To investigate the denaturation of an enzyme by heat.
|
PROCEDURE
- Place yeast solution in a beaker and place into the water bath at 1000C.
- Add the heated yeast and the buffer to a graduated cylinder.
- Add hydrogen peroxide to another cylinder.
- Stand the cylinders in a water bath until the desired temperature (250C) is reached
- Add the hydrogen peroxide into the cylinder containing the yeast and buffer.
- Note the presence or absence of foam formation and record.
- Repeat the experiment with yeast solution that was not boiled and compare results.
|
|
2008 Q9
Sample Answers
2008 Q9
- i – the pH at which the enzyme works best
ii – a denatured enzyme experiences a changed shape and loss of function
- i – enzyme used – catalase
ii – substrate – hydrogen peroxide
iii –
- 1In one graduated cylinder add hydrogen peroxide
- To the other, add enzyme, pH10 buffer and washing up liquid
- Place cylinders in water bath of boiling water for 10 minutes
- Control – place cylinders with identical content into water bath at 20 degrees for 10 minutes
- Mix tube A and Tube B.
- Start stopwatch and record foam at 2 minute intervals
*draw a diagram if needed*
Iv – Control – bubbles form as oxygen is produced
Denatured enzymes don’t produce bubbles as no reaction occurred to produce oxygen