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2.1Unit 2: Cells, Development, Biodiversity and Conservation

SNAB Cell Structure & Organisation — IAL Edexcel Modular Revision Notes & Topical Questions

5 min read 12 parts Lesson 3 of 8 1 quiz

📚 IAL Edexcel Modular Hub / Topical Revision
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Curriculum Equation Key قوانين الرقم الهيدروجيني والاتزان الأيوني - pH & Acid-Base Equilibrium FormulasFast Exam Solution
pH = -log[H⁺] | pOH = -log[OH⁻] | pH + pOH = 14 | [H⁺][OH⁻] = 10⁻¹⁴
Word Equation & Conditions: الرقم الهيدروجيني = -لوغاريتم تركيز أيون الهيدروجين | pH + pOH = 14
Location & Specifications: الاتزان الأيوني، كيمياء 3 ثانوي، التحصيلي، و AP Chemistry.
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Lesson summary

2.1 Cell Structure and Organisation — IAL EDEXCEL MODULAR notes: Describe eukaryotic and prokaryotic cell structure, the levels of organisation of cells, and the use of light and electron microscopes.Cell theory — Schleiden and Schwann proposed in 1837 that all living organisms a…

  • Common features
  • Differences
  • Ultrastructure
  • Eukaryotic cells
  • Cell surface membrane
  • Mitochondria

Part 1 of 10Cell theory

Cell theory
Cell theory
  • Schleiden and Schwann proposed in 1837 that all living organisms are made of cells.
  • All living organisms consist of one or more cells.
  • Cells are the basic functional unit of living organisms.
  • New cells are produced from pre-existing cells.
Common features
  • Common features all cells have a cell surface membrane, cytoplasm, DNA and ribosomes.
Differences
  • Differences prokaryotes have no internal membranes and smaller ribosomes, whereas eukaryotes have membrane-bound organelles and larger ribosomes.
Ultrastructure
Ultrastructure the internal structures of a cell seen under a microscope.

Part 2 of 10Eukaryotic cells: surface membrane, nucleus and mitochondria

Eukaryotic cells
  • Eukaryotic cells they have membrane-bound organelles including a nucleus and 80S ribosomes.
  • Animal cells have centrioles and sometimes microvilli, which increase surface area for absorption.
  • Plant cells have a cellulose cell wall, a large permanent vacuole and chloroplasts.
Cell surface membrane
  • Cell surface membrane a partially permeable phospholipid bilayer about 10 nm wide that controls exchange between the cell and its environment.
Nucleus
  • Nucleus it is surrounded by a double membrane, the nuclear envelope, with pores.
  • Pores let mRNA and ribosomes out and enzymes (such as DNA polymerase) and signalling molecules in.
  • It contains chromatin, made of linear DNA wound around histone proteins.
  • The nucleolus is a dark region where ribosomes are produced.
Mitochondria
  • Mitochondria they are the site of aerobic respiration and are just visible with a light microscope.
  • A double membrane with an inner membrane folded into cristae surrounds a matrix containing respiratory enzymes.
  • The matrix also holds circular mitochondrial DNA and ribosomes needed for replication of mitochondria.

Part 3 of 10Ribosomes, endoplasmic reticulum, Golgi, lysosomes and centrioles

1Ribosomes
  • Ribosomes they have no membrane and are made of rRNA and protein in almost equal amounts, made in the nucleolus.
  • They are the site of translation.
  • 80S ribosomes occur in eukaryotes, and 70S ribosomes in prokaryotes, mitochondria and chloroplasts.
2Rough endoplasmic reticulum (RER)
  • Rough endoplasmic reticulum (RER) folded membrane continuous with the nuclear envelope and covered in ribosomes that processes proteins made on them.
3Smooth endoplasmic reticulum (SER)
  • Smooth endoplasmic reticulum (SER) folded membrane without ribosomes that produces, processes and stores lipids, carbohydrates and steroids.
4Golgi apparatus
  • Golgi apparatus a regular stack of flattened membrane sacs that modifies proteins and lipids and packages them into vesicles.
  • The cis face lies near the RER and the trans face near the cell surface membrane.
5Lysosomes
  • Lysosomes vesicles containing hydrolytic enzymes that break down waste materials and worn-out organelles.
  • They are used in immune cells and in programmed cell death (apoptosis).
6Centrioles
  • Centrioles hollow microtubule structures, absent from plants and fungi, with two at right angles forming a centrosome that organises spindle fibres.

Part 4 of 10Protein production and secretion

1
Transcription of the gene occurs in the nucleus.
2
Ribosomes on the RER make proteins by translation, and the proteins pass into the RER lumen.
3
The protein is folded and processed in the RER, then carried in a vesicle to the Golgi apparatus.
4
The Golgi modifies the protein and packages it into vesicles.
5
Vesicles carry the protein to the cell surface membrane for secretion, for example insulin, or to lysosomes or other organelles.
  • Free ribosomes
    • they make proteins that stay in the cytoplasm.

Part 5 of 10Prokaryotic cells

Prokaryotic cells
Prokaryotes
  • Prokaryotes bacteria are much smaller than eukaryotic cells.
  • The cytoplasm has no membrane-bound organelles.
  • Ribosomes are smaller (70S).
  • There is no nucleus, only a single circular chromosome free in the cytoplasm and not associated with proteins.
  • The cell wall contains murein (peptidoglycan).
Optional structures
  • Optional structures plasmids (DNA loops), capsules, flagella, pili and mesosomes.
    • (folds of the cell membrane)
FeatureProkaryotic cellEukaryotic cell
NucleusAbsentPresent
DNACircular, free, no histonesLinear, with histones
Ribosomes70S80S
OrganellesNo membrane-bound organellesMembrane-bound organelles
Cell wallMureinCellulose (plants) or chitin (fungi); none in animals

Part 6 of 10Levels of organisation

Specialised cells
  • Specialised cells cells become adapted for a function,
    • such as intestinal epithelial cells for absorption, red blood cells for oxygen transport and xylem cells for water transport.
Tissue
Tissue a group of cells working together to perform a particular function, such as epithelial or muscle tissue.
Organ
Organ a group of tissues working together, such as the heart or a leaf (palisade mesophyll, spongy mesophyll and vascular tissue).
Organ system
Organ system a group of organs working together, such as the circulatory system or the digestive system.

Part 7 of 10Light microscopy and preparing slides

Light microscope
  • Light microscope light passes through a thin specimen on a slide and is focused by objective and eyepiece lenses.
  • Parts are the eyepiece lens, objective lenses, stage, light source and coarse and fine focus.
Liquid specimen
  • Liquid specimen place drops on the slide and lower a coverslip gently to avoid air bubbles.
Solid specimen
  • Solid specimen cut a small piece, peel a very thin layer so light passes through, stain it and add a coverslip.
  • Some tissues are fixed with formaldehyde, dehydrated in ethanol, impregnated with paraffin or resin, sliced thinly, then de-waxed and stained.
Using the microscope
  • Using the microscope always start on the low power objective to find the specimen and avoid damaging the lens.
  • A drop of water prevents the specimen drying out.
  • A blurry image may need the low power lens, coarse focus or a thinner specimen.
Limitations
  • Limitations structures look different in different planes of section, light microscopes cannot see small structures and preparation may alter cells.

Part 8 of 10Staining and biological drawings

  • Stains
    • most colours in light micrographs come from stains, except green chloroplasts.
    • Differential staining uses several dyes to show different tissues.
StainWhat it colours
Methylene blueAnimal cell nuclei blue
IodineStarch blue-black
Toluidine blueTissues with DNA and RNA blue
PhloroglucinolLignin red or pink
Drawing conventions
  • Drawing conventions a title, the magnification, a sharp pencil on plain white paper, single clear lines, no shading and no sketching.
  • The drawing fills the page, shows well-defined structures in proper proportion and draws only what is visible.
  • Label lines are ruled, do not cross, have no arrowheads and touch the part labelled.
Plan drawings
  • Plan drawings low-power drawings of tissues that never show individual cells, unlike cell drawings made at high power.

Part 9 of 10Magnification and measuring size

Magnification
Magnification image size ÷ actual size, with both measured in the same units.
  • Total magnification equals eyepiece magnification (often ×10) multiplied by objective magnification.
  • Convert mm to µm by multiplying by 1000.
Eyepiece graticule
  • Eyepiece graticule an engraved ruler in the eyepiece with no fixed units that must be calibrated for each objective lens.
  • A stage micrometer with divisions of 0.01 mm (10 µm) is used to find the size of one graticule unit.
  • Once calibrated, the graticule measures objects in the field of view.

Part 10 of 10Electron microscopes

  • Resolution = the ability to distinguish two separate points; magnification is limited by resolution.
    • Light microscope resolution is limited by the long wavelength of light.
    • Electrons have a much smaller wavelength, so electron microscopes resolve closer points and show organelles, viruses and DNA.
    • Electron microscopy needs dead specimens in a vacuum, giving a snapshot such as chromosomes at stages of mitosis.
FeatureTEMSEM
BeamTransmitted through a thin specimenScanned across the surface
Image2D, shows internal structures; denser parts appear darker3D, shows surface
ResolutionVery highLower than TEM
SpecimenMust be thinNeed not be thin

Key terms

TermMeaning
UltrastructureThe internal structure of a cell seen with an electron microscope.
ResolutionThe ability to distinguish two separate points.
TissueA group of cells working together to perform a function.
OrganelleA specialised part of a cell with a particular function.
MureinGlycoprotein (peptidoglycan) forming the bacterial cell wall.
GraticuleAn engraved scale in the eyepiece used with a stage micrometer to measure size.
Transmission electron microscopeMicroscope that sends electrons through a thin specimen to show internal structure.
Scanning electron microscopeMicroscope that scans electrons over a surface to give a 3D image.

Avoid these mistakes

1
Including size as a structural difference between prokaryotic and eukaryotic cells — size is not a structural feature.
2
Confusing magnification and resolution — resolution is how clearly two points are separated.
3
Forgetting to convert units before calculating magnification — convert so image and actual size use the same unit.
4
Calling the cell surface membrane the cell wall — a wall is a separate outer layer in plants, fungi and bacteria.

Last updated:

Cambridge 9700 AS Biology Core Formula

Magnification Triangle & Unit Conversion

Formula: M = I / A  ⇔  A = I / M  ⇔  I = M × A

Units: 1 mm = 1,000 μm = 1,000,000 nm.
Rule: Convert Image size (ruler mm) to μm by ×1,000 before dividing by Actual size.

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