2013 HSC COURSE

HSC biology, physics, economics, english & four unit mathematics

HSC biology, physics, economics, english & four unit mathematics

Oliver Williams

Oliver Williams

Kartei Details

Karten 417
Sprache English
Kategorie Allgemeinbildung
Stufe Mittelschule
Erstellt / Aktualisiert 10.04.2013 / 10.09.2024
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experiment on structures in plants that assist the in conservation of water 

aim: to investigate structures in plants that assist in the conservation of water

risk: cacti has sharp spines that may cause injury. As such wear gloves when handling

materials 1x cacti sample 1x banksia sample 1x spinifex grass sample 1x magnifying glass 1x pencil 

method: 1. use the magnifying glass to observe samples 2. identify and sketch features that assist with water conservation 

 

independant variable 

variable that the experimenter changes 

dependant variable 

variable that the experimenter measures 

xylem tissue

tissue in plants responsible for the unidirectional passive movement of water from roots to shoots.

structure: 1. arranged end to end to form a continuous column 2. pits to allow sideways movement of water 3. narrow lumen to increase height that water can reach 4. walls thick with lignin to increase strength 5. composed of dead cells (doesnt absorb water)

Osmoregulators 

able to regulate salt water concentration and keep it constant regardless of changes in the external environment

osmoconformers 

body fluids isotonic (same concentration as the environment) 

unable to adjust internal salt water concentration 

carries out enantiostasis

Phloem tissue

living tissue responsible to the bilateral movement of organic substances in plants from source to sink 

composed of: 1. sieve tube elements and compagnion cells linked end to end 2. sieve tube plates perforated with pores linked by plasmodesmata 

James watson contribution to determining the structure of DNA

suggested with crick that DNA molecule was made up of 2 chains of nucleotides each in a helix by one going up and the other going down

realised that A - T pair held togethor by 2 hydrogen bonds was identical to G - C pair  - therefore these pairs of bases could serves as rungs on the twisting ladder of DNA

Francis crick contribution to determining the structure of DNA

deduced that the matching base pairs of which there were similar amounts interlocked in the middle of the double helix to keep the distance between the chains constant 

Relative importance of Watson and Crick in determining the structure of DNA

Concluded that the DNA molecules was made up of 2 chains of nucelotides, bonded in a double helix shape with one going up and the other going down

Rosalind franklin contribution to the determination of the structure of DNA 

Produced the "world's best" X ray diffraction images of DNA 

Extracted fine DNA fibers than ever before and arranged them in paralled bundles before studying reaction to humid conditions 

Found her images showed that the 'wet' form of DNA had the characteristics of a helix

Rosalind Franklin relative importance in the determining of DNA structure 

X ray diffraction images became the basis of watsons and cricks conclusion 

Showed that the chains of nucleotides in DNA were in the shape of helixes - crucial to watsons and cricks conclusions 

Maurice wilkins contribution to the determining of DNA structure 

Found DNA could exist in 2 forms depending on humidity of surrounding air

deduced that the phosphate part of DNA was on the outside 

Showed watson one of franklins X ray diffraction images giving vital information

Relative importance of Maurice wilkins to the determining of DNA structure 

Enabled the combination of Franklins images and Watsons and Cricks research leading to watsons and cricks conclusion on the structure 

Impact of collaboration and communication on the determination of DNA structure 

Franklin's reluctance to share her works ultimately meant she was not directly credited for her work and the discovery of the structure was retarded 

Good collaboration between watson and crick helped find a quicker solution

Principle of segregation 

for any particular trait the pair of alleles / factors each each parent seperate and only one allele / factor passes from each parent to an offspring 

principle of independant assortment 

different pairs of alleles are passed to offspring interpendant of one another

e.g. if a pea plant inherits purple flower its is no more likely to inherit yellow seeds 

roles of Sutton and Boveri in identifying the importance of chromosomes

 

  • Two scientists are credited with the discovery of the role of chromosomes in 1902. They were the German scientist Theodor Boveri and the American microbiologist Walter Sutton.
  • Boveri worked on sea urchins and showed that their chromosomes were not all the same and that a full complement was required for the normal development of an organism.
  • Sutton worked on grasshoppers and showed that their chromosomes were distinct entities. He said even though they duplicate and divide they remain as a distinct structure. He associated the behaviour of chromosomes with Mendel's work on the inheritance of factors and concluded that chromosomes were the carriers of hereditary units.
  • Together their work became known as the Sutton-Boveri chromosome hypothesis.

Chemical nature of chromosomes and genes

 

  – Each chromosome is made up of about 60% protein and 40% DNA – The DNA is coiled tightly around a protein core (histone proteins) – A gene is a section on a chromosome, made up of DNA – DNA is further made up made up of a particular sequence of bases – Different genes are different lengths (diameter of locus), hence differing lengths of DNA.

Structure of DNA

 

DNA (deoxyribonucleic acid): - A double stranded helix - Made up of sub-units called nucleotides, each nucleotide is made up of a phosphate, a deoxyribose sugar and a nitrogenous base. - The four different nitrogenous bases are adenine, thymine, guanine, and cytosine - Adenine pairs with thymine (A-T) and guanine with cytosine (G-C) - A single DNA strand is made up of a chain of nucleotides (a polynucleotide) where the phosphate and sugar alternate as the backbone of the strand  

Meiosis

Meiosis is the process of division in which sex cells are produced(ie gamates)

In the process half the number of chromosomes are in each sex cell (compared to a normal cell)

occurs in the sex organs 

Jelly snakes model

models the process of meiosis using jelly snakes to represent chromosomes   

cell with diploid number of 2 (2 pairs of 2 chromosomes) 1 pair short homologous 1 pair long homologous with each chromsome in the homologous pair a different colour

Chromosomes were doubled keeping colours consistant (copy attached to original at centromere) 

crossing over was modelled between homologous chromosomes by breaking off pieces from the homolougous chromatid and rejoining to the other homologous chromatid

random segregation was modelled as each homologous pair lined up at the equator in random order 

The homologous chromosomes then moved away from each other to the poles of the cell by the spindle

cytokinesis occurs 

Chromosomes are once again drawn to the equator and then the chromatid are seperated drawn by the spindle to the poles 

cytokinesis 

4 cells each with 2 seperate chromosomes 

Advantages of jelly snakes model

Colours of the snakes helped understand the idea of homologous chromosomes and made crossing over clear as well as the random segregation of chromosomes (different possibilities)

The snakes being soft and sticky demonstrated crossing over clearly 

Moving the snakes around to simulate movement in meiosis helped to understand the dynamic nature of the process 

The snakes could be resized to make chromosome pairs different sizes 

 

 relationship between the structure and behaviour of chromosomes during meiosis and the inheritance of genes

  • Chromosomes are made of DNA. Genes are coded within the DNA on the chromosomes. Meiosis in four genetically different sex cells (due to crossing over and random segregation) that are haploid, (ie contain half the chromosome number of the original cell) thereby creating 4 possibilities for the inheritance of genes

Gamete formation and sexual reproduction in genetic variation

Gamete formation results in the halving of the chromosome number (n) (diploid to haploid) and sexual reproduction results in combining gametes (haploid to diploid) to produce a new diploid organism (2n).

The processes involved in forming this new organism result in variability of the offspring as not only does 2 different genetic makeups combine through sexual reproductioon, but in gamete formation each sex cell is also genetically different each other due to random segregation and crossing over during meiosis

experiment: demonstrating the effect of environment on phenotype 

aim: to demonstrate the effect of the environment on the phenotype of bean sprouts 

hypothesis: The different environmental condition will result in different phenotypes 

risk: spilt water is a slipping hazard and may cause injury. As such clean up any split water immeadiatly 

materials 100 x bean sprouts 10 x plastic contrainer 1x cotton wool 1 x 1L water 1x light impermiable sheet 

method: 1x place a layer of cotton wool into each of the plastic containers 2. soak cotton so that it is damp 3. place 10 bean sprouts into each container equally spaced 4. store 5 containers under the light impermiable sheet and 5 in a light abundant area 5. leave for 2 days and return 6. record results 

 process of DNA replication 

1. DNA double helix unwound by helicase enzyme 

2. DNA unzips to form two seperate strands 

3. Complementary nucleotides are brought over by DNA enzyme polymerase and form hydrogen bonds with the single strands resulting in two identical strands of DNA

4. DNA double helix rewinds 

DNA replication 

takes place during interphase in preparation for nuclear division that occurs during meiosis or mitosis 

Ensures daughter cells receive a copy of DNA from parent cells in asexual reproduction and mitosis and half the genetic information in meiosis

Semi conservative (each new double helix has one original and one new strand)

DNA and the production of polypeptides 

DNA carries the instruction for making a polypeptide and therefore a protein 

RNA is used to transcribe the message from DNA (as it is small enought to fit through the nuclear pore to the ribosome) it does so through helicase enzyme unwinding the enzyme, and RNA polymerase building a complementary strand of mRNA

The ribosomes translates the DNA sequence 3 bases at a time and tRNA (transfer RNA) molecule brings over the corrosponding amino acid (the amino is based on the mRNA condon) 

Peptide bonds form between neighbouring amino acids

tRNA molecule is released back into the cytoplasm

Chain of amino acids form a polypeptide chain

sequence stops when ribsosome reaches a stop sequence and starts again when it reaches a start condon 

Simple model: DNA production of polypeptides 

DNA ---> transcription ---> RNA ---> translation ---> polypeptide 

Relationship between a polypeptide and a protein 

Polypeptides are the basic units of proteins 

Sometimes more than one polypeptide chain is needed to create a protein (and therefore more than one gene may be needed to create a protein)

polypeptide 

A chain of amino acids 

How changes in DNA sequences can result in changes in cell activity

 

simple substitution for a single base pair on a strand of DNA will result in a different amino acid codon forming a different polypeptide.   If one base pair is lost from the sequence there will be a shift along the DNA molecule producing different polypeptides.

Beedle and tatum 

 

hypothesized that if there really was a one-to-one relationship between genes and specific enzymes, it should be possible to create genetic mutants that are unable to carry out specific enzymatic reactions.   To test this theory, they exposed spores of Neurospora crassa (a bread mold) to X-rays or UV radiation and studied the resulting mutations.   The mutant molds had a variety of special nutritional needs. Unlike their normal counterparts, they could not live without the addition of particular vitamins or amino acids to their food.    Genetic analysis showed that each mutant differed from the original, normal type by only one gene and biochemical analysis showed a build up of the substrate the enzyme normally used     These results led them to the one gene/one enzyme hypothesis, which states that each gene is responsible for directing the building of a single, specific enzyme.   Subsequent work has led to further refinement of this hypothesis. We now know that a gene infact codes for a particular polypeptide rather than a protein and a protein can be composed of multiple polypeptides (e.g. Hb). Its also been shown that proteins dont just code for enzymes, but are also coded for structural uses 

how mutations can lead to new alleles 

 

  • Any change in the base sequence in DNA by mutations may result in different polypeptides being produced and therefore a new allele
  • if the mutation occurs in the sex cells of the organism the mutated code may be passed off to offspring
  • The offspring may therefore have a new allele/s from the changed protein/s depending on the effect of the mutation

effect of mutations 

depending on types of mutations mutations may have:

no effect - as mutation produces the same amino acid 

neutral effect - eye colour

harmful effect - e.g. sickle cell anaemia 

beneficial effect - e.g. sickle cell anaemia immunity to HIV

Chromosomal mutations 

Changes in the number and/or structure of entire chromosomes 

may occur during meiosis when homologous chromosomes dont seperate properly 

e.g. down's syndrome (trisome 21)

Causes of mutations 

inheritance from parents (if mutation occurs in sex cells)

environmental damage (radiation)

mistakes when DNA is compied 

modern day natural selection example DDT 

insecticide DDT was used to eradicate maleria carrying mosquito 

however widespread use cause resistance to occur arising from a mutation in a single genen DDT-R  (occured in the sex cellsand was passed on)

evidence for the mutagenic nature of radiation

A mutagen is a natural or human-made agent (physical or chemical) which can alter the structure or sequence of DNA.

Mutagens can be carcinogens (cancer causing) or teratogens (birth defects causing).

 

Beadle and Tatum used X-rays to produce mutations in bread mould in the formulation of their “one – gene one – polypeptide” hypothesis.   The atomic bombs dropped on Hiroshima and Nagasaki also increased the evidence for mutations caused by radiation. There was a tenfold increase in cancer deaths directly after the bombs were dropped.   Rosalind franklin died very young after using x ray cyrstalography to examine DNA structure   Mutagens may cause death in the individual but unless they affect the sex cells the effect is not passed on to the next generation.