Topic 2: Beetroot core practical Flashcards

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1
Q

Beetroot cells contain large red pigment molecules called _________ in their _________.

A

betalains

vacuole

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2
Q

Normally, the betalains cannot pass through the ________ ________ (tonoplast) or the _______ _________. These membranes are not __________ to betalains.

A

vacuole membrane

cell membrane

permeable

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3
Q

But when beetroot cells are exposed to certain temperatures or put in alcohol this disrupts the vacuole membrane and the cell membrane (they become _________) and betalains can ______ through these membranes and leave the cell.

A

permeable

diffuse

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4
Q

Define diffusion in terms of betalains

1 point

A
  1. the betalains move from where they are in HIGH concentration inside the cell, to where they are in LOWER concentrations outside the cell, down the concentration gradient.
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5
Q

What happens when there is no longer a diffusion gradient? (in terms of betalains diffusing)
(2 points)

A
  1. Eventually an equilibrium will be reached between the inside of the cell and the outside of the cell
  2. even though the betalains are moving through the disrupted membrane in both directions, there is no NET movement (movement happens at the same rate in both directions).
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6
Q

What is the aim of the beetroot practical?

1 point

A
  1. To investigate the effect of temperature on the permeability of beetroot membranes
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7
Q

The _______ _____ the solution, the more betalain molecules have been able to move through the vacuole and cell membranes, so the more disrupted the membranes are and the ________ the membrane ____________.

A

darker pink

greater

permeability

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8
Q

Key Summary: What is the method for the beetroot practical?

7 steps

A
  1. Tissue named (e.g. beetroot, red cabbage) – controlled variable - pieces cut to same surface area & from same species of beetroot & same part of beetroot.
  2. Soak overnight and rinse to wash betalains off the beetroot pieces.
  3. Place one beetroot piece in water in at each temperature.
  4. Independent variable = temperature - 5 different temperatures for validity + control (normal temperature for beetroot) so 6 in total - 0, 10, 20, 30, 40, 50 (or alcohol concentrations – 0%, 1%, 2%, 3%, 4%, 5%) using {water bath to maintain different temperatures / dilution of same alcohol stock solution}.
  5. Controlled variable eg. same length of TIME in water bath – same {time of 30 minutes/ VOLUME of water in tube} – measure with pipette 5cm^3 (same temperature using water bath at 10⁰C if changing {ethanol/alcohol} concentration).
  6. Dependent variable = measure absorbance using a colorimeter, with blue-green filter, as a measure of membrane permeability (higher absorbance = higher membrane permeability).
  7. Repeat 5 times FOR EACH TEMPERATURE – identify anomalies, obtain 3 concordant results, calculate mean, increases reliability.
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9
Q

A _____ ______ filter ( ____ nm) is used - wavelength of light that the pink solution absorbs the most. This maximises the ________ of the results.

A

blue green

490

accuracy

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10
Q

A beam of ______ passes through the ______, through the _________ ________ and to the _________. The meter records the amount of _______ absorbed by the ________.

A

light

filter

beetroot solution

photocell

light

solution

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11
Q

The more concentrated (darker) the pink solution, the _______ the absorbance.

A

higher

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12
Q

(the effect of temperature on membrane permeability in beetroot practical)
Below 0 degrees C, ___ _________ may form and pierce the membrane, this may __________ the membrane permeability.

A

ice crystals

increase

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13
Q

Key Summary: What is the effect of temperature on membrane permeability?
(5 steps)

A
  1. INCREASED KINETIC ENERGY INCREASES MOVEMENT OF PHOSPHOLIPIDS
  2. Membrane PROTEINS ARE DENATURED (look at data if given to determine temperature at which this happens)
  3. More denaturation of proteins and disruption of membrane at higher temperatures
  4. Vacuole membrane and cell membrane break down, so are disrupted and become more permeable to betalains
  5. Betalains can escape FROM THE VACUOLE AND THE CELL through vacuole and cell membranes
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14
Q

(beetroot practical)
Name the independent variable (1 point)

How can it be varied? (2 points)

What is the control? (1 point)

A
  1. temperature
  2. 5 different temperatures + 1 control
  3. Using WATER BATHS at 0, 10, 20, 30, 40, 50 degrees C.
  4. control - usual temperature for growing beetroot (10 degrees C)
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15
Q

(beetroot practical)
Name the dependent variable (1 point)

How can it be measured? (1 point)

A
  1. % absorbance of the solution around the beetroot piece

1. Measured using a COLORIMETER

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16
Q

Why is using a colourimeter (to measure the % absorbance of the solution around the beetroot piece) better than just deciding which solution is darkest by eye?
(2 points)

A
  1. Colourimeter gives QUANTITATIVE data - numbers (colours are qualitative data)
  2. LESS SUBJECTIVE (as different people could rank colours differently)
17
Q

(beetroot practical)
What are the controlled organism variables?
(7 points)

A
  1. SAME SURFACE AREA (size) of beetroot pieces - measured using cork borer and ruler
  2. same species of beetroot - ideally cloned plants, so genetically identical
  3. same age of beetroot – seeds sown and beetroot picked at same time
  4. same growth conditions eg. soil pH, soil minerals
  5. same part of beetroot used eg. core
  6. same storage temperature
18
Q

Betalains are released when {cells / vacuole membranes} are cut and damaged, even though the membrane permeability has not changed.

How can we make sure there are no betalains on the surface of the beetroot piece before it is placed in the water? (1 point)

What if there are betalains on the surface of the beetroot piece when it is placed in the water? (1 point)

A
  1. SOAK AND RINSE BEETROOT PIECES to remove betalains from damaged (cut) cells before placing in water
  2. if they are not washed they would make the solution darker pink (higher absorbance), suggesting a higher permeability than there actually is
19
Q

How is the surface area of beetroot pieces controlled? (1 point)

A
  1. Cut cylinders or cubes to the same size using a cork borer, ruler and sharp scalpel
20
Q

Why is the surface area of beetroot pieces controlled? (2 points)

A
  1. If the area is larger there is more {surface area / more tissue} for betalains to be lost from,
  2. so solution will be darker (higher absorbance)
21
Q

How is the same beetroot {part/age/species/storage temperature} controlled? (3 points)

A
  1. grow beetroot plants from seeds from same packet.
  2. sown and harvested at the same time.
  3. stored in same conditions.
22
Q

Why is the beetroot {part/age/species/storage temperature} controlled? (1 point)

A
  1. Different {beetroots/parts of beetroot/ages} may have different {numbers or sizes of cells/number of betalains}
23
Q

(beetroot practical)
What are the controlled procedural variables & how are they controlled?
(3 points)

A
  1. Same VOLUME of water - 5cm3 measured using graduated pipette
  2. Incubation time - 30 minutes measured using stopclock
  3. Same {wavelength/filter} in colorimeter - set to 490nm
24
Q

(beetroot practical)
What are the controlled environmental variables & how are they controlled?
(1 point)

A
  1. SAME pH OF WATER that beetroot pieces are placed in - use a BUFFER
25
Q

Why is the volume of water in the test tube controlled? (1 point)

A
  1. If there is more water, the solution will be diluted more and solution will be lighter (lower absorbance)
26
Q

Why is the incubation time controlled? (1 point)

A
  1. If longer time there is more time for betalains to diffuse into water and solution will be darker (higher absorbance)
27
Q

Why is the pH of water in the test tube controlled? (1 point)

A
  1. pH may affect membrane proteins, making membrane more permeable
28
Q

(beetroot practical)]
Cut eight 1cm length sections of beetroot (same surface area) from a single beetroot. Soak in distilled water overnight.

What is the {purpose/justification} of this step?
(2 points)

A
  1. Soak and rinse beetroot pieces – to remove betalains released when cells are damaged(before placing in water),
  2. as they would make solution darker pink (higher absorbance)
29
Q

(beetroot practical)
Place eight labelled boiling tubes, containing 5cm^3 distilled water, into water baths (at 0, 10, 20, 30, 40, 50 C) and leave for 5 minutes. Place one beetroot section into each boiling tube and leave for 30 minutes.

What is the {purpose/justification} of this step?
(2 points)

A
  1. Leave for 5 minutes for water in tube to reach temperature of water bath
  2. Leave for 30 minutes for temperature to have an effect on membranes and any betalains to diffuse into water
30
Q

(beetroot practical)
Remove beetroot sections from boiling tubes, do not squeeze, and discard.

What is the {purpose/justification} of this step?
(1 point)

A
  1. Squeezing may damage cells or force more betalains out of beetroot
31
Q

(beetroot practical)
Switch on colorimeter, set it to read percentage absorbance and the filter to blue-green.

What is the {purpose/justification} of this step?
(1 point)

A
  1. Blue-green filter (490nm) - wavelength of light that the pink solution absorbs the most - maximises accuracy of results
32
Q

(beetroot practical)
Measure 2cm^3 of distilled water into a cuvette. Place in colorimeter. Make sure light is shining through the smooth side. Calibrate colorimeter to read absorbance for clear water.

What is the {purpose/justification} of this step?
(1 point)

A
  1. To calibrate the colourimeter
33
Q

(beetroot practical)
Place 2cm^3 of the beetroot solution into a cuvette and take a reading for absorbance.

What is the {purpose/justification} of this step?
(1 point)

A
  1. Absorbance gives a measure of how dark the solution is. Darker solution = more betalains = membrane more disrupted = more permeable
34
Q

(beetroot practical)
Repeat readings for all temperatures

What is the {purpose/justification} of this step?
(1 point)

A
  1. Identify anomalies, calculate mean, increases reliability
35
Q

If the effects of alcohol on membrane permeability was investigated instead of temperature, what would need to be changed? (4 points)

A
  1. Independent variable is alcohol (ethanol) concentration (%) - 0, 10, 20, 30, 40, 50%
  2. Controlled variable is temperature & volume of ethanol
  3. Temperature controlled by water bath at optimum temperature for beetroot membranes (e.g. 15 degrees C)
  4. Temperature controlled because temperature affects membrane permeability. If temperature increases, the rate of diffusion increases and solution will be darker (higher absorbance) after 30 minutes.
36
Q

Key Summary: How does {ethanol/alcohol} concentration effect the membrane permeability?
(5 points)

A
  1. ethanol causes the membrane to be disrupted (look at data to determine which concentration this happens at)
  2. ethanol DISSOLVES THE PHOSPHOLIPIDS
  3. ethanol DENATURES MEMBRANE PROTEINS
  4. the vacuole membrane and cell membrane break down, so are disrupted and become more permeable to betalains
  5. betalains can escape FROM THE VACUOLE AND THE CELL THROUGH VACUOLE AND CELL MEMBRANES
37
Q

List the experimental design question checklist (7 points)

A
  1. IV Independent variable - how many and range
  2. C Control (if applicable) + why it is needed
  3. DV Dependent variable + how it is measured (equipment and brief method)
  4. CVO/E Controlled variables – organism + environment - use the word ‘same’ and state equipment and value
  5. M Method – key details to make design hang together
  6. R Repeats + why they are needed
  7. S Safety (if relevant) - pair points – risk + how to minimise