T2 Cells Flashcards

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1
Q

Name the process by which prokaryotic cells divide. 1 mark

A

Binary fission

Reject fusion

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2
Q

Name two structures present in plant cells that are not present in animal cells. 1 mark

A
  1. Chloroplasts / plastids
  2. Cell wall
  3. Cell vacuole
  4. Starch grains / amyloplasts;
    Any 2 for 1 mark
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2
Q

Give one advantage of viewing a biological specimen using a transmission electron
microscope compared with using a scanning electron microscope. 1 mark

A

Higher resolution
or
View internal structure

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2
Q

A biologist prepared a sample of organelles labelled C from liver. He used the following method.
1. Added to the liver tissues an ice-cold, buffered solution with the same water potential as the liver tissue.
2. Mixed the liver and solution in a blender.
3. Filtered the mixture from the blender.
4. Spun the filtered liquid in a centrifuge at a low speed. A pellet appeared in the bottom
of the centrifuge tube.
5. Poured off the liquid above the pellet into a second centrifuge tube and spun this at a
higher speed to obtain the sample of organelles labelled C.
(c) Explain why the solution the biologist used was ice-cold, buffered and the same water
potential as the liver tissue (step 1) 3 marks

A
  1. Ice-cold – Slows / stops enzyme activity to prevent digestion of organelles /
    mitochondria;
  2. Buffered – Maintains pH so that enzymes / proteins are not denatured;
    Reject reference to cells
  3. Same water potential – Prevents osmosis so no lysis / shrinkage of organelles /
    mitochondria / C;
    Ignore damage
    For each mark must link reason to relevant property
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3
Q

Eukaryotic cells produce and release proteins.
Outline the role of organelles in the production, transport and release of proteins from eukaryotic cells.
Do not include details of transcription and translation in your answer. 4 marks

A
  1. DNA in nucleus is code (for protein);
  2. Ribosomes/rough endoplasmic reticulum produce (protein);
    Accept rER for ‘rough endoplasmic reticulum’
  3. Mitochondria produce ATP (for protein synthesis);
  4. Golgi apparatus package/modify;
    OR
    Carbohydrate added/glycoprotein produced by Golgi apparatus;
    Accept body for ‘apparatus’
  5. Vesicles transport
    OR
    Rough endoplasmic reticulum transports;
  6. (Vesicles) fuse with cell(-surface) membrane;
    Accept exocytosis at cell membrane
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3
Q

Starting with some lettuce leaves, describe how you would obtain a sample of undamagedchloroplasts. Use your knowledge of cell fractionation and ultracentrifugation to answer this question. 6 marks

A
  1. Chop up (accept any reference to crude breaking up);
  2. Cold;
  3. Buffer solution;
  4. Isotonic / same water potential;
  5. Filter and centrifuge filtrate;
  6. Centrifuge supernatant;
  7. At higher speed;
  8. Chloroplasts in (second) pellet;
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3
Q

  Name the fixed position occupied by a gene on a DNA molecule 1 mark

A

Locus/Loci

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3
Q

Describe how you could make a temporary mount of a piece of plant tissue to observe the
position of starch grains in the cells when using an optical (light) microscope. 4 marks

A
  1. Add drop of water to (glass) slide;
  2. Obtain thin section (of plant tissue) and place on slide / float on drop of water;
  3. Stain with / add iodine in potassium iodide.
  4. Allow any appropriate method that avoids trapping air bubbles
  5. Lower cover slip using mounted needle.
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3
Q

The student produced the sucrose solutions with different concentrations from a
concentrated sucrose solution.
Name the method she would have used to produce these sucrose solutions. 1 mark

A

Dilution series
Accept serial dilution

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4
Q

Describe how a gene is a code for the production of a polypeptide. Do not include
information about transcription or translation in your answer. 3 marks

A
  1. (Because) base/nucleotide sequence;
  2. (In) triplet(s);
  3. (Determines) order/sequence of amino acid sequence/primary structure (in
    polypeptide);
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5
Q

Trexall is a drug that can be used to slow the development of various forms of cancer.
Trexall slows cell division by interacting with an enzyme called dihydrofolate reductase (DR).
DR is involved in making nucleotides; the substrate for DR is folic acid.
Use the information provided to suggest how Trexall slows cell division. 3 marks

A
  1. (Trexall acts as a) competitive inhibitor
    OR
    (Trexall) competes (with folic acid/substrate) for/is able to fit into/binds at active site (on dihydrofolate reductase / enzyme);
    Reject Trexall and folic acid have the same shape
  2. Less folic acid/substrate attaches
    OR
    Fewer enzyme-substrate complexes;
    Accept folic acid/substrate is prevented from binding
    3.Fewer/not enough nucleotides available for DNA replication;
    Accept fewer/not enough nucleotides available during interphase/for semi-conservative replication/to add to (all) template strands/for
    transcription
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6
Q

Mitosis is important in the life of an organism. Give two reasons why 2 marks

A
  1. Growth / increase in cell number;
    Ignore growth of cells
  2. Replace cells / repair tissue / organs / body;
    Ignore repair cells
    Reject bacteria
  3. Genetically identical cells;
    ‘Produces 2 genetically identical cells’ does not reach MP1 as well
    as MP3
  4. Asexual reproduction / cloning;
    Allow example or description
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7
Q

In which phase of the cell cycle does DNA replication take place?
1 mark

A

Interphase

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8
Q

Describe the role of the spindle during mitosis 2 marks

A

Attachment of centromeres / chromosomes / chromatids; Separation of centromeres /
chromatids / chromosomes;

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9
Q

Meiosis also occurs during the life cycle of organisms. What is the importance of meiosis?
2 marks

A

Halves chromosome number / haploid;
Diploid / full number restored at fertilisation;
Allow correct reference to variation

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10
Q

A student prepared a stained squash of cells from the root tips of garlic to calculate a mitotic
index. He:
1. cut the end 5 mm from 10 garlic roots
2. placed the root tips into a Petri dish containing 5 cm3
of hydrochloric acid for 12 minutes
3. rinsed the root tips in distilled water
4. placed one of the root tips on a microscope slide and added toluidine blue stain
5. placed a coverslip onto the microscope slide, and gently pressed the coverslip downwards on the root tip
6. observed the root tip using an optical microscope.
7.
(a)  Suggest why the student soaked the root tips in hydrochloric acid in step 2. 2 marks

A
  1. To break down links between cells/cell walls
    OR
    To separate cells/cell walls
    OR
    To break down/hydrolyse cellulose/cell wall;
  2. Allowing the stain to pass/diffuse into the
    cells
    OR
    Allowing the cells to be (more easily)
    squashed;
  3. To stop mitosis;
11
Q

Describe how a phagocyte destroys a pathogen present in the blood. 3 marks

A
  1. Engulfs;
    Accept endocytosis
    OR
    Description
    Ignore ‘taken in’
  2. Forming vesicle/phagosome and fuses with lysosome;
  3. Enzymes digest/hydrolyse;
    Accept lysozymes for ‘enzymes’
12
Q

Give two types of cell, other than pathogens, that can stimulate an immune response. 2 marks

A
  1. (Cells from) other organisms/transplants;
  2. Abnormal/cancer/tumour (cells);
  3. (Cells) infected by virus;
    Accept ‘own cells’ if autoimmune response suggested
    Accept APCs
    Accept non-self
13
Q

What is the role of the disulfide bridge in forming the quaternary structure of an antibody? 1 mark

A

Joins two (different) polypeptides;
Accept holds/attaches
Accept ‘prevents polypeptide chains separating’

14
Q

In Europe, viruses have infected a large number of frogs of different species. The viruses are
closely related and all belong to the Ranavirus group.
Previously, the viruses infected only one species of frog.
3.
(a) Suggest and explain how the viruses became able to infect other species of frog.
2 marks

c. Describe how the B lymphocytes of a frog would respond to vaccination against Ranavirus.
You can assume that the B lymphocytes of a frog respond in the same way as B
lymphocytes of a human.
Do not include details of the cellular response in your answer. 3 marks

A

  1. Mutation in the viral DNA/RNA/genome/genetic material;
Accept named examples mutations
2. Altered (tertiary structure of the) viral attachment protein;
Accept ‘antigen’ for ‘attachment protein’
Accept causes antigenic variability
3. Allows it/attachment protein/virus to bind (to receptors of other species);
Accept descriptions of binding eg is complementary

  1. B cell (antibody) binds to (viral) specific/complementary receptor/antigen;
    Accept B cell forms antigen-antibody complex
  2. B cell clones
    OR
    B cell divides by mitosis;
  3. Plasma cells release/produce (monoclonal) antibodies (against the virus);
  4. (B/plasma cells produce/develop) memory cells;
    Accept B cell undergoes clonal selection/expansion
15
Q

Name two techniques the scientists may have used when analysing viral DNA to determine
that the viruses were closely related 1 mark

A

For one mark, accept any two of the following:
*   The polymerase chain reaction
*   Genetic/DNA fingerprinting
*   (Gel) electrophoresis
*   DNA/genome sequencing;
Accept PCR for polymerase chain reaction
Accept autoradiography
Accept DNA hybridisation
Accept compare DNA/base sequence for ‘DNA sequencing’
Ignore compare mRNA base sequence
Ignore compare amino acid sequence
Ignore DNA probes

16
Q

Determining the genome of the viruses could allow scientists to develop a vaccine.
Explain how. 2 marks

A
  1. (The scientists) could identify proteins (that derive from the genetic code)
    OR
    (The scientists) could identify the proteome;
  2. (They) could (then) identify potential antigens (to use in the vaccine);
    Reject if answer suggests vaccine contains antibodies
17
Q

What is a monoclonal antibody?
1 mark

A

(Antibodies with the) same tertiary structure
OR
(Antibody produced from) identical/cloned plasma cells/B cells/B lymphocytes;
Accept in context of single plasma/B cell/B lymphocyte
Reject: genetically identical antibody

18
Q

After a disease is diagnosed, monoclonal antibodies are used in some medical treatments.
Give one example of using monoclonal antibodies in a medical treatment. 1 mark

A

Accept any one suitable use, eg
Targets/binds/carries drug/medicine to specific cells/antigens/receptors
OR
Block antigens/receptors on cells;
Accept cancer/diseased cells (as a specific cell).
Ignore medical diagnosis/pregnancy/ PSA/ELISA test

19
Q

Describe the role of antibodies in producing a positive result in an ELISA test 4 marks

A

1.   (First) antibody binds/attaches /complementary (in shape) to antigen;
2.   (Second) antibody with enzyme attached is added;
3.   (Second) antibody attaches to antigen;
Accept (second) antibody attaches to (first) antibody (indirect ELISA test).
4.   (Substrate/solution added) and colour changes;
Only award if enzyme mentioned.

20
Q

When a person is bitten by a venomous snake, the snake injects a toxin into the person.
Antivenom is injected as treatment. Antivenom contains antibodies against the snake toxin.
This treatment is an example of passive immunity.
Explain how the treatment with antivenom works and why it is essential to use passive
immunity, rather than active immunity. 2 marks

A
  1. (Antivenom/Passive immunity) antibodies bind to the toxin/venom/antigen and
    (causes) its destruction;
    For ‘bind’ accept ‘attach’, ignore ‘attack’.
    For ‘destruction of toxin’ accept agglutination or phagocytosis.
    Ignore reference to antibodies ‘neutralising toxin/stopping damage’
    Reject reference to ‘killing’ toxin/venom.
  2. Active immunity would be too slow/slower;
    Accept ‘passive immunity is fast er’, not simply ‘passive immunity is
    fast’
21
Q

During vaccination, each animal is initially injected with a small volume of venom. Two
weeks later, it is injected with a larger volume of venom.
Use your knowledge of the humoral immune response to explain this vaccination
programme. 3 marks

A
  1. B cells specific to the venom reproduce by mitosis;
    Accept in context of primary or secondary immune response.
    Credit idea of specificity if given once in relation to T or B cell.
    Accept a description for specificity.
    Accept ‘clone’ for ‘reproduce by mitosis’.
    ‘Clonal selection of B cells’ = MP1.
  2. (B cells produce) plasma cells and memory cells;
  3. The second dose produces antibodies (in secondary immune response) in higher
    concentration and quickly
    OR
    The first dose must be small so the animal is not killed;
    Accept ‘a lot of antibody’ for ‘higher concentration of antibody’.
22
Q

A high mutation rate of a virus makes it difficult to develop a vaccine. Explain why. 3 marks

A
  1. (High mutation rate leads to) antigens change/antigenic
    variability;
    Accept (high mutation rate leads to) changes in base sequence
    coding for antigen;
  2. Vaccine contains specific antigen;
  3. Antibodies not complementary to (changed) antigen / won’t bind to
    (changed) antigens;
23
Q

Describe how HIV is replicated 4 marks

A
  1. Attachment proteins attach to receptors on helper T cell/lymphocyte;
  2. Nucleic acid/RNA enters cell;
  3. Reverse transcriptase converts RNA to DNA;
  4. Viral protein/capsid/enzymes produced;
  5. Virus (particles) assembled and released (from cell);
24
Q

Describe how the human immunodeficiency virus (HIV) is replicated once inside helper T
cells (TH cells). 4 marks

A
  1. RNA converted into DNA using reverse transcriptase;
    Reject ‘messenger’ or ‘m’ before RNA
  2. DNA incorporated/inserted into (helper T cell) DNA/chromosome/genome/nucleus;
  3. DNA transcribed into (HIV m)RNA;
    Accept descriptions of transcription
  4. (HIV mRNA) translated into (new) HIV/viral proteins (for assembly into
    viral particles);
    Accept descriptions of translation
    Accept named viral protein, eg capsid
    Reject viral cells
25
Q

Describe the structure of the human immunodeficiency virus (HIV).
4 marks

A

1.   RNA (as genetic material);
Reject nucleus/DNA/plasmids.
2.   Reverse transcriptase;
3.   (Protein) capsomeres/capsid;
Reject capsule.
4.   (Phospho)lipid (viral) envelope
OR
Envelope made of membrane;
Reject if HIV has a cell membrane or a cell wall.
5.   Attachment proteins;
Accept gp41 and/or gp 120.
Accept glycoprotein.
Accept description of attachment protein.
Ignore ‘receptor protein’.
Ignore cytoplasm.