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All living things are made from cells they are a basic unit of structure
Smallest unit of life
Derived from pre-existing cells by division
Original cell
Contain a blueprint for growth, development & behaviour
theory
Site of all metabolism
1 nm
10 nm
100 nm
1m
up to 10 m
up to 100 m
2.1.5 Calculate the linear magnification of drawings and the actual size of
specimens in images of known magnification.
2.1.6 Explain the importance of the surface area to volume ratio as a factor limiting
cell size.
Volume increases at a faster rate than surface area. As volume increases, the surface area :
volume ratio decreases and the cells interior has decreasing access to the external
environment. The cell becomes less efficient as substances must be transported in & out.
Diffusion in/ out is much slower.
2.1.7
The properties are worth more than the sum of individual parts.
2.1.8
2.1.9 State that stem cells retain the capacity to divide and have the ability to
differentiate along different pathways.
Stem cells are pluripotent and can produce differentiate into many cells.
2.1.10
Bone marrow cells can be harvested before chemotherapy and replaced afterwards to ensure
the patient has an ample supply of red and white blood cells, as the stem cells found in bone
marrow are killed during chemotherapy.
2.2.1 Draw and label a diagram of the ultrastructure of Escherichia coli (E. coli) as
an example of a prokaryote.
2.2.2 Annotate the diagram from 2.2.1 with the functions of each named structure.
2.2.3
Escherichia Coli
Cell Wall
Plasma
Membran
e
Pili
Ribosome
s
Cytoplas
m
Flagella
2.3.1 Draw and label a diagram of the ultrastructure of a liver cell as an example
of an animal cell.
2.3.2 Annotate the diagram from 2.3.1 with the functions of each named structure.
2.3.3 Identify structures from 2.3.1 in electron micrographs of liver cells.
Rough
Endoplasmi
c Reticulum
Lysosome
Plasma
Membrane
Ribosomes
Golgi
Nucleus
Mitochondri
Contains ribosomes.
Synthesises proteins for use
outside the cell
Break down waste & cellular
debris using digestive
enzymes
Controls entry & exit
Semi permeable
Synthesise proteins according
to RNA orders.
Free floating or on RER
Two subunits
Processes materials produced
in the cell for intra/extra
cellular use
Control centre of the cell
Contains hereditary
information
Site of respiration converts
Prokaryotes
Naked DNA in the cytoplasm
No mitochondria
Shorter ribosomes (70S)
Fewer organelles
Plant
Made from cellulose
Animal
none
Chloroplasts
Vacuole
Centrosome
Plasticity/ Cell shape
Energy storage
Starch
none
Small temporary vacuoles
Outside nucleus
Rounded, able to change
shape
Glycogen
Structure
Integral Protein
Phospholipid Bilayer
Cytoskeleton
Glycoprotein
Peripheral Protein
Cholesterol
Function
Permanent, allows facilitated diffusion & active transport (if it is a
channel)
Two layers of globular proteins, allows selective entry and exit
Scaffold of fibrous proteins
Protein with polysaccharide attached, acts as receptor
Temporary, allows entry (outer) & exit (inner) for specific
substances
Reduces fluidity
2.4.2 Explain how the hydrophobic and hydrophilic properties of phospholipids help
to maintain the structure of cell membranes.
The phospholipids are made from a phosphate group connected to a glycerol and two fatty
acid tails.
The phosphate head is hydrophilic; they are attracted to water
The fatty acid tails are hydrophobic; they are repelled by water.
In a watery environment, the phospholipids will automatically form a bilayer as above.
The cell will therefore remain stable but allow flexibility, as the phospholipids are in a fluid.
2.4.3 List the functions of membrane proteins.
Proteins are used as hormone binding sites, electron carriers, pumps for active transport,
receptors, channels for passive transport, and enzymes
Passive diffusion unaided movement of particles from an area of high concentration to low
concentration
Osmosis unaided movement of water through a semi-permeable membrane from an area of
high water potential to low water potential.
2.4.5 Explain passive transport across membranes by simple diffusion and
facilitated diffusion.
Passive Diffusion
Particles move through the semi-permeable lipid bilayer through simple diffusion until the
concentration on both sides is even. Hydrophobic molecules diffuse inwards through this
method.
Facilitated Diffusion
Channel proteins allow hydrophilic & charged molecules in (inside of cell is hydrophobic)
2.4.7 Explain how vesicles are used to transport materials within a cell between the
rough endoplasmic reticulum, Golgi apparatus and plasma membrane.
Proteins are synthesised in the rough endoplasmic reticulum by ribosomes. Vesicles transport
the protein to the golgi apparatus, and then to the plasma membrane. The vesicle fuses with
the membrane and expels its contents outside the cell. This is exocytosis. The membrane
then pinches inwards and the vesicle detaches. This is endocytosis.
2.4.8 Describe how the fluidity of the membrane allows it to change shape, break
and re-form during endocytosis and exocytosis.
The phospholipids which make up the membrane are in a fluid state. This allows them to
move, change shape, and allow vesicles to fuse with it. This is critical during endocytosis and
exocytosis as it means that substances are able to enter & exit the cell.
2.4.6 Explain the role of protein pumps and ATP in active transport across
membranes.
Active transport is used to transport substances against a concentration gradient. The protein
pump requires energy to open and close, which it receives from ATPs. Note that protein
pumps are specific.
2.5.1 Outline the stages in the cell cycle, including interphase (G 1, S, G2), mitosis
and cytokinesis
and in plants, a
2.5.2 State that tumours (cancers) are the result of uncontrolled cell division and
that these can occur in any organ or tissue.
2.5.3 State that interphase is an active period in the life of a cell when many
metabolic reactions occur, including protein synthesis, DNA replication and an
increase in the number of mitochondria and/or chloroplast
2.5.4Describe the events that occur in the four phases of mitosis (prophase,
metaphase, anaphase and
telophase).
Interphase
1.
2.
3.
4.
5.