Required Practicals Flashcards

1
Q

How to investigate the effects of osmosis on plant tissue

A
  1. Peel the potato as the skin can affect osmosis
  2. Produce three cylinders of potato using cork borer
  3. Trim the cylinders to the same length using a scalpel
  4. Measure length of each cylinder using ruler and measure the mass of each cylinder using a balance
  5. Place each cylinder into a test tube and add 10cm3 of a 0.5 molar sugar solution to first test tube
  6. Add 10cm3 of a 0.25 molar sugar solution to the second test tube and 10cm3 of distilled water to the third test tube
  7. Leave the potato cylinders overnight to allow osmosis to take place
  8. Remove the potato cylinders and gently roll them on paper towel to remove any surface moisture
  9. Measure length and mass of cylinders again and use the results to calculate the percentage change
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2
Q

How do you calculate percentage change

A

Change in value/original value x 100

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3
Q

How to carry out the test for starch

A
  1. Grind food sample with distilled water using a mortar and pestle
  2. Transfer paste to a beaker and add more distilled water and stir so the chemicals in the food dissolve in water
  3. Filter the solution to remove suspended food particles
  4. place 2cm3 of food solution into a test tube
  5. Add a few drops of iodine solution
  6. If starch is present then iodine solution will turn from orange to blue black
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4
Q

How do you test for sugars

A
  1. Grind food sample with distilled water using a mortar and pestle
  2. Transfer paste to a beaker and add more distilled water and stir so the chemicals in the food dissolve in water
  3. Filter the solution to remove suspended food particles
  4. Place 2cm3 of food solution into a test tube
  5. Add 10 drops of Benedict’s solution
  6. Place the test tube containing the solution into a beaker and Half fill the beaker with hot water from the kettle and leave it for 5 minutes
  7. If sugars are present the solution will turn from blue to brick red
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5
Q

How to test for protein

A
  1. Grind food sample with distilled water using a mortar and pestle
  2. Transfer paste to a beaker and add more distilled water and stir so the chemicals in the food dissolve in water
  3. Filter the solution to remove suspended food particles
  4. Take 2cm3 of food solution and place into a test tube
  5. Add 2cm3 of biuret solution
  6. If proteins are present then the solution will turn from blue to purple
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6
Q

How to test for lipids

A
  1. Grind food sample with distilled water using a mortar and pestle
  2. Transfer paste to a beaker and add more distilled water and stir so the chemicals in the food dissolve in water but do not filter solution
  3. Transfer 2cm3 of solution to a test tube
  4. Add a few drops of distilled water and a few drops of ethanol
  5. Gently shake the solution
  6. If lipids are present then the solution will turn from colourless to form a white cloudy emulsion
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7
Q

How to set up and use a microscope

A
  1. Place your prepared slide onto the stage and use the clips to hold it in place
  2. Select the lowest power objective lens
  3. Use the coarse focussing knob to move the stage up, just below the objective lens
  4. Look down the eyepiece and slowly use the coarse focussing knob to move the slide downwards until the image is roughly in focus
  5. Use the fine focussing knob to adjust the focus until you get a clear image
  6. If you need to see the slide with greater magnification, swap to higher powered objective lens and repeat the steps until focus.
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8
Q

Culturing microorganisms

A
  1. Clean the bench using disinfectant solution to kill by microorganisms that could contaminate our culture
  2. Sterilise an inoculating loop by passing it through a Bunsen burner flame
  3. Open a sterile agar plate near a Bunsen burner flame
  4. Spread the chosen bacteria evenly over the gar plate using the inoculating loop
  5. Place sterile filter paper discs containing different types or concentrations of antibiotics onto the plate, evenly distributed
  6. Attach Petri dish lid to the plate using adhesive tape
  7. Place plate upside down onto an incubator
  8. Incubate plate at 25*C for at least 48 hours
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