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3.1 Unit 2 Topic 3 Cells, Reproduction and Development
3.1 Unit 2 Topic 3 Cells, Reproduction and Development
Advanced Subsidiary
Unit 2
Topic 3: Cell Structure, Reproduction
and Development.
10 2
3
1. Eye-piece Lens (x10)
4 2. Arm
3. Coarse Adjustment / Focusing Knob
4. Fine Adjustment / Focusing Knob
8 5. Light Source / Illuminator / Mirror
6. Power switch
7. Foot / Base
8. Condenser / Iris Diaphragm
9. Mechanical Stage
10. Objective Lens ( x4, x 10, x40, x100)
11. Revolving Nose
7 12. Rotating Head
5 13. Body Tube
6
DESCRIBE HOW YOU WOULD USE A LIGHT
MICROSCOPE TO OBSEVE A SPECIMEN ON A
PREPARED SLIDE. (6marks)
• Place the microscope on a firm bench.
• Rotate the revolving nose and click the low power objective lens, x4, into
position.
• View through the eye-piece lens of x10 and switch on the light / adjust
the mirror to see a bright field of view.
• Keep the prepared slide on the stage of the microscope and clamp the
slide with the stage clips.
• Adjust the mechanical stage knob to bring the specimen into view.
• Adjust the diaphragm for optimum illumination.
• Rotate the coarse adjustment knob to focus the specimen.
• Use the fine adjustment knob to bring the specimen to a sharp focus.
Place the microscope View through the
on a firm bench. eye-piece lens of x10
and switch on the
light / adjust the
mirror to see a
bright field of view.
Adjust the
mechanical
Stage knob to
bring the
Keep the prepared slide on specimen into view
the stage of the microscope
and clamp the slide with the
stage clips
Adjust the iros Rotate the coarse adjustment Use the fine adjustment knob
diaphragm for knob to focus the specimen to bring the specimen
optimum illumination to a sharp focus
DESCRIBE HOW YOU WOULD PREPARE A LEAF
TISSUE TO STUDY THE CELLS UNDER A LIGHT
MICROSCOPE
• Peel off the outer most layer of an onion carefully, using a pair of
forceps.
• Place the peeled layer in a watch glass containing water. Make certain
that the onion peel does not roll or fold.
• Using a scalpel or a thin blade, cut a square piece of the onion peel.
• Remove the thin transparent skin from the inside curve of a small piece
of raw onion and place it on a drop of iodine solution on a clean slide.
• Cover the peel with a coverslip ensuring that no bubbles are formed.
• Using a piece of tissue paper wipe off any excess iodine solution /
methylene blue remaining on the slide.
• Observe the onion skin under low power of the microscope and then
under high power.
• Draw a neat diagram of 5-10 cells of the typical cells you can see
ONION CELLS STAINED WITH METHYLENE BLUE.
ELECTRON MICROSCOPE
• The EM uses a beam of electrons to form an image.
• The electrons are scattered by the specimen and
electromagnetic or electrostatic lenses focus the
electron beam to form an image.
• Since the wavelength gets smaller, the resolution
becomes bigger and specimens less than 1nm
(1x10-9m or 0.0001µm) could be seen clearly.
• The preparation of the specimen involves chemical
preservation, freeze-drying, freeze fracturing,
embedding, sectioning, and mounting on a metal
grid.
ADVANTAGES OF AN ELECTRON
MICROSCOPE
1. Has huge powers magnification and
resolution.
DISADVANTAGES OF AN ELECTRON
MICROSCOPE
1. Living material can not be studied
since the specimens are examined
in a vacuum and electrons could be
scattered to produce a blurred
image of the specimen.
2. Preparation of specimen involves
skills and the treatment the
specimen undergoes could result in
artefacts.
3. Electron microscopes are very
expensive and a trained technician
is needed.
4. The instrument is very large and
must be kept at a constant
temperature and pressure with an
internal vacuum.
The diagram shows
the silhouette of a
Golden Eagle reduced
16 times.
AMYLOPLAST
MITOCHONDRION
PLASTIDS
Plastids are organelles found only in plants. There
are three different types:
CENTRIOLES. RIBOSOMES
TRIPLETS OF 9 BUNDLES MADE OF A SMALLER AND
WITH 2 AT THE CENTRE LARGER SUBUNIT CONSISTING
AND OCCUR IN PAIRS AT OF rRNA AND PROTEIN
RIGHT ANGLES TO EACH OTHER
NUCLEUS
Description Function
• Organelle surrounded by • Chromatin is made from
nuclear envelope containing proteins and DNA. The pores
pores. Contains Chromatin and allow substances (RNA) to
a structure called the nucleolus move between the nucleus and
cytoplasm. The nucleolus
makes ribosomes.
LYSOSOME
Description Function
• A round organelle surrounded • Contains digestive enzymes.
by a membrane. Described as They are kept separated from
the ‘suicide bags’ since the cytoplasm by the surrounded
rupture of lysosome and membrane, but can be used
liberation of its contents could digest invading cells or to
digest its own cell. This is break down worn out
called apoptosis, the components of the cell.
programmed cell death.
VESICLE
Description Function
• A small fluid- filled sac in • Transports substances in and
cytoplasm, surrounded by a out of the cell (via the cell
membrane membrane) and between
organelles. Some are formed
by the Golgi apparatus or the
endoplasmic reticulum, while
others are formed at the cell
surface.
RIBOSOME
Description Function
• A very small organelle that • The site where proteins are
floats freely in the cytoplasm made.
or is attached to the rough • Clamps the mRNA in position
endoplasmic reticulum. for translation
• Made of rRNA and Protein.
ENDOPLASMIC RETICULUM
Description Function
• Smooth Endoplasmic • The smooth ER synthesis and
Reticulum is a system of processes lipids.
membranous tubular cavities • Rough ER folds the proteins
called cisternae filled with that have been made at the
fluid. ribosomes into 3D / Tertiary
• Rough endoplasmic reticulum structure by the formation of
is similar but covered in Hydrogen, Ionic and
ribosomes Disulphide bonds.
POST TANSLATIONAL MODIFICATION
• Proteins are made at the Ribosomes.
Ribosomes of Rough ER make proteins and
are sexcreted by exocytosis or attached to the
cell membrane.
• Free Ribosomes in the cytoplasm make
proteins that stay in the cytoplasm.
• As the polypeptide chain produced moves
through cisternae of rER, it’s folded into 3D /
Tertiary structure by the formation of
Hydrogen, Ionic and Disulphide bonds.
• Then they’re transported from the ER to the
Golgi apparatus in transport vesicles.
• At the Golgi apparatus proteins may
undergoes further processing (sugar chains
trimmed or more added to make it
glycoprotein, addition of lipid makes it
lipoprotein)
• The proteins enter more vesicles to be
transported around the cell. e.g. extracellular
enzymes (like digestive enzymes) move to the
cell surface and are secreted. (Exocytosis)
MITOCHONDRION
Description Function
• They’re usually oval-shaped. • The site of aerobic respiration
They have a double membrane where ATP is produced. They
- the inner one is folded to are found in large numbers in
form structures called cristae. the cells that are very active
Inside is the matrix which and require a lot of energy.
contains enzymes for
respiration
GOLGI APPARATUS
Description Function
• A group of fluid filled, closely • It processes and packages
packed, parallelly curved new lipids and proteins. It also
flattened sacs called cisternae. makes lysosomes.
Vesicles are often seen at the
edges of the sacs.
As the polypeptide chain moves
through the cisternae of RER,
the protein is folded into its
3D/tertiary structure by the
formation of hydrogen, ionic
and disulphide bonds.
The protein
is secreted
out by
In Golgi body, the polypeptide
exocytosis,
chain is modified into glycoprotein
as the
by the addition of
carbohydrate or vesicle fuses
lipoprotein by the with the
addition of lipids membrane
and bursts
open
POST TRANSLATIONAL
MODIFICATION
CENTRIOLE
Description Function
• Hollow cylinders containing a • Involved in the separation of
ring of microtubules (tiny chromosomes during cell
protein cylinders) division.
• Triplets of 9 bundles with 2 at
the centre and occur in pairs
at right angles to each other.
THREE STRUCTURES THAT CHLOROPLASTS
AND MITOCHODRIA HAVE IN COMMON
• Both have a double membrane / envelope
• Both have 70s ribosomes
• Both have circular DNA 70s
Circular DNA
1. Stack of curved
cisternae Modification of proteins
2. Surrounded by many
vesicles
Rough Endoplasmic 1.
Reticulum
2.
Chloroplast 1.
Site of photosynthesis
2.
The table below describes some structures found in eukaryotic
cells. Complete the table by writing the name of the structure
in the box next to its description. (4 marks)
Cytoplasm
Photosynthetic
Cell wall membrane
(murein/peptidoglycan)
Plasmids
Circular DNA/
Nucleoid Mesosomes-for
aerobic
respiration
70s ribosomes
Pilus
Flagellum
STRUCTURE OF A TYPICAL PROKARYOTE
1. NUCLEAR ZONE (NUCLEOID)
• The region of cytoplasm that contains the genetic
material (DNA).
• There is no nuclear envelope surrounding the DNA.
• DNA is circular in shape, contains about 5000 genes, the
bacterial genome, which codes for all structural and
functional proteins and enzymes.
• DNA is not associated with histone proteins ( DNA
associated with histone form chromosomes in
eukaryotic cells). So there is no true chromosomes in
prokaryotes.
Muramic acid Acetylglucosamine
Peptide bond
Tetra-
petide
chain
CHRISTIAN GRAM 1884.
Diplococcus
• Cocci (ball-shaped)
• Streptococcus mutans
Streptococcus
• Bacillus (rod-shaped)
• Clostridium botulinum
•Capsule
•Cell wall
•Ribosomes
•Nucleoid
•Plasmid
•Flagella
•Pili
Flagellum
•Cytoplasm 65
Slime layer / Capsule
➢ Slime layer, a loose
soluble covering,
prevents the cell
from desiccation and
helps it stick to food
or other cells
➢Capsule is more
structured and
compact, prevents
phagocytes engulfing
Flagellum
them. Both found in
pathogenic bacteria. 66
Cell wall
➢Thick outer
covering that
maintains the overall
shape of the
bacterial cell
➢Made of
peptidoglycan /
murien.
Flagellum
67
Ribosomes
➢ Non-membranous
organelle where
proteins are made
Flagellum
68
Nucleoid
➢ A ring
made up of
DNA containing
5000 genes
Flagellum
69
Structure of a Bacterial Cell
Plasmid
➢ Small circular DNA Plasmid
capable of
autonomous
replication.
➢An ideal candidate in
gene technology as a
vector
➢Carries very few
genes such as that for
antibiotic resistance,
Flagellum
ability to utilize certain
nutrients. 70
Ribosomes
Plasmid
➢ Non-membranous
organelle where
proteins are made
Flagellum
71
Structure of a Bacterial Cell
Flagella
➢A whip-like tail that
Plasmid
some bacteria have for
locomotion
➢Aerobic bacteria
move towards a source
of oxygen showing a
positive aerotactic
movement,
photosynthetic bacteria
move towards light
showing a positive Flagellum
phototactic movement. 72
DIFFERENCES BETWEEN PROKARYOTIC AND
EUKARYOTIC CELLS
Ribosomes
Centrioles
Starch grains
Nucleus