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Cell structure
A2.2.1. Cells as the basic structural unit of
all living organisms
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A2.2.5. Prokaryote cell structure
(Pro means before and karyon means nucleus.)
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3. Common organelles for plant and animal cells
•Ribosomes are the protein factories of the cell.
•Endoplasmic reticulum (ER) is involved in protein and vital lipids production.
•Golgi apparatus stores and transports the processed in the cell proteins.
•Mitochondria are the site of cellular respiration where glucose molecules are transformed into
energy molecules.
•Lysosomes contain enzymes for breaking down components of cells. They are important in cell
death, in breaking down old organelles.
•Nucleolus- the site of production of ribosomes.
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4. Additional organelles in plant cells
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https://www.youtube.com/watch?v=URUJD5NEXC8
A2.2.7. Processes of life in unicellular
organisms
• All living things carry out seven basic functions integral to survival:
• Metabolism – Living things undertake essential chemical reactions
• Reproduction – Living things produce offspring, either sexually or
asexually
• Sensitivity – Living things are responsive to internal and external
stimuli
• Homeostasis – Living things maintain a stable internal environment
• Excretion – Living things exhibit the removal of waste products
• Nutrition – Living things exchange materials and gases with the
environment
• Growth / Movement – Living things can move and change shape
or size
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A2.2.8. Differences in eukaryotic cell
structure between animals, fungi, and plants
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Eukaryotic Cells Comparison
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A2.2.9. Atypical cell structure in eukaryotes
• Red Blood Cells:
• Red blood cells have no nucleus or mitochondria when they are
mature (the organelles are ejected to allow more haemoglobin to
be stored)
• Without any genetic material, red blood cells cannot
independently replicate and new cells must be continually
produced within the bone marrow
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• Sieve Tube Elements:
• Sieve elements that line the phloem in plants are interconnected
by plasmodesmata into supracellular assemblies that transverse
the length of a plant
• These sieve elements also lack nuclei and have few organelles,
relying on local companion cells for survival
• Phloem sieve tube elements challenge the idea that multicellular
structures are composed of anatomically independent cells
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• Striated Muscle Fibres:
• Individual muscle cells fuse together to form long striated
muscle fibres
• These fibres are surrounded by a continuous plasma
membrane and possess multiple nuclei
• Striated muscle fibres challenge the idea that all living things
are comprised of discrete cell units
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• Aseptate Fungal Hyphae:
• Fungi may have filamentous structures called hyphae, which are
used for nutrient absorption and growth
• Hyphal cells are typically separated by internal walls (septa), but
some hyphae are not partitioned and have a continuous
cytoplasm (with multiple nuclei)
• Aseptate fungal hyphae challenge the idea that living structures
are composed of autonomous cells
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A2.2.10. Cell types and cell structures viewed
in light and electron micrographs
• Light microscopes possess low magnification and resolution,
but can view living specimens in their natural colors
• Eukaryotic cells will be much larger than prokaryotic cells but
without staining, only nuclei and chloroplast will likely be visible
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• Electron microscopes possess higher magnification but can
only view dead specimens in monochrome (false color can be
applied)
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Types of organelles
a. Nucleus
•The nucleus is a double membrane structure with
pores that stores the genetic material (DNA)
•Within the nucleus, a specific region called the
nucleolus is responsible for ribosome assembly
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b. Mitochondria
• Mitochondria are responsible for ATP
production via the process of aerobic cell
respiration
• It has an inner membrane that is highly folded
into cristae in order to increase the SA:Vol
ratio
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c. Endoplasmic reticulum
•The ER is a membranous network that synthesises
and transports materials via vesicles
•The smooth ER synthesises lipids, while the rough ER
synthesises proteins (via ribosomes)
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d. Golgi complex
•The Golgi apparatus is an assembly of folded
membranes responsible for material secretion
•Material is sorted, stored, modified and exported
from the cell within vesicles (exocytosis)
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e. Vesicles
•Vesicles are membranous containers involved in the
transport and storage of materials
•Peroxisomes are involved in the oxidation of lipids and
the digestion of toxic metabolites
•Lysosomes are responsible for the breakdown of
cellular wastes and pathogenic debris
•Vacuoles are comparatively larger containers that store
excess fluid and regulate pH
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f. Chloroplasts (in plants)
•An organelle responsible for photosynthesis
(converting light energy into chemical energy)
•Chloroplasts use the photosynthetic pigment
chlorophyll to absorb and utilize light energy
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g. Centrosomes (in animals)
•Centrosomes are composed of paired centrioles
•They contribute towards cell division in animal cells
(plants and fungi use other structures)
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A2.2.11. Drawing and annotation based
on electron micrographs
a. Prokaryote: Bacteria
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b. Eukaryote: Animal Cell
•When drawing animal cells, the following should be included:
•The nucleus should be a double membrane structure with pores
•The ER network should be shown as connected membranes, but
Golgi membranes should be unconnected
•Ribosomes should be drawn as filled in dots and labelled as 80S
in size
•Mitochondria should be sausage-shaped and the inner
membrane highly folded (into cristae)
•Lysosomes and secretory vesicles should all look the same
(except for the labelling)
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c. Eukaryote: Plant Cell
•When drawing animal cells, the following should be
included:
•A large central vacuole should be included that
occupies significant space within the cell
•A cell wall made of cellulose should be included as a
thicker line external to the plasma membrane
•Chloroplasts should be double-membrane structures
with internal stacks of flattened discs (grana)
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https://www.youtube.com/watch?v=B-CnLnOHijY&list=PLEnRjfGdbEtKRMdp_x5ywmUCRd6vVJNwU&index=2
A2.2.2. Microscopy skills
• 1. Using a Light Microscope
• Most light microscopes include both an ocular lens
(~10×) and objective lens (~10×; 40×; 100×)
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• 2.Calculating magnification and actual cell
size
• A photo taken down a microscope is called a
micrograph.
• To find the magnification of a micrograph or a drawing
we need to know two things:
- the size of the image (in the drawing or the
micrograph)
- the actual size of the specimen.
This formula is used for the calculation:
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https://www.youtube.com/watch?v=oSd7Dlx56Xg&t=271s
• In order to calculate magnification, both image
size and actual size must be in the same units
• Metric conversions can be applied according
to the following table:
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• 3. Calculating cell size- examples
• Worked example 1
• The length of an image is 30 mm. It represents a
structure that has an actual size of 3 µm. Determine
the magnification of the image.
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Worked example 2
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• Worked example 3
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A2.2.3. Developments in
microscopy
• 1. Light Microscopy
• Light microscopes can be used to view living
specimens in their natural colours
• These microscopes use glass lenses to bend light in
order to magnify images (extent of magnification is
determined by the lenses used)
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• 2. Electron Microscopy
• Electron microscopes can generate images at
a much higher magnification but cannot view living
specimens in natural color
• These microscopes use electromagnets to focus
electrons and produce monochromatic images (to
which false color may be applied)
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Surface area to volume ratio
• Cells need to produce chemical energy ( via
chemical metabolic reactions) to survive and this
requires the exchange of materials with the
environment.
• The rate of metabolism of a cell is a function of
its volume (larger cells need more energy to sustain
essential functions)
• The rate of material exchange is a function of
its surface area (large membrane surface allows
more material movements)
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Calculating SA/Vol ratio
volume (units3)
surface area (units2)
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15. Surface area to volume ratio importance to
cell functions
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