CELLS : MARK SCHEME ANSWERS Flashcards

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1
Q

Explain why it is not possible to determine the identity of the structures
labelled X using an optical microscope. (2)

A
  1. Resolution (too) low;
  2. Because wavelength of light is (too) long.
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2
Q

U. marinum cells ingest bacteria and digest them in the cytoplasm.
Describe the role of one named organelle in digesting these bacteria (3)

A
  1. Lysosomes;
  2. Fuse with vesicle;
  3. releases hydrolytic enzymes
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3
Q

Give two structures found in all prokaryotic cells and in all eukaryotic cells.(2)

A
  1. Cell(-surface) membrane;
  2. Ribosomes;
  3. Cytoplasm;
  4. DNA
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4
Q

Describe how a sample of chloroplasts could be isolated from leaves. (4)

A

1.Break open cells/tissue and filter
OR
Grind/blend cells/tissue/leaves and filter;
2. In cold, same water potential/concentration, pH controlled solution;
3. Centrifuge/spin and remove nuclei/cell debris;
4. (Centrifuge/spin) at high(er) speed, chloroplasts settle out;

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5
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)

A
  1. DNA in nucleus is code (for protein);
  2. Ribosomes/rough endoplasmic reticulum produce (protein);
  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
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6
Q

Suggest why a nucleus is not visible in above image. (1)

A

A section/slice (so nucleus in another part of cell)
OR
(Nucleus) not stained;
1

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7
Q

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

A

Higher resolution
OR
View internal structures;

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8
Q

Name an organelle found in both a chloroplast and a prokaryotic cell. (1)

A

(70S) Ribosome;
Reject: (80S) Ribosome
1

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9
Q

A biologist separated cell components to investigate organelle activity. She
prepared a suspension of the organelles in a solution that prevented
damage to the organelles.
Describe three properties of this solution and explain how each property
prevented damage to the organelles. (3)

A
  1. (Ice) cold to prevent/reduce enzyme activity;
    For 1, 2 and 3 reject context of cell
  2. Buffered to prevent denaturing of enzyme/protein;
    Accept description of buffer.
    Accept: prevent change of tertiary structure.
  3. Same water potential/ Ψ to prevent lysis/bursting (of organelle);
    Accept: isotonic for same water potential.
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10
Q

Contrast how an optical microscope and a transmission electron
microscope work and contrast the limitations of their use when studying
cells. (6)

A
  1. TEM use electrons and optical use light;
  2. TEM allows a greater resolution;
  3. (So with TEM) smaller organelles / named cell structure can be
    observed
    OR
    greater detail in organelles / named cell structure can be
    observed;
  4. TEM view only dead / dehydrated specimens and optical (can)
    view live specimens;
  5. TEM does not show colour and optical (can);
  6. TEM requires thinner specimens;
  7. TEM requires a more complex/time consuming preparation;
    8.TEM focuses using magnets and optical uses (glass) lenses;
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11
Q

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

A
  1. Chloroplasts / plastids
  2. Cell wall
  3. Cell vacuole
  4. Starch grains / amyloplasts;
    Any 2 for 1 mark
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12
Q

Explain why the biologist used a blender and then filtered the mixture
(steps 2 and 3).

A
  1. Break open cells / homogenise / produce homogenate;
  2. Remove unbroken cells / larger debris;
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13
Q

The second centrifuge tube was spun at a higher speed to obtain the
sample of organelles labelled C (mitochodria) in the diagram (step 5).
Suggest why. (1)

A
  • Mitochondria / organelle C less dense than nucleus / organelle in first pellet;
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14
Q

DNA and RNA can be found in bacteria.
Give two ways in which the nucleotides in DNA are different from the
nucleotides in RNA (2)

A
  1. DNA contains thymine and RNA contains uracil;
  2. DNA contains deoxyribose and RNA contains ribose.
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15
Q

No organelles are visible in the cytoplasm of this red blood cell.
Suggest why. (1)

A

Cytoplasm of red blood cell filled with haemoglobin.

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16
Q

Before the cell was examined using the electron microscope, it was stained. This stain caused parts of the structure of the cell-surface
membrane to appear as two dark lines.
Suggest an explanation for the appearance of the cell-surface membrane
as two dark lines. (3)

A
  1. Membrane has phospholipid bilayer;
  2. Stain binds to phosphate / glycerol;
  3. On inside and outside of membrane.
    Accept phospholipid head / protein
17
Q

Describe and explain two features you would expect to find in a cell specialised for
absorption.(2)

A

Any of the 2:
1. Folded membrane/microvilli so large surface area (for absorption);
2. Large number of cotransport/carrier/channel proteins so fast rate (of
absorption)
3. Large number of mitochondria so make (more) ATP (by respiration) ( for active transport)
4. Membrane-bound (digestive) enzymes so maintains concentration gradient (for fast absorption);

18
Q

Describe how amino acids join to form a polypeptide so there is always NH2 at one end and COOH at the other end.
You may use a diagram in your answer

A
  1. One amine/NH2 group joins to a carboxyl/COOH group to form a peptide bond;
  2. (So in chain) there is a free amine/NH2 group at one end and a free
    carboxyl/COOH group at the other
  3. Each amino acid is orientated in the same direction in the chain.
19
Q

The student kept constant:
* the mass of fresh blueberries
* the volume of extraction solvent
* the time for the mixture to stand.
Name two other variables the student should have kept constant during this investigation. (2)
investigation = A student investigated how to extract anthocyanins from blueberries

A
  1. Temperature;
  2. Agitation/mixing/stirring;
  3. Source/age/type of blueberries;
  4. Crushing of the blueberries;
  5. Rinsing of the blueberries prior to mixing;
  6. Concentration of ethanol/acid
20
Q

A different student did this investigation. He did not have a colorimeter.
Describe a method this student could use to prepare colour standards and use them to give
data for the total anthocyanin extracted. (3)

A
  1. Use known concentration of blueberry juice/extract OR of anthocyanin/pigment (solution) OR of (extraction) solvent to be added to blueberries;
  2. Prepare dilution series;
  3. Compare (results) with colour standards to give score/value/concentration;
21
Q

Give two similarities in the movement of substances by diffusion and by osmosis. (2)

A
  1. (Movement) down a gradient / from high concentration to low concentration;
  2. Passive / not active processes;
22
Q

Explain the advantages of lipid droplet and micelle formation (3)

A
  1. Droplets increase surface areas (for lipase / enzyme action);
  2. (So) faster hydrolysis / digestion (of triglycerides / lipids);
  3. Micelles carry fatty acids and glycerol / monoglycerides to / through membrane / to (intestinal epithelial) cell;
23
Q

suggest how the Golgi apparatus is involved in the absorption of lipids (3)

A
  1. Golgi (apparatus);
  2. Modifies / processes triglycerides;
  3. Combines triglycerides with proteins;
  4. Packaged for release / exocytosis
    OR
    Forms vesicles
24
Q

Sodium ions from salt (sodium chloride) are absorbed by cells lining the gut. Some of these
cells have membranes with a carrier protein called NHE3.
NHE3 actively transports one sodium ion into the cell in exchange for one proton (hydrogen
ion) out of the cell.
Use your knowledge of transport across cell membranes to suggest how NHE3 does this. (3)

A
  1. Co-transport;
  2. Uses (hydrolysis of) ATP;
  3. Sodium ion and proton bind to the protein;
  4. Protein changes shape (to move sodium ion and / or proton across the
    membrane);
25
Q

High absorption of salt from the diet can result in a higher than normal concentration of salt
in the blood plasma entering capillaries. This can lead to a build-up of tissue fluid.
Explain how. (2)

A
  1. (Higher salt) results in lower water potential of tissue fluid;
  2. (So) less water returns to capillary by osmosis (at venule end);
  3. (Higher salt) results in higher blood pressure / volume;
  4. (So) more fluid pushed / forced out (at arteriole end) of capillary
26
Q

Describe how an ATP molecule is formed from its component molecules.(4)

A

mention these points:
1.2.: Accept for 2 marks correct names of three components adenine, ribose/pentose,
three phosphates;
3. Condensation reaction
4. ATP synthase

27
Q

Name and describe five ways substances can move across the cell-surface membrane into a cell(5)

A
  1. (Simple) diffusion of small/non-polar molecules down a concentration gradient;
  2. Facilitated diffusion down a concentration gradient via protein carrier/channel;
  3. Osmosis of water down a water potential gradient;
  4. Active transport against a concentration gradient via protein carrier using ATP;
  5. Co-transport of 2 different substances using a carrier protein;
28
Q

The movement of substances across cell membranes is affected by
membrane structure. Describe how (5)

A

Any 5 of these points:
1. Phospholipid (bilayer) allows movement/diffusion of non-polar/lipid-soluble substances;
2. Phospholipid (bilayer) prevents movement/diffusion of polar/ charged/lipid-insoluble substances
3. Carrier proteins allow active transport;
4. Channel/carrier proteins allow facilitated diffusion/co-transport;
5. Shape/charge of channel / carrier determines which substances move;
6. Number of channels/carriers determines how much movement;
7. Membrane surface area determines how much diffusion/movement;
8. Cholesterol affects fluidity/rigidity/permeability;