RP - The effect on PH on Enzyme activity
1) Put a drop of iodine solution into every well of a spotting tile.
2) Place a Bunsen burner on a heat-proof mat, and a tripod and gauze over the
Bunsen burner. Put a beaker of water on top of the tripod and heat the water until it is 35 °C. Try to keep the temperature of
mixture sampled every 30 seconds
the water constant throughout the experiment.
3. Use a syringe to add 1 cm° of amylase solution and 1 cm° of a buffer solution with a pH of 5 to a boiling tube. Using test tube holders, put the tube into the beaker. Using test tube holders, put tube in the beaker of the water and wait for 5 minutes
4. Next, use a different syringe to add 5 cm of a starch solution to the boiling tube.
5. Immediately mix the contents of the boiling tube and start a stop clock.
6. Use continuous sampling to record how long it takes for the amylase to break down all of the starch To do this, use a dropping pipette to take a fresh sample from the boiling tube every 30 seconds and put a drop into a well. When the iodine solution remains browny-orange, starch is no longer present.
7. Repeat the whole experiment with buffer solutions of different pH values to see how pH affects the time taken for the starch to be broken down.
8. Remember to control any variables each time (e.g. concentration and volume of amylase solution) to make it a fair test.