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Describe how DNA profiling could be carried out to show that these snakes are different species. (4)
M1: DNA obtained from two types of snakes
M2: {PCR/ restriction enzymes} used to produce fragments of DNA
M3: Gel electrophoresis used to analyse the DNA
M4: Gel electrophoresis used to separate the fragments of DNA
More differences in the patterns of bands produced would indicate that the snakes are different species
Describe the changes that occur inside a body in the first week after death. (3)
M1: Body temperature falls
M2: Rigor mortis/ stiffening of the muscles
M3: Autolysis/ breakdown of cells by enzymes in the body
M4: Putrefaction/ discolouration/ bloating (allow: accumulation of gases)
Microorganisms are also found on a dead body.
Describe the role of decomposers, such as microorganisms, in the carbon cycle. (2)
M1: Decomposers break down organic material
M2: Decomposers respire
M3: releasing CO2 into the atmosphere
Devise a procedure, using electrophoresis, to compare the amplified DNA from these two types of human.
M1: {restriction enzymes/ endonuclease} used to cut DNA into fragments
M2: DNA samples are loaded into agarose gel
M3: {electric current is passed through/ potential difference is applied across} the gel
M4: Markers are added to visualise the gel
M5: The positions of the bands produced can be compared
Explain the effect of ambient temperature on the rate of decomposition. (3)
M1: An increase in temperature will increase the rate of {decay/ decomposition}
M2: An increase in temperature increases enzyme activity
M3: An increase in temperature increases growth rate of {bacteria/ fungi/ decomposers}
Describe how one PCR cycle would increase the quantity of DNA present. (3)
M1: heat to 90-98 C {to break hydrogen bonds between DNA strands/ separate the strands of DNA} - denaturation
M2: {joining of primers/ annealing} at 50-75 C
M3: {elongation/ extension/ addition of nucleotides}/ DNA polymerase involved in formation of phosphodiester bonds
M4: To double the quantity of the DNA
Describe the infection control practices hospitals have introduced. (3)
M1: Hand wash stations
M2: doctors/ nurses not to wear {ties/ watches/ long sleeves}
M3: Testing patients for antibiotic resistant bacteria before admission/ {isolation/ quarantine} of infected patients
M4: Increased washing of bedding/ disinfection of {beds/surfaces}
Inflammation is a non-specific response to an infection. Explain how changes in the blood vessels result in the redness and swelling seen at the site of inflammation. (4)
M1: Histamines are released
M2: Histamines cause {arterioles to dilate/ vasodilation}
M3: Which increase the blood flow to the site causing redness
M4: Histamines also cause the permeability of the membranes to increase
M5: Allowing blood plasma to {leave the capillary/ enter the tissues} causing oedema/ swelling
Describe how HIV particles are able to enter T helper cells. (3)
M1: {glycoproteins/ GP120} on the surface of the virus
M2: bind to CD4 receptors on the surface of the T-helper cells
M3: Viral envelope fuses with the cell membrane of the T-helper cell
M4: Viral RNA enters the cell
Explain why the destruction of T helper cells causes the symptoms of AIDS. (4)
M1: Lack of T-helper cells reduce cytokine production
M2: Therefore reducing {cloning/ activation} of B cells
M3: Reducing antibody production
M4: There is an increased risk of opportunistic infections(eg TB)
Explain why the presence of microorganisms on the skin and in the gut helps to prevent pathogenic organisms multiplying in the body. (3)
M1: Flora in the gut and skin are better adapted to the conditions
M2: Therefore they can outcompete pathogenic organisms
M3: Bacteria in the gut secrete {chemicals/ lactic acid} which help to destroy pathogens
A person who has been vaccinated becomes infected with HPV-16. Explain the role of the T cells in the body of this person. (3)
M1: A vaccinated person will have memory T-cells
M2: Memory T cells recognise antigens specific to the HPV-virus
M3: T-helper cells that activate {B-cells/ T killer cells}
M4: Formation of T-killer cells destroy cells infected with the virus
Explain why there are relatively few species of bacteria in the stomach. (2)
M1: Because pH in the stomach is too low for the enzymes of most bacteria to suffer
M2: Bacteria that live the the stomach have adaptations that enable them to survive.
State what is meant by the term bacteriostatic. (1)
A substance which can {inhibit the growth/ prevent multiplication} of bacteria
Explain the role of T cells in the immunity to the Ebola virus that develops following the use of this vaccine. (3)
M1: T helper cell bind to {protein/ antigen} on the APC
M2: Therefore leading to production of {active T helper cells/ T memory cells}
M3: The T helper cells activate the B cells to {divide/ become} cells capable of producing antibodies
M4: The memory cells cells remain in the body so antibodies can be produced quickly on re-infection
Explain how a bone marrow stem cell can give rise to red blood cells. (4)
M1: By differentiation
M2: Due to certain stimuli
M3: Which causes {some genes genes of haemoglobin} to be activated
M4: {mRNA/ haemoglobin} produced from activated genes
M4: Removal of nucleus/ produce a biconcave shape
M. tuberculosis bacteria can remain dormant in the body after infection.
Explain why these dormant bacteria are not destroyed by the immune system. (3)
M1: the bacteria are inside {macrophages/ phagocytes}
M2: This bacterium has a thick waxy cell wall
M3: Lysosomes cannot fuse with phagocytic vacuole/ bacteria not destroyed by enzymes
M4: Bacteria within tubercles cannot be destroyed
Describe how amplified samples of DNA can be prepared for analysis using gel electrophoresis. (3)
M1: DNA is cut into fragments
M2: {radioactive tracers/ fluorescent tags} attached to DNA (allow stains such as dye)
M3: Fragments of DNA loaded onto agarose gel/ samples placed in wells
M4: Electric current passed through the gel/ potential difference set up through buffer/ across gel
Explain why antibiotics cannot be used to treat influenza. (2)
M1: Because influenza is (caused by) a virus
M2: Antibiotics target {prokaryotes / bacteria} (ALLOW: treat bacterial infections)
M3: Structure of a virus is different to that of a {prokaryote / bacteria}
Devise a procedure to determine the similarities of the RNA of a particular virus which has many strains (hence differences in its RNA) in saliva collected from different people. (4)
M1: {isolate / extract} RNA from (saliva) samples
M2: Amplify the {RNA/DNA/nucleic acid} by PCR (ALLOW (reverse) transcribe RNA to DNA and amplify DNA)
M3: Cut the {RNA/DNA/nucleic acid} into fragments (using restriction enzymes)
M4:(separate fragments using) gel electrophoresis
M5: More similar the {banding / profile} (of the fragments) the more closely related the strain
Describe how M. tuberculosis bacteria evade the immune system. (2)
M1: (M tuberculosis) survive inside macrophages
M2: (M tuberculosis) {survive / remain dormant} in tubercles
M3: (M tuberculosis) {inhibit T helper cells / supress the (acquired) immune response}
State what is meant by the term transcription factor. (1)
Is a protein that controls {activation/ transcription} of gene