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Biology AS Notes AQA

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Biological Molecules:
Example of Biological molecules?
Carbohydrates, proteins, Lipids, DNA, ATP, Water and inorganic
ions
What is a monomer?
Amino acid is a monomer.
What are polymers?
Long chain of monomers joined together
Building blocks of carbohydrates?
Monosaccharides
Carbohydrate Structure
Carbon, hydrogen +oxygen
●
Carbohydrate Functions?
●
●
Chemical bond has a lot of energy which makes it a ​good
energy source​ in plants and animals.
Energy Store ​(starch in plants and glycogen in animals)
Structure​ is soluble making it easy to transport around a
cell.
What type of sugar is glucose?
Hexose (monosaccharide w/6 carbon atoms)
2 types of glucose?
Alpha and Beta glucose
Condensation​ between 2 monomers between OH groups
releasing water. Forming a ​glycosidic ​bond.
Reaction which joins
monosaccharides?
Bond formed when 2
monosaccharides/carbohydrates join? Glycosidic​ bond forms
How do you form a disaccharide?
2 monosaccharides ​joined together by a ​glycosidic bond​ ​- in
condensation​ reaction.
● Removes ​a ​water ​molecule
How is maltose (disaccharides)
formed?
Alpha Glucose + Alpha Glucose
How is Sucrose (disaccharides)
formed?
Alpha Glucose + Fructose
How is Lactose formed?
Beta Glucose + Galactose
What reaction breaks down polymers?
Hydrolysis​ reaction -- ​addition of water
● Breaking down into monomers
What is the test for testing reducing
sugars?
Add ​Benedict's solution​ (blue) and ​heat in warm water bath​.
● If Reducing sugar then it turns ​brick red
Test for Non-reducing sugars?
What are polysaccharides?
Examples of polysaccharides?
Structure of starch?
Heat w/ benedict’s solution - when no change detected carry
out:
● Add ​dilute HCl + heat (breaks glycosidic bond)​.
● Then​ sodium hydrogencarbonate​ (neutralise), then
benedict's test -turn brick red
2 or more monosaccharides joined together​ by condensation Glycosidic bond formed.
●
●
●
Long straight chain ​of 2 ​Alpha glucose​ ​which is coiled.
● Found in only ​plants
●
Feature of Starch?
●
What is the test for Starch?
Starch - energy stored in plants
Glycogen - energy stored in animals
Cellulose - cell wall of plants
●
●
Insoluble​ in water so ​water potential is not affected
easily transportable & doesn’t diffuse out of the cell.
Coiled​ so compact = good for storage
Add ​iodine​ ​solution​.
If present then it will turn ​orange to blue-black​.
What is Glycogen used for?
Main energy storage for animals
Structure of Glycogen?
● Polymer of alpha glucose joined by glycosidic bonds
Long, highly branched​ straight chains of alpha glucose
Feature of Glycogen?
●
●
●
Side branches​- quick release of energy for respiration.
Very ​compact​ molecule so good for storage +
Insoluble​ so doesn't affect water potential
Structure of Cellulose?
Long, ​unbranched chain of beta glucose​ forming ​Straight
chains
Features of Cellulose?
Straight chains are c​ross linked by hydrogen bonds​ forming
microfibrils​ ​providing ​strength and rigidity.
Types of Lipids?
Structure of Triglycerides?
How are triglycerides formed?
●
●
Triglycerides
Phospholipids
●
●
4 molecules​ overall
One molecule glycerol​ +
Fatty acid tails​ joined by
ester bonds
Condensation​ of ​fatty acid and glycerol ​molecule.
● Ester bond​ ​formed + water released.
Difference between Unsaturated and
Saturated triglycerides?
●
Saturated​ ​don't have double bonds ​between carbon
atoms.
Unsaturated have at least one double bond​.
●
1 Glycerol + 2 Fatty acid and 1 Phosphate group
●
Phosphate​ group is ​hydrophilic
(head attracts water)
Fatty acid tails ​(​hydrophobic​) so
forms a ​barrier to prevent water
soluble molecules to pass
through membrane​.
This forms​ phospholipid bilayer
●
What is Phospholipids structure?
●
Feature of Phospholipids?
●
Long hydrocarbon tail containing lot of chemical energy
-energy released when they're broken.
Structure linked to functions of Lipids?
Also insoluble as tail is hydrophobic so doesn't affect water
potential.
Uses for lipids?
-Water proofing
-Storage
-Membranes
-Energy store
-Energy Source
What is the test for lipids?
Emulsion​ ​test​:
1.​Shake​ substance w/​ethanol​ + ​add water
2.Should show as a ​milky emulsion
Importance of water molecules to
organisms?
1. Strong Cohesion​: Water has hydrogen bonds. When
water freezes it becomes ice and floats due to hydrogen
bonds.
2. High Specific Heat Capacity​: Lots of energy required to
separate water molecules due to hydrogen bonds.
3. Metabolite​: B
​ reaks down ​molecules by ​hydrolysis​ ; used
in photosynthesis; ​condensation​ ​reactions​. Also an
important ​solvent
4. Large latent heat of evaporation- ​cooling effect through
evaporation.
What are the base of proteins?
Amino​ ​acids​ are the monomers
How are dipeptides formed?
2 amino acids join ​together by ​condensation
What are polypeptides?
● Many amino acids join​ together.
By ​condensation
What are proteins made up of?
Contains ​1 or more polypeptides
What do amino acids contain?
There are 20 different amino acids and they all differ in the R
variable group.
Amino acids are linked by ​condensation​ reactions.
Water​ is ​released​.
Forms ​peptide bonds.
How are peptide bonds formed
between amino acids?
What is the primary structure of
proteins ?
Sequence of amino acids.
● Polypeptide chain held by peptide bonds
What is the secondary structure of
proteins ?
●
●
Primary structure ​coils into alpha helix
Held together by ​hydrogen bonds
What is the tertiary structure?
●
●
●
Coiled further.
3D structure
Held together by ​disulfide/hydrogen/ionic bonds
What is the Quaternary structure?
Types of proteins are there?
Made up of ​more than 1 polypeptide chain
●
●
globular (haemoglobin)
fibrous
Function of proteins?
EATS
●
●
●
●
How do enzymes break down large
molecules?
The ​substrate binds to the enzyme​ (active
site,complementary) , ​forming a ​enzyme-substrate
complex​.
-By condensation (removing water)
-The ​binding of the substrate​ and enzyme ​places stress on the
bonds (hydrogen)
-then the molecules ​separate​.
What is the test for proteins?
Biuret test:
● Add ​sodium hydroxide solution
● Then ​Copper (II) Sulfate ​(should turn ​purple​ if Protein
present)
● if proteins ​not​ ​present​ then it​ stays blue​.
Enzymes break down food molecules
Antibodies (in immune systems)
Transport proteins (in cell membranes)
Structural proteins
●
What are enzymes?
●
Biological catalysts​ which provide an alternate pathway
and ​lowers activation energy​.
●
Lock Key​ theory- ​active​ ​site​ is ​rigid​. Substrate must be
exactly ​complementary to form ES complexes​.
Induced-Fit​ - ​active site changes​ ​shape​ slightly,
substrate binds with active site​ to form E-S complexes.
Compare lock and key with induced
fit?
●
What makes enzymes specific?
●
●
Has a ​specific active site ​shape.
Only ​complementary substrates ​can be binded w/ a
​ ctive
site ​to form Enzyme substrate complex.
What is active site of the enzyme
determined by?
●
●
Tertiary structure
If substrate different then ​cannot form ES complex.
1.
2.
3.
4.
As​ temp increases​,​ kinetic energy increases
More successful collisions​ as molecules are faster
More E-S ​formed
increased rate of reaction
(until optimum)
After ​optimum​ ​bonds​ in
tertiary structure ​breaks
(hydrogen, disulfide, ionic)
Active site changes
shape; so no longer
complementary
ES complex cannot be formed
Enzyme​ ​denature
5.
Effect of temperature on enzyme
activity?
6.
7.
8.
●
Effect of pH on enzyme activity?
●
●
●
●
Effect of substrate concentration on
enzyme activity?
●
●
What are competitive inhibitors?
What are non-competitive inhibitors?
Increase in substrate, increases the chance​ of successful
collisions
More Enzyme Substrate Complexes formed ; ​increase
R.O.R
Continues ​until the enzyme's active sites are saturated/
full​= ​maximum rate of reaction
●
●
●
●
Increase in enzyme concentration​, increases the ​chance
of successful collision
Forms E-S complex
Increase rate of reaction.
Continues until all substrates have been used up​.
Then R.O.R decreases.
●
●
●
●
Molecules with same shape to substrate​ molecules
Complementary shape to active site
Binds to active site​, ​blocking the active​ ​site​.
Preventing ES complex to be formed​.
●
●
Binds​ to enzyme​ away from active site
Causes ​active site to change shape​ (no more
complementary)
Less ES complex formed ​as tertiary structure has
changed.
Increasing concentration doesn’t make a difference.
●
Effect of enzyme concentration on
enzyme activity?
If ​pH away from optimum​,
bonds in tertiary structure
break
Active site changes shape
No longer forms ES
complexes
Enzyme denature
●
●
Nucleic Acids
What are DNA and RNA?
What do DNA and RNA do?
Function of DNA?
Function of RNA?
What are ribosomes made up of?
Nucleic acids
●
●
Carry information
Made of proteins
●
Deoxyribonucleic acid​- used to ​store genetic
information.
●
Ribonucleic acid- main function is to​ transfer genetic
information from DNA to ribosomes​ to make proteins
●
RNA and Amino acids
●
●
●
Deoxyribose sugar
Phosphate group
Nitrogen containing one of
the organic bases; Adenine,
cytosine, guanine or thymine
●
●
●
Ribose sugar
Phosphate group
Nitrogen containing
one of the organic
bases ; adenine, uracil,
Cytosine, Guanine
Building block of DNA?
Building block of RNA?
RNA molecule is a ​relatively
short polynucleotide chain.
●
How does a dinucleotide form?
●
How are polynucleotides formed?
How is the Double helix of DNA
formed?
Many mononucleotides joined together in condensation
●
●
1.
2.
Structure/Properties of DNA?
3.
4.
5.
How do organic bases help stabilise
DNA? **
What does Semi-conservative
replication allow?
What does semi-conservative
replication do?
Condensation reaction​ between the phosphate​ group​ of
one nucleotide and another sugar.
Joined together by​ ​phosphodiester bond
●
When ​2 polynucleotide chains are held together by
hydrogen bonds
Between ​complementary base pairs
2 nucleotide chain joined by​ hydrogen bonds​; allowing for
molecules to unzip to replicate easily​; hydrogen bonds
make it ​more stable
Complementary base pairing​; allowing for a
​ ccurate
replication​ between 2 polynucleotides.
A-T, C-G pairing means ​equal amounts of bonding
Polynucleotide can​ twist to form DNA double helix​;
makes it ​more stable as less damaged caused​. Also
more compact
Long & twisted so store lots of information
●
Hydrogen bonds between base pairs holds 2 strands
together​.
Many hydrogen bonds formed increasing the strength.
●
Genetic continuity between generations of cells
Half of original DNA is built onto a new DNA strand.
What is the process of
semiconservative replication of DNA?
1. DNA helicase ​breaks the ​hydrogen bonds​ between the
complementary bases in the polynucleotide strands
2. Double helix unwinds​; 2 strands formed
3. Free complementary nucleotides ​bind t​ o the exposed
bases on the template strand.
4. DNA polymerase​ joins ​nucleotides ​to form a strand
What is ATP?
●
●
Adenosine Triphosphate
Source of energy in a cell​ during respiration
●
●
Glucose converts its energy to produce ATP.
ATP then releases in small quantities of energy for e.g.
Respiration
How is energy produced from ATP
using glucose?
Ribose sugar; 3 phosphate groups; adenine group
What is the structure of ATP?
What is the synthesis of ATP?
What can the inorganic phosphate be
used for which is produced during
synthesis of ATP?
What is the re-synthesis of ADP and
Pi?
What is the biological importance/
Uses of ATP?
What is the uses of ATP in organisms?
● ATP is broken down/hydrolysed into ADP​;
● This is a ​hydrolysis reaction (adding water​)
● An ​inorganic phosphate​ is catalysed by ​ATP hydrolase​.
ATP + H20 --> ADP + Pi + Energy
●
●
●
●
Pi released can be used for ​phosphorylation of other
compounds
This makes them ​more reactive.
Condensation reaction ​of ADP and Pi.
This reaction is catalysed by enzyme ​ATP synthase ​during
photosynthesis and respiration​.
Remember ​RIPS
● ReSynthesized rapidly in cells
● Immediate source of energy​; as only one bond required
to break. Also, provides a lot of energy.
● Phosphorylation of other compounds​ making them more
reactive
● Small​, ​manageable amounts of energy released​.
●
●
●
●
Maintain body temp
Cell division
Protein synthesis
DNA replication
Section 2: Cells
How to measure the diameter of
organelles using microscope?
●
●
●
Measure with eyepiece graticule
Calibrate with stage micrometer
Repeat and calculate means
What is Magnification?
Shows how much ​bigger an image appears​ than the specimen.
What is resolution?
Shows the clarity of the image;
-Also determines by how well a microscope distinguishes between
2 points which are close together.
What is formula for magnification?
magnification = image size/ actual size
1 mm=1,000 micrometre = 1,000,000nm
What is an optical microscope?
●
●
Uses light to shine through sample.
Used to measure the ​size of an object
Advantage of Optical microscopes?
●
●
●
Inexpensive
Portable
Minimum training required
Drawbacks of Optical microscopes?
●
●
Low magnification + resolution
Specimen have to be ​stained
●
Uses​ electromagnets to transmit electron beams
through a sample
Denser ​parts of the specimen​ absorb more electrons and
appear darker
What is a Transmission electron
microscope (TEM) ?
What is the advantage of TEM?
Limitations of TEM?
What is scanning electron
microscope?
Advantage of SEM?
Disadvantage of SEM?
●
●
TEM has the highest resolution and magnification​ of all
microscopes.
●
●
●
●
●
Expensive and Large
Specimen​ has to be ​dead
Specimen has to be in a ​vacuum
Staining​ is required to see specimen.
Specimen has to be ​thin
●
Fires a ​beam of electrons at a specimen​.
○ The electrons are ​knocked off any surface​ it hits
●
●
Produces a​ 3D image
Magnification ​and​ resolution ​is​ bette​r ​than​ ​optical
microscope.
●
●
●
Specimen must be ​dead
Must be in a ​vacuum
It is ​large​ and ​expensive
Used to ​separate organelles​ from different cells
What are the 3 main steps of cell
fractionation?
1.​Homogenisation
2.​Filtration
3.​Ultracentrifugation
What is the process of
homogenization?
What conditions are required for cell
fractionation?
●
●
Vibrate​ the cells
This process ​breaks plasma membranes​ and ​releases
organelles into solution​.
●
●
Solution must be ​cold​; to ​reduce enzyme activity
Isotonic​ (​same water potential​);​ prevent organelles to
burst or shrink.
Buffered​; ​maintain a pH
●
Why is isotonic important?
What is the step of ultracentrifugation?
●
●
●
Maintains the ​same water potential
No movement of water ​by osmosis
So ​allows cells ​to ​not change shape
●
Cell fragments ​put in a t​ est​ ​tube​ and spun in a ​centrifuge
at a​ low speed
Heaviest organelles​ go to the ​bottom​ and​ form a layer of
sediment
Fluid​ at t​ op​ ​removed​ and ​spun at faster speeds​ to
separate​ ​lighter​ organelles.
●
●
Eukaryotic cell structure in animals:
What is the function of the nucleus?
What is the function of cell-surface
membrane?
Nucleus​ controls the​ cell's activity
● Contains​ ​genetic​ ​material​ to make e.g. proteins
● Contains chromosomes
● Makes RNA ​and​ Ribosomes
● Contains ​linear DNA
●
●
Made up of ​proteins and lipids
It allows the ​movement of substances into​ and ​out​ of
cells
●
●
●
Oval shaped
Folded membrane
forms Crista
Matrix​ contains
DNA, ribosomes,
proteins and
lipids
●
●
Site of ​Aerobic respiration;​ ​ATP​ is ​produced​.
Found in cells which require a lot of energy
●
Surface covered with ribosomes
●
Modifies​ and ​transports proteins​ which are made by
ribosomes
●
Has​ no ribosomes
What is the structure of Mitochondria?
What is the function of Mitochondria?
What is the structure of Rough
Endoplasmic Reticulum?
Function of Rough ER?
Structure of Smooth ER?
Function of Smooth ER?
●
Synthesis​ and p
​ rocesses​ ​lipids​ + ​carbohydrates
Structure of ribosomes?
●
●
There are​ 2 types of ribosomes​; 80S & 70S
80S in eukaryotic and 70S in prokaryotic
Function of Ribosomes?
●
Site of ​Protein synthesis
Structure of Golgi Apparatus?
●
Vesicles can often seen on the edges.
Function of Golgi Apparatus?
●
●
●
Processes​ and ​packages​ new l​ ipids​ and p
​ roteins
Makes lysosomes.
Forms vesicles
What are lysosomes?
Associated with tissue break down
Eukaryotic cell structure in Plants:
Structure of Chloroplasts?
●
●
Only found in ​plant cells
Double membrane
Function of chloroplasts?
●
Site of Photosynthesis
Structure of Vacuole?
●
Fluid filled sac
Function of Vacuole?
●
●
Only​ found in ​plants
Fluid​ ​contains​ ​water
Structure of cellulose cell wall?
●
●
Rigid structure ​which ​surrounds the cells​ in plants.
Made​ of c
​ ellulose
Function of cellulose?
●
Supports cells​ and​ prevents them​ from ​changing​ ​shape
What are tissues?
Group of eukaryotic cells​ ​working​ ​together​ to perform a
particular function​;
e.g. Epithelial tissue
How are Organs formed?
● Different tissues working together​ to form ​organs​;
different organs make up organ system.
●
Prokaryotic cell structure:
What are Prokaryotic cells?
Type of organisms e.g. bacteria; ​doesn't have nucleus​.
●
●
●
What are the differences between
Eukaryotic and Prokaryotic cells?
●
●
●
●
Prokaryotic cells are much smaller than Eukaryotic
cells
E cells ​have c
​ ell walls
In P cells they have ​circular DNA molecules called
plasmids
Cytoplasm which doesn't contain membrane-bound
organelles ​e.g mitochondria.
Smaller ribosomes​ in P cells- 70s
Cell wall made of murein​; a ​glycoprotein​. whereas
animals only have membranes and plants have cellulose
P cells have ​flagella
What do many prokaryotic cells have?
●
●
●
One or more ​Plasmids​ (loops of DNA)
Capsule​ surrounding cell
One or more ​flagella​.
How do prokaryotic cells divide?
Process of ​binary fission​:
1. Circular DNA​ and ​plasmids replicate
2. Division of ​cytoplasm produces 2 daughter cells​, each
with 1 copy of circular DNA.
3. Forms ​2 identical daughter cells​.
What is a virus?
Acellular​; not a cell as they are ​non living​.
● Viruses invade and reproduce inside cells of other
organisms.
-Contains ​genetic material
-​Attachment protein​; allowing them to stick onto a host cell
-Capsid​ around the core.
What is the structure of a virus?
How do viruses replicate themselves?
●
●
●
●
They are ​acellular so cannot divide + require host cell
They attach onto ​host plasma membrane
Inject DNA or RNA into host cell
Infected ​host cell replicates​ the virus particles.
●
Cell cycle when ​Eukaryotic cell divides to produce 2
(identical) daughter cells, each with identical copies of
DNA​.
●
●
●
Growth,
Asexual reproduction
Tissue repair.
What is mitosis?
What is Mitosis needed for?
Remember ​IPMAT : ​Interphase, Prophase, Metaphase,
Anaphase, Telophase.
What is the process of Mitosis?
What occurs in Interphase?
●
●
DNA unravels and replicates in the ​nucleus​.
Organelles also replicate.
●
Stays the same ​as 2 daughter cells formed.
Process of mitosis?
What happens to the number of
chromosomes in mitosis?
What is the role of spindle?
What is cancer?
How does an uncontrolled cell division
occur?
1. Attaches to the centromere of chromosome
2. Causes ​separation ​of the ​chromosomes
Uncontrolled, rapid cell divisio​n leading to formation of tumors
and cancer.
●
Mutation
What are some cancer treatments?
-Surgery​ = aim to remove tumor
-Chemotherapy​ = Using drugs to prevent dividing cancer cells
- Treatment given as regular doses to allow time for normal healthy
cells to recover in number
-Radiotherapy​ = Radiation used to destroy cancer cells
Transport across cell membranes
What do cell membranes do?
What are cell membranes composed
of?
They act as a ​barrier​ between the cell and the environment;
controlling​ which ​substances enter and leave the cell​.
Lipids, proteins + carbohydrates
Several different components and these membrane constituents
are constantly moving.
Components; Phospholipids, Cholesterol, Proteins, Glycoproteins,
Glycolipids (receptors)
What does the fluid mosaic include?
What is the feature of cholesterol?
Restricts movement of other molecules ​moving up the
membrane.
-Maintains the shape
-Provides more rigidity
●
What is the process of simple
diffusion?
What type of process is diffusion?
What is simple diffusion determined
by?
●
●
Movement of molecules from area of high
concentration to lower concentration​;
Until it reaches ​dynamic equilibrium ​(evenly distributed)
Down the concentration gradient
Passive​ process meaning​ no energy ​is required
●
●
●
●
Surface​ ​area​ (e.g. folding)
Thickness​ of membrane
Concentration gradient
Temperature (more ke = more movement)
How does large surface area allow for
fast rate of diffusion?
●
Larger area for molecules/particles to diffuse into cell
-Oxygen
What does simple diffusion let through
-Carbon Dioxide
the membrane?
-Fat-soluble vitamins
What is Facilitated diffusion?
Faster than simple diffusion
● Used to ​transport large​ and ​polar molecules. e.g.
fructose, glucose.
● Uses channel proteins & carrier proteins
●
How do carrier proteins work in
facilitated diffusion?
●
●
Large molecules binds with carrier protein ​- on cell
surface
Protein changes shape ​allowing the molecule to be
transported through the cell
Molecule detaches​ from transporter protein and ​protein
reverts to original shape
What is the process of osmosis?
Diffusion of water molecules​ ​from an​ ​area of high water
potential to an area of low water potential.
-Through a​ ​partially permeable membrane​.
What has the highest water potential
and what does this mean?
Pure water​- meaning water will diffuse from the water molecules
into an area with lower water potential.
What occurs when plant cell is
surrounded by pure water?
What is the process of active
transport?
Process of active transport?
Describe the process of cotransport of
glucose?
●
●
●
●
Swells​ but no burst
Cell wall prevents it from bursting
Made of cellulose- strong material
Cell is ​turgid
Movement​ of ​molecules and ions from low to high
concentration​;
● Using ​energy
● Against the concentration gradient​;
● Uses ​carrier protein
Molecules ​bind ​to carrier protein
ATP ​is ​hydrolysed​ into ​ADP ​& ​Pi & energy
Pi and energy causes ​carrier proteins to change shape​.
Carrier protein ​releases ​the molecules to the other side of
the membrane (high conc)
5. Carrier protein releases the Pi to revert to original shape.
1.
2.
3.
4.
1. Glucose moves in with sodium (into epithelial cells);
2. Via​ channel protein
3. Sodium removed ​(from epithelial cells) by a​ctive
transport
4. Into blood;
5. Maintaining low concentration of sodium (in epithelial cell) /
maintaining sodium concentration gradient (between lumen
and epithelial cells);
6. Glucose moves into blood;
7. By (facilitated) diffusion;
The epithelial cells that line the small
intestine are adapted for the
absorption of glucose. Explain how?
Cell recognition and Immune system
What are pathogens?
How do pathogens cause disease?
How do foreign cells get recognised?
What is a phagocyte?
What is the process of
Phagocytosis?**
● Disease causing microorganisms
e.g. bacteria. virus, fungi
●
●
Produce toxins
Damage self cells
●
Every molecule has a specific molecule​ on its ​surface
that identifies it.
●
White blood cell​ which ​ingests​ and ​destroys​ ​pathogens
by a process called ​phagocytosis​.
Found in​ blood and tissues​; are the first​ cells to respond
to an immune system
●
●
What is an antigen?**
●
Protein​ ​on the surface of pathogens which stimulate an
immune response.
Causing antibody production/ immune response
What is antigenic variability and how
does it affect disease prevention? **
●
●
Antigen alters shape
So ​no antibodies formed
What are the roles of
antigen-presenting cells during cell
mediated response?
●
Phagocytes present antigens onto its surface for T
cells to bind together.
What is the role of T- lymphocytes in
cell mediated immunity?
T cells complementary​ ​bind​ onto the ​antigen​ on the
phagocyte's surface​;
● When binded, this ​activates other T cells to divide
rapidly​ by mitosis and form genetic​ clone T cells​.
●
What can cloned T-helper cells do?
●
●
Activate cytotoxic T cells which ​kill abnormal and foreign
cells​.
T-helper cells ​stimulate the production of B cells​ to
produce​ ​antibodies
Stimulate ​phagocytosis in phagocytes
1.Each ​B cell have a different shaped antibody​ which means it
can bind with different types of antigens
2.When ​antibody on the surface of B cell is complementary to
an antigen- they bind together.
What is the process of Clonal selection
3.When binded this ​activates B-cells to rapidly divide into
inc. B cells?
plasma cells​.
4.The plasma cells ​mainly produces antibodies which are
complementary to the antigens ​and;
produces ​memory cells​.
Why are producing memory cells
important? **
What is an antibody?
●
Proteins with specific binding sites to the antigen​.
●
●
●
Has ​4 polypeptide chains​ so has a ​quaternary structure
Variable region​ where ​specific antigens​ can ​fit​ onto it.
Hinge region​; allowing flexibility and binding to multiple
antigens.
●
Antibody has​ 2 binding sites​ so can​ bind 2 pathogens​ at
the same time.
Foms ​Antigen-Antibody complex​ causing ​clumps of
pathogens​ to form.
Phagocyte binds to antibodies ​and ​digests the
pathogens​ at once.
Structure of antibody?
Why can antibody only recognise 1
antigen? **
Process of Agglutination?
●
●
Explain how antibodies were produced
when the mice were injected with
sheep red blood cells?**
What is the primary immune response?
What are plasma cells?
●
●
●
●
●
T cell attaches to antigen of pathogen
T cell activates immune system;
T cell divides & produces T helper cells
T helper cells trigger B cells to produce antibodies
B cells divides ​producing plasma cells​ making
antibodies + memory cells
●
●
Identical to B cells.
Form antigen-antibody complex with pathogens.
●
What occurs during secondary immune
response?
●
●
If same ​pathogen enters the body; immune system will
respond faster​.
Clonal selection occurs faster. ​Memory B cells are
activated​ and​ divides into plasma cells​ to ​produce
correct antibody.
Memory T cells are​ activated and divide into correct T
cells​ to k
​ ill cells carrying antigen​.
What are vaccines?
Ethical issues of vaccines?
-Use of animals
-Pathogen might still be active
-Antigenic variation may occur
-Religious obligations
Vaccines protect people against
disease. Explain how.
Describe how giving vaccine leads to
production of antibody?
What is active immunity?
Production​ of ​antibodies by individuals own immune
system
eg. natural after disease
● artificial​ (after ​vaccination​)
What is passive immunity ?
● Introduction of a​ntibodies from an outside source
-eg. from​ mother through breastfeeding ​or placenta
-artificial (injection)
●
What are the differences between
active and passive immunity?
Human Immunodeficiency Virus which causes AIDS
What is the structure of HIV?
Process of HIV replication in T cells?
1. ​HIV attaches​ onto receptor molecules on ​host T helper cell
2. ​Capsid released into cel​l, where it ​uncoated and releases
genetic material (RNA)​ into the cell's​ cytoplasm
3. ​Reverse transcriptase​ converts ​viruses RNA to DNA
4.​ Viral DNA​ is integrated into h
​ ost DNA
5. New RNA is made and virus is released.
How does HIV cause the symptoms of
AIDS?
-HIV remains ​suspended at low levels for many years
-​Aids then develops after many years.
-Aids ​progresses to decrease the number of immune system
cells further and symptoms become serious​.
-During late stages;​ patients can develop serious infections​.
●
What are monoclonal antibodies?
●
One type of antibody complementar​y to ​one type of
antigen
Made same plasma cells​.
Tests using monoclonal antibodies are
specific. Use your knowledge of
protein structure to explain why?
What are the uses of monoclonal
antibodies?
-​Medical diagnosis;
-Allows for ​attaching an antigen to an antibody to recognise a
disease
Ethical issues of monoclonal
antibodies?
-expensive
-side effects
-Mice dies after testing
How do antibiotics work?
Why are antibiotics ineffective against
viruses?
●
●
They disrupt cell wall
Stops DNA replication
●
●
Antibiotics ​only target bacterial enzymes
Viruses don't have their own enzymes and ribosomes so
cannot be inhibited
Virus don't have a cell wall
●
What is the ELISA test?
-Allows you to see if a patient has antibodies to a certain antigen.
e.g. pathogenic infections
How is the ELISA test used?
1. Antibody used which has an enzyme attached.
2. Enzyme can react with a substrate to produce a colured product.
3. if colour change is present then the certain antigen or antibody is
present.
Section 3: Organisms exchange with
their environment
●
●
They have a ​large surface area to volume ratio
Thin surface (​short diffusion distance​)
Why can’t Animals/ Plants perform
exchange via surface ?
●
●
●
●
Small surface area to vol ratio
Long ​diffusion distance
Impermeable surface to prevent pathogens entering
Decrease water loss
Surface area:Vol ratio compared to
large and small organism?
●
●
Small​ organisms have a ​large SA:Vol ratio
Large organisms have a small SA: Vol ratio
Features for good exchange?
●
●
●
Large surface area
Thin surface
Large concentration gradient (faster diffusion)
●
Gills​ made up of ​gill filaments + gill lamellae​ (providing
large surface area for gas exchange​).
Lamellae + filaments have a ​thin epithelium for fast rate
of diffusion + short diffusion distance & ​are ​permeable​.
Why can single cell organisms
(microorganism) exchange directly via
surface?
Structure of gills in fish?
●
●
●
●
What is the countercurrent flow in
fish?
●
●
Blood and water flow in opposite directions​.
Maintains a large concentration gradien​t between ​water
and blood​.
Conc. of oxygen in water is always highe​r so ​O2
diffuses into blood of fish​.
Along the length of the gill
This increases the O2 conc in blood of the fish.
●
●
●
●
●
●
Structure of tracheal system in
insects?
Adapted features of insects to prevent
water loss?
●
●
●
How is gas exchanged in plants?
How does stomata prevent/allow gas
exchange?
Controlling water loss in plants?
●
Waterproof​, ​waxy cuticle​ all over body and ​exoskeleton
to prevent water loss by ​evaporation​.
Spiracles open & close​.
Main site is​ mesophyll cells​.They have l​arge surface area
so can absorb light​.
Gas can move in ​and​ out through stomata​.
○ These are ​found​ on the ​epidermis of leaf
●
●
They ​open and close to reduce water loss.
Guard cells ​control​ ​opening​ and ​clmosing​ of the
stomata
●
●
Water enters​ making cells ​turgid​.
If cell begins to​ lose water; then becomes flaccid ​and
closes the pore​s.
Stomata close at night to prevent water loss
●
●
●
Adaptations of Xerophytic plants?
O2 moves into ​through spiracles ​and connects to the
trachea​.
Down conc. Gradient
Trachea connect​ to ​tracheoles​ which are ​thin
Tracheoles attach directly to ​respiring tissues ​(deliver O2
and remove CO2)
CO2 moves down its concentration gradient ​towards the
spiracles​.
Insects use ​rhythmic abdominal movements​ to ​move​ ​air
in and out.
●
●
●
waxy cuticles
reduced surface area to volume ratio for reduced water loss
through transpiration
layers of hair
reduced no. of stomata
closing stomata when water availability is low
Structure of human gas exchange?
Human gas exchange
occurs in the lungs.
1. Air enters through
the trachea
2. Trachea splits into
2 bronchi
3. Each​ ​bronchus
branch​ into smaller
bronchioles
4. Bronchioles​ end in
air sacs​ called
alveoli
Trachea -> Bronchi -> Bronchus -> Bronchioles -> alveoli
●
Key features of the gas exchange
system?
●
●
●
●
What type of process is breathing?
Trachea/Bronchi​ supported by​ rings of cartilage​ for
support
○ Cartilage is ​C​ ​shaped​ for ​flexibility and prevent
collapse
Bronchioles ​wall are made from ​smooth muscle
Alveoli​ are one cell thick so ; short d.d and fast d/ pathway
Ventilation means constant blood supply by capillaries so
steep conc. gradient maintained.
large no.of alveoli so large surface area
-active process (using energy)
Stages of inhalation?
1.
2.
3.
4.
5.
6.
External intercostal muscles contract
Ribs​ moves ​upwards and outwards
Diaphragm contract ​causing it to ​fatten
Volume​ in chest ​Increases
Pressure in chest lower ​than ​atmospheric pressure
Air moves into lungs
Stages of exhalation?
1. External intercosta​l muscles ​relax ; internal intercostal
muscles contract
2. Diaphragm relaxes​ (Dome shape) and ​moves upwards
3. Volume of ches​t cavity ​decreases
4. Pressure greater​ than a​tmospheric pressure
5. So ​air moves out of lungs
Pv (pulmonary ventilation) = tidal volume x breathing rate
Formula for pulmonary ventilation?
Exchange of gases in lungs
-tidal volume = volume of air breathed in/out in ​one breath
-breathing rate = number of breaths per minute
-Pulmonary Ventilation = volume of air breathed in/out per minute
-large no.of alveoli and are folded in lungs so large SA for
exchange
● -​O2 diffuses out of alveoli through the alveolar
epithelium
●
Risk factors for lung disease?
What is digestion?
How are carbohydrates digested?
How is lipid digested?
-smoking
-air pollution
-infections
-occupations
●
Hydrolysis of​ large molecules into smaller molecules
which can be ​absorbed across cell membranes
1.
2.
3.
4.
Amylase converts (Starch) to maltose:
Maltase;
Maltose to glucose;
Hydrolysis Of glycosidic bond
●
Lipase​ breaks lipids into ​monoglycerides and 2 fatty
acids
Lipase​ produced in pancreas + released in small
intestine
Bile salts​ produced in liver ​emulsify lipids into small
droplets called micelles
●
●
How is protein digested?
What is the structure of ileum?
Proteins are broken down by peptidases:
● Endopeptidases​ hydrolyse the internal peptide bonds.
Found in stomach
● Exopeptidases​; hydrolyse at the ​end of the protein
producing dipeptides​. Found in small intestine
● Dipeptidases​; membrane bound and ​hydrolyse peptide
bonds between dipeptides​ into ​single amino acids
●
●
●
●
Describe the process of cotransport of
glucose?
And ​through capillary endothelium ​and into haemoglobin
in blood by ​diffusion.
Thin walls (reduced/ distance)
Villi and microvilli increase surface area for diffusion
Muscles move food along the ileum to maintain diffusion
gradient
Well supplied with blood vessels.
8. Glucose moves in with sodium (into epithelial cell);
9. Via channel protein
10. Sodium removed (from epithelial cell) by active transport
11. Into blood;
12. Maintaining low concentration of sodium (in epithelial cell) /
maintaining sodium concentration gradient (between lumen
and epithelial cell);
13. Glucose moves into blood;
14. By (facilitated) diffusion;
Mass transport
What is structure of haemoglobin?
Protein with a ​quaternary structure
● Contains ​haem group​ allowing ​oxygen to be binded
Role of haemoglobin in transport of
oxygen?
Explain how oxygen is loaded,
transported and unloaded in the blood.
**
●
●
●
Transport oxygen
haemoglobin + oxygen <==> oxyhaemoglobin
Oxygen can bind ​reversibly ​allowing it to be loaded ​in
the ​lungs​ and ​unloaded in respiring body tissues.
1. Haemoglobin carries oxygen / has a high affinity for oxygen
/ oxyhaemoglobin;
2. Loading / uptake / association in lungs;
3. at ​high pO​2​;
4. Unloads / dissociates / releases to respiring cells / tissues;
5. at low pO​2​;
6. Unloading linked to higher carbon dioxide (concentration);
●
●
●
Each molecule of ​haemoglobin can carry up to four
oxygen molecules
Can ​change shape for further oxygen binding​ to be easy
Haemoglobin has ​High Affinity in the lungs​ – ​due to high
partial pressure of oxygen​ and low partial pressure of
carbon dioxide, so ​haemoglobin loads/associates
oxygen in the lungs​ and becomes saturated (full)
What is meant when haemoglobin has
a high affinity
for oxygen?
●
What is the effect of carbon dioxide
concentration
on the dissociation of
oxyhaemoglobin? (Bohr effect)
Why does foetal haemoglobin have a
slightly higher affinity for oxygen than
adult hemoglobin?
●
●
Greater conc. of carbon dioxide​; the​ more readily it
releases its oxygen​.
When ​cells respire,​ they ​produce carbon dioxide raising
pCO2​.
This ​increases the rate of oxygen unloading +
dissociation curve shifts to the right
So it​ insures foetus can get oxygen​ from maternal group through
the placenta.
Important:
● Curve to the ​left
● So greater association due to low partial pressure of
oxygen in the placenta.
Has a​ high affinity​, curve to the ​left​, therefore it can rea​dily
Affinity of Organisms in a Low Oxygen
associate oxyge​n at the​ low oxygen partial pressures
Environment?
Affinity of active organisms ?
Low affinity, curve to the right​;
-So more ​oxygen can be unloaded​ to meet to cell's demand ​for
more respiration
●
Affinity of small organisms?
●
●
Low affinity​ due to ​large surface area to vol ratio​; curve
moves to the right.
Therefore ​greater heat loss ​& respiration needs to occur to
generate heat.
So ​unloads​ enough oxygen for cells demand of oxygen
What is the advantage of oxygen
dissociation curve shifting to the right
during vigorous exercise?
Allows them to survive in particular environments
Why do organisms have different types
-Organisms which live in an area of low oxygen have haemoglobin
of haemoglobin?
with high affinity of oxygen
Circulatory system in mammals?
What is the structure of the heart?
What is coronary artery?
Supplies blood to the heart
What is the aorta?
Connected to ​left atrium ​and ​carries oxygenated blood to all
parts of the body.
What is the vena cava?
Connected​ to ​right atrium​ and ​carries deoxygenated blood
back ​from the tissues of the body.
What is the pulmonary artery?
Connected to the ​right ventricle​ and c
​ arries deoxygenated
blood to the lungs​ where CO2 is
removed and oxygen is replenished.
What is the pulmonary vein ?
Brings oxygenated blood​ back ​from​ the ​lungs
What does the left ventricle allow?**
Has a​ thick, muscular wal​l which can​ contract and pump the
blood around the body​;
● w​/ ​high blood pressure around the body
What does the left atrioventricular
valves do?
Stops the blood from flowing backwards​ ​into​ the ​atrium​ when
ventricles contract
What does the semilunar valves do?
Links ​ventricles to pulmonary artery
● Prevents backflow​ of ​blood​ ​into​ the ​heart
What happens in the process of
diastole (relaxation of
the heart)?
1. ​Blood enters atria,​ ​increasing​ the ​pressure​.
● Causing ​pressure to be higher in atria than ventricles
2. ​Blood​ starts ​moving​ ​from atria into the ventricles​ by ​ ​ the
atrioventricular valves​.
What happens in the process of atrial
systole? (contraction)
1.​Atria contract ​causing a ​greater decrease in volume; so
further pressure increase.
2.Remaining ​blood is forced from atria into the ventricles​.
What happens in the process of
Ventricular systole (contraction of
ventricles)?
1.​Ventricle volume decreases​; so ​pressure increases ​causing
the ventricles to contract
2.​Atrioventricular valves are forced shut
3.​Semilunar valve​ are ​forced open​ as blood enters the arteries
4.Pressure begins to decrease in ventricles causing Semilunar
valves to shut preventing reverse blood flow
How is a heartbeat initiated and
coordinated? **
Explain how the heart muscle and the
heart valves maintain a one-way flow of
blood from the left atrium to the aorta.
Formula for Cardiac Output?
CO = Stroke Volume x Heart Rate
● stroke volume = volume of blood pumped out of the heart in
one beat
● heart rate = number of beats per minute
● Cardiac Output = volume of blood pumped out of the heart
in one minute
How does blood travel from heart to
rest of body?
Artery → Arterioles → Capillary → Vein
●
What is the structure of arteries?
●
Walls​ are​ thick and muscular​. Also has ​elastic tissue to
stretch and recoil ​as the heart beat which helps maintain
high pressure
Endothelium is folded ​also allowing it to stretch. Means it
maintains a high pressure
What is the function of arteries?
●
●
Maintain high pressure​ of the blood
Muscle​ withstand pumping of heart
What is the structure of arterioles?
●
●
Thicker muscle layer than arteries ​to allow blood flow
Thinner elastic tissue as ​blood pressure is lower
What is the function of arterioles?
●
Deliver blood from arteries to the capillaries
What is the structure of capillaries?
What is the function of capillaries?
● Smallest blood vessel
-Narrow​ ​diameter​ ; 1 cell thick
●
●
Delivers nutrients ​to the body tissues
Removing the waste product​s of metabolism
●
●
●
●
Wide lumen
Layers of collagen,​ smooth muscle
Contains ​one-way flow valves
Less elastic tissu​e as there is ​little pressure
Advantages of capillaries being
narrow?
Structure of veins?
Functions of veins?
Transports​ deoxygenated blood back to the heart at low
pressures
●
What is the process of tissue fluid
formation?
Valves prevent low pressure blood from flowing in the
wrong direction.
1. At the arteriole end of the capillary, there is a ​high
hydrostatic pressure ​which ​forces water and solutes
out ​in​ blood plasma through the thin capillary wall​.
2. Large proteins remain in capillary.
3. Tissue fluid​ contains n
​ utrients​ and ​oxygen​ surrounds
body cells.
4. At the ​venule end of the capillary​ there is a h​igh oncotic
pressure​ in the​ tissue fluid which means some solutes
drain back into the capillaries​.
5. There is are ​proteins ​in the capillary so lowers water
potential
6. Hence, water moves back into capillary by osmosis.
7. Rest of tissue fluid drains into the ​lymphatic system​.
Why does high blood pressure causes Increased Hydrostatic pressure​, so​ more tissue fluid is
accumulation of
formed​;
tissue fluid?
Not as much can be returned to the circulatory system.
Adaptations of Xerophytic plants?
Transports water​ and mineral​ from the roots up to the leaves​ in
the ​xylem tissue
What occurs in the Xylem in plants?
What is the structure of the xylem?
How does water move up the stem
through the xylem? (transpiration
pull)**
Why does the diameter of trunk
decrease during midday?
What are the factors affecting rate of
transpiration?
What does an increased humidity in air
cause?
What is the structure of phloem?
●
●
●
●
●
Tubes with ​no end walls
Continuous water flow
No cytoplasm
Allows easy flow of water
Lignin for support
1. water ​evaporates / transpires​ from leaves;
2. reduces water potential in cell
3. water is drawn out of xylem;
4. Transpiration creates tension
5. cohesive forces between water molecules;
6. water pulled up as a column;
Diameter of trunk ​minimal at warmest
Stomata open in light → more water loss;
Water evaporates more​ when warm
Hydrogen-bonding between water molecules / ​cohesion​ ( /
described) ​between water molecules​;
5. Adhesion (described) between water molecules and walls
of xylem vessels;
6. (Xylem) ​pulled​ inwards by faster flow of water / ​pulled​ in by
tension;
1.
2.
3.
4.
1.​Light Intensit​y: Greater light intensity; faster the rate
2.​Temperature​: High temp; faster rate as molecules have more
energy SO faster transpiration / by evaporation
3.​Humidity​: Lower humidity faster rate
4.​Wind​: Greater wind faster rate; more water molecules blows
away
1.
2.
3.
4.
5.
Increased humidity leads to decreased transpiration;
High humidity means more water in the air
increased water potential;
reduced diffusion gradient / water potential gradient;
Slower rate of water loss / less evaporation;
Sieve tube elements​; no nucleus; elongated tubes
Companion cells​; contains nucleus; mitochondria for ATP
production
What is the mechanism of
translocation?
1. At ​source sucrose is actively (transported) into the
phloem
2. By companion cells;
3. Lowers water potential in phloem​ ​and​ water enters by
osmosis​;
4. (Produces) ​high (hydrostatic) pressure;
5. Mass​ flow/transport towards sink/roots/storage tissue;
6. At sink/roots sugars are removed/unloaded;
Section 4: Genetic information,
variation and relationships between
organisms
What is a Gene?**
How does a Gene/Exon code for a
Protein?
What is meant by degenerate genetic
code? **
What is meant by a codon? **
● Length of DNA which codes for a single polypeptide.
● Gene is a sequence of ​triplets​.
● Made out of intron and exon
-intron​ = n
​ on-coding DNA ​(function e.g. turns gene on or off)
-exon​ = ​coding DNA​ (codes for protein)
-made out of a sequence of bases
-each 3 bases code for 1 amino acid (called triplet code)
● Therefore, sequence of bases determines ​sequence of
triplet ​codes which determine the sequence of AAs
= polypeptide chain/primary structure (folds to secondary, then to
tertiary/quaternary)
An amino acid (Gly) coded by more than one triplet/codon
●
●
3 bases on mRNA
That code for a protein
Why are stop codons required? **
To stop translation
Hence, ribosome detatches to polypeptide
What is meant by locus of DNA?
●
Position​ where a ​gene occupies​ on a ​DNA molecule​.
How does a mutation / change in DNA
sequence lead to a non-functional
enzyme? **
-change in base sequence
-change in sequence of AAs
-change in primary structure
-change in hydrogen/ionic/disulfide bonds
-change in tertiary structure (3D shape)
-change in active site shape
-substrate no longer complementary
-can no longer form enzyme-substrate complex
How is a protein assembled?
-By transcription and translation
-transcription​ = production of a ​single stranded complementary
copy of a gen​e (called ​mRNA​)
-translation​ = use ​sequence of codons on mRNA to assemble
protein ​(tRNA brings in AAs)
DNA vs RNA?
-deoxyribose sugar vs ribose sugar
-thymine vs uracil
-double stranded (DNA) vs single stranded
-one type vs two types (mRNA and tRNA)
●
●
●
What is mRNA?
●
●
●
messenger RNA
single stranded complementary copy of a gene
carries the code for assembling protein (on DNA called
triplet code, on mRNA called codon)
Linear
No base pairing
No hydrogen bonds
Differences between DNA and mRNA?
●
●
What is tRNA?
●
●
●
●
transfer RNA
single stranded RNA folded over into a ​'clover leaf' shape
(held by ​hydrogen bonds between the bases​)
has an AA attachment site on the top
has ​3 specific bases​ on the bottom (anticodon)
anticodon binds to ​complementary codons on mRNA
Contains hydrogen bonds
Difference between mRNA and tRNA?
What is Transcription?
Difference between pre-mRNA and
mRNA?
Transcription is the process of p​roducing a single stranded copy of
a gene (called mRNA​)
● DNA Helicase breaks the hydrogen bonds ​between
complementary bases in the gene
● The double strand of the​ gene unwinds
● leaves 2 separate strands (1 coding strand and 1 template
strand)
● Complementary ​RNA nucleotides bind to exposed bases
on the template strand
● RNA Polymerase​ joins the ​nucleotides ​together to form
mRNA
● Forms ​pre-mRNA ​(contains introns and exons)
● The copies of the ​introns are removed by ​splicing
● leaves mRNA
●
pre-mRNA contains exons mRNA contains only introns
●
●
Change ​in the s
​ equence​ of chromosomes
May cause a change in ​amino acid s​ equence in the
encoded polypeptide
What is Translation? **
What is Mutation?
What is a Gene Mutation?
A change in the ​base sequence of DNA
● 2 types of mutation ​substitution​ ​and insertion/deletion
● Substitution​; ​replace​ one b
​ ase for another​ (could
change structure of protein OR remain same OR may code
for stop codon so no protein formed)
● Substitution alters only ​one codon which maybe a
degenerate
● Insertion​;​ adding a base​, ​deletion​; ​removing a base
both insertion/deletion causes ​frameshift​, all the triplet
codes after the mutation changes, so normal polypeptide
chain/protein ​not produced​.
What causes mutation?
Random or due to mutagens (e.g. chemicals, ​radiation​)
What are mutagenic agents?
What is a homologous pair of
chromosomes?
What is a Chromosome Mutation?
●
Increase ​rate of mutation​.
●
Carry the same genes
In animals,​ homologous pair of chromosome do not separate
in meiosis, so either inherit ​one extra or one less chromosom​e
called ​non-disjunction
Why might not all mutations result in a
change to the amino acid sequence of
encoded polypeptide? **
●
What does Meiosis produce?
●
●
4 genetically different
cells​, h
​ aploid​ (half the
amount of
chromosome/DNA)
Haploid allows for
chromosome number ​to
constant at each
generation
For cell fusion/ joining of
gametes
be
Benefits of Meiosis?
●
Produces gametes which will be used in sexual
reproduction in animals & plants
(2 gametes fuse to form a zygote, zygote develops into organisms)
Stages of Meiosis?
Interphase/Meiosis I/Meiosis II/Cytokinesis
What happens to the chromosomes in
meiosis?
●
●
Interphase?
After crossing over they produce ​new combination of
alleles
Separation of chromosomes causes ​varying ​combination
of chromosomes
G1: protein synthesis
S: ​DNA replication​ (doubles set of DNA)
G2: ​organelle synthesis
Meiosis I?
Prophase I: ​DNA coils to form chromosomes​,​ nucleus breaks
down​, ​spindle fibres form​, c
​ rossing​ ​over​ occurs
Metaphase I: ​homologous pair of chromosomes line up in
middle​ of cell and ​attach to spindle fibre​ via ​centromere
Anaphase I: ​spindle fibres pull, homologous pair of
chromosomes separate to opposite sides by independent
Meiosis II?
Prophase II: DNA coils to form chromosomes, nucleus breaks
down, spindle fibres form
Metaphase II: chromosomes line up in middle of cell and attach to
spindle fibre via centromere
Anaphase II: spindle fibres pull, centromere splits, sister
chromatids move to opposite sides by independent assortment
Telophase II: chromatids uncoil, nucleus reforms (left with 4
genetically different nuclei)
Cytokinesis?
separating cell into 4​ (each receives a nucleus and
organelles/cytoplasm)
How does Meiosis produce Variation?
**
What is an allele? **
●
Different version of a gene
●
●
Occurs in ​Prophase I o​f Meiosis I
Chromosome from a Homologous pair twist around each
other.
Causing​ section of ​chromatids to break and rejoin with
chromatid from sister chromosome
What is crossing over? **
●
What is independent assortment?
What happens to DNA mass in
meiosis?
- in Anaphase I of Meiosis I – th​e homologous pairs of
chromosomes separate
- in Anaphase II of Meiosis II – the chromatids separate
- independent assortment​ produces a mix of alleles from
paternal and maternal chromosomes in gamete
quarters
What happens to Chromosome number Halves
in meiosis?
Module 4:
How does courtship behaviour
increase probability of successful
mating?
1. Recognition of ​same species
2. Recognition of opposite genders
●
●
●
Disruption / Isolation causing
speciation?
●
●
●
●
What is stabilising selection?
●
●
Isolation​ of two populations
variation already present due to mutations;
different environmental conditions leading to different
features and hence different alleles
different frequency of alleles;
separate gene pools / no interbreeding;
No change in environmental conditions
The population ​on the extreme ​die out as they are not well
adapted
The ​range of population decreases
There is an increase in population which are very well
adapted.
Selection against one extreme
● Shifted towards a favoured extreme
● Favours one characteristic
● The extreme population of the characteristic die
●
Directional selection?
What is a species?
Species richness?
What is Hierarchical Classification?
What is Binomial Naming System?
A group of organisms that can produce fertile offspring
No. of different species in a community
-
l​arge groups divided into smaller groups​ with ​no overlap
domain, kingdom, phylum, class, order, family, genus, species
​member of groups ​have similar ​common features
using Genus name and Species name to name organism
Genus name first in capital, Species name second in lower
case
e.g. tiger = Felix tigris
What is Phylogenetic Classification?
●
Based on ​evolutionary relationships​ – how closely related
different species are and how ​more recent common
ancestor they are
●
Amino acid sequence can be used to see which organisms
have similar sequences so put together OR similar DNA
sequence OR mRNA sequence
If large difference then they diverged many years ago / not
related.
●
What is Biodiversity?
What is Species Diversity?
●
●
-
variety in an ecosystem
variety of habitats and variety of species
number of different species
number of individuals for each species
●
●
What is Genetic Diversity?
●
●
Benefit of high species diversity?
The larger number of individuals in a species, the larger the
genetic diversity ​due to a greater gene pool
Difference in gene pools / genes OR difference in DNA
base sequence
Crossing over increases genetic diversity since it
causes sections to have different alleles.
This leads to new combinations of alleles.
-Stable ecosystem
- each species is less likely to become extinct (due to high genetic
diversity)
- & if a species does become extinct it will not affect the food chain
as there are other species available
How to measure Species Diversity for
an area?
Species Diversity Index
takes into account the number of different species and how
many individuals there are for each species
the larger the species diversity index, the larger the species
diversity
How does deforestation lower species
diversity?
-
(deforestation is the removal of trees for wood & space)
decreases plant species diversity
less variety of habitats
less variety of food sources
decreases animal species diversity
How does agriculture/farming lower
species diversity?
-
deforestation to make space for farm
only grow a few plants & keep a few animal species
selectively breed plants & animals
use pesticides to kill other species
What is Classification?
What is Variation?
Types of Variation?
Causes of Intraspecific Variation?
placing organisms into groups
difference in characteristics between organisms
intraspecific = differences between organisms of the same species
interspecific = differences between organisms of different species
Genetic Factors = same genes but different alleles (allele are
different type/forms of genes)
Environmental Factors
Causes of Interspecific Variation?
Genetic Factors = different genes and different alleles
Environmental Factors
Types of Characteristics?
Discontinuous and Continuous
Properties of Discontinuous
Characteristics?
Characteristics fall into certain groups with no overlap (e.g. blood
group) – determined by genetics only (a single gene)
Properties of Continuous
Characteristics?
What is natural selection and
adaptation? **
What are the 2 types of selection?
What is stabilising selection?
Characteristics show a range (e.g. height) – determined by
genetics (a few genes, polygenes)
and environment
variation in population of species
(genetic diversity/genetic variation/variety in gene pool)
new alleles arise by random mutation
environment applies a selection pressure on the population
those with favourable characteristics/favourable
alleles/selection advantage/better adapted survive, the others die
[natural selection]
the ones that survive will reproduce, passing on their
favourable alleles
if this happens for many generations, then that characteristic
will become most common – the allele will become more frequent
[adaptation]
stabilising and directional
when the environment favours those with the most common
characteristic – those on the extreme dies out
the common characteristic increases in proportion
the range (standard deviation) will reduce
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