Module 2. Cell structure - (set 2) Flashcards

[Spec point: 2.1.3] microscopes (10 cards)

1
Q

Define Magnification

A
  • The number of times greater image is than size of the real (actual) object
  • Magnification = size of image / size of real object
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2
Q

Define Resolution

A

minimum distance apart 2 objects can be to be distinguished as separate objects

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3
Q

A scientist prepared a suspension of 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 marks]
[5.6 - JUN19] [AS]

A
  1. (Ice) cold to prevent/reduce enzyme activity;
  2. Buffered to prevent denaturing of enzyme/protein;
    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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4
Q

Explain why the solution the biologist used was ice-cold, buffered and the same water
potential as the liver tissue
(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
    Ignore damage
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5
Q

Describe and explain how cell fractionation and ultracentrifugation can be used to isolate mitochondria from a suspension of animal cells.
(5)

A
  1. Cell homogenisation to break open cells;
  2. Filter to remove (large) debris/whole cells;
  3. Use isotonic solution to prevent damage to mitochondria/organelles;
  4. Keep cold to prevent/reduce damage by enzymes / use buffer to prevent protein/enzyme denaturation;
  5. Centrifuge (at lower speed/1000 g) to separate nuclei/cell fragments/ heavy organelles;
  6. Re-spin (supernatant / after nuclei/pellet removed) at higher speed to get mitochondria in pellet/at bottom;
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6
Q

A biologist prepared a sample of organelles labelled C from liver.
Explain why the biologist used a blender and then filtered the mixture.
[2 marks]
[14d PMT]

A
  1. Break open cells / homogenise / produce homogenate;
  2. Remove unbroken cells / larger debris;
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7
Q

Describe how a sample of chloroplasts could be isolated from leaves.
[4 marks]
[5.1 - JUN21]

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; Accept isotonic, buffered
  3. Centrifuge/spin and remove nuclei/cell debris;
  4. (Centrifuge/spin) at high(er) speed, chloroplasts settle out;
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8
Q

Skin cells may be studied with a transmission electron microscope or an optical microscope. Explain the **advantages **and limitations of using a transmission electron microscope to study cells.
(6)

A
  1. TEM uses (beam of) electrons;
  2. These have short wavelength;
  3. Allow high resolution/greater resolution/Allow more detail to be seen/greater useful magnification;
  4. Electrons scattered (by molecules in air);
  5. Vacuum established;
  6. Cannot examine living cells;
  7. Lots of preparation/procedures used in preparing specimens/ fixing/staining/sectioning;
  8. May alter appearance/result in artefacts;
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9
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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10
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. Lower cover slip using mounted needle.
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