O Level'S: BIOLOGY (5090)
O Level'S: BIOLOGY (5090)
O Level'S: BIOLOGY (5090)
BIOLOGY (5090)
Chapter #1
The Cells
The Cells
The Cells
*Key Definition: “Cell is the basic unit of
life that makes up living things.”
The Light Microscope
• The light microscope has 2 convex lenses, with magnification up to
x1500.
• The eyepiece lens (ocular lens) is usually x10 and there is a choice of
objective lenses. (usually x4, x10 and x40), set in a nose piece which
can be rotated (turned around)
• Light from a mirror or a bulb is projected through the specimen
placed on a microscope slide.
• The light passes through the objective and eyepiece lenses,
magnifying the image so you can see the detail of the specimen.
• You can use coarse and fine focus knobs to make the image clearer.
• Images produced by a light microscopes are called photo micrographs
How to use a microscope
1) Adjust mirror and slide to stage.
2) Switch to lower magnification and focus.
3) Increase magnification and focus & repeat for highest
magnification.
4) Draw cell diagram with a sharp pencil.
(Draw to scale and include magnification)
The Electron Microscope
• An electron microscope is a microscope that uses
a beam of electrons as a source of illumination.
• The Electron microscope produces a detailed
image. (not clear)
• It has more resolution than the light microscope.
• It always produces black and white images.
• Images produced by an electron microscope are
called electron micrographs.
• You need a screen or a computer to look at the
images produced.
Characteristics Light Microscope Electron Microscope
1) Magnification x1500-2000 upto x10,000,000
2) Resolution 200nm 0.5nm
3) Image produced visible light rays electron beam
4) Image focused by glass objective lens electromagnetic lenses
5) Image viewed by glass ocular lenses fluoroscent screen
6) Specimen placed on glass slide copper mesh
7) Organisms maybe alive always dead
8) Specimen requires not always stain/treatment requires stains/beam
9) Images colour coloured images black and white
How to make a slide (plant cell)
1) An onion is cut into quarters.
2) One of the fleshy scale leaves is removed.
3) Snapping leaf backwards exposes the epidermis.
4) A thin inner layer of epidermis is peeled off.
5) Epidermis is placed on slide and covered with 2-3 drops of
distilled water.
6) Coverslip is then lowered and placed over it.
7) A drop of stain is put at one end of slide.
8) Stain is drawn over specimen using a small piece of filter paper
9) Draw adjacent cells out of a photomicrograph of a plant tissue.
(make sure to make double outline to show cell walls)
How to make a slide (animal cell)
1) Take a piece of liver e.g: chicken liver.
2) Crush the chicken liver make a thin film of it.
3) Place it on a microscope slide
4) Add a dye: methylene blue or iodine and then
place a coverslip on it and examine it.
5) Draw 4 cells out of a photomicrograph of a liver
cell.
(don’t draw double line as an outline of the cell because it has no cell walls)
Cutting Structures for Samples
Precautions:
1) Eye Protection must be worn.
2) Take care when using a scalpel.
3) Follow your teachers guidance.
4) Take care using the stains:
(iodine solution and methylene blue stains can stain
the skin and clothes).
Practical #1
Onion Epidermal Cells
• Preparing a slide of onion epidermis layer:
1. Peel off the epidermal layer of the curly onion leaf using forceps.
2. Peel it from the incurve of the onion bulb.
3. Place the epidermal tissue on a glass microscope slide.
4. Using a scapel, cut out 1cm square of tissue & arrange it in slide’s centre.
5. Add 2-3 drops of iodine solution.
6. Support a cover slip with one edge resting near to the angle of 45°
7. Gently lower the cover slip over the onion tissue avoiding any air bubbles.
8. Leave the slide for about 5 minutes, this allows the iodine solution stain to
react with the specimen. ( stains the cell nuclei: pale yellow and starch grains
blue)
9. Place the slide on to the microscope stage, choose the lowest power
objective lens and focus on the specimen.
10. Increase the magnification using the other objective lenses, under high
power resolution the cells are observed.
Practical #2
Plant’s with chloroplast
• Preparing a slide of cells with chloroplast:
1. Using forceps, remove a leaf from a moss plant.
2. Place the leaf in the center of the microscope slide and add 1-
2 drops of water.
3. Place a cover slip over the leaf. Using forceps, a mounted
needle or wooden splint, support a coverslip with one edge,
resting near to the cheek cell sample at an angle of 45°. Gently
lower the coverslip over the tissue. Avoid trapping air bubbles.
4. Examine the cells with high power objective lenses of a
microscope.
5. The green color chloroplasts will be seen.
Practical #3
Human Cheek Cells
Examining a slide of human cheek cells:
1. Precautions: treat contaminated items with disinfectants or by
autoclaving.
2. Rinseyour mouth with water to remove extra fragments of food
3. Take a cotton bud from a freshedly open pack.
4. Rub the cotton bud lightly on the inside of your cheeks and gums to
collect cheek cells from saliva.
5. Rub that cotton bud on the center of a clean microscope slide, leaving a
sample of saliva.
6. Repeat if the sample is too small. Then drop the cotton bud in to a
container of absolute alcohal or disinfectant.
7. Add 2-3 drops of methylene blue dye. (stains parts of cheek cells making
nuclei more visible)
8. Using forceps, a mounted needle or wooden splint, support a coverslip
with one edge, resting near to the cheek cell sample at an angle of 45°.
Gently lower the coverslip over the tissue. Avoid trapping air bubbles.
9. Leave slide for few minutes for methylene blue to react with specimen.
10. Place the slide on to the microscope stage, choose the lowest power
objective lens and focus on the specimen. Increase the magnification
slightly.
Practical #4
Human Skin Cells
• Preparing human skin cells slide:
1. Wash your wrist well, then press some transparent sticky
tape on to the cleaned area of skin.
2. Remove the tape and stick it to a microscope slide.
3. Place the slide on the microscope stage.
4. Using forceps, a mounted needle or wooden splint, support
a coverslip with one edge, resting near to the cheek cell
sample at an angle of 45°. Gently lower the coverslip over
the tissue. Avoid trapping air bubbles.
5. Look for cells. You should be able to see nuclei in them.
6. If you add methylene blue stain to the sample, the nuclei
will take the stain making it more distinct.
Practical #5
Liver Cells
• Preparing Liver cells slide:
1. Take a piece of liver e.g: chicken liver.
2. Crush the chicken liver make a thin film of it.
3. Place crushed liver sample on a microscope slide.
4. Using forceps, a mounted needle or wooden splint,
support a coverslip with one edge, resting near to
the cheek cell sample at an angle of 45°. Gently
lower the coverslip over the tissue. Avoid trapping
air bubbles.
5. Add a dye: methylene blue or iodine and then
place a coverslip on it and examine it.
Specification#2: “Draw diagrams to represent observations of
the animal and plant cells examined above.”
Specification#2: “Draw diagrams to represent observations of the
animal and plant cells examined above.”
1. Capsule
2. Cell Wall
3. Plasma Membrane
4. Cytoplasm
5. Ribosomes
6. Plasmid
7. Pilli
8. Flagella
9. Nucleoid Circular DNA
Structure
1. Bacterial Cells are called prokaryotes.
2. Very small organisms/ uni cellular/ single cells/ not often
more than 0.1mm in length/ 1000x smaller than plant cell.
3. It can only be seen under a high magnification microscope.
4. It’s cell wall is madeup of peptidoglycan - a complicated
mixture of proteins, carbohydrate (sugar) and lipids.
5. It may or may not have a gelatin capsule around it.
6. Inside the cell wall is the cytoplasm, which may contain
granules small particles of glycogen, lipids and other food
reserves.
7. Loop of DNA in coiled present inside it/ no nucleus.
8. Large no. of ribosomes float freely in the cytoplasm.
(smaller than the ribosomes present in animal & plant cell)
9. Some have one or more flagella for locomotion and some
plasmids sometimes.
Functions
1. Capsule- A protective layer.
2. Cell Wall- Prevents the cell from bursting, allows
water and salts to pass through this freely permeable
membrane.
3. Cell Membrane- Prevents Cell content from escaping
& controls what enters or leaves the cells.
4. Cytoplasm- Contains all cell orgnelles inside it.
5. Circular DNA- Controls cell division/ cell
development and cell activities.
6. Plasmids- Contain genes that carry genetic
information to help the process of the survival and
reproduction of bacterium.
7. Ribosomes- a site of protein synthesis/ makes
proteins inside a bacterium cell.
Bacterium Cell Division
Ribosomes Small, Circular Structures Inside the cytoplasm A site of protein synthesis/ makes
proteins inside a bacterium cell.