| Dr. William H. Heidcamp, Biology Department, Gustavus Adolphus College
http://homepages.gac.edu/~cellab/chpts/chpt5/ex5-5.html
Materials
- Enzyme Extract
- 8 mM DOPA pH 6.6
- Incubators or Water baths adjusted to 10, 15, 20, 25, 30, 35 and 40° C 6
- Spectrophotometer and Cuvettes
- Stopwatch
Procedure
- Set up a series of test tubes each containing 2.5 ml of 8 mM DOPA buffered to a pH = 6.6. Place one tube in an ice bath or incubator adjusted to the following temperature; 10, 15, 20, 25, 30, 35 and 40° C
- Add 0.5 ml of an appropriately diluted enzyme extract (to yield 10 micromoles dopachrome in 3-5 minutes) to each of a second series of tubes. Place one each in the corresponding temperature baths. Allow all of the tubes to temperature equilibrate for 5 minutes. Do not mix the tubes.
- Beginning with the 10° C tube, and with the spectrophotometer adjusted to 475 nm and properly blanked, pour the enzyme (0.5 ml @ 10° C ) into the tube containing the DOPA and begin timing the reaction. Mix thoroughly. Note the time to reach the end point equivalent to the conversion of 10 micromoles of substrate.
- Repeat Step 3 for each of the listed temperatures, complete the following and plot the data.
Temperature (° C )
|
Time (Minutes) |
Micromoles of Dopachrome |
Velocity (Micromoles/Minute) |
10
|
|
10
|
|
15
|
|
10
|
|
20
|
|
10
|
|
25
|
|
10
|
|
30
|
|
10
|
|
35
|
|
10
|
|
40
|
|
10
|
|
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