2.2 Water

Structure

  • 2 hydrogen and 1 oxygen, bonded covalently.
  • Non-equal sharing of electrons.
  • 8 protons (Oxygen) vs. 1 proton (Hydrogen).
  • Oxygen’s 8 protons attract electrons more strongly.
  • So “O” becomes slightly +ve and “H” becomes slightly -ve.
  • Causes a slight potential charge - hence the molecule is polar.
  • Hydrogen bonding between water molecules.

Properties of Water

  • Cohesion (molecules stick to each other).
  • Adhesion (Molecules stick to other surfaces).
  • Thermal Properties:
    • High specific heat capacity.
    • High latent heat of vaporisation.
    • High boiling point.
  • Universal solvent - Polar nature can interrupt intramolecular forces and cause dissociation in other molecules.

Methane vs Water

Property Methane Water
Formula CH4 H2O
Molar Mass 16 18
Bonding single covalent single covalent
Polarity non-polar polar
Density (gcm-1) 0.46 1
Specific Heat Capacity (Jg-1 oC-1 2.2 4.2
Latent Heat of Vaporisation (Jg-1) 760 2257
Melting Point (oC) -182 0
Boiling Point (oC) -160 100

Water as a Coolant

  • Sweat is secreted by glands in the skin.
  • The high specific heat of vaporisation causes the water in sweat to take away a lot of heat from the tissues in the body when evaporating.
  • This helps cool the body during periods of intense activity.
  • Similarly, dogs pant and plants transpire.

Transport in Blood Plasma

Water transports the following in blood:

  • Sodium Chloride - ion dissolves as Na+ and Cl-
  • Amino acids - polar molecules, solubility depends on R group
  • Glucose - polar
  • Oxygen - non-polar, but dissolves sparingly, haemoglobin in the blood coverts to oxyhaemoglobin to increase carrying capacity
  • Fat molecules - non-polar, so form lipoproteins. Lipoproteins consist of phospholipid on the outside and fat on the inside, thus helps transport.
  • Cholesterol - Lipoproteins, as they are non-polar

Sources

  • Class notes
  • Biology - Course Companion - Andrew Allott and David Mindorff - Oxford 2014

Enzymes

Active Sites and Enzymes

  • Enzymes are globular proteins that speed up reactions
  • They convert substrates to products
  • All substrates bind to the active site of its enzymes, the shape of the active site and the substrate are complementary
  • The shape of the active site is determined by the arrangement and bonding between amino acids that make up the enzyme

Enzyme Activity

  • Enzyme activity is determined by the rate of collisions between the active site and the substrate

Factors affecting enzyme activity

1) Temperature

  • As thermal energy increases, the particles are given more kinetic energy
  • So they move around more and faster, so the chances of collision increase, and enzyme activity increases
  • But if the temperature gets too high, the bonds between the amino acids break, altering the shape of the enzyme
  • So the substrate is no longer complementary to the active site and the reaction can’t be catalysed.
  • This is reversible upto a certain temperature, but causes permanent denaturation after that

enter image description here

2) pH

  • pH is a measure of hydrogen ion concentration
  • Too many or too little ions can denature the enzyme by altering it’s bonding
  • different enzymes have different optimum pHs depending on their environment

enter image description here

3) Substrate Concentration

  • If there is more substrate present, more reactions can be catalysed simultaneously, so rate of reaction would increase
  • But if the substrate concentration is too high, all the active sites would have already been occupied, so the rate of reaction would no longer increase

enter image description here

Immobilized Enzymes

  • Present in industries and nature
    • For example, on a glass surface, alginate beads, or on the wall of the villi
  • Advantages in industry:
    • Enzyme can easily be seperated from products, prevents contamination
    • Enzymes can be recycled easily (cost \downarrow)
    • Immobilization lowers sensitivity of enzymes to pH and temperature, so the rate at which they are degraded goes down, so can be replaced less often
    • Substrates are exposed to higher enzyme concentrations, so rate increases

Use of Immobilized Enzymes in Producing Lactose Free Milk

  • Lactose is a sugar naturally present in milk
  • It can be broken down by the enzyme lactase
  • LactoseGlucose+Galactose\text{Lactose} \rightarrow \text{Glucose} + \text{Galactose}
  • Some people are lactose intolerant so cannot consume lactose
  • So this reaction is used to produce Lactose-Free Milk
  • Galactose and Glucose are sweeter than lactose, so less sugar needs to be added to dairy products made from Lactose Free Milk
  • Galactose and Glucose crystallize less, giving a smoother texture for ice creams
  • Bacteria ferment Glucose and Galactose quicker, so less time required for making yogurt

enter image description here

References

  • Class Notes
  • Oxford University Press BIOLOGY 2014 Edition
  • ScienceAid
  • Pathwayz
  • Philpot Education

DNA Replication, Transcription and Translation

CENTRAL DOGMA

Transcription, nucleus
Translation, ribosome
DNA
RNA
Polypeptide

Genetic Code

  • Universal to all organisms
  • Nuclear DNA consists of single copy genes + regions of highly repetitive sequences
  • Exons (coding sequences) and Introns (Non-Coding)
  • 4 bases: A, T, G and C

Replication

Replication of DNA is semi-conservative, dependent on complementary base pairing

  • Two strands of double helix separate
  • Each original strand is template for new strand
  • Complementary nucleotides are added one by one
  • Since part of original strand remains, replication is semi-conservative
  • Complementary bases from hydrogen bonds with each other, stabilising the structure
  • Complementary Base Pairing: one base always pairs with another
  • A with T & G with C

Nature of Science: evidence for theory of semi-conservative replication

  • Meselson and Stahl
    • Used 15N, a rare isotope of nitrogen
    • Has 1 more neutron than 14N isotope, making it denser
    • Developed caesium chloride density gradient centrifugation
    • Method to separate the strands based on density, substance became concentrated at level corresponding to its density, creating a gradient
    • Cultured E. Coli, 14 generations, with 15N
    • Under ultraviolet light, after centrifugation, dark bands were seen
    • First Generation band was exactly in between original E. Coli and E. Coli with only 15N in their DNA.

Helicase

  • Unwinds the double helix
  • Separates two strands by breaking the hydrogen bonds (between complementary bases)
  • Uses energy from ATP
  • Structure: 6 globular proteins, in donut shape
  • Unwinding whilst separating

DNA Polymerase

  • Uses pre-existing strand as template
  • Links nucleotides together to form new strand (one at a time)
  • Enzyme brings nucleoside triphosphate, attaching them in the 5’ to 3’ direction
  • Covalent bond between phosphate group of free nucleotide and sugar of nucleotide on template strand
  • High degree of fidelity

Application: Polymerase Chain Reaction (PCR)

  • Used to make many copies of DNA sequence
  • If DNA heated to high temperature hydrogen bonds between complementary base pairs breaks.
  • When cooled, these can from again; called re-annealing
  • Steps (Cycle, repeated)
    • heated to 95 degrees celsius for 15 seconds
    • DNA cooled quickly to 54 degrees
    • Short strands of single stranded DNA present, called primers
    • Bind rapidly to target sequences; prevent re-annealing
    • Copying then starts from these primers
    • Enzyme TaqDNA Polymerase used
    • obtained from bacteria Thermus aquaticus found in hot springs
    • Will not denature in high temperatures
    • Adds nucleotides to template strands
    • Next cycle is started by heating to 95 degrees again
    • DNA is amplified

Transcription

  • Synthesis of mRNA copies from the DNA base sequence by RNA polymerase
  • RNA is single stranded; transcription occurs on only one strand
  • Enzyme involved: RNA Polymerase
  • Binds to promoter site
  • Moves along strand (5’ to 3’ direction) separating DNA into single strand and covalently bonding ribonucleoside triphosphate
  • No thymine in RNA, replaced with Uracil (U)
  • Once this is complete, RNA Polymerase separates from DNA strand and double helix reforms
  • Transcription stops at terminator site
  • DNA Strand that has the same base sequence is called Sense Strand
  • Anti-Sense Strand is what is copied from, complementary bases

Translation

  • synthesis of polypeptides on ribosomes
  • ribosomes are a binding site and catalyse the synthesis
  • Ribosome Structure
    • complex structure of proteins and ribosomal RNA
    • small and large subunit
    • 1 binding site for mRNA (on small subunit)
    • 3 binding sites for tRNA (on large subunit)
  • amino acid sequence determined by mRNA according to genetic code
  • what protein is translated depends on requirements of cell + function of cell
  • example: insulin secretory cells, make many copies of mRNA needed to synthesise insulin
  • tRNA (transfer RNA): involved in de-coding base sequence of mRNA in amino acid sequence
  • mRNA binds to small subunit; molecule of tRNA with anticodon complementary to first codon can be translated
  • second tRNA with anticodon complementary to second codon binds to ribosome active site
  • Ribosome transfers amino acids carried by 1st tRNA to the amino acid of 2nd tRNA by making a new peptide bond
  • 2nd tRNA now has di-peptide
  • another tRNA binds with complementary anti-codon to next part of sequence
  • cycle continues until stop codon; then polypeptide is released
  • ribosome can be re-used

Codons and Anticodons

  • DNA transcribed in triplets
  • Codons ( 3 bases on mRNA) correspond to one amino acid in polypeptide
  • there are 4 bases; 20 required amino acids; therefore codon of 3 bases creates ideal possibility of 4x4x4 = 64 combinations
  • different codons can code for same protein
  • Degenerate code; reduce impact of base-substitution mutation
  • START CODON: AUG, promoter site
  • amino acid is carried on tRNA
  • translation depends on complementary base pairing between codons on mRNA and anticodons on tRNA
  • mRNA has sequence of codons that specified amino acid sequence
  • anticodon is complementary this codon

enter image description here

Cell Respiration

  • controlled release of energy in the form of ATP by breaking down organic compounds
  • one of the 7 necessary functions of life
  • main source is carbohydrates and lipids, but sometimes amino acids if proteins are excess in the diet.

Adenosine Tri-Phosphate

  • considered to be the universal energy carrier
  • transfers chemical energy in an immediately available form for use of metabolic processes.
  • releases energy by splitting ATP into ADP (di-phosphate) by hydrolysis

Structure of ATP
Image result for structure of atp

  • nucleotide derivative
  • purine base (Adenine) + pentose sugar (ribose) + 3 phosphates groups attached to the 5’ carbon

When energy from ATP is used in cells, its becomes converted to dissipated heat energy. Hence, continual source of ATP is required.

Anaerobic Respiration

  • glucose is broken down in the absence of oxygen resulting in a smaller yield of ATP.
  • products of anaerobic respiration vary based on organism
  • useful in 3 situations:
    • short but rapid burst of ATP/ energy
    • oxygen supplies have run out for the cell
    • environments deficient in oxygen
Yeast and Plants
Animals
Anaerobic Respiration
Alcoholic Fermentation
Lactic Acid Fermentation
glucose-> ethanol + carbon dioxide
glucose-> lactic acid

2.9 - Photosynthesis

  • Photosynthesis:- Metabolic pathway which uses carbon dioxide and water to produce carbohydrates and oxygen, in the presence of sunlight.
  • 6CO2 + 6H2O --> C6H12O6 + 6O2
  • Glucose gets converted into starch and cellulose.
  • Leaves are green because they reflect green.
  • Endothermic as energy is needed to be absorbed from light (and then stored in the form of carbohydrates).

Absorption and Action Spectra

Absorption Spectrum

  • Shows the absorbance of light by photosynthetic pigments for all wavelengths
  • "Chlorophyll a**"** absorbs mostly violet and orange.
  • "Chlorophyll b" absorbs mostly blue and yellow.
  • "Carotenoids" absorb mostly blue-green and violet.

Absorption Spectrum
Absorption Spectrum, source

Action Spectrum

  • Shows the rate of photosynthesis for wavelengths of light as a % of the maximum rate.

Action Spectrum
Action Spectrum, source

Limiting Factors

Light Intensity

  • As light increases, more energy is absorbed for the reaction.
  • Until another factor becomes the limiting factor.
  • Light too dim closes the stomata.

Temperature

  • Photosynthesis is an enzyme controlled reaction.
  • So there is an optimum temperature for the enzymes and stomata to stay open.

Carbon Dioxide Concentration

  • As CO2 concentration increases, rate increases.
  • Till an optimum point, the levels out.

Limiting Factors
Limiting Factors, source

Oxygen Production

  • Photolysis: The splitting of water molecules in the presence of light to produce oxygen, electrons, and protons (hydrogen ion).
  • H2O --> 4e- + 4H+ + O2
  • This increased O2 in the air and helped oxygen dependent life to develop.

Sources

Genes

  • A gene is the unit of heredity. It is defined as a length of
    DNA
    that codes for a single protein that aids in the
    determination of a specific trait or characteristic of the
    phenotype.
  • Genes occupy a specific position on one chromosome - locus

Alleles

  • variant form of a gene
  • can be two or more alleles for a gene
  • occupy the respective, equivalent loci on homologous chromosomes
  • differ from each other by slight variations in gene sequence

Homozygous - both homologous chromosomes carry identical alleles for the gene of interest
Heterozygous - each homologous chromosome carries a different allele for the gene of interest

Mutation

  • random change in DNA base sequence
  • errors in copying or induced by other physical, chemical or biological agents (mutagens)
  • can include single base pair changes to large sections of chromosomes
  • gametic mutations can be inherited
  • somatic mutations are eliminated once the body dies.

Diseases caused by mutations
Cystic fibrosis: chloride transport protein - disruption in glands that lead to symptoms like chronic lung infections
Sickle Cell Anemia:

  • mutation in beta chain of haemoglobin (Hb) molecule
  • substitution of one base leading to placement of hydrophobic amino acid instead of hydrophilic one.
  • inherited disorder
  • red blood cells deform into sickle shapes, which affects movement through capillaries
  • reduces circulation and blocks small vessels

Genome

the whole of the genetic information in an organism

The Human Genome Project

  • entire base sequence of the human genes
  • rich mine of data
  • allowed for understanding of protein coding regions
  • “junk DNA”
  • comparisons with other genomes for evolutionary history

References

  • Class notes
  • Oxford University Press BIOLOGY 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Chromosomes

Prokaryotic Chromosomes

Most prokaryotes have one naked chromosome, made out of of a single circular DNA molecule, which is present in the nucleoid. This means there is only one copy of each gene.

Plasmids:

  • small, extra DNA molecules
  • also circular and naked
  • consists of genes not required for basic life but for use in special circumstances (e.g. antibiotic resistance)
  • replicates independently of the main chromosome and can be passed between individuals through conjugation

Eukaryotic Chromosomes

  • linear, wound around proteins known as histones
  • multiple sets of chromosomes
  • specific positioning of the gene (loci)
  • homologous chromosomes - carry same sequence of genes (one is paternal and the other is maternal)
  • become visible during replication due to supercoiling
  • number of chromosomes is a characteristic feature of specie

Haploid nuclei vs. Diploid nuclei: Haploid nuclei only have one copy of each gene/ chromosome (n), while diploid nuclei have two copies of each gene/chromosome due to homologous chromosomes (2n).

Karyograms

  • Dividing cells are stained to produce a banding pattern on each chromosome
  • A micrograph is taken of the chromosomes that can be seen
  • Chromosomes are arranged according to size, structure, banding and position of centromere.

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

3.3 Meiosis

  • Meiosis: The division of one diploid nucleus to produce four haploid nuclei.
  • Four haploid nuclei are produced:
    • Cells divide twice.
    • Resulting in 4 daughter cells, each with half as many chromosomes as the parent cell.
  • Half the number of chromosomes because:
    • Sexual life cycle with fusion of gametes is allowed.
    • Chromosome number stays constant across generations after fusion of gametes.
    • Causes evolution.

Haploid Gametes

  • Reduces the number of chromosomes by half.
  • Produces genetic variability, as each gamete is different so two offspring from the parent are never identical.
  • Two divisions: Meiosis I and Meiosis II. Chromosomes are duplicated in interphase prior to Meiosis I.

Interphase

  • DNA replication in S Phase.
  • Replicated chromosomes attach to each other via centromere.
  • Attached chromosomes are known as sister chromatids.
  • Further growth to prepare for meiosis.

Meiosis I

Prophase I

  • Supercoiling + Condensation
  • Nuclear membrane dissolves, centrioles go to poles.
  • Bivalent formation (synapsis), formation of chiasmata (points of crossing over).
  • Crossing over between non-sister chromatids. Results in recombination of alleles - source of genetic variation.
  • Crossing Over: The mutual exchange of genes between two non-sister chromatids resulting in genetic variation.
  • Centrioles start moving to poles

Metaphase I

  • Bivalents line up at equator of cell. Spindle microtubules attach to the centromeres.
  • Random Orientation occurs:
    • Each chromosome of a bivalent is attached only to one pole.
    • Orientation of bivalents (direction they face) is random - equal chance of chromosome attaching to either pole.

Anaphase I

  • Disjunction occurs
    • Homologous Chromosomes are pulled apart. Splitting known as Reduction Division
    • One pair moves to each pole.

Telophase I

  • Nuclear membrane reforms.
  • Chromosomes uncoil.
  • Cytokinesis I occurs.
  • 2 haploid daughter cells formed.

Meiosis 1
Meiosis 1, source

Meiosis II

Prophase II

  • Chromosomes condense.
  • Nuclear membrane dissolves.
  • Centrioles move to poles.

Metaphase II

  • Chromosomes line up at equator of cell.
  • Spindle fibres attach to centromeres.

Anaphase II

  • Spindle fibres contract, chromosome splits at centromere.
  • Chromosomes pulled to opposite poles.

Telophase II

  • Chromosomes reach opposite poles.
  • Nuclear membrane reforms.
  • Cytokinesis occurs.
  • Four new haploid nuclei are formed.

Meiosis 2
Meiosis 2, source

Non-Disjunction and Down Syndrome

  • If chromosomes do not separate properly, it is known as Non-Disjunction
    • Failure in Anaphase I (Homologous Pairs) - four effected cells
    • Failure in Anaphase II (Sister Chromatids) - two effected cells
  • This causes one gamete to have more/less chromosomes than usual,
  • When gametes fuse, there are three copies of that chromosome instead of two - known as trisomy, only one chromosome is known as monosomy.
  • Examples:
    • Down Syndrome (Trisomy 21) - short stature, cardiac issues, shorter lifespan, often sterile, sometimes show mental retardation.
    • Klinefelter’s Syndrome (XXY males) - unusually small testes, sterile, enlarged breasts.

Detecting Chromosomal Abnormalities

Method 1 - Amniocentesis

  • Amniotic fluid is sampled from the amniotic sac.
  • Fetal DNA is examined for genetic abnormalities.
  • 1% chance of miscarriage.
  • Can detect gender as well, so not allowed in some countries.

Method 2 - Chorionic Villus Sampling

  • The chorion is a membrane apart of the placenta.
  • It has cells with villi.
  • Villi are sampled and cultured.
  • Karyotype is carried out.
  • Can be done earlier in pregnancy than amniocentesis
  • 2% chance of miscarriage
  • Can detect gender.

Karyotype - The number and visual appearance of the chromosomes in the cell nuclei of an organism or species.

Sources

Inheritance

Mendel and his Pea Plant Experiments

  • studied pea plants to show the inheritance of traits (specific characteristics of the individual)
  • proposed that inheritance was due to the transmission of discrete units -> referring to genes
  • Genotype: entire genetic makeup of an organism consisting of genes that influence the phenotype
  • Phenotype: observable characteristics of the individual as a result of the genotype
  • Gamete: haploid cells that are the product of meiosis and hence carry only one allele of each gene. Two gametes fuse during fertilization to form a zygote that can develop into a diploid individual.

Mendel’s Laws of Inheritance

  1. Particulate Inheritance
    Characteristics of parents are passed to offspring through discrete entities - genes
  2. Law of Segregation
    During gametic meiosis, two alleles of each gene will separate into different haploid daughter nuclei. (No gamete can have two alleles of the same gene)
  3. Law of Independent Assortment
    Allele pairs will separate independently of how other pairs are separating, in the case of unlinked genes

GENES TO BE KNOWN FOR PEA PLANT

Gene Dominant Allele Recessive Allele
Height of plant Tall [TT, Tt] Dwarf [tt]
Flower Colour Purple [PP, Pp] White [pp]
Flower Position Axial [AA, Aa] Terminal [aa]
Seed Shape Round [RR, Rr] Wrinkled [rr]
Seed colour Yellow [YY, Yy] Green [yy]
Pod Colour Green [GG, Gg] Yellow [gg]

Monohybrid Crosses

Cross in which the inheritance of one characteristic is observed over many generations

Dominance

Dominance: when the allele has an effect on the phenotype both in heterozygous and homozygous states
Recessive: when the allele has an effect on the phenotype only in homozygous state.
Example:

Test cross: Cross that is carried out to find an unknown genotype by breeding with a homozygous recessive parent

Always remember to include genotypic and phenotypic frequencies or ratios as a conclusion for each Punnet grid/ square present.

Codominance

In codominance, neither allele is recessive to the other such that both alleles are independently expressed in the heterozygous state.

E.g.
coat colour for cattle : Red, White, Roan
coat colour for Icelandic horses: Black, White, Brown
flower colour for Mirabilis jalapa: Red, White, Pink

The intermediate phenotype is important as it is expressed in the heterozygous genotype.

Multiple Alleles

A Multiple Allele system occurs when there are more than two alleles that code for the same specific trait.
E.g. Human ABO blood group system

IA and IB are codominant.
i is recessive to both

Genotype Phenotype
IAIA A
IAi A
IAIB AB (codominance)
IBIB B
IBi B
ii O (recessive)

Genetic Disorders

  1. Present in autosomal genes (recessive) -Cystic Fibrosis
    Similar to regular monohybrid crosses
  2. Present in autosomal genes (dominant) -Huntington’s Disease
    Similar to regular monohybrid crosses
  3. Present in autosomal genes (codominant) -Sickle cell anaemia
    Intermediate phenotype is when there is a mix of regularly shaped and sickle shaped RBCs in the blood, which has been naturally selected in areas prone to malaria as the sickle cell allows for resistance against the disease, without killing the individual with sickle cell anaemia
  4. Present in allosomal genes/ sex chromosomes -Hemophilia + Red-green colour blindness
    Disease allele is present on non-homologous area of the X chromosome and hence males (XY) do not have another paired allele to mask the effect of the disease allele.

Pedigree Charts

graphic illustration of inheritance patterns

Most important representations are followed universally. All pedigree charts, however, may not indicate clearly a carrier.

Mutations

  • radiation
  • mutagenic chemicals
  • random change to the base sequence of a gene
  • change the structure of the protein formed
  • can prevent the synthesis of protein
  • affects the cell in a range of intensities (e.g. cancer)
  • mutations in somatic (body) cells are eliminated when the individual dies
  • mutations in sex cells (gametes) lead to genetic disorders that can be inherited

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

3.5 - Genetic Modification and Biotechnology

Gel Electrophoresis

  • Samples of DNA/protein are inserted into gel wells.
  • Gel is placed in conducting fluid; current is passed through.
  • Molecules move based off of charge.
  • Smaller molecules move further - can fit through gel’s pores.
  • Used for separation of DNA/protein fragments.
  • DNA is negatively charged.

DNA Profiling

  1. DNA samples taken and amplified through PCR
  2. Restriction enzymes fragment DNA at specific base sequences in each sample
  3. Fluorescent markers bind to specific base triplets in the DNA fragment so results can be seen
  4. Samples undergo gel electrophoresis. Electric current pushes fragments along the gel
  5. Heavier fragments stay close to origin, smaller ones move further
  6. Banding pattern shows up for each DNA sample
  • Used in Forensic Investigations and Paternal Matching.
    enter image description here
    Banding Patterns shown above, source

Variable Number Tandem Repeats (VNTRs)

  • These are short base sequences that show variation between individuals in terms of number of repeats.
  • These are highly repetitive sequences - useful for DNA profiling due to uniqueness.

Genetic Modification

  • Genetic code is universal so genes can be transferred between species. All organisms use the same bases.
  • Each codon produces the same amino acid in transcription & translation, regardless of species/organism.
  • So the sequence of amino acids in polypeptides remains unchanged.

Gene Transfer

  • Restriction enzymes cut the desired gene from DNA.
  • Ligase joins human insulin gene to plasmid.
  • Recombinant plasmid is inserted back into host cell, and now expresses that gene, producing desired protein.

Transferring genes

  • mRNA transcript encoding desired protein obtained from eukaryotic cell. Made into cDNA (complementary DNA made with reverse transcriptase enzyme).
  • mRNA is easier to extract (no histones) and inserted genes are ready to be spliced - have no introns.
  • Bacterial enzyme and cDNA are cut with the same restriction enzymes, forming complementary sticky ends.
  • DNA Ligase seals eukaryotic sequence into bacterial plasmid.

Examples of Genetically Modified Organisms (GMOs)

GMO Description
Golden Rice Rice modified with daffodil genes to have more beta-carotene, which body converts to Vitamin A
Salt-resistant Tomatoes Tomatoes modified to grow well in saline soils
Bt Corn Corn modified with a bacterial insecticide gene so that it produces insect toxins within its cells
Factor IX Sheep Sheep modified with human clotting factor IX gene so that they produce clotting factor in their milk for hemophiliacs
Round Up Ready Soy Soybeans modified with a herbicide resistance gene so farmers can spray fields and kill weeds, not soybean plants
Rainbow Papaya Papaya modified with viral genes that make it immune to the Papaya Ringspot Virus

Cloning

  • Clones; A group of genetically identical organisms.
  • Asexual reproduction always results in clones.
  • Clones are rarer in sexually reproducing organisms (eg monozygotic twins).
  • Clones can occur in very large numbers (eg potatoes) but can be traced to the original parent cell.
  • Example: A single garlic bulb will clone itself to produce many identical bulbs in growing season.

Somatic Cell Nuclear Transfer (SCNT)

  1. Somatic cells taken from adult organism and cloned and grown in low-nutrient medium. This inactivates genes to wipe out previous patterns of differentiation
  2. Unfertilised egg cells are taken from that species’ female and nuclei are removed
  3. Cultured somatic cells and anucleated egg cells are placed side-by-side and zapped with a small electric pulse to fuse them together
  4. Fused egg cells containing cell nucleus develop into embryos. Seven days later, they are implanted into a surrogate mother
  • Cloning low success rates, Dolly the sheep was successful 1 out of 29 times.

Sources

Evidence for Evolution

Evolution occurs when heritable characteristics of a species change.
Mechanism - selection (natural or artificial)

  • Fossils
    • chronological sequence matches expected evolution sequence
    • bacteria, simple algae first --> fungi and worms --> vertebrates
    • sequence fits with the ecology of the group and time period
    • fossils link with existing organisms as likely ancestors
  • Evidence from Selective Breeding
    • selective breeding of domestic animals demonstrate evolution due to artificial selection
    • speciation from domesticated animals and their wild counterparts
    • proves existance of evolution but does not prove the natural mechanism of evolution
  • Homologous structures
    • Homologous structures are superficially different in appearance and specific functionality but structurally and evolutionary similar
    • same origin (ancestor) that evolved to perform different functions more appropriate for the specie (Adaptive radiation)
    • converse of homologous is analogous structures
      • superficially similar in appearance and functionality
      • different in structure and evolution
      • convergent evolution
    • E.g. pentadactyl limbs of mammals, birds, amphibians, and reptiles
  • Speciation
    • formation of new species from a common ancestral population due to isolation
    • proves that each separated population evolved differently and now cannot interbreed
  • Patterns of Variation
    • across geographical range
    • continuous range in variation of speciation, across an area
    • provides evidence for constant evolution into origin of new species
      • species are not unchanging distinct populations
      • instead they gradually evolve over time and space
    • E.g. industrial melanism for Biston betularia in polluted industrial area (light vs dark phenotype, lichen covered vs. lichen dead tree trunks)

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Written with StackEdit.

Natural Selection

Natural Selection depends on variation of phenotype, resulting in certain characteristics that are more suitable to a particular circumstance/ situation

Sources of Variation

  • Mutation causes new alleles of genes to be formed, enlarging gene pool
  • Meiosis introduces new combinations of alleles resulting in varied phenotypes, due to crossing over and independent orientation of bivalents
  • Sexual reproduction involves fusion of gametes from male and female. The pairing of parents introduces variation as well.

Adaptations

  • characteristics of an individual that make it suitable to survive in its environment
  • develop over time due to evolution
  • develop by natural selection
  • do not take place during one lifetime but instead over generations

Overproduction of offspring also add to the selective pressure required for natural selection and evolution to occur. There is an overall trend in living organisms to produces more number of offspring than environment can support. This leads to competition for resources and space, which makes more advantageous adaptations necessary for survival (survival of the fittest), causing these genes to be passed onto the next generation.


Differential survival and repoduction
Inheritance of advantageous characteristics
Progressive Change
  1. Better adapted individuals survive and produce more offspring than less well adapted which die/ produces less offspring.
  2. The advantageous variation of those who survive and reproduce is inherited by offspring
  3. Increases the frequency of these selected characteristics, decreases frequency of other alleles
  4. Over generations, the overall characteristics of the population change to favor this selected phenotype/ allele.

Examples: Galapagos Islands: beaks of finches living in different islands AND antibiotic resistance in bacteria

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition

Written with StackEdit.

Classification of Biodiversity

Binomial Naming System

  • universal among biologists
  • local names may differ around the world, prevents international cooperation
  • ‘science is an international venture’
  • consists of two parts: genus name and species name
  • some rules
    • genus: uppercase letter begins with; species name begins with lowercase letter [ Homo sapiens ]
    • in typed text, binomial name is in italics
    • after it has been used once in a text, the genus name can be abbreviated to the initial letter [ H. sapiens ]
    • earliest published name (from 1753 for plants or 1758 for animals) is correct

Hierarchy of Taxa

  • taxonomists classify species using this hierarchy
  • going up this hierarchy, larger numbers of species are included, and they share fewer and fewer features
Domain
Kindgdom
Phylum
Class
Order
Family
Genus
Species
  • use acronym: Did King Philip Come Over For Good Soup?
Feature Bacteria Archaea Eukaryota
Histones associated with DNA naked DNA, not associated with proteins associated with proteins similar to histones present
Presence of Introns absent present sometimes present
Structure of Cell Walls made of peptidoglycan present, not made of peptidoglycan sometimes present, not made of peptidoglycan
Cell Membrane glycerol-ester lipid; side chain is unbranched; D-form of glycerol glycerol-ester lipid; side chain is unbranched; L-form of glycerol glycerol-ester lipid; side chain is unbranched; D-form of glycerol
  • archaeans are found in mostly extreme condition (far below ocean surface, hot springs etc)
  • viruses belong to none of these domains; not considered ‘living’ although they have genetic code

Eukaryote Classification

  • natural classification: genus, and accompanying taxa, consist of all the species that have evolved from one common ancestral species
    • convergent radiation could make organisms appear superficially related [DISADVANTAGE]
    • adaptive radiation could make closely related species seem different [DISADVANTAGE]
    • species are easier to classify (with new molecular methods, refer to 5.4) [ADVANTAGE]
    • features of closely related species are easy to predict as they are similar (example vestigial organs for mammals) [ADVANTAGE]
  • unnatural classification: species with similar features are grouped together, regardless of ancestry [birds, bats and insects classified together due to their wings]
    • this form of classification is misleading, as most organisms grouped together may not even be similar (apart from the feature(s) they share)
  • Taxonomists sometimes reclassify groups of species when new evidence shows that a previous taxon contains species that have evolved from different ancestral species.

SKILL: reading dichotomous keys

Plant Phyla

  • Bryophyta [relate to moss]
    • vegetative organs: rhizoids, but no true roots. Some have simple stem/leaves, others have thallus.
    • vascular tissue: no xylem or phloem
    • cambium: absent; no trees or shrubs
    • pollen not produced
    • no seeds produces
    • no ovules or ovaries
    • no fruits
Image Identification
enter image description here no stem, root, large leaves; usually no flowers; grow near the ground/ water sources

  • Filicinophyta [relate to ferns]
    • root, stem and leaves usually present
    • xylem and phloem present
    • cambium: absent; no trees or shrubs
    • pollen not produced
    • no seeds produces
    • no ovules or ovaries
    • no fruits
Image Identification
abc leafs as fronds; never trees/shrubs

  • Coniferophyta [relate to conifers]
    • root, stem and leaves usually present
    • xylem and phloem present
    • cambium: present; allows secondary thickening of stems and development of trees and shrubs.
    • pollen produced in male cones
    • ovules in female cones
    • seeds produced and dispersed
    • no fruits
Image Identification
enter image description here presence of cone; thin sharp leaves; tree

  • Angiospermophyta [relate to flowering plants]
    • root, stem and leaves usually present
    • xylem and phloem present
    • cambium: present; allows secondary thickening of stems and development of trees and shrubs.
    • pollen produced by anthers
    • ovules enclosed in ovary of flowers
    • seeds produced and dispersed
    • fruits produces for dispersal of seeds
Image Identification
enter image description here flower, fruit, clear stem + leaves

Animal Phyla

NOTE: no diagrams necessary, only provided for understanding of anatomical differences

  • Porifera [relate to sea sponges]
    • no mouth or anus
    • no symmetry
    • internal skeletal needles called spicules for skeleton
    • pore over surface through which water is drawn for filter feeding
Image Identification
enter image description here pores over surface, irregular shape

  • Cnidaria [relate to jellyfish]
    • only mouth
    • radial symmetry
    • soft [except hard coral, CaCO3 secreted]
    • tentacles arranged in ring around mouth, stinging cells
Image Identification
enter image description here tentacles around mouth, no regular skeleton

  • Platyhelminthes [relate to flatworms]
    • only mouth
    • bi-lateral symmetry
    • soft, no skeleton
    • flat, thin bodies, shape of a ribbon; no blood system or system for gas exchange
Image Identification
enter image description here flat body, ribbon shape

  • Mollusca [relate to snail/octopus]
    • mouth and anus
    • bi-lateral symmetry
    • shell made of CaCO3
    • mantle, secretes the shell; rasping radula for feeding
Image Identification
enter image description here hard outer shell (exception octopus)

  • Annelida [relate to leeches]
    • mouth and anus
    • bi-lateral symmetry
    • internal cavity, fluid under pressure
    • ring-shaped segments, blood vessels often visible
Image Identification
enter image description here bristles present on body, ring like segments

  • Arthropoda [relate to insects]
    • mouth and anus
    • bi-lateral symmetry
    • external skeleton, made of chitin
    • segmented body, joints between sections
Image Identification
enter image description here segmented body

Chordata (Vertebrates)

Bony ray-finned fish Amphibians Reptiles Birds Mammals
Scales which are bony plates in skin Soft moist skin, permeable to water and gas Impermeable skin; scales of keratin Skin + Feathers, of keratin Skin + Follicles with hair made of keratin
Gills covered by operculum, gill slit Simple lungs, small folds and moist skin for gas exchange Lungs with extensive folding (increase surface area) Lungs with para-bronchial tubes; ventilated with air-sac Lungs with alveoli; ventilate with diaphragm and ribs
No limbs Tetrapods + pentadactyl limbs Tetrapods + pentadactyl limbs Tetrapods + pentadactyl limbs Tetrapods + pentadactyl limbs
Fins, supported by rays Four legs when adult Four legs (exception: snakes) Two legs, two wings Four legs (or two wings/ arms and two legs)
Eggs and sperm released for external fertilisation Eggs and sperm released for external fertilisation Sperm passed into the female for internal fertilisation Sperm passed into the female for internal fertilisation Sperm passed into the female for internal fertilisation
Remain in water throughout lifecycle Larval stage: water; adult life: usually land Females lay eggs with soft shell Females lay eggs with hard shell Give birth to young live; feed with mild from mammary glands
Swim bladder containing gas for buoyancy Eggs coated in protective jelly Teeth of one type, no living parts Bill/Beak no teeth Teeth of two kinds, living core
Do not maintain constant body temperature Do not maintain constant body temperature Do not maintain constant body temperature Maintain constant body temperature Maintain constant body temperature

Cladistics

Clades

  • group of organisms that have evolved from a common ancestor;
  • species can evolve and split to form new species (speciation)
  • these groups share common characteristics due to common ancestor (derived characteristics)
  • evidence gained from base sequence of gene (or constituent amino acids of proteins)

Molecular Clocks

  • sequence differences accumulate gradually over time
  • positive correlation between number of differences between species and time since they diverged
  • evidence suggests the rate of mutations occurring is roughly constant, can be used to estimate time of diversion

Analogous or Homologous?

  • homologous structures are similar due to ancestry
    • pentadactyl limbs
  • analogous structures are similar due to convergent evolution
    • human eye and octopus eye (similarities in structure and function, evolved independently)
  • similarities in analogous and homologous structures can be misleading; for this reason morphology is rarely used to classify organisms

Cladograms

  • tree diagrams that show the most probable sequence of divergence in clades
  • when two clades branch off, it is called a node
  • primate cladograms
  • reclassification
  • (NOS: falsification, one theory of superseded by another)
  • reclassification of figwort family, using evidence of cladistics

Digestion and Absorption

  • system to break down large insoluble molecules, to small soluble particles that can be absorbed
  • requires surfactants to break up lipid droplets and enzymes to catalyse reactions
  • Glandular cells in the lining of the stomach and intestines produce the enzymes
  • Surfactants and other enzymes are secreted by accessory glands that have ducts leading to the digestive system
  • Controlled, selective absorption of the nutrients takes place in the small intestine and colon
  • Some small molecules (alcohol) diffuse through the stomach lining

enter image description here
(diagram necessary for drawing and labelling)

Structure Function
Mouth control of eating and swallowing; mechanical digestion of food by chewing and mixing saliva (lubricant); enzymes that start starch digestion
Oesophagus movement of bolus by peristalsis from mouth to stomach
Small Intestine final stage of digestion of lipids, carbohydrates, proteins and nucleic acids; neutralising acids from stomach; absorption of nutrients
Stomach Churning and mixing with secreted water and acid (kills foreign bacteria and pathogens); initial stages of protein digestion
Pancreas secretion of lipase, amylase and protease
Liver Secretion of surfactants in bile to break up lipid droplets
Gall Bladder Storage and regulated release of bile
Large Intestine Re-absorption of water, further digestion of carbohydrates by symbiotic bacteria; formation and storage of faeces

Structure of wall of Small Intestine

  • wall is made of layers of living tissue
  • four layers
    • serosa: outer coat
    • muscle layers: longitudinal muscle and (inside it) circular muscle
    • sub-mucosa: tissue layer with blood and lymph
    • mucosa: the lining of the small intestine; epithelium that absorbs nutrients on its inner surface

enter image description here

Peristalsis

  • contraction of circular and longitudinal muscle layers
  • in small intestine mixes the food with enzymes and helps move it
  • circular and longitudinal are smooth muscle; relatively short cells, not elongated fibres
  • exerts continuous moderate force with short periods of vigorous contraction
  • Contraction of circular muscles constricts the gut; prevents it from being pushed back towards the mouth (always specify direction )
  • Contractions are controlled unconsciously
  • In oesophagus, moves quickly in continuous wave
  • In gut, movement is slower
  • Peristalsis only occurs in one direction, away from the mouth
  • main function of peristalsis in the intestine is churning of the semi-digested food to mix it with enzymes
  • speed up process of digestion

Pancreatic Juice

  • pancreas secretes enzymes into the lumen of small intestine
  • pancreas contains two types of gland tissue
    • Small groups of cells secrete the hormones insulin and glucagon
    • remainder of the pancreas synthesises and secretes digestive enzymes into the gut
    • mediated by hormones synthesised in stomach and enteric nervous system
    • Small groups of gland cells cluster round tubes called ducts

enter image description here

  • digestive enzymes secreted by pancreatic gland cells on ribosomes in rER
  • process in Golgi Apparatus and secreted by exocytosis
  • ducts merge to form larger ducts; large volume secreted
  • Enzymes: amylase to digest starch, lipases to digest triglycerides and phospholipids and proteases to digest proteins and peptides.

Digestion in the Small Intestine

  • Enzymes digest most macromolecules in food into monomers in the small intestine
  • hydrolysis reactions
    • starch digested to maltose by amylase
    • triglycerides are digested to fatty acids and glycerol / monoglycerides by lipase
    • phospholipids are digested to fatty acids, glycerol and phosphate by phospholipase
    • proteins and polypeptides are digested to shorter peptides by protease
  • The wall of the small intestine produces a variety of other enzymes
  • most remain immobilised in the plasma membrane of epithelium cells lining
  • Examples include:
Substrate Enzyme Product(s)
DNA and RNA nucleases nucleotides
maltose maltase glucose
lactose lactase glucose, galactose
sucrose sucrase glucose, fructose
peptides exopeptidases dipeptide remains
dipeptides dipeptidases amino acids
  • Cellulose is not digested and passes on to the large intestine; dietary fibre

Villi and Digestion

  • Villi increase the surface area of epithelium over which absorption is carried out
  • Absorption : process of taking substances into cells and the blood is called
  • area is increased by the presence of villi (x10)
  • Villi : small finger-like projections of the mucosa

Absorption by Villi

  • Villi absorb monomers formed by digestion as well as mineral ions and vitamins
  • epithelium: permeable enough to allow useful nutrients to pass through, a barrier to harmful substances
  • If harmful substances pass through the epithelium they are removed from the blood and detoxified by the liver

Methods of Observation

  • Different methods of membrane transport are required to absorb different nutrients
  • The nutrients must first be absorbed into epithelium cells through the part of the plasma membrane
  • Examples include simple diffusion, facilitated diffusion, active transport and exocytosis
    • Triglycerides must be digested before they can be absorbed.
    • The products of digestion are fatty acids and monoglycerides, which can be absorbed into villus epithelium cells by simple diffusion ( can pass between phospholipids in the plasma membrane )
    • Fatty acids are also absorbed by facilitated diffusion as there are fatty acid transporters, which are proteins in the membrane
    • Once inside the epithelium cells, fatty acids are combined with monoglycerides to produce triglycerides, which cannot diffuse back out
    • Triglycerides coalesce with cholesterol to form droplets, which become coated in phospholipids and protein
    • These lipoprotein particles are released by exocytosis through the plasma membrane on the inner side of the villus epithelium cells.They then either enter the lacteal or enter the blood capillaries.
    • Glucose cannot pass through the plasma membrane by simple
      diffusion because it is polar and therefore hydrophilic.
    • Sodium–potassium pumps in the inwards-facing part of the plasma membrane pump sodium ions by active transport from the cytoplasm to the interstitial spaces inside the villus and potassium ions in the opposite direction
    • Sodium–glucose co-transporter proteins in the microvilli transfer a sodium ion and a glucose molecule together from the intestinal lumen to the cytoplasm of the epithelium cells; passive but depends concentration gradient created by pumps
    • Glucose channels allow the glucose to move by facilitated diffusion from the cytoplasm to the interstitial spaces inside the villus and on into blood capillaries in the villus

Digestion of Starch

  • Starch is a macromolecule, composed of many α-glucose monomers
  • Must be digested in the small intestine to allow absorption
  • Any 1,4 bond in starch molecules can be broken by amylase
  • Because of the specificity of its active site, amylase cannot break 1,6 bonds in amylopectin.
  • Maltase, glucosidase and dextrinase digest maltose, maltotriose and dextrins into glucose
  • The blood in these venules is carried via the hepatic portal vein to the liver, where excess glucose can be absorbed by liver cells

NOS: Modelling Physiological Processes

  • dialysis tubing can be used to model absorption in the intestine
  • dialysis tubing made from cellulose.
  • pores in the tubing allow water and small molecules or ions to pass through, but not large molecules.
  • These properties mimic the wall of the gut: permeable to small rather than large particles.
  • Dialysis tubing can be used to model absorption by passive diffusion and by osmosis
  • It cannot model active transport and other processes that occur in living cells

Gas Exchange

Ventilation

  • maintains concentration gradients of oxygen and carbon dioxide between air in alveoli and blood flowing in capillaries
  • In humans gas exchange occurs in small air sacs called alveoli inside the lungs
  • Gas exchange happens by diffusion between air in the alveoli and
    blood flowing in the adjacent capillaries
  • The gases only diffuse because there is a concentration gradient (air in the alveolus has a higher concentration of oxygen and a lower concentration of carbon dioxide than the capillary )
  • Process of maintaining these concentration gradients by pumping fresh air and removing stale air is called ventilation
  • Ventilation Experiments
    • Ventilation rate: count inhalation/exhalation, pressure sensor
    • Tidal volume/spirometer

Structure of Alveoli

enter image description here

Adaptations

  • numerous alveoli (large surface area)
  • flattened layer of thin cells (diffusion distance decreases)
  • dense network of capillaries
  • moist lining (gases can dissolve)
  • diffusion of oxygen down the concentration gradient

Type 1 Pneumocytes

  • Type I pneumocytes are extremely thin alveolar cells
  • Large total surface area for diffusion
  • The wall of each alveolus has a single layer of cells (epithelium)
  • Reduced diffusion distance (adaptation)

Type 2 Pneumocytes

  • Type II pneumocytes secrete a solution with surfactant
  • Creates a moist surface inside the alveoli to prevent the sides from adhering (reducing surface tension)
  • film of moisture allows oxygen in the alveolus to dissolve and then diffuse to the blood in the alveolar capillaries
  • Surfactant
    • structure similar to that of phospholipids
    • form a monolayer on the surface of the moisture
    • hydrophilic heads facing the water and the hydrophobic tails facing the air
    • reduces the surface tension
    • prevents the water from causing the sides of the alveoli to adhere
    • helps to prevent collapse of the lung
  • premature babies are often born with insufficient pulmonary surfactant
  • can suffer from infant respiratory distress syndrome

Airway for Ventilation

  • Air enters the ventilation system through the nose or mouth and then passes down the trachea
  • rings of cartilage in its wall to keep it open even when air pressure inside is low
  • Air is carried to the bronchi and then to the alveoli in bronchioles
  • bronchioles have smooth muscle fibres in their walls

Pressure Changes

  • pressure and volume are inversely related
  • Muscle contractions cause the pressure inside the thorax to drop below atmospheric pressure (air rushes into lungs, inspiration)
  • Muscle contractions cause the pressure inside the thorax to rise above atmospheric pressure (air rushes out lungs, expiration)

Antagonistic Muscles

  • Muscles do work when they contract by exerting a pulling force (tension) that causes a particular movement (become shorter)
  • Muscles lengthen while they are relaxing, but this happens passively (no work done)
  • can only cause movement in one direction
  • Antagonistic pair of muscles : When one muscle contracts and causes a movement, the second muscle relaxes and is elongated by the first; then the opposite happens;
Process Muscle Inspiration Expiration
volume and pressure changes N/A Volume in thorax increases, pressure decreases Volume in thorax decreases, pressure increases
movement of diaphragm diaphragm diaphragm contracts; moves downward and pushes abdomen wall out diaphragm relaxes; can be pushes upwards into a more domes shape
abdomen wall muscles Muscles in the abdomen wall relax allowing pressure from the diaphragm to push it out Muscles in the abdomen wall contract pushing the abdominal organs and diaphragm upwards
movement of rib-cage External intercostal muscles contract, pulling the ribcage upwards and outwards relax and are pulled back into their elongated state
Internal intercostal muscles relax and are pulled back into their elongated state contract, pulling the ribcage inwards and downwards

Epidemiology

  • Obtain evidence for theories
  • W.R.T understanding causes of cancer
  • Epidemiology is the study of the incidence and causes of disease
  • Based on observation, not experimentation
  • survey data is collected that allows the association
  • A correlation between a risk factor and a disease does not prove that the factor causes the disease (confounding factor)
  • usually necessary to collect data on many factors apart from the one being investigated

Lung Cancer

  • Causes of Lung Cancer
    • smoking
    • passive smoking
    • air pollution
    • radon gas
    • asbestos, silica
  • Consequences of Lung Cancer
    • difficulties with breathing
    • persistent coughing
    • coughing up blood
    • chest pain
    • loss of appetite/ weight loss
    • general fatigue
  • Metastasis
  • Surgery, Chemotherapy, Radiotherapy

Emphysema

  • total surface area for gas exchange is reduced
  • smaller number of larger air sacs with much thicker walls
  • lungs also become less elastic, so ventilation is more difficult
  • Phagocytes inside alveoli prevent lung infections by engulfing bacteria and produce elastase (protein-digesting enzyme)
  • An enzyme inhibitor called alpha 1-antitrypsin (A1AT) prevents elastase and other proteases from digesting lung tissue
  • In smokers, the number of phagocytes in the lungs increases and they produce more elastase
  • Genetic factors affect the quantity of A1AT produced
  • damage to alveoli is usually irreversible
  • patient lacks energy, shortness of breath

Transcription [AHL]

Nucleosomes + Super-Coiling

  • DNA in eukaryotes are associated with histone proteins
  • Nucleosomes Consists of octamer, DNA combination, attached to a H1 Histone

enter image description here

  • Served to protect DNA from damage and allow long lengths of DNA to be super-coiled
  • Supercoiling
    • allows chromosome to be mobile in mitosis and meiosis
    • supercoiled DNA cannot be transcribed for protein synthesis
    • allows genes to be turned on and off
  • DNA consists of single copy genes and regions of highly repetitive sequences (Exons, coding sequences and Introns, non-coding sequences)
  • While Introns were thought to be “junk DNA” they are now know to serve a purpose
    • production of rRNA and tRNA
    • genetic fingerprinting
    • factors that regulate gene expression
    • telomeres [ protective function; DNA cannot be replicated all the way to the end so telomeres prevent loss of important genes]

Regulation of Transcription

  • Operator: region of DNA that can regulate transcription
  • Promoter: non-coding DNA with function; binding site of RNA Polymerase
  • Gene Expression and Transcription need to be regulated to control what proteins get synthesised and what don’t
  • Example in Prokaryotes: lactose metabolism, negative feedback
  • Factors that help in these are promoters, enhancers and silencers
  • Both environmental factors and cellular function play a role in which proteins are synthesised
  • Nucleosomes in Transcription
    • chemical modification of the tails of histones is an important factors in determining whether a gene will be expressed
    • Addition of **acetyl, methyl or phosphate group **
    • Example: histone acetylation neutralises positive charge; allows for less condensed structures & higher levels of transcription
    • chemical modification of histone tails can either activate or deactivate genes by decreasing/ increasing the accessibility of the gene to transcription factors
    • usually addition of an acetyl group means increased transcription, while the addition of methyl group means reduced transcription
    • SKILL : analysing changes in DNA methylation patterns

enter image description here

Epigenetics

  • Chemical modifications are called epigenetic tags
  • sum of these tags are called an epigenome
  • provide understanding of environmental factors affecting inheritance
  • when 2 reproductive cells (sperm, egg cell) with epigenetic tags meet, epigenome is erased through reprogramming
  • 1% is not erased, called imprinting
  • example of imprinting is gestational diabetes

Direction of Transcription

  • occurs in 5’ to 3’ direction
  • 3 stages: initiation, elongation and termination
  • begins at promoter site; site of binding for RNA Polymerase

Operators

DNA Sequence Binding Protein Function
enhancer activator increases rate of transcription
silencer repressor decreases rate of transcription
promoter RNA Polymerase initiates transcription

Post-transcriptional Modification

  • eukaryotic cells modify mRNA after transcription
  • in prokaryotes, translation and transcription is coupled [no nuclear membrane]
  • cell membrane in eukaryotes allows for significant post transcriptional modification before mature transcript exits nuclear
  • examples of modification: removing introns
Transcription
post-transcriptional modification
DNA
pre mRNA
mature mRNA
  • RNA splicing includes:
    • removing introns
    • splicing all/some remaining exons together
    • addition of 5’ cap
    • polyA tail added
  • Splicing of mRNA increases number of different proteins an organism can produce [particular exon may or not be including, increasing combinations]

Application: Morphogens

  • determine body patterns during embryonic development
  • diffuse across surface, in varied concentrations
  • regulate production of transcriptional factors
  • change rate of growth of different cells, creating ideal body shape like size of fingers, hands etc.

Translation

Component Structure

Ribosomes

  • Large unit (50S) and small unit (30S).

  • Made of proteins and ribosomal RNA (rRNA).

  • Three binding sites for tRNA: exit site (E), peptidyl site § and aminoacyl site (A).

  • Two tRNA molecules can bind at the same time.

  • Has a binding site for mRNA on the surface of the ribosome (for your visualisation, think lower surface).

tRNA

  • Have sections that become double-stranded because of complementary base-pairing.

  • Clover shaped with 3 loops: one is an anticodon loop.

  • The base sequence CCA at the 3’ end on top for attachment of amino acid.

tRNA activation

  • Each tRNA recognised by tRNA-activating enzymes that attaches specific amino acid to that tRNA – uses ATP.

  • 20 different tRNAs, 20 different amino acids, and 20 different activating enzymes.

  • ATP and amino acids bind to enzyme.

  • Amino acid is activated (it gets energy) by hydrolysis of ATP (makes AMP which is adenosine monophosphate and pyrophosphate) and covalent bonding of AMP to enzyme.

  • tRNA binds to active site of enzyme, amino acid binds to attachment site on tRNA and AMP is released: energy released to charge tRNA.

  • Energy from bond later used to attach amino acid to growing peptide chain.

Initiation

  • assembly of components involved
  • small ribosomal subunit binds to mRNA at the binding site (start codon AUG)
  • initiator tRNA with methionine
  • large ribosomal subunit also binds such that initiator tRNA is on the P site
  • the next codon signals for the appropriate tRNA to bind to the a site.
  • peptide bond forms between the two amino acids

Elongation

  • ribosome moves down mRNA
  • tRNA from P site is now in the E site
  • tRNA from A site is now in the P site
  • first tRNA, now in E, is released
  • while a new tRNA, according to complementary base pairing joins to the A site
  • peptide bond forms again
  • series of repeated steps until the end of the mRNA

Termination

  • reaches a stop codon with no amino acid
  • polypeptide is released

Note that direction of translation is 5’ to 3’ of the mRNA strand.

Free and Bound Ribosomes

  • Proteins are synthesised in both ER and cytosol.

  • Proteins are usually needed for mitochondria or chloroplasts = free ribosomes.

  • Proteins needed for lysosomes, ER, Golgi apparatus, plasma membranes, outside cell = ER bound ribosomes.

Structures of Proteins

  • Primary structure: just peptide bonds between amino acids to form a polypeptide.

  • Secondary structure: alpha-helices and beta-pleated sheets due to hydrogen bonding between N-H and C-O of peptide bond.

  • Tertiary structure: folding of polypeptide due to interactions with R-groups: +ve and -ve charged R-groups interact, polar R-groups interact with each other, hydrophobic amino acids orient IN while hydrophilic OUT, and some R-groups form disulphide bridges.

  • Quaternary structure: the way polypeptides fit together; only in proteins with more than one polypeptide.

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Written with StackEdit.

Metabolism

Metabolic pathways are cycles or chains of enzyme- catalyzed reactions.

Enzymes and Activation Energy

  • increase rate of reaction such that speed of metabolic processes are fast enough to sustain life
  • substrate binds to active site
  • altered to reach transition state
  • binding lowers energy level
  • activation energy is reduced, increasing rate

Inhibitors

  • Competitive
    bind to active site
    can be both reversible (Affected by conc.) and non reversible

malonate inhibits succinic dehydrogenase from catalyzing succinic acid

sulphonamide drugs inhibits folic acid synthetase from catalyzing P amino benzanoic Acid into folates

  • Non - competitive
    bind to allosteric site
    reversible

Cyanide inhibits Cytochrome oxidase from catalyzing cytochromes

Nerve Gas/ Metallic ions inhibits acetylcholine esferase from catalyzing Acetylcholine

  • End Product/ Allosteric
    end product as inhibitor
    prevents buildup of intermediate compounds

isoleucine inhibits Threonine deaminasefrom catalyzing threonine into isoleucine

ATP inhibits phosphofructose kinase from catalyzing Glucose into hexose bi-phosphate

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Written with StackEdit.

Cell Respiration

  • heavily dependent on oxidation and reduction reactions between compounds
  • substances known as electron carriers link redox by accepting and donating electrons when required
  • main electron carrier in respiration is nicotinamide adenine dinucleotide (NAD)
  • NAD++2HNADH+H+NAD^+ + 2H \rightarrow NADH + H^+
  • Phosphorylation reactions is the addition of a phosphate molecule (PO43-)
  • makes the organic compound less stable and more reactive i.e. activation
  • Hydrolysis of ATP as an exergonic reaction to release energy for couple metabolic endergonic and non-spontaneous reactions

Process

Glycolysis

  • occurs in the cytoplasm
  • does not require oxygen
  • has two phases: 1) energy requiring and 2) energy producing

  1. Glucose (6C) is rearranged and phosphorylated with 2 phosphate groups to produce Fructose 1,6 biphosphate (6C). Energy is required: 2 ATP --> 2 ADP

  2. Lysis: Fructose biphosphate is split into half: DHAP (3C) and Glycerate-3-phosphate. Glycerate-3-phosphate continues in the next step but the other compound, DHAP, is easily converted into Glycerate-3-phosphate to continue as well.

  3. Series of reactions, oxidation by de-hydrogenation. to convert Glycerate-3-phosphate (3C) into pyruvate (3C) which releases energy. 2 ADP --> 2 ATP and NAD+ --> NADH + H+ per 3C molecule, therefore twice as much per glucose molecule

enter image description here

  • occurs in the matrix of the mitochondria
  • does not require oxygen
  • links glycolysis to Kreb’s cycle

  1. De carboxylation, therefore CO2 is released (waste), and de-hydrogenation of pyruvate molecules (3C) to form Acetyl CoA (2C). Reduces NAD+ + --> NADH + H+ per pyruvate molecule, so two molecules per glucose molecule.

enter image description here

Kreb’s cycle/ Citric Acid cycle

  • a cyclic progression of reaction using acetyl CoA as its fuel
  • redox reactions release energy carried in the form of electron carriers, NADH and FADH2.
  • occurs in the matrix of the mitochondria
  • no oxygen required
  • runs twice per glucose molecule

  1. Acetyla CoA (2C) combines with oxaloacetate (4C) to form citrate (6C)
  2. Citrate (6C) is de-carboxylated into alpha ketoglutanate (5C) reducing NAD+ --> NADH + H+.
  3. Alpha ketoglutanate (5C) is de-carboxylated into a (4C) compound, oxalosuccinate, reducing NAD+ --> NADH + H+.
  4. This (4C) compound undergoes a series of configuration changes resulting in more release of energy and electron carriers.

NAD+ --> NADH + H+
FAD + H2 --> FADH2
ADP + Pi --> ATP

  1. The last (4C) compound, oxaloacetate is eventually regenerated from oxalosuccinate, to continue reacting with incoming Acetyl CoA, looping the process into a cycle.
  2. Decarboxylation produces CO2 (waste)

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Electron Transport Chain

  • Occurs on the the cristae, folds of the inner mitochondrial membrane
  • transfer of electrons between proteins
  • coupled with proton pumping to create gradient
  • sets up for chemiosmosis that allows for ATP production
  • oxygen required

  1. Chain of proteins arranged on the cristae in order from least electronegative to most.
  2. Electron carrier approaches the first protein on the chain and becomes oxidised to release 2e- : NADH + H+ --> NAD+ + 2H+ + 2e-
  3. Each electron carrier protein gets oxidized and reduced in turn, passing on electrons to the next, more electronegative, protein in the chain.
  4. This process releases energy to pump protons, H+, from the matrix into the intermembrane space.
  5. Due to the small volume and the membrane impermeability to protons, a concentration gradient of protons build up quickly with the high concentration in the intermembrane space.
  6. Oxygen, being the most electronegative when compared to the protein, is present in the matrix, is the final electron acceptor.

Chemiosmosis

  • diffusion of the protons
  • catalyses oxidative phosphorylation of ADP into ATP
  • final stage
  • also requires oxygen
  • occurs across the inner mitochondrial membrane and in the matrix

  1. Protons move done concentration gradient from within intermembrane space into matrix through specific channel proteins
  2. The channel proteins, termed ATPase, also acts as an enzyme that is activated by the passage of the protons.
  3. Head of the protein rotates, allowing Pi to bind to it, catalysing the phosphorylation: ADP + Pi --> ATP
  4. The reduced oxygen in the matrix is needed to bind with the incoming free protons, forming water (waste product). This maintains concentration gradient.

Yield

Each NADH run by the ETC ~= 3 ATP
Each FADH2 tun by the ETC ~= 2 ATP

Glycolysis Link Kreb’s Cycle ATP equivalent totally
ATP 2 x 2 2
NADH 2 2 6 30
FADH2 x x 2 4

Total: 38 ATP per glucose molecule broken down in aerobic respiration.

Structure and Function of Mitochondria

  1. Outer membrane : separates contents from rest of cell for a compartments with ideal conditions
  2. Inner membrane : supports ETC, allows for proton concentration buildup, contains ATPase
  3. Cristae : projections to increase surface are available for oxidative phosphorylation
  4. Matrix : contains enzymes for link reactions and Kreb’s cycle
  5. Intermembrane space : small volume for easy and fast buildup of protons for chemiosmosis
  6. 70S Ribosomes and DNA : evidence for endosymbiosis theory

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Written with StackEdit.

Photosynthesis

  • consists of light dependent and light independent reactions
  • takes place in chloroplast in leaf cells

Light Dependent

  • inter-membrane space of thylakoids

  • produces reduced NADP and ATP

  • convert light energy to chemical energy

  • 3 overall steps

    • excitation of light system by light (photo-activation)
    • production of ATP through electron transport chain
    • reduction of NADP+
  • Photo-activation

    • absorption of light by photosystems generates excited electrons
    • light harvesting arrays (in thylakoids) + reaction centres
    • Photosystem II is the first to be activated ( 680nm wavelength of light); Photosystem I (700 nm wavelength)
  • Photolysis

    • excited electrons from PS II are transferred to an electron transport chain;
    • electron acceptor in this chain is called plastoquinone
    • as they pass through the chain, lose energy, used to move H+ into the lumen of thylakoid from stroma
    • splitting of water molecule to generate electrons in LDR
    • chlorophyll is not powerful oxidising agent
    • 2H2O --> O2 + 4H+ + 4e- [water-splitting enzyme]
    • oxygen waste product, diffuses out of leaf
    • When the electrons reach the end of the chain of carriers they are passed to plastocyanin, a water-soluble electron acceptor in the fluid
  • Production of NADPH

    • Photosystem I, at reaction centre, excited electrons move down their own electron transport change
    • energy used by NADP reductase (enzyme)
    • reduces NADP to NADPH, into stroma
    • electron for PS I comes from plastocyanin; non cyclic photo-phosphorylation
  • Production of ATP (Photophosphorylation)

    • H+ ions will diffuse passively through ATP synthase due to gradient built up
    • chemiosmosis (higher to lower concentration, from thylakoid space to stroma)
    • ATP synthase is channel + enzyme; rotating head creates energy for phosphorylation
    • ADP converted to ATP

Light Independent Reaction

Calvin’s Cycle (Stroma)

  • 3 RuBP (5C) (Rubisco Bisphosphate) undergo carbon fixation due to rubisco (enzyme)
  • This compound formed (6C) (name not necessary) is split in half to form 6 Glycerate-3- Phosphate (labelled 3-PGA)

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  • This compound is reduced to TP, or triose phosphate; as they are reduced (addition of H+), NADPH is oxidised to complete the redox reaction. Energy for this comes from ATP

enter image description here

  • Now we have 6 Triose phosphate; 1 goes to being 3 Carbon molecules of glucose molecule
  • Other 5 used in regeneration of RuBP
    • RuBP is a 5C compound
    • We have 5x3 compound
    • therefore we can make 3 RuBP;
  • energy from regeneration comes from ATP; complete the cycle
  • 2 full cycles to make one glucose molecule

enter image description here

Chloroplast Structure and Function

  • adapted to its function in photosynthesis
  • Feature
    • double membrane (chloroplast envelope)
    • extensive internal membrane system (thylakoid)
    • small fluid spaces inside thylakoid
    • colourless fluid in chloroplast: stroma (many enzymes)
    • stacks of thylakoids: grana
  • strcuture/ function relationship
Structure Function
chloroplasts absorb light pigment molecules; arranged in photosystems in thylakoid membrane; large area of thylakoid ensure large surface area of absorption; stacks (Grana) allow more light to be absorbed
ATP by phosphorylation proton gradient required between inside and outside of thylakoid; volume of fluid in it is small, so gradient can be built up quickly;
many chemical reaction during Calvin’s cycle stroma has high concentration of required enzymes; ATP and reduced NADP, needed for the Calvin cycle, are easily available because the thylakoids, distributed through the stroma

Sources

  • Biology - Course Companion - Andrew Allott and David Mindorff - Oxford 2014
  • YouTube @Cheryl Hickman
  • Khan Academy
  • BioNinja

Meiosis

Interphase

  • Chromatin looks like a string of beads because of lengths of DNA wound around histone proteins and separated by lengths of DNA.

  • G1: Cell enlarges.

  • S: Chromosomes replicate: there are two chromatids on each chromosome now; they are genetically identical.

  • G2: centrioles replicate.

Meiosis I

Prophase I

  • Homologous pairs pair up.

  • So there are four chromatids attached together.

  • This is called synapsis and the two pairs together make four chromatids.

  • The structure formed is called a bivalent or tetrad.

  • In eukaryotic cells, usually a synaptonemal complex is formed (protein structure that forms between homologous chromosomes (two pairs of sister chromatids).

  • Crossing over of homologous pairs occurs.

  • A junction is created where one chromatid in each homologous chromosome breaks and rejoins with a non-sister chromatid – occurs at random positions and can be several.

  • Chiasma: the point of contact between these two chromatids of homologous chromosomes. There can be many such points – chiasmata.

  • Importance of crossing over: increased stability of bivalents at chiasmata AND it creates new combinations of genes, also decoupled linked genes, leading to independent assortment.

  • Occurs at the same position on the two chromatids involved.

  • Chromosomes condense (shorten by supercoiling)

  • Nucleolus dissipates.

  • Centrioles migrate to the poles of the cell.

  • Spindle microtubules are growing from the poles of the cell.

Metaphase I

  • Spindle microtubules from the centrioles attach to the centromeres of the chromosomes.

  • The pole to which each chromosome is attached depends on which way the bivalent is facing – called orientation and it is random.

  • Bivalents align at the equator of the cell.

  • Nuclear envelope disintegrates.

Anaphase I
  • Microtubules shorten and pull bivalents apart and one chromosome of each pair moves to each pole. Important note: centromeres are not divided. This process is called disjunction.
Telophase I
  • Nuclear envelopes reforms.

  • Chromosomes uncoil.

Cytokinesis occurs and in the interphase between meiosis I and meiosis II and centrioles replicate but nothing else replicates.

Meiosis II

Prophase II

  • Chromosomes condense again.

  • Centrioles migrate to poles of the daughter cells as the spindle fibre network reforms.

Metaphase II

  • Nuclear envelope disintegrates.

  • Spindle microtubules attach themselves to the centromeres of the chromosomes.

  • Chromosomes align in the equator of the cell.

Anaphase II

  • Nuclear envelope disintegrates and chromatids are moved to opposite poles.

  • Haploid cells are created

Telophase II

  • Chromatids reach opposite poles.

  • Nuclear envelope reforms.

Cytokinesis occurs.

Meiosis and Genetic Variation

  • Mendel’s First Law: the Law of Segregation states that two alleles of every gene that occurs during meiosis separate (i e there is a 50% chance a particular allele is in a sex cell). Linked genes are more unlikely to separate because their loci are near each other.

  • Random orientation: bivalents face poles of the cell randomly and the orientation of one bivalent doesn’t affect that of another. It is the process that generates genetic variation among genes that are on different chromosome types.

  • Mendel’s Second Law: the Law of Independent Assortment states that the alleles of two genes will pass into gametes without influencing each other.

Crossing over: exchange of genetic materials forms new combinations (recombination).

References

  • Class notes
  • Oxford IB Diploma Programme BIOLOGY Course Companion 2014 Edition
  • BIOZONE Student Workbook IB Biology Second Edition

Written with StackEdit.

10.3 - Gene Pools and Speciation

Gene Pool:- The total collection of different alleles in an interbreeding population.

Allele Frequency and Evolution

  • Allele Frequency:- The proportion of all copies of a gene that is made up of a particular gene variant.
  • New combinations of alleles lead to new phenotypes that can be selected for/against by the environment.
    • This leads to evolutionary change.

Patterns of Evolution and Selection

  • Selective pressures need to change for evolution.
  • Type of evolution depends on the phenotypes that experience the greatest pressure.

Directional Selection

  • Population changes as one range of variation is better adapted.
  • For example - bird beaks are better longer and harder, so they evolve till the population has longer and harder beaks.

Directional Stabilisation

Stabilising Selection

  • Selection Pressures remove extreme varieties.
  • For example - Human baby birth weight.
    • Too heavy = difficult to deliver through pelvis. (babies would die during delivery).
    • Too light = lose heat too quickly. (babies would die).

Stabilising Selection

Disruptive Selection

  • Selection pressures act to remove intermediate varieties.
  • For example - Grass close to a quarry with metal contaminated soil.
    • One population will be metal tolerant and slow growing.
    • The other won’t be metal tolerant and will grow slower.

Disruptive Selection
Sources for graphs

Reproductive Isolation

  • Inability of a species to breed with a related species due to some factors (see below).
  • Only promotes selection in sexually reproducing organisms

Temporal Isolation

  • Mating seasons/times do not coincide
  • For example - different pollination times for flowers

Ecological Isolation

  • Organisms in the same area, but different habitats/conditions.
  • For example - Plant A survives in alkaline soil vs. Plant B in acidic

Behavioural Isolation

  • Organisms that mate based off of courting behaviour/pheromones will only mate with those who perform the best mating behaviour (eg dancing, fighting, etc.).
  • So it can prevent two organisms from mating.

Rate of Speciation

Phyletic Gradualism

  • Evolution occurring at a constant pace. Gradual Change.
  • Due to accumulation of mutations.

Punctuated Equilibrium

  • Long periods of stability followed by sudden changes
  • Fossil record supports this
  • Rapid evolution due to major environmental changes like a meteor

Polyploidy

  • Non-disjunction can occur during meiosis in humans.
  • Individual can end up with an extra chromosome or missing chromosomes.
  • Total non-disjunction: One of the two cells produced during Meiosis I gets all of the chromosomes.
  • Tetraploid offspring cannot mate with diploid organisms, so speciation has occurred
  • More common in plants
    • increased size, resistance to disease and overall vigour in plants.

Sources

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