SlideShare ist ein Scribd-Unternehmen logo
1 von 40
B2 Topic 2
B2.1 – Plant and Animal Cells
7 Organelles Function
Cell Membrane Controls movement into and out of the cell.
Nucleus Contains DNA. Controls the cell
Cytoplasm Where chemical reactions take place.
Mitochondria Where respiration occurs.
Cell Wall Made of CELLULOSE. Supports the cell.
Vacuole Contains CELL SAP. Helps support the plant by keeping the cell rigid
Chloroplast Contains CHLOROPHYLL. Absorbs LIGHT. Where photosynthesis takes place
Plant and animal cells can be
studies in greater detail using a
light microscope.
Light passes through a thin slice of
the specimen. Lenses magnify the
specimen many times.
B2.2 – Inside Bacteria
4 Organelles Function
Chromosomal DNA A giant loop of DNA containing most of the genetic material.
Plasmid DNA Small loops of DNA that carry extra information.
Flagella Long whip like structures that aid movement.
Cell Wall Provides support but is more flexible than a plant. Not made
of cellulose.
2 types of DNA
Microscopes have improved in last 350 years.
Light microscopes can magnify 1500x.
Electron microscopes can magnify 2000000x.
Electron microscopes produce very clear
images.
Electron microscopes show more detail of the
specimen.
B2.3 - DNA
Key Definition
A gene is a section of DNA that codes
for a specific protein.
DNA is made up of two strands
coiled to form a double helix.
The two strands are linked by
complementary bases held together
by weak hydrogen bonds.
Adenine (A) pairs with Thymine (T)
Cytosine (C) pairs with Guanine (G)
B2.4 – Extracting DNA
1. Chop onion or peas into chunks.
2. Grind in a pestle and mortar.
3. Mix together with washing up liquid, salt and water and
stir.
4. Incubate the mixture at 60 degrees Centigrade for 15
minutes in a water bath.
5. Filter the mixture through filter paper into a boiling tube.
6. Take ice cold alcohol and pour it slowly down the side of
the boiling tube. The alcohol will form a transparent layer
on top of the liquid, as the alcohol is less dense.
7. You will see the DNA between the two liquid layers.
B2.5 – DNA Discovery
London - Maurice Wilkins & Rosalind Franklin using X-rays to
study DNA structure. From the patterns made they could work
out how the atoms were arranged.
Cambridge – Watson & Crick were building a model of DNA using
data from other scientists. They were given a copy of Franklins
photographs which enabled them to crack the code. Franklin
didn’t know they had the photo.
Watson and Crick published their paper with the structure of
DNA but didn’t acknowledge the photograph they used
Watson and Crick were awarded the Nobel Prize with Maurice
Wilkins but Rosalind Franklin had already died so did not get the
prize.
B2.5 – DNA Discovery
The Human Genome Project –
International Project.
3 billion bases that make up the
human genome were sequenced.
It took 13 years and scientists
collaborated using IT to store and
share data.
All humans have 99.9% of their
DNA in common.
5 Implications of the HGP
1. Improved genetic testing for
disorders.
2. New ways of finding new
genes that may increase risk
of certain diseases.
3. New treatments and cures
for diseases.
4. New ways of looking at
changes in the genome over
time.
5. Personalised medicines that
work with a particular
genotype.
B2.6 – Genetic Engineering
Know this process!
Definition - The process of removing a gene from one organism and inserting it into
the DNA of another.
B2.6 – Genetic Engineering
Example Advantages Disadvantages
Beta carotene in
golden rice to
reduce vitamin
A deficiency in
humans
1. Beta carotene used to make vitamin
A
2. Vitamin A will reduce death and
blindness.
1. Could cross breed with wild rice and
contaminate wild rice DNA
2. Levels of beta carotene in Golden
Rice might not be high enough to
make a difference
3. Can be expensive to buy
4. Produces sterile seeds so farmers
have to buy them every year
The production
of human insulin
by GM bacteria
1. Can be used by vegans
2. Supply not affected by animal
diseases
3. Supply not affected by demand for
meat
4. Can be made in vast quantities
5. Cheaper
1. Bacteria produce insulin slightly
differently so may not work for
some people
The production
of herbicide
resistant crops
1. Reduces amount of crop spraying 1. Herbicide resistant weeds can
develop
2. Cross pollination with wild plants
3. Potential loss of biodiversity
B2.7 – Mitosis and
Meiosis
Mitosis
• The production of two
daughter cells with identical
sets of chromosomes in the
nucleus as the parent cell.
• Results in the formation of
two genetically identical
diploid cells.
• Occurs during growth and
repair and asexual
reproduction
Meiosis
• The production of four
daughter cells, each with
half the number of
chromosomes as the parent
cell.
• Results in the formation of
genetically different haploid
gametes.
• Occurs when making
gametes only.
Definitions
Haploid – Having one set of chromosomes.
Diploid – Having two sets of chromosomes.
Gamete – the sex cells (sperm and egg)
At fertilisation, haploid gametes join to form a diploid zygote.
B2.8 - Clones
How to produce a clone
1. Remove a diploid nucleus
from a body cell
2. Enucleate an egg cell
3. Insert diploid nucleus into
enucleated egg cell.
4. Stimulate the diploid
nucleus to divide by mitosis.
5. Implant into surrogate
mother.
Cloning – An example of asexual
reproduction.
Enucleate – Remove the nucleus
B2.8 - Clones
Advantages of
Cloning
Disadvantages of
Cloning
Risks of Cloning
1. Can make a
genetically
identical copy of
an animal with
desirable
characteristics.
2. Can be used to
make copies of
GM animals to
guarantee all
offspring have
the trait.
1. Cloned animals
often die young.
2. Cloned animals
often age more
quickly.
3. Complicated
process.
1. Very few
embryos develop
properly resulting
in deformities.
B2.9 – Stem Cells
Advantages of Stem Cell
Research
Disadvantages of Stem Cell
Research
Risks of Stem Cell Research
1. Embryonic stem cells can
develop into almost every
type of human cell.
2. Bone marrow stem cells
can be used to treat
lukaemia.
3. Adult stem cells may be
used in future instead of
embryonic stem cells.
1. Embryonic stem cells can
come from leftover
embryos from fertility
treatments.
2. Risk of rejection if not
from a patients own stem
cells.
3. Could lead to tumours
forming.
1. Technology could be used
illegally.
2. Risk of the unknown – long
term effects may not be
shown for years.
Key definitions
Stem Cell - An unspecialised cell that can divide to produce more stem cells or
different types of specialised cell.
Differentiate – Become specialised.
Embryonic Stem Cell – Can differentiate into almost any cell type.
Adult Stem Cell – Can differentiate into only a few cell types.
Specialised Cell – a cell with a particular function e.g. neurone, red blood cell.
B2.10–ProteinManufacture
B2.10 Protein Manufacture
Transcription
1. DNA double helix unzips.
2. The complementary mRNA strand is made in the nucleus and
passes out through a pore.
Translation
1. mRNA attaches to the ribosome.
2. A triplet of bases on the mRNA (codon) code for a specific amino
acid.
3. tRNA transfers amino acids to the ribosome.
4. Amino acids link together to form polypeptides.
RNA is single stranded but DNA is double stranded.
RNA contains Uracil (U) instead of thymine (T)
Each amino acid is
coded for by 3
specific bases. DNA
is a triplet code.
B2.11 - Mutations
1. Each protein has its own specific number and
sequence of amino acids.
2. This is coded for by the DNA.
3. Therefore, each protein is a different shape and
has a different function e.g. an enzyme.
4. Mutations change the sequence of the bases,
and therefore the shape of the protein.
5. Most mutations are harmful.
6. Radiation and some chemicals in cigarette
smoke are mutagens and cause mutations.
Mutation – A change in the sequence of bases in the
genetic code.
B2.12 - Enzymes
These are examples of enzyme catalysed reactions:
1. DNA Replication – One enzyme unzips the two strands
of DNA, the other joins the new bases together to
make the new double stranded molecule.
2. Protein Synthesis – RNA Polymerase makes the mRNA
strand from the DNA template.
3. Digestion – Many enzymes break larger molecules
down into smaller ones in digestion. This happens
outside of the body. Stain digesting enzymes in
washing powders break down stain in clothes.
Microorganisms excrete enzymes onto food to break
them down outside the body and then absorb the
products.
Enzymes are biological catalysts. They speed up reactions.
B2.13 – Enzymes and Temperature
Factors that affect enzyme activity:
1. Temperature
2. pH
3. Substrate Concentration.
Enzymes are SPECIFIC to their substrate. They only catalyse
specific reactions in specific conditions. They have a specific
shaped active site.
Enzyme activity can be measured by measuring the speed at
which a product is made e.g. a gas, or the speed at which a
substrate is used up e.g. stain digestion.
B2.14 – Enzyme Action
As temperature
increases, so does
enzyme activity, up to
40oC. After 40oC the
active site is denatured
and the reaction stops.
As substrate concentration
increases, so does enzyme
activity, up to a point where the
number of active sites becomes
limiting. The only way to speed
up the reaction after this is to
increase the number of active
sites.
Enzymes will only work
at a specific pH. Either
side of this optimum
pH, the enzyme will
denature and not
work.
Enzymes can never be killed. They can
only be denatured, which is where the
shape of the active site changes.
B2.14 – Enzyme Action
Enzymes work like a lock and key
Lock and Key Enzyme and Substrate
One key will only fit one lock. One substrate will only fit one enzyme.
The key fits the lock. The substrate fits the active site
The key unlocks the lock. The substrate is changed in the enzyme
Wrong key won’t fit the lock. Wrong substrate won’t fit the active site.
B2.15 Aerobic Respiration.
• All organisms are made of cells
• Energy released by respiration
• Cells that move more need more energy.
• Exercise = more energy needed.
Key Terms:
Respiration - the release of energy from
food molecules that act as fuel for the cell.
Diffusion - when substances move from an
area of high concentration to an area of low
concentration.
Glucose + Oxygen = Carbon Dioxide + Water
Aerobic respiration = uses oxygen to release energy from glucose.
How does it get delivered?
• Glucose and oxygen diffuse from capillaries to respiring cells
• Carbon dioxide diffuses from respiring cells to capillaries
• Capillaries - smallest vessel that carries blood between cells/ one cell thick
• Substances move by diffusion down a concentration gradient = the diffusion
pathway.
• Respiring cells = oxygen and glucose levels fall as they are used up in
aerobic respiration/ Carbon dioxide levels increase.
• Gas exchange = the transfer of gases.
B2.16 investigating The effects of
exercise.
• Exercise = increase heart rate and has to pump
blood faster to the muscles.
• Causes breathing rate to increase and get deeper.
Why?
• Cells need more oxygen and glucose as they need
more energy.
• Cells produce more carbon dioxide as a result
which needs to be removed.
B2.17 Anaerobic respiration
• Anaerobic respiration = respiration without oxygen
• Glucose is broken down to supply energy to the muscles
• Releases less energy then aerobic and produces Lactic Acid
• Amount of blood pumped around the body depends on the stroke volume and the
heart rate.
• Exercise = increase in heart rate and stroke volume.
• Lactic Acid needs to be broken down = oxygen used to break it down into carbon
dioxide and water.
• The requirement of this oxygen to break down the lactic acid is called excess post-
exercise oxygen consumption (EPOC)
Glucose  lactic acid
Cardiac output = stroke
volume x heart rate.
B2.18 Photosynthesis.
• Photosynthesis = plants make their own food
• Uses light energy to produce glucosefrom carbon dioxide and water
• Glucose stored as starch
• Starch = lots of glucose molecules joined together.
• Digestion breaks down starch = glucose
• Chlorophyll = green found in chloroplasts absorbs light for
photosynthesis.
• Variegated leaves = the green parts of a leaf contain the chlorophyll.
Carbon dioxide + water  glucose + oxygen
Light and chlorophyll
2.20 Factors that effect the rate of
photosynthesis.
3 factors that effect photosynthesis.
• Carbon dioxide
• Light
• Temperature
• All 3 are needed at optimum amount for photosynthesis to be at its best.
• The limiting factor is the one that is in short supply…..you may have lots of CO2 the right
temperature but little light this means photosynthesis will be slow.
Limiting factor =
something can affect
the rate of
photosynthesis.
Adaptations of a leaf.
Upper epidermis = tightly packed cells = lots of
chloroplasts = lots of photosynthesis.
Air spaces = provide large surface for cells to
exchange with gases in the air.
Lower epidermis = contain stomata.
Stomata = open and close to allow gases into
the leaf. Located underside of the leaf.
Open in response to light.
Allow Carbon dioxide in and lets out oxygen
and water vapour.
3 Adaptations
Has stomata for gas exchange
(carbon dioxide, oxygen,
water vapour)
Contains chlorophyll in
chloroplasts to absorb light.
Large surface area to absorb
most amount of light.
Root HairCell
• Job of root = anchor plant
and take up nutrients.
• Root hair found on surface
of root.
• Role – to absorb water
and dissolved minerals.
• Adaptation = large surface
area.
B2.21 Water Transport
• Roots absorb nitrates and mineral ions
dissolved in water by Active transport.
This needs energy from respiration
• Water transported by xylem
• Nutrients transported by phloem
Key Definitions
• The loss of water from the leaves drives
transpiration.
• Transpiration – the movement of water
through a plant and the loss of water
throught he leaves.
• Osmosis = movement of water from an area
of low concentration to an area of high
concentration through a partially permeable
membrane.
B2.22 Investigating Osmosis
Osmosis
Water can move across cell membranes because
of osmosis. For osmosis to happen you need:
two solutions with different concentrations and
a partially permeable membrane to separate them
B2.23 Organisms and their
environment
Key Terms
• Environment = an organisms
surroundings including the soil, air,
water and other organism in the area.
• Biodiversity = the different plants and
animals in an area.
• Ecosystem = an area in which all the
living organisms and all the non living
organism form a relationship in order
to survive.
• Habitat = where the plants and
animals are found/living.
• Population = the number of animals in
a given area.
• Sampling = looking at small proportion
of the plants and animals.
Sampling techniques =
• 1) Pooter = used to catch animals.
• 2) Sweep net = can catch flying
animals.
• 3) Pond net = to catch aquatic
animals.
• 4) pit fall traps = buried in the
ground…the organisms fall in.
• 5) quadrats = used to sample the
population size of plants = random
sampling or systematic sampling. =
placing the quadrat at regular
intervals along a line.
B2
Topic 3 Common Systems
B2.25 Fossils and evolution
Keywords
• Fossil record – The collection of fossils identified from different periods of time that can be
interpreted to form a hypothesis about the evolution of life on Earth.
• Fossil – The preserved traces or remain of an organism which lived a very long time ago
• Pentadactyl – five fingered organism
Facts:
• The moon is 30 ‘earths’ away
• The sun is 11,000 ‘earths’ away
Fossils
• Fossils from different periods of time show organisms have changed gradually = evolution.
• Fossil record has gaps
– Soft tissues decay not forming fossils
– Hard parts of organisms could have been destroyed
– Many fossils are buried too deep to be found
• Scientists using incomplete data sometimes make mistakes
• More fossils = more accurate conclusions
Evidence for Evolution
• Internal bones of all vertebrate’s limbs are similar
• Fossils of limbless vertebrates have the same five fingered structure
• All vertebtates evolved from one common ancestor
• Evolution of the limbs is due to adaptation to how the organisms lived and moved,
B2.26 Growth
Keywords
• Percentile – The value of a variable below which a certain percentage of observations fall.
• Stem Cell – An unspecialised cell that can divide to produce more stem cells or different kinds of specialised cells
• Differentiate – Specialise, develop into different kinds of cell, as in cells that become nerve, muscle or bone cells
• Elongation – getting longer
Facts
• Growth is when an organisms
increases in size, length and
mass
• To monitor growth of babies we
check
– Head circumference
– Weight
– Height
• Each child is compared to a chart
to determine which percentile of
the population they are in.
• Growth involves 2 things
– Increase in the number
of cells
– Increase in the size of
cells
Growth in Plants
• Grow all through their lives
• Cells divide in the Meristem – behind the tip of the root and shoot
• Cells also elongate
• Older meristem cells differentiate to become specialised for example:
– Palisade leaf cell
– Root hair cell
Growth in Animals
• Cell division
• Animals stop growing when they become adults
• Stem cells are undifferentiated
• Stem cells can specialise into all other cells
• Adults have very few stem cells (only in blood and
skeletal tissues)
• Most animals cannot regrow limbs or body parts.
Components
• Plasma
– Fluid part of blood
– Transports carbon dioxide, hormones and waste
– Pale yellow
• Red blood cells
– No nucleus = more room for haemoglobin
– Made in the bone marrow.
– Contain red pigment haemoglobin which carries oxygen
Oxygen + Haemoglobin Oxyhaemoglobin
– Oxygen is carried in the blood to the tissues for aerobic respiration
– Biconcave disc = large surface area to volume ratio for faster diffusion of oxygen
• White blood cells
– An important part of the immune system
– Some produce antibodies (proteins that bind to microbes and destroy them)
– Others surround and destroy foreign cells
– All have a nucleus
– Made in the bone marrow
– All have a nucleus
• Platelets
– Tiny fragments of cells (no nuclei)
– Clump together to form clots
– Protect the body by stopping bleeding and forming a scab to stop microbes entering.
B2.27 Blood
B2.28 The heart
• Deoxygenated blood (low
oxygen levels)
• Pumped to the lungs (by
right ventricle) to collect
oxygen
• Oxygenated blood
returns to heart (Left
side)
• Pumped to the body cells
and tissues (by left
ventricle)
• Left and right side work
together at the same
time
• Valves prevent backflow
of blood
• Tendons stop valves
turning inside out
Septum
Thicker wall as it
pumps blood all
around the body
B2.29 The circulatory system
3 types of blood vessel:
Arteries
• Carry blood away from the heart
• Have thick muscular walls
• Have small internal lumen
• Blood under high pressure
Veins
• Carry blood to the heart
• Thin walls
• Larger internal lumen
• Blood under low pressure
• Valves to prevent blood flowing
backwards
Capillaries
• Wall is one cell thick
• Very low blood pressure
• Allows diffusion between blood
and tissues
B2.30 The
digestive
system
churns
Peristalsis
• Muscles contract
in waves to move
food along the
alimentary canal (
a muscular tube
running from
your mouth to
your anus)
B2.31 Breaking
down food
Keywords
Enzyme – a protein molecule made by living cells that speeds up the rate of a
reaction
Emulsion – a mixture in which particles of one liquid are suspended in another
liquid.
Digesting proteins Digesting
Carbohydrates
Digesting Fats
Enzyme
involved
Proteases (e.g.
pepsin)
Carbohydrases (e.g.
amylase)
Lipases
Broken down
into…
Amino acids Simple sugars
(glucose)
Glycerol and Fatty acids
Where it occurs Stomach first then
small intestine
Mouth and small
intestine
Small Intestine
Additional
features
Pepsin has an
optimum pH of 2
(perfect for
stomach acid)
Amylase is
denatured by
stomach acid
• Bile from the gall bladder
breaks down large fat globules
into droplets with a larger
surface area to help lipase.
• We say bile emulsifies the fat.
• Bile also neutralises the
stomach acid.
B2.32 Villi
Inside the Small Intestine
1. Digested food passes into blood by diffusion
2. Bigger surface areas = more diffusion
3. Finger-like folds called Villi increase surface area of small intestine
Features of a Villus to speed up diffusion
1. Good network of capillaries moving absorbed nutrients
2. Low concentration of food
3. Steep concentration gradient maintained
4. Wall is a single cell layer (shorter distance
to diffuse)
Keywords
Villi – finger like projections in the small intestine.
Diffusion – movement of particles from an area of high concentration to
an area of low concentration down a concentration gradient.
B2.34 Probiotics and Prebiotics – Functional foods
Prebiotics
• Substances the body cannot digest
• They act as food for the beneficial bacteria
• Oligosaccharides are a common form of prebiotic (contained in tomatoes, onions and asparagus)
• Also found in specially made dairy foods and sold as capsules
• Increasing evidence supports their positive effect on health
Plant Stanol Esters
• Oily substances in plants
• Stop the small intestine absorbing cholesterol
• Lowers blood cholesterol
• Use in many foods like yogurt and spreads.
Probiotics
• Live bacteria – friendly or beneficial
• Bifidobacteria or Lactobacillus
• They produce lactic acid in your gut and companies claim they improve health
• NOT ENOUGH EVIDENCE to support the claims they are effective

Weitere ähnliche Inhalte

Was ist angesagt?

Biology2 120721041928-phpapp02
Biology2 120721041928-phpapp02Biology2 120721041928-phpapp02
Biology2 120721041928-phpapp02cpugh5345
 
1biologyeocreviewnotes all
1biologyeocreviewnotes all1biologyeocreviewnotes all
1biologyeocreviewnotes allkonnerhouse
 
#1 B1 topic 1 - classification (part 1 of 2)
#1 B1 topic 1 - classification (part 1 of 2)#1 B1 topic 1 - classification (part 1 of 2)
#1 B1 topic 1 - classification (part 1 of 2)Mr. Science
 
Cambridge Pre-U Biology - 1.3 DNA Replication
Cambridge Pre-U Biology - 1.3 DNA ReplicationCambridge Pre-U Biology - 1.3 DNA Replication
Cambridge Pre-U Biology - 1.3 DNA Replicationmrexham
 
Cell parts
Cell partsCell parts
Cell partshubbard
 
Biology Review
Biology ReviewBiology Review
Biology ReviewErin Mucci
 
Introduction of dna into non bacterial cells
Introduction of dna into non bacterial cellsIntroduction of dna into non bacterial cells
Introduction of dna into non bacterial cellsSD Syed
 
AQA Unit 1 AS Biology
AQA Unit 1 AS BiologyAQA Unit 1 AS Biology
AQA Unit 1 AS BiologyJosh Wanklyn
 
Macromolecule human awareness
Macromolecule  human awarenessMacromolecule  human awareness
Macromolecule human awarenessPaula Mills
 
Ls1 afet semester test 1 memo 2012
Ls1 afet semester test 1 memo 2012Ls1 afet semester test 1 memo 2012
Ls1 afet semester test 1 memo 2012portia201182750
 
Bm 2 review 2010
Bm 2 review 2010Bm 2 review 2010
Bm 2 review 2010farrellw
 

Was ist angesagt? (18)

Biology2 120721041928-phpapp02
Biology2 120721041928-phpapp02Biology2 120721041928-phpapp02
Biology2 120721041928-phpapp02
 
1biologyeocreviewnotes all
1biologyeocreviewnotes all1biologyeocreviewnotes all
1biologyeocreviewnotes all
 
B1 poster summary_
B1 poster summary_B1 poster summary_
B1 poster summary_
 
#1 B1 topic 1 - classification (part 1 of 2)
#1 B1 topic 1 - classification (part 1 of 2)#1 B1 topic 1 - classification (part 1 of 2)
#1 B1 topic 1 - classification (part 1 of 2)
 
cell
cellcell
cell
 
Cambridge Pre-U Biology - 1.3 DNA Replication
Cambridge Pre-U Biology - 1.3 DNA ReplicationCambridge Pre-U Biology - 1.3 DNA Replication
Cambridge Pre-U Biology - 1.3 DNA Replication
 
Cell parts
Cell partsCell parts
Cell parts
 
AP Bio Ch 1 PowerPoint
AP Bio Ch 1 PowerPointAP Bio Ch 1 PowerPoint
AP Bio Ch 1 PowerPoint
 
Biology Review
Biology ReviewBiology Review
Biology Review
 
Life and cells
Life and cellsLife and cells
Life and cells
 
19 lecture viruses
19 lecture viruses19 lecture viruses
19 lecture viruses
 
cell parts
cell partscell parts
cell parts
 
Introduction of dna into non bacterial cells
Introduction of dna into non bacterial cellsIntroduction of dna into non bacterial cells
Introduction of dna into non bacterial cells
 
Cell Parts
Cell PartsCell Parts
Cell Parts
 
AQA Unit 1 AS Biology
AQA Unit 1 AS BiologyAQA Unit 1 AS Biology
AQA Unit 1 AS Biology
 
Macromolecule human awareness
Macromolecule  human awarenessMacromolecule  human awareness
Macromolecule human awareness
 
Ls1 afet semester test 1 memo 2012
Ls1 afet semester test 1 memo 2012Ls1 afet semester test 1 memo 2012
Ls1 afet semester test 1 memo 2012
 
Bm 2 review 2010
Bm 2 review 2010Bm 2 review 2010
Bm 2 review 2010
 

Ähnlich wie B2 revision powerpoint

A Study On Bacterial Transformation
A Study On Bacterial TransformationA Study On Bacterial Transformation
A Study On Bacterial TransformationJessica Myers
 
4.6 Biotechnology And Genetic Engineering
4.6 Biotechnology And Genetic Engineering4.6 Biotechnology And Genetic Engineering
4.6 Biotechnology And Genetic EngineeringPatricia Lopez
 
4.4 Biotechnology And Genetic Engineering
4.4 Biotechnology And Genetic Engineering4.4 Biotechnology And Genetic Engineering
4.4 Biotechnology And Genetic EngineeringPatricia Lopez
 
Genetic Engineering lab micro health ppt
Genetic Engineering lab micro health pptGenetic Engineering lab micro health ppt
Genetic Engineering lab micro health pptalhamily556677
 
Genome evolution discussion questions
Genome evolution discussion questionsGenome evolution discussion questions
Genome evolution discussion questionsabhiagphd
 
Genetic engineering & Plasmids 08 (tim) - Copy.ppt
Genetic engineering & Plasmids 08 (tim) - Copy.pptGenetic engineering & Plasmids 08 (tim) - Copy.ppt
Genetic engineering & Plasmids 08 (tim) - Copy.pptDrmahmoudAhmedabdeen1
 
Biology - Chp 13 - Genetic Engineering - PowerPoint
Biology - Chp 13 - Genetic Engineering - PowerPointBiology - Chp 13 - Genetic Engineering - PowerPoint
Biology - Chp 13 - Genetic Engineering - PowerPointMr. Walajtys
 
Chapter 4 Explain How Bacterial Plasmids Differ From...
Chapter 4 Explain How Bacterial Plasmids Differ From...Chapter 4 Explain How Bacterial Plasmids Differ From...
Chapter 4 Explain How Bacterial Plasmids Differ From...Melissa Luster
 
Describe how the structure of the DNA double helix was discovered. E.pdf
Describe how the structure of the DNA double helix was discovered.  E.pdfDescribe how the structure of the DNA double helix was discovered.  E.pdf
Describe how the structure of the DNA double helix was discovered. E.pdfarchanadesignfashion
 
Biology review
Biology reviewBiology review
Biology reviewErin Mucci
 
Unit7_MolecularGenetics
Unit7_MolecularGeneticsUnit7_MolecularGenetics
Unit7_MolecularGeneticsaurorabiologia
 
Recombinant Dna technology, Restriction Endonucleas and Vector
Recombinant Dna technology, Restriction Endonucleas and Vector Recombinant Dna technology, Restriction Endonucleas and Vector
Recombinant Dna technology, Restriction Endonucleas and Vector Dr. Priti D. Diwan
 
Bacterial growth & metabolism
Bacterial growth & metabolism Bacterial growth & metabolism
Bacterial growth & metabolism Aishwarya Hajare
 
2010 semester exam review
2010 semester exam review2010 semester exam review
2010 semester exam reviewBrandeisBiology
 
What Are The Three Postulates Of Cell Theory
What Are The Three Postulates Of Cell TheoryWhat Are The Three Postulates Of Cell Theory
What Are The Three Postulates Of Cell TheoryErica Baldwin
 
Unit 7 :Molecular Genetics
Unit 7 :Molecular GeneticsUnit 7 :Molecular Genetics
Unit 7 :Molecular Geneticsaurorabiologia
 

Ähnlich wie B2 revision powerpoint (20)

Genetic engineering
Genetic engineeringGenetic engineering
Genetic engineering
 
A Study On Bacterial Transformation
A Study On Bacterial TransformationA Study On Bacterial Transformation
A Study On Bacterial Transformation
 
4.6 Biotechnology And Genetic Engineering
4.6 Biotechnology And Genetic Engineering4.6 Biotechnology And Genetic Engineering
4.6 Biotechnology And Genetic Engineering
 
4.4 Biotechnology And Genetic Engineering
4.4 Biotechnology And Genetic Engineering4.4 Biotechnology And Genetic Engineering
4.4 Biotechnology And Genetic Engineering
 
Genetic Engineering lab micro health ppt
Genetic Engineering lab micro health pptGenetic Engineering lab micro health ppt
Genetic Engineering lab micro health ppt
 
Biotechnology
BiotechnologyBiotechnology
Biotechnology
 
Genome evolution discussion questions
Genome evolution discussion questionsGenome evolution discussion questions
Genome evolution discussion questions
 
Genetic engineering & Plasmids 08 (tim) - Copy.ppt
Genetic engineering & Plasmids 08 (tim) - Copy.pptGenetic engineering & Plasmids 08 (tim) - Copy.ppt
Genetic engineering & Plasmids 08 (tim) - Copy.ppt
 
Biology - Chp 13 - Genetic Engineering - PowerPoint
Biology - Chp 13 - Genetic Engineering - PowerPointBiology - Chp 13 - Genetic Engineering - PowerPoint
Biology - Chp 13 - Genetic Engineering - PowerPoint
 
Chapter 4 Explain How Bacterial Plasmids Differ From...
Chapter 4 Explain How Bacterial Plasmids Differ From...Chapter 4 Explain How Bacterial Plasmids Differ From...
Chapter 4 Explain How Bacterial Plasmids Differ From...
 
Describe how the structure of the DNA double helix was discovered. E.pdf
Describe how the structure of the DNA double helix was discovered.  E.pdfDescribe how the structure of the DNA double helix was discovered.  E.pdf
Describe how the structure of the DNA double helix was discovered. E.pdf
 
Biology review
Biology reviewBiology review
Biology review
 
DNA Cloning Lesson
DNA Cloning LessonDNA Cloning Lesson
DNA Cloning Lesson
 
Unit7_MolecularGenetics
Unit7_MolecularGeneticsUnit7_MolecularGenetics
Unit7_MolecularGenetics
 
Recombinant Dna technology, Restriction Endonucleas and Vector
Recombinant Dna technology, Restriction Endonucleas and Vector Recombinant Dna technology, Restriction Endonucleas and Vector
Recombinant Dna technology, Restriction Endonucleas and Vector
 
Bacterial growth & metabolism
Bacterial growth & metabolism Bacterial growth & metabolism
Bacterial growth & metabolism
 
2010 semester exam review
2010 semester exam review2010 semester exam review
2010 semester exam review
 
What Are The Three Postulates Of Cell Theory
What Are The Three Postulates Of Cell TheoryWhat Are The Three Postulates Of Cell Theory
What Are The Three Postulates Of Cell Theory
 
Unit 7 :Molecular Genetics
Unit 7 :Molecular GeneticsUnit 7 :Molecular Genetics
Unit 7 :Molecular Genetics
 
Rdna ppt presntation
Rdna ppt presntationRdna ppt presntation
Rdna ppt presntation
 

Mehr von Hannah Evans

P2 revsion powerpoint
P2 revsion powerpointP2 revsion powerpoint
P2 revsion powerpointHannah Evans
 
C2 revision powerpoint
C2 revision powerpointC2 revision powerpoint
C2 revision powerpointHannah Evans
 
P3 revision powerpoint
P3 revision powerpointP3 revision powerpoint
P3 revision powerpointHannah Evans
 
C3 revision powerpoint
C3 revision powerpointC3 revision powerpoint
C3 revision powerpointHannah Evans
 
P1 revision powerpoint
P1 revision powerpointP1 revision powerpoint
P1 revision powerpointHannah Evans
 
C1 revision powerpoint
C1 revision powerpointC1 revision powerpoint
C1 revision powerpointHannah Evans
 
B1 Powerpoint.pptx
B1 Powerpoint.pptxB1 Powerpoint.pptx
B1 Powerpoint.pptxHannah Evans
 

Mehr von Hannah Evans (7)

P2 revsion powerpoint
P2 revsion powerpointP2 revsion powerpoint
P2 revsion powerpoint
 
C2 revision powerpoint
C2 revision powerpointC2 revision powerpoint
C2 revision powerpoint
 
P3 revision powerpoint
P3 revision powerpointP3 revision powerpoint
P3 revision powerpoint
 
C3 revision powerpoint
C3 revision powerpointC3 revision powerpoint
C3 revision powerpoint
 
P1 revision powerpoint
P1 revision powerpointP1 revision powerpoint
P1 revision powerpoint
 
C1 revision powerpoint
C1 revision powerpointC1 revision powerpoint
C1 revision powerpoint
 
B1 Powerpoint.pptx
B1 Powerpoint.pptxB1 Powerpoint.pptx
B1 Powerpoint.pptx
 

Kürzlich hochgeladen

CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service 🪡
CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service  🪡CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service  🪡
CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service 🪡anilsa9823
 
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCESTERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCEPRINCE C P
 
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral AnalysisRaman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral AnalysisDiwakar Mishra
 
Formation of low mass protostars and their circumstellar disks
Formation of low mass protostars and their circumstellar disksFormation of low mass protostars and their circumstellar disks
Formation of low mass protostars and their circumstellar disksSérgio Sacani
 
Cultivation of KODO MILLET . made by Ghanshyam pptx
Cultivation of KODO MILLET . made by Ghanshyam pptxCultivation of KODO MILLET . made by Ghanshyam pptx
Cultivation of KODO MILLET . made by Ghanshyam pptxpradhanghanshyam7136
 
Nanoparticles synthesis and characterization​ ​
Nanoparticles synthesis and characterization​  ​Nanoparticles synthesis and characterization​  ​
Nanoparticles synthesis and characterization​ ​kaibalyasahoo82800
 
Unlocking the Potential: Deep dive into ocean of Ceramic Magnets.pptx
Unlocking  the Potential: Deep dive into ocean of Ceramic Magnets.pptxUnlocking  the Potential: Deep dive into ocean of Ceramic Magnets.pptx
Unlocking the Potential: Deep dive into ocean of Ceramic Magnets.pptxanandsmhk
 
Disentangling the origin of chemical differences using GHOST
Disentangling the origin of chemical differences using GHOSTDisentangling the origin of chemical differences using GHOST
Disentangling the origin of chemical differences using GHOSTSérgio Sacani
 
Orientation, design and principles of polyhouse
Orientation, design and principles of polyhouseOrientation, design and principles of polyhouse
Orientation, design and principles of polyhousejana861314
 
Broad bean, Lima Bean, Jack bean, Ullucus.pptx
Broad bean, Lima Bean, Jack bean, Ullucus.pptxBroad bean, Lima Bean, Jack bean, Ullucus.pptx
Broad bean, Lima Bean, Jack bean, Ullucus.pptxjana861314
 
Grafana in space: Monitoring Japan's SLIM moon lander in real time
Grafana in space: Monitoring Japan's SLIM moon lander  in real timeGrafana in space: Monitoring Japan's SLIM moon lander  in real time
Grafana in space: Monitoring Japan's SLIM moon lander in real timeSatoshi NAKAHIRA
 
A relative description on Sonoporation.pdf
A relative description on Sonoporation.pdfA relative description on Sonoporation.pdf
A relative description on Sonoporation.pdfnehabiju2046
 
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...jana861314
 
Botany 4th semester series (krishna).pdf
Botany 4th semester series (krishna).pdfBotany 4th semester series (krishna).pdf
Botany 4th semester series (krishna).pdfSumit Kumar yadav
 
Presentation Vikram Lander by Vedansh Gupta.pptx
Presentation Vikram Lander by Vedansh Gupta.pptxPresentation Vikram Lander by Vedansh Gupta.pptx
Presentation Vikram Lander by Vedansh Gupta.pptxgindu3009
 
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...Labelling Requirements and Label Claims for Dietary Supplements and Recommend...
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...Lokesh Kothari
 
Natural Polymer Based Nanomaterials
Natural Polymer Based NanomaterialsNatural Polymer Based Nanomaterials
Natural Polymer Based NanomaterialsAArockiyaNisha
 
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...ssifa0344
 
Recombinant DNA technology (Immunological screening)
Recombinant DNA technology (Immunological screening)Recombinant DNA technology (Immunological screening)
Recombinant DNA technology (Immunological screening)PraveenaKalaiselvan1
 

Kürzlich hochgeladen (20)

CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service 🪡
CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service  🪡CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service  🪡
CALL ON ➥8923113531 🔝Call Girls Kesar Bagh Lucknow best Night Fun service 🪡
 
CELL -Structural and Functional unit of life.pdf
CELL -Structural and Functional unit of life.pdfCELL -Structural and Functional unit of life.pdf
CELL -Structural and Functional unit of life.pdf
 
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCESTERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
 
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral AnalysisRaman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis
Raman spectroscopy.pptx M Pharm, M Sc, Advanced Spectral Analysis
 
Formation of low mass protostars and their circumstellar disks
Formation of low mass protostars and their circumstellar disksFormation of low mass protostars and their circumstellar disks
Formation of low mass protostars and their circumstellar disks
 
Cultivation of KODO MILLET . made by Ghanshyam pptx
Cultivation of KODO MILLET . made by Ghanshyam pptxCultivation of KODO MILLET . made by Ghanshyam pptx
Cultivation of KODO MILLET . made by Ghanshyam pptx
 
Nanoparticles synthesis and characterization​ ​
Nanoparticles synthesis and characterization​  ​Nanoparticles synthesis and characterization​  ​
Nanoparticles synthesis and characterization​ ​
 
Unlocking the Potential: Deep dive into ocean of Ceramic Magnets.pptx
Unlocking  the Potential: Deep dive into ocean of Ceramic Magnets.pptxUnlocking  the Potential: Deep dive into ocean of Ceramic Magnets.pptx
Unlocking the Potential: Deep dive into ocean of Ceramic Magnets.pptx
 
Disentangling the origin of chemical differences using GHOST
Disentangling the origin of chemical differences using GHOSTDisentangling the origin of chemical differences using GHOST
Disentangling the origin of chemical differences using GHOST
 
Orientation, design and principles of polyhouse
Orientation, design and principles of polyhouseOrientation, design and principles of polyhouse
Orientation, design and principles of polyhouse
 
Broad bean, Lima Bean, Jack bean, Ullucus.pptx
Broad bean, Lima Bean, Jack bean, Ullucus.pptxBroad bean, Lima Bean, Jack bean, Ullucus.pptx
Broad bean, Lima Bean, Jack bean, Ullucus.pptx
 
Grafana in space: Monitoring Japan's SLIM moon lander in real time
Grafana in space: Monitoring Japan's SLIM moon lander  in real timeGrafana in space: Monitoring Japan's SLIM moon lander  in real time
Grafana in space: Monitoring Japan's SLIM moon lander in real time
 
A relative description on Sonoporation.pdf
A relative description on Sonoporation.pdfA relative description on Sonoporation.pdf
A relative description on Sonoporation.pdf
 
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...
Traditional Agroforestry System in India- Shifting Cultivation, Taungya, Home...
 
Botany 4th semester series (krishna).pdf
Botany 4th semester series (krishna).pdfBotany 4th semester series (krishna).pdf
Botany 4th semester series (krishna).pdf
 
Presentation Vikram Lander by Vedansh Gupta.pptx
Presentation Vikram Lander by Vedansh Gupta.pptxPresentation Vikram Lander by Vedansh Gupta.pptx
Presentation Vikram Lander by Vedansh Gupta.pptx
 
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...Labelling Requirements and Label Claims for Dietary Supplements and Recommend...
Labelling Requirements and Label Claims for Dietary Supplements and Recommend...
 
Natural Polymer Based Nanomaterials
Natural Polymer Based NanomaterialsNatural Polymer Based Nanomaterials
Natural Polymer Based Nanomaterials
 
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...
TEST BANK For Radiologic Science for Technologists, 12th Edition by Stewart C...
 
Recombinant DNA technology (Immunological screening)
Recombinant DNA technology (Immunological screening)Recombinant DNA technology (Immunological screening)
Recombinant DNA technology (Immunological screening)
 

B2 revision powerpoint

  • 2. B2.1 – Plant and Animal Cells 7 Organelles Function Cell Membrane Controls movement into and out of the cell. Nucleus Contains DNA. Controls the cell Cytoplasm Where chemical reactions take place. Mitochondria Where respiration occurs. Cell Wall Made of CELLULOSE. Supports the cell. Vacuole Contains CELL SAP. Helps support the plant by keeping the cell rigid Chloroplast Contains CHLOROPHYLL. Absorbs LIGHT. Where photosynthesis takes place Plant and animal cells can be studies in greater detail using a light microscope. Light passes through a thin slice of the specimen. Lenses magnify the specimen many times.
  • 3. B2.2 – Inside Bacteria 4 Organelles Function Chromosomal DNA A giant loop of DNA containing most of the genetic material. Plasmid DNA Small loops of DNA that carry extra information. Flagella Long whip like structures that aid movement. Cell Wall Provides support but is more flexible than a plant. Not made of cellulose. 2 types of DNA Microscopes have improved in last 350 years. Light microscopes can magnify 1500x. Electron microscopes can magnify 2000000x. Electron microscopes produce very clear images. Electron microscopes show more detail of the specimen.
  • 4. B2.3 - DNA Key Definition A gene is a section of DNA that codes for a specific protein. DNA is made up of two strands coiled to form a double helix. The two strands are linked by complementary bases held together by weak hydrogen bonds. Adenine (A) pairs with Thymine (T) Cytosine (C) pairs with Guanine (G)
  • 5. B2.4 – Extracting DNA 1. Chop onion or peas into chunks. 2. Grind in a pestle and mortar. 3. Mix together with washing up liquid, salt and water and stir. 4. Incubate the mixture at 60 degrees Centigrade for 15 minutes in a water bath. 5. Filter the mixture through filter paper into a boiling tube. 6. Take ice cold alcohol and pour it slowly down the side of the boiling tube. The alcohol will form a transparent layer on top of the liquid, as the alcohol is less dense. 7. You will see the DNA between the two liquid layers.
  • 6. B2.5 – DNA Discovery London - Maurice Wilkins & Rosalind Franklin using X-rays to study DNA structure. From the patterns made they could work out how the atoms were arranged. Cambridge – Watson & Crick were building a model of DNA using data from other scientists. They were given a copy of Franklins photographs which enabled them to crack the code. Franklin didn’t know they had the photo. Watson and Crick published their paper with the structure of DNA but didn’t acknowledge the photograph they used Watson and Crick were awarded the Nobel Prize with Maurice Wilkins but Rosalind Franklin had already died so did not get the prize.
  • 7. B2.5 – DNA Discovery The Human Genome Project – International Project. 3 billion bases that make up the human genome were sequenced. It took 13 years and scientists collaborated using IT to store and share data. All humans have 99.9% of their DNA in common. 5 Implications of the HGP 1. Improved genetic testing for disorders. 2. New ways of finding new genes that may increase risk of certain diseases. 3. New treatments and cures for diseases. 4. New ways of looking at changes in the genome over time. 5. Personalised medicines that work with a particular genotype.
  • 8. B2.6 – Genetic Engineering Know this process! Definition - The process of removing a gene from one organism and inserting it into the DNA of another.
  • 9. B2.6 – Genetic Engineering Example Advantages Disadvantages Beta carotene in golden rice to reduce vitamin A deficiency in humans 1. Beta carotene used to make vitamin A 2. Vitamin A will reduce death and blindness. 1. Could cross breed with wild rice and contaminate wild rice DNA 2. Levels of beta carotene in Golden Rice might not be high enough to make a difference 3. Can be expensive to buy 4. Produces sterile seeds so farmers have to buy them every year The production of human insulin by GM bacteria 1. Can be used by vegans 2. Supply not affected by animal diseases 3. Supply not affected by demand for meat 4. Can be made in vast quantities 5. Cheaper 1. Bacteria produce insulin slightly differently so may not work for some people The production of herbicide resistant crops 1. Reduces amount of crop spraying 1. Herbicide resistant weeds can develop 2. Cross pollination with wild plants 3. Potential loss of biodiversity
  • 10. B2.7 – Mitosis and Meiosis Mitosis • The production of two daughter cells with identical sets of chromosomes in the nucleus as the parent cell. • Results in the formation of two genetically identical diploid cells. • Occurs during growth and repair and asexual reproduction Meiosis • The production of four daughter cells, each with half the number of chromosomes as the parent cell. • Results in the formation of genetically different haploid gametes. • Occurs when making gametes only. Definitions Haploid – Having one set of chromosomes. Diploid – Having two sets of chromosomes. Gamete – the sex cells (sperm and egg) At fertilisation, haploid gametes join to form a diploid zygote.
  • 11. B2.8 - Clones How to produce a clone 1. Remove a diploid nucleus from a body cell 2. Enucleate an egg cell 3. Insert diploid nucleus into enucleated egg cell. 4. Stimulate the diploid nucleus to divide by mitosis. 5. Implant into surrogate mother. Cloning – An example of asexual reproduction. Enucleate – Remove the nucleus
  • 12. B2.8 - Clones Advantages of Cloning Disadvantages of Cloning Risks of Cloning 1. Can make a genetically identical copy of an animal with desirable characteristics. 2. Can be used to make copies of GM animals to guarantee all offspring have the trait. 1. Cloned animals often die young. 2. Cloned animals often age more quickly. 3. Complicated process. 1. Very few embryos develop properly resulting in deformities.
  • 13. B2.9 – Stem Cells Advantages of Stem Cell Research Disadvantages of Stem Cell Research Risks of Stem Cell Research 1. Embryonic stem cells can develop into almost every type of human cell. 2. Bone marrow stem cells can be used to treat lukaemia. 3. Adult stem cells may be used in future instead of embryonic stem cells. 1. Embryonic stem cells can come from leftover embryos from fertility treatments. 2. Risk of rejection if not from a patients own stem cells. 3. Could lead to tumours forming. 1. Technology could be used illegally. 2. Risk of the unknown – long term effects may not be shown for years. Key definitions Stem Cell - An unspecialised cell that can divide to produce more stem cells or different types of specialised cell. Differentiate – Become specialised. Embryonic Stem Cell – Can differentiate into almost any cell type. Adult Stem Cell – Can differentiate into only a few cell types. Specialised Cell – a cell with a particular function e.g. neurone, red blood cell.
  • 15. B2.10 Protein Manufacture Transcription 1. DNA double helix unzips. 2. The complementary mRNA strand is made in the nucleus and passes out through a pore. Translation 1. mRNA attaches to the ribosome. 2. A triplet of bases on the mRNA (codon) code for a specific amino acid. 3. tRNA transfers amino acids to the ribosome. 4. Amino acids link together to form polypeptides. RNA is single stranded but DNA is double stranded. RNA contains Uracil (U) instead of thymine (T) Each amino acid is coded for by 3 specific bases. DNA is a triplet code.
  • 16. B2.11 - Mutations 1. Each protein has its own specific number and sequence of amino acids. 2. This is coded for by the DNA. 3. Therefore, each protein is a different shape and has a different function e.g. an enzyme. 4. Mutations change the sequence of the bases, and therefore the shape of the protein. 5. Most mutations are harmful. 6. Radiation and some chemicals in cigarette smoke are mutagens and cause mutations. Mutation – A change in the sequence of bases in the genetic code.
  • 17. B2.12 - Enzymes These are examples of enzyme catalysed reactions: 1. DNA Replication – One enzyme unzips the two strands of DNA, the other joins the new bases together to make the new double stranded molecule. 2. Protein Synthesis – RNA Polymerase makes the mRNA strand from the DNA template. 3. Digestion – Many enzymes break larger molecules down into smaller ones in digestion. This happens outside of the body. Stain digesting enzymes in washing powders break down stain in clothes. Microorganisms excrete enzymes onto food to break them down outside the body and then absorb the products. Enzymes are biological catalysts. They speed up reactions.
  • 18. B2.13 – Enzymes and Temperature Factors that affect enzyme activity: 1. Temperature 2. pH 3. Substrate Concentration. Enzymes are SPECIFIC to their substrate. They only catalyse specific reactions in specific conditions. They have a specific shaped active site. Enzyme activity can be measured by measuring the speed at which a product is made e.g. a gas, or the speed at which a substrate is used up e.g. stain digestion.
  • 19. B2.14 – Enzyme Action As temperature increases, so does enzyme activity, up to 40oC. After 40oC the active site is denatured and the reaction stops. As substrate concentration increases, so does enzyme activity, up to a point where the number of active sites becomes limiting. The only way to speed up the reaction after this is to increase the number of active sites. Enzymes will only work at a specific pH. Either side of this optimum pH, the enzyme will denature and not work. Enzymes can never be killed. They can only be denatured, which is where the shape of the active site changes.
  • 20. B2.14 – Enzyme Action Enzymes work like a lock and key Lock and Key Enzyme and Substrate One key will only fit one lock. One substrate will only fit one enzyme. The key fits the lock. The substrate fits the active site The key unlocks the lock. The substrate is changed in the enzyme Wrong key won’t fit the lock. Wrong substrate won’t fit the active site.
  • 21. B2.15 Aerobic Respiration. • All organisms are made of cells • Energy released by respiration • Cells that move more need more energy. • Exercise = more energy needed. Key Terms: Respiration - the release of energy from food molecules that act as fuel for the cell. Diffusion - when substances move from an area of high concentration to an area of low concentration. Glucose + Oxygen = Carbon Dioxide + Water Aerobic respiration = uses oxygen to release energy from glucose. How does it get delivered? • Glucose and oxygen diffuse from capillaries to respiring cells • Carbon dioxide diffuses from respiring cells to capillaries • Capillaries - smallest vessel that carries blood between cells/ one cell thick • Substances move by diffusion down a concentration gradient = the diffusion pathway.
  • 22. • Respiring cells = oxygen and glucose levels fall as they are used up in aerobic respiration/ Carbon dioxide levels increase. • Gas exchange = the transfer of gases.
  • 23. B2.16 investigating The effects of exercise. • Exercise = increase heart rate and has to pump blood faster to the muscles. • Causes breathing rate to increase and get deeper. Why? • Cells need more oxygen and glucose as they need more energy. • Cells produce more carbon dioxide as a result which needs to be removed.
  • 24. B2.17 Anaerobic respiration • Anaerobic respiration = respiration without oxygen • Glucose is broken down to supply energy to the muscles • Releases less energy then aerobic and produces Lactic Acid • Amount of blood pumped around the body depends on the stroke volume and the heart rate. • Exercise = increase in heart rate and stroke volume. • Lactic Acid needs to be broken down = oxygen used to break it down into carbon dioxide and water. • The requirement of this oxygen to break down the lactic acid is called excess post- exercise oxygen consumption (EPOC) Glucose  lactic acid Cardiac output = stroke volume x heart rate.
  • 25. B2.18 Photosynthesis. • Photosynthesis = plants make their own food • Uses light energy to produce glucosefrom carbon dioxide and water • Glucose stored as starch • Starch = lots of glucose molecules joined together. • Digestion breaks down starch = glucose • Chlorophyll = green found in chloroplasts absorbs light for photosynthesis. • Variegated leaves = the green parts of a leaf contain the chlorophyll. Carbon dioxide + water  glucose + oxygen Light and chlorophyll
  • 26. 2.20 Factors that effect the rate of photosynthesis. 3 factors that effect photosynthesis. • Carbon dioxide • Light • Temperature • All 3 are needed at optimum amount for photosynthesis to be at its best. • The limiting factor is the one that is in short supply…..you may have lots of CO2 the right temperature but little light this means photosynthesis will be slow. Limiting factor = something can affect the rate of photosynthesis.
  • 27. Adaptations of a leaf. Upper epidermis = tightly packed cells = lots of chloroplasts = lots of photosynthesis. Air spaces = provide large surface for cells to exchange with gases in the air. Lower epidermis = contain stomata. Stomata = open and close to allow gases into the leaf. Located underside of the leaf. Open in response to light. Allow Carbon dioxide in and lets out oxygen and water vapour. 3 Adaptations Has stomata for gas exchange (carbon dioxide, oxygen, water vapour) Contains chlorophyll in chloroplasts to absorb light. Large surface area to absorb most amount of light.
  • 28. Root HairCell • Job of root = anchor plant and take up nutrients. • Root hair found on surface of root. • Role – to absorb water and dissolved minerals. • Adaptation = large surface area. B2.21 Water Transport • Roots absorb nitrates and mineral ions dissolved in water by Active transport. This needs energy from respiration • Water transported by xylem • Nutrients transported by phloem Key Definitions • The loss of water from the leaves drives transpiration. • Transpiration – the movement of water through a plant and the loss of water throught he leaves. • Osmosis = movement of water from an area of low concentration to an area of high concentration through a partially permeable membrane.
  • 29. B2.22 Investigating Osmosis Osmosis Water can move across cell membranes because of osmosis. For osmosis to happen you need: two solutions with different concentrations and a partially permeable membrane to separate them
  • 30. B2.23 Organisms and their environment Key Terms • Environment = an organisms surroundings including the soil, air, water and other organism in the area. • Biodiversity = the different plants and animals in an area. • Ecosystem = an area in which all the living organisms and all the non living organism form a relationship in order to survive. • Habitat = where the plants and animals are found/living. • Population = the number of animals in a given area. • Sampling = looking at small proportion of the plants and animals. Sampling techniques = • 1) Pooter = used to catch animals. • 2) Sweep net = can catch flying animals. • 3) Pond net = to catch aquatic animals. • 4) pit fall traps = buried in the ground…the organisms fall in. • 5) quadrats = used to sample the population size of plants = random sampling or systematic sampling. = placing the quadrat at regular intervals along a line.
  • 31. B2 Topic 3 Common Systems
  • 32. B2.25 Fossils and evolution Keywords • Fossil record – The collection of fossils identified from different periods of time that can be interpreted to form a hypothesis about the evolution of life on Earth. • Fossil – The preserved traces or remain of an organism which lived a very long time ago • Pentadactyl – five fingered organism Facts: • The moon is 30 ‘earths’ away • The sun is 11,000 ‘earths’ away Fossils • Fossils from different periods of time show organisms have changed gradually = evolution. • Fossil record has gaps – Soft tissues decay not forming fossils – Hard parts of organisms could have been destroyed – Many fossils are buried too deep to be found • Scientists using incomplete data sometimes make mistakes • More fossils = more accurate conclusions Evidence for Evolution • Internal bones of all vertebrate’s limbs are similar • Fossils of limbless vertebrates have the same five fingered structure • All vertebtates evolved from one common ancestor • Evolution of the limbs is due to adaptation to how the organisms lived and moved,
  • 33. B2.26 Growth Keywords • Percentile – The value of a variable below which a certain percentage of observations fall. • Stem Cell – An unspecialised cell that can divide to produce more stem cells or different kinds of specialised cells • Differentiate – Specialise, develop into different kinds of cell, as in cells that become nerve, muscle or bone cells • Elongation – getting longer Facts • Growth is when an organisms increases in size, length and mass • To monitor growth of babies we check – Head circumference – Weight – Height • Each child is compared to a chart to determine which percentile of the population they are in. • Growth involves 2 things – Increase in the number of cells – Increase in the size of cells Growth in Plants • Grow all through their lives • Cells divide in the Meristem – behind the tip of the root and shoot • Cells also elongate • Older meristem cells differentiate to become specialised for example: – Palisade leaf cell – Root hair cell Growth in Animals • Cell division • Animals stop growing when they become adults • Stem cells are undifferentiated • Stem cells can specialise into all other cells • Adults have very few stem cells (only in blood and skeletal tissues) • Most animals cannot regrow limbs or body parts.
  • 34. Components • Plasma – Fluid part of blood – Transports carbon dioxide, hormones and waste – Pale yellow • Red blood cells – No nucleus = more room for haemoglobin – Made in the bone marrow. – Contain red pigment haemoglobin which carries oxygen Oxygen + Haemoglobin Oxyhaemoglobin – Oxygen is carried in the blood to the tissues for aerobic respiration – Biconcave disc = large surface area to volume ratio for faster diffusion of oxygen • White blood cells – An important part of the immune system – Some produce antibodies (proteins that bind to microbes and destroy them) – Others surround and destroy foreign cells – All have a nucleus – Made in the bone marrow – All have a nucleus • Platelets – Tiny fragments of cells (no nuclei) – Clump together to form clots – Protect the body by stopping bleeding and forming a scab to stop microbes entering. B2.27 Blood
  • 35. B2.28 The heart • Deoxygenated blood (low oxygen levels) • Pumped to the lungs (by right ventricle) to collect oxygen • Oxygenated blood returns to heart (Left side) • Pumped to the body cells and tissues (by left ventricle) • Left and right side work together at the same time • Valves prevent backflow of blood • Tendons stop valves turning inside out Septum Thicker wall as it pumps blood all around the body
  • 36. B2.29 The circulatory system 3 types of blood vessel: Arteries • Carry blood away from the heart • Have thick muscular walls • Have small internal lumen • Blood under high pressure Veins • Carry blood to the heart • Thin walls • Larger internal lumen • Blood under low pressure • Valves to prevent blood flowing backwards Capillaries • Wall is one cell thick • Very low blood pressure • Allows diffusion between blood and tissues
  • 37. B2.30 The digestive system churns Peristalsis • Muscles contract in waves to move food along the alimentary canal ( a muscular tube running from your mouth to your anus)
  • 38. B2.31 Breaking down food Keywords Enzyme – a protein molecule made by living cells that speeds up the rate of a reaction Emulsion – a mixture in which particles of one liquid are suspended in another liquid. Digesting proteins Digesting Carbohydrates Digesting Fats Enzyme involved Proteases (e.g. pepsin) Carbohydrases (e.g. amylase) Lipases Broken down into… Amino acids Simple sugars (glucose) Glycerol and Fatty acids Where it occurs Stomach first then small intestine Mouth and small intestine Small Intestine Additional features Pepsin has an optimum pH of 2 (perfect for stomach acid) Amylase is denatured by stomach acid • Bile from the gall bladder breaks down large fat globules into droplets with a larger surface area to help lipase. • We say bile emulsifies the fat. • Bile also neutralises the stomach acid.
  • 39. B2.32 Villi Inside the Small Intestine 1. Digested food passes into blood by diffusion 2. Bigger surface areas = more diffusion 3. Finger-like folds called Villi increase surface area of small intestine Features of a Villus to speed up diffusion 1. Good network of capillaries moving absorbed nutrients 2. Low concentration of food 3. Steep concentration gradient maintained 4. Wall is a single cell layer (shorter distance to diffuse) Keywords Villi – finger like projections in the small intestine. Diffusion – movement of particles from an area of high concentration to an area of low concentration down a concentration gradient.
  • 40. B2.34 Probiotics and Prebiotics – Functional foods Prebiotics • Substances the body cannot digest • They act as food for the beneficial bacteria • Oligosaccharides are a common form of prebiotic (contained in tomatoes, onions and asparagus) • Also found in specially made dairy foods and sold as capsules • Increasing evidence supports their positive effect on health Plant Stanol Esters • Oily substances in plants • Stop the small intestine absorbing cholesterol • Lowers blood cholesterol • Use in many foods like yogurt and spreads. Probiotics • Live bacteria – friendly or beneficial • Bifidobacteria or Lactobacillus • They produce lactic acid in your gut and companies claim they improve health • NOT ENOUGH EVIDENCE to support the claims they are effective