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Step 1
Cut 20 potato discs as a source of catalase
Step 2
Boil 10 of the potato discs for five minutes and leave the other 10 unboiled
Step 3
The unboiled discs will act as the control for comparison
Step 4
Add each set of discs to two identical tubes of catalase plus washing-up liquid plus pH buffer at 40°C
Step 5
measure the rate of enzyme activity by the height of foam after two minutes
Step 6
A typical result would be unboiled = 2cm of foam and boiled = 0 cm foam
Conclusion
Boiling has denatured the enzyme