  • Definition (3 keywords): system of INTERCONNECTED, FLATTENED, MEMBRANOUS SACS (called cisternae; one = cisterna).

Functions of RER:

  1. Involved in protein synthesis via translation (because of ribosomes).
  2. Protein folding (= post-translational modification) — many polypeptide chains fold together in the correct orientation to give a protein.
  3. Packages the protein into vesicles and transports it to the Golgi body (like gift-wrapping before handing over — it can't just eject it).

(v) Golgi apparatus / Golgi body

RERcisternae INTERCONNECTED+ ribosomes on surface GolgiSEPARATE stack, no ribosomes,swollen ends → vesicles
RER vs Golgi — two structural differences: continuity & ribosomes
  • A stack of flattened membranous sacs (cisternae); each sac has a swelling at its end where a vesicle pinches off (like flaky skin peeling) — the swollen end forms the vesicle, which then pinches off and repeats.
  • Unlike ER the sacs are not interconnected (stacked like books) and have no ribosomes.

Functions of Golgi body: (1) protein modification (2) packages proteins into vesicles for secretion (3) production of lysosomes.

Careful: RER folding = making the protein. Golgi modification = adding other molecules to a protein that is already complete ("add a ribbon & card to the gift").

When folding is complete in the RER, a fully folded protein molecule (made of polypeptide chains) is formed → it goes to the Golgi, where other biological molecules are attached to form conjugated molecule(s) = molecules created when 2 distinct molecules from different categories combine.

protein + = conjugated protein
lipids (short chain attached) → lipoprotein
sugars (carbohydrates) → glycoprotein

Naming trick: the main molecule is the last word (the "surname"); the short chain attached is the prefix. Same logic: peptidoglycan = carbohydrate (glycan) main + peptide chain attached.

Why modify proteins? Important (1) for the protein to function properly and (2) for the protein to be delivered to its specific destination.

Pathway: final modified protein is packaged in vesicles → used inside the cell, or moved to the cell membrane and secreted out (e.g. enzymes, peptide hormones like insulin / glucagon).

NUCLEUSDNA→mRNA RER ribosometranslate+fold→protein GOLGImodify + package vesicle: usedin celllysosome(special vesicle) secretedout of cell pathway: nucleus → ribosome/RER → Golgi → vesicles

(vi) Lysosomes

  • Spherical, single-membrane-enclosed organelle; a specialised Golgi vesicle (released into the cytoplasm).
  • Contains an array of hydrolytic (digestive) enzymes at a low (acidic) pH — each enzyme has an optimum pH; these work best in acid.
  • Hydrolytic enzymes are proteins → made in RER, modified & packaged by Golgi (recall!).
worn-out organelle digestedlysosome
Autophagy
acid leaks → cell bursts
Autolysis
bacteriumforeign particle digested
Phagocytosis

Functions of lysosome:

  1. Autophagy — ordered and purposeful digestion of cell organelles (auto = self, phagy = digestion). Happens automatically when an organelle is worn out → beneficial to the cell.
  2. Autolysis — self-destruction of cells: digestive enzymes leak out of the lysosome and start destroying the cell (acid is toxic) = "lysosomal cell death".
  3. Phagocytosis — digestion of foreign particles that got into the cell, e.g. bacteria.
Why "suicide sacs"? Enzymes are proteins; digestive → hydrolytic enzymes → they need an acidic environment. If that acidic content leaks into the cytoplasm ⇒ cell death / cell lysis occurs — therefore lysosomes are also called "suicide sacs".

(vii) Smooth endoplasmic reticulum (SER)

  • Responsible for synthesis of lipids — e.g. steroids (steroidal hormones: oestrogen, progesterone, testosterone). (Peptide hormones such as insulin & glucagon are protein-based → RER/Golgi, not SER.)
  • System of interconnected flattened membranous sacs (cisternae) — same structure as RER but no ribosomes → smooth; also called "agranular ER".
  • Detoxification (e.g. alcohol, toxins) — liver cells have a lot of SER.
  • No ribosomes ⇒ no translation / no protein synthesis or modification in the SER.
SER — smooth sacs
RER — orange dots = ribosomes

(viii) Mitochondria

Head vs tail: head of the stalked particle (ATP synthase) always points to the matrix; tail points to the intermembrane space.
  • Double membrane: smooth outer membrane + folded inner membrane. Folds = cristae (singular crista). Plural mitochondria / singular mitochondrion.
  • 2 compartments: intermembrane space (IMS) (gap between membranes) and matrix (inner medium).
  • Stalked particles (lollipop-shaped) on the cristae; head = enzyme ATP synthase → makes ATP.
  • Has its own circular (naked) DNA — no membrane round it, so not a nucleus — and 70S ribosomes.
  • DNA + ribosomes ⇒ can do transcription & translation ⇒ protein synthesis ⇒ a self-replicating organelle.
  • Production of ATP via aerobic respiration ("powerhouse"). ATP = energy currency; the only form of energy cells can use for active processes.
outer membrane inner membrane(folded) cristae =folds of innermembrane circular DNA70S ribosomes MATRIX intermembrane space (IMS) ● orange lollipops = stalked particles (ATP synthase heads face matrix)
intermembrane spacetailhead =ATP synthasematrix
stalked particle

Matrix contains soluble enzymes for respiration. Cristae give a large surface area for enzyme reactions. Cells use ATP from respiration for energy-requiring processes.

(ix) Chloroplast (plants — self-replicating organelle)

  • Only in autotrophic cells (auto = self; they make their own food); green pigment = chlorophyll (gives leaves their green colour).
  • Double membrane (outer + inner) with an intermembrane space; own circular DNA and 70S ribosomes ⇒ self-replicating (protein synthesis possible).
  • Thylakoid = one flattened disc (coin-like); granum (plural grana) = stack of thylakoids; grana joined by inter-granal lamellae. (Granum = singular, grana = plural.)
  • Stalked particles on the thylakoid membranes (head = ATP synthase) → ATP is made.
  • Chlorophyll in the thylakoid/grana → light energy is absorbed / trapped there.
  • Stroma = the surrounding medium → site of the light-independent reaction.
outer membraneinner membrane circular DNA70S ribosomes (orange dots) intermembrane space = gap between the 2 membranes granum (stack)thylakoidsgranum inter-granal lamellae STROMA stroma = site of light-independent (dark) reaction
chloroplast ultrastructure — 3 compartments: IMS, stroma, thylakoid space
granum = stack1 thylakoid + stalked particles
granum = stack of thylakoids = site of LIGHT-DEPENDENT reaction (ATP made)
Photosynthesis (2 stages): Light-dependent (grana/thylakoids; photophosphorylation) → light energy → ATP · Light-independent / dark (stroma; Calvin cycle) → ATP used to make carbohydrate (glucose). Plant can make food even without light because of the 2nd stage. (Names are A2 knowledge — only the sites are needed.)

Chloroplasts convert solar (light) energy into chemical (food) energy by photosynthesis.

10. Mitochondria vs Chloroplast

Structural similarities
  • 70S ribosomes
  • circular DNA
  • 2–10 µm in size
  • stalked particles (ATP synthase) — mito: on cristae, heads → matrix · chloroplast: on thylakoid membrane, heads → stroma
  • double membrane (outer, inner, IMS)
Functional similarity

Both produce ATP using the enzyme ATP synthase.

Functional differences
  • Mito: ATP via aerobic respiration
  • Chloroplast: ATP via photosynthesis (light-dependent reaction)
Mitochondria Chloroplast
2 compartments: IMS + matrix 3 compartments: IMS + stroma + thylakoid (space)
Cristae (folds of inner membrane) give large surface area for enzyme reactions Thylakoid membrane gives large surface area for enzyme reactions
Sausage-shaped Oval / spherical
Matrix has soluble enzymes for respiration Stroma has soluble enzymes for photosynthesis
Inner membrane is folded (cristae) Inner membrane is not folded

Tip: the folds (cristae) are why mitochondria look "sausage-like"; a chloroplast's membranes are smooth and round.

11. Plant-only Structures

(x) Cellulose cell wall

  • Outermost covering of a plant cell; made of the polysaccharide cellulose (poly = many; built from cellulose fibres in a criss-cross mesh).
  • The gaps in the mesh are pores → anything small enough passes → fully permeable (no filtering). Cellulose fibres are highly tensile (can bear huge pressure — like a PVC pipe vs a thread).
porecellulose fibre mesh
pores → permeable

Functions:

  1. Mechanical strength → prevents cell lysis (animal cells burst if too much water enters; the wall resists swelling — turgor).
  2. Protects the protoplasm from invading micro-organisms (pores too small for bacteria/viruses).
  3. Maintains shape — structural framework, mechanical support (like a building's framework) → definite regular shape.
  4. Permeable for diffusion; helps absorption of minerals & solutes with water in root-hair cells.
  5. May also serve as a reservoir for food.
Two boundaries: plant cell has wall (1st gate, fully permeable) + membrane (2nd gate, selective) = the cell boundary. Substances must cross both.
cell wallcell membranecytoplasm

(xi) Large permanent vacuole & tonoplast (only in plant cells)

  • Contents of the vacuole = cell sap (glucose, sucrose, amino acids, water, nutrients, metabolic waste).
  • Cell sap is enclosed by a membrane called the tonoplast — selectively permeable, regulates entry/exit of substances into/out of the cell sap, so waste/nutrients don't leak into the cytoplasm and disturb enzymes.

Functions of the large permanent vacuole:

  • Storage site for useful substances (glucose, amino acids, water) and waste (metabolic waste products).
  • Vacuolar turgidity pushes the chloroplasts to the edge of the cell ⇒ maximises light absorption ⇒ increases efficiency of photosynthesis (light travels a shorter distance).
  • Turgidity supports the plant cell and maintains its shape.
nucleus ↘VACUOLE(cell sap)chloroplasts pushed to the edgetonoplast = vacuole membrane
big turgid vacuole → nucleus & chloroplasts squeezed to the periphery

(xii) Plasmodesmata

Definition: made up of cytoplasmic strands which run transversely across the walls of a plant cell — channels where the cell wall & membrane boundary is absent between 2 adjacent plant cells (singular plasmodesma).

Analogy: neighbours build an internal door between their houses instead of going out the gate and ringing the bell → quicker.
plant cell 1plant cell 2vacuoleplasmodesmacytoplasm continuous
cell wall + membrane (= cell boundary) are absent at the plasmodesma

Functions: (1) transport of water, sugars, amino acids, proteins, hormones etc. between adjacent cells; (2) rapid communication between adjacent cells because substances do not have to cross the cell boundary (cell wall & membrane). Cytoplasm is a semi-fluid (sol-gel).

12. Cytoskeleton & Microtubules

(xiii) Cytoskeleton — "skeleton of the cell" (structural framework)

Component Diameter Note
① Microtubules 10–25 nm (largest) tubulin protein; hollow
② Intermediate filaments 7–10 nm
③ Microfilaments 3–7 nm (smallest) actin filament, myosin, tropomyosin

Functions of cytoskeleton:

  1. Structural support and gives shape to a particular cell.
  2. Intracellular movement of organelles.
  3. Plays a part in cell division through centrioles.
  4. Muscle cell contraction (via actin & myosin microfilaments).
  5. Movement of an entire cell via flagellum (e.g. sperm cell).

(1) Microtubule structure & assembly

α-tubulinβ-tubulin monomerstubulin dimer(α+β) many dimers polymerise= PROTOFILAMENT 13 protofilaments in a ring= MICROTUBULEhollow cylinder · 10–25 nm (≈25 nm) α + β → tubulin (hetero)dimer → protofilament (any number of dimers) → 13 protofilaments = hollow cylindrical microtubule
  • Microtubules are made of tubulin protein, 2 types: α-tubulin and β-tubulin.
  • 1 α + 1 β = tubulin dimer (heterodimer, since the two units differ).
  • Numerous dimers polymerise into a long chain = protofilament — no fixed number of dimers (board example: 4 or 8).
  • 13 protofilaments join into a hollow cylinder = microtubule — here the number 13 is fixed. Cross-section ≈ 25 nm.

13. Centrioles, Cilia, Flagella, Microvilli

★ Centrioles (near the nucleus)

  • Only in animal cells (absent in plants; usually absent in fungi). Made up of microtubules.
  • Always exist as a pair at right angles to each other, close to the nucleus — never a single one.
  • Arise from MTOCs (microtubule organising centres) — regions where microtubules assemble. The most common MTOC = centrosome (the region holding the 2 centrioles).
  • Arrangement: "9 + 0" = 9 microtubule triplets around a hollow centre (triplets linked by connecting fibrils).
  • 3 microtubules = 1 triplet; 9 × 3 = 27 microtubules (each microtubule = 13 protofilaments).
Function: cell division — formation of the spindle fibre (spindle fibres are made of microtubules; details in Chapter 5, mitosis).
hollow
centriole cross-section: 9 triplets, centre empty = 9+0
2 centrioles at 90° = centrosome
pair at right angles

★ Cilium (plural cilia)

  • Small, slender, hair-like projections on the surface of some cells (e.g. lungs/airways, oviduct/fallopian tubes — wave to move mucus / the ovum).
  • A centriole moves to the cell surface membrane and is modified into a basal body (the part beneath the membrane) which templates the formation of the cilium. The cilium = outgrowth of microtubules enclosed by the cell membrane.
  • Cross-section (axoneme): "9 + 2" = 9 doublets around 2 central singlets.
  • Each doublet: A microtubule (complete circle, 13 filaments) + B microtubule (incomplete, 11 filaments). A carries dynein arms (outer + inner) pointing toward the neighbouring B.
  • Dynein = motor protein: converts the chemical energy of ATP into mechanical energy → arms grip the adjacent doublet, push/slide it, release, grip again (rhythmic wave). If the doublets were not attached they would just slide past each other.
axoneme (cilium T.S.) = 9 + 29 outer doublets(A: 13 filaments,B: 11 filaments)2 central singletsdynein arms on A →→ B doublet 1 doublet 2ATP → dynein arm grips,slides neighbour up, releases ↑ sliding force → bending
9+2 axoneme · dynein arms (powered by ATP) slide adjacent doublets → movement
cilium (9+2) — microtubules,covered by cell membranecell surface membranebasal body (modifiedcentriole: 9 triplets)
centriole → basal body (below membrane) → cilium (outgrowth above)
Centriole Cilium / eukaryotic flagellum
arrangement 9 + 0 (triplets) 9 + 2 (doublets + 2 singlets)
location inside cell, no membrane covering outgrowth beyond the cell; covered by cell membrane
job spindle fibres in cell division movement (dynein + ATP)

★ Eukaryotic flagellum

Long tail-like projection used for locomotion of the whole cell (e.g. sperm cell); structure, dynein arms and movement are identical to cilia: 9 + 2, with a basal body (BB) and enclosed by the cell membrane. Not the same as the bacterial flagellum (made of flagellin protein; see prokaryotes).

BBeukaryotic flagellum (9+2)sperm / cell
one long flagellum vs many short cilia

★ Microvilli (brush border)

Finger-like membrane protrusions (projections) supported by the actin cytoskeleton. Function: increases the surface area for faster absorption via diffusion, osmosis and/or active transport (e.g. epithelial cells lining the small intestine; cells have many mitochondria, ER, Golgi, lysosomes).

microvilli↑ surface areanucleus
absorptive epithelial cell with brush border

14. Structure of a Prokaryotic Cell (Bacteria)

Always unicellular; oldest and simplest living cells; ubiquitous (found everywhere), huge numbers. Size 1–5 µm.

slimy capsule →peptidoglycan cell wall →(murein) cell membrane →(wall + membrane = cell boundary) circular DNAcytoplasm70S ribosomes plasmidflagellumpili / sex pili
always present: wall, membrane, circular DNA, 70S ribosomes, cytoplasm · sometimes: capsule, plasmid, flagellum, pili (a printed diagram also shows a mesosome)
ALWAYS present (5): peptidoglycan cell wall · cell membrane · circular (naked) DNA · 70S ribosomes · cytoplasm.
MAY OR MAY NOT be present: plasmid · slimy capsule · flagellum · pili.
Structure Details / function
Peptidoglycan cell wall (murein) peptide chain attached to carbohydrate (glycan = main molecule). Bacteria need water/moisture → wall gives mechanical support and prevents osmotic lysis (osmosis = passive movement of water); (ii) protection against phagocytes. With the membrane = cell boundary.
Cell membrane regulates entry & exit of substances; semi-permeable (filter).
Circular DNA genes code for bacterial proteins; no free ends; naked (no histones), free in cytoplasm, no nuclear membrane → no true nucleus. Does transcription.
70S ribosomes protein synthesis via translation. DNA + ribosomes ⇒ bacteria make their own proteins/enzymes.
Cytoplasm contains soluble enzymes for vital life processes (e.g. respiration — no mitochondria, enzymes do it in cytoplasm/membrane).
Plasmid small fragment of extra genetic material (double-stranded ring DNA). Serves as a vector in genetic engineering (cut the ring with a restriction enzyme, insert the desired gene → bacterium makes a new protein; Ch. 8).
Slimy capsule protective layer of polysaccharides + protein (sticky). (i) gives pathogenicity (disease-causing ability — only capsulate bacteria are virulent); (ii) protects against phagocytosis (and bacteriophage attachment); helps stick to surfaces.
Flagellum made of the protein flagellin; locomotion (whip-like movement).
Pili / sex pili hollow tubular external structures of pilin protein; transfer of DNA between prokaryotic cells by conjugation ("Bluetooth / AirDrop" of genes).
Linear vs circular DNA: eukaryote DNA is linear (5′ and 3′ ends) and wrapped around histone proteins; prokaryote / mitochondrial / chloroplast DNA is circular and naked (no ends, no histones).

15. Modes of Transmission of Bacterial Genes

Vertical transmission

Parent → offspring (genetic material from a parent organism to offspring). In bacteria = asexual reproduction by binary fission: 1 cell → 2 → 4 → 8 … (≈20 min each). Daughter cells are genetically identical (no 2nd parent). No mitosis/meiosis because those are nuclear divisions and bacteria have no nucleus.

Horizontal transmission = genetic recombination

Transmission of genetic material from one bacterium to another of the same or different species (e.g. E. coli → Vibrio cholerae). Not reproduction — it brings variation. 3 types: ① Transformation ② Transduction ③ Conjugation.

∞binary fission → identical daughter cells
vertical: binary fission
  • Transformation: random uptake of bacterial gene/DNA present in the surroundings through the cell boundary.
  • Transduction: a virus (bacteriophage) transfers genetic material from one bacterium to another (viral vector — phage picks up donor DNA in A, injects it into B). Bacteriophage = virus that "eats" (phage) bacteria.
  • Conjugation: bacterial genes are transferred from one bacterium to another through the conjugation tube (mating-pair formation) built by the sex pili.
bacterium Abacterium Bphage carries A's DNATRANSDUCTION (viral vector)
conjugation tube (sex pilus)DNA passes donor → recipientCONJUGATION

16. Comparison: Prokaryote · Animal · Plant

Property Bacteria / prokaryotes Animal Plant
Cellular organisation unicellular multicellular multicellular
★ Cell wall peptidoglycan absent cellulose
DNA circular / naked DNA (no histones) linear, wrapped around histones linear, wrapped around histones
Nucleus absent present present
Membrane-bound organelles absent (no RER, SER, mitochondria, Golgi, chloroplast) present present
Reproduction asexual only — binary fission both sexual & asexual observed both sexual & asexual observed
Cell division binary fission (no mitosis/meiosis) mitosis & meiosis mitosis & meiosis
Ribosomes 70S 80S (mitochondria: 70S) 80S (mito & chloroplast: 70S)
Flagella present (some) absent (except sperm — cell-type specific) absent
Average size 1–5 µm 10 µm – 100 µm

★ Fungi (eukaryotes) have a chitin cell wall. Eukaryotic DNA: helical DNA wrapped around histone protein. Why no mitosis/meiosis in bacteria? Both are nuclear divisions and there is no true nucleus. Prokaryotes are ~10× smaller than eukaryotic cells and evolved first.

17. Viruses (average size 20–300 nm)

Acellular = absence of cellular life/organelles. Viruses are not in the 5-kingdom classification and are treated as non-living.
  • A cell needs cell membrane + genetic material + protoplasm. A virus has only genetic material (cell membrane? ✗ · genetic material ✓ · protoplasm ✗) → acellular particle/species.
  • Why non-living? no cytoplasm · no ribosomes · no metabolism (no enzymes, no ATP, no respiration). Outside a host cell they are inactive particles that use no energy; they only become active inside a host.
  • They hijack the protein-synthesis machinery of the host cell to make viral proteins. All viruses are parasitic.
genomeenvelopecapsid
virus: genome + capsid (made of capsomeres) ± envelope
Part Details
Genome — compulsory genetic information, either DNA or RNA, never both; 4 types: ss DNA, ds DNA, ss RNA, ds RNA
Capsid — compulsory protein coat made of protein sub-units capsomeres. Roles: ① protects the genetic material ② helps attachment to host cells
Envelope — some only phospholipid membrane taken from the host cell's membrane when the virus leaves. With envelope = enveloped (e.g. HIV); without = non-enveloped / naked (e.g. polio, rhino virus)

How a virus replicates (e.g. a DNA virus)

  1. Virus attaches to the host cell (via capsid) and enters; capsid breaks up, releasing the genome into the host cytoplasm.
  2. Viral DNA is transcribed into viral mRNA using the host's DNA polymerase (in host nucleus) — the virus has no enzymes of its own.
  3. Viral mRNA attaches to host ribosomes → translation → viral proteins (capsomeres).
  4. Viral genomes + capsids assemble into many new viruses (replication).
  5. Host cell fills up, bursts (lysis) and dies — hence all viruses are parasitic (a parasite harms its host, like a malarial mosquito).
virus injects genomeDNA polymerasehost nucleusviral mRNAhost ribosomes make viral proteinsviral protein (capsomeres)
host cell machinery (HC) hijacked: host DNA polymerase + host ribosomes → viral mRNA → viral proteins

18. Organelle Sizes & Quick Recap

Organelle (largest → smallest) Size
Nucleus 5–10 µm
Chloroplast 5–7 µm
Mitochondria 0.5 to 3 µm
Nucleolus 0.2 to 3.5 µm
Lysosomes 0.1 to 1.2 µm
Golgi body 1 µm
SER 50 nm
RER 20–30 nm
Ribosomes 20–30 nm
Mnemonic: "Nobody Can Make Noodles Like Chef Ramsay" → Nucleus · Chloroplast · Mitochondria · Nucleolus · Lysosome · Centrioles · Ribosomes (board's order; note: "Chef" = centrioles there — the table above has Golgi/SER/RER between lysosome and ribosomes).
✓ Quick Recap — Cell Structure
  • M = I/A (MIA); I = M×A; no units; same units top & bottom · eye sees 50–100 µm
  • LM: light, ×1500, live+dead, colour, cheap · EM: e⁻, ×250 000, dead only, B&W, vacuum, expensive · TEM 2D thin / SEM 3D surface
  • Resolution ≈ ½ λ: LM 200 nm (λ 400), EM 0.5 nm (λ 1) · total mag = eyepiece × objective
  • Prokaryote: unicellular, no true nucleus, no membrane organelles, 70S, circular naked DNA, peptidoglycan wall, binary fission, 1–5 µm
  • Eukaryote: true nucleus, membrane organelles, 80S, linear DNA + histones, 10–100 µm
  • Plant only: cellulose wall · chloroplast · large permanent vacuole (tonoplast, cell sap) · plasmodesmata · Animal only: centrioles, lysosomes
  • Nucleus = transcription, control centre · nucleolus = makes ribosomes · ribosome = translation · RER = translate + fold + package · Golgi = modify (conjugated proteins) + package + lysosomes · SER = lipids/steroids + detox · lysosome = autophagy, autolysis, phagocytosis · mitochondria = ATP (aerobic respiration, cristae/ATP synthase, matrix) · chloroplast = photosynthesis (grana light-dep., stroma light-indep.)
  • Mito vs chloroplast: both 70S, circular DNA, 2–10 µm, stalked particles, double membrane · 2 vs 3 compartments · cristae vs thylakoids · sausage vs oval
  • Cytoskeleton: MT 10–25 nm > IF 7–10 nm > MF 3–7 nm · microtubule = 13 protofilaments of α/β tubulin dimers · centriole 9+0 (27 MTs) · cilium/flagellum 9+2 (dynein + ATP)
  • Virus: acellular, genome (DNA or RNA) + capsid (± envelope), parasitic, hijacks host machinery, 20–300 nm