- Enzyme extract
- 0.1 M citrate buffer, pH 4.8
- 10 mL pipette
8 mM DOPA
- Spectrophotometer and cuvettes
- Ice bath
- To determine the kinetic effects of the enzyme reaction, first, determine an
appropriate dilution of your enzyme extract. This will produce a reaction
rate of 5–10 micromoles of DOPA converted per minute. Prepare a serial
dilution of your enzyme extract. Place 9.0 mL of citrate buffer into each of
3 test tubes. Label the tubes 1/10, 1/100, and 1/1000.
- Pipette 1.0 mL of your enzyme extract into the first of these tubes (the one
labeled 1/10) and mix by inversion.
- Pipette 1.0 mL of the 1/10 dilution into the second tube (labeled as 1/100)
and mix by inversion.
- Pipette 1.0 mL of the 1/100 dilution into the third tube (labeled as 1/1000)
and mix by inversion.
- Place all of the dilutions in the ice bath until ready to use.
- If not already done, turn on a spectrophotometer, adjust to 475 nm, and
blank with a tube containing 2.5 mL of citrate buffer and 0.5 mL of enzyme
- Add 2.5 mL of 8 mM DOPA to each of 4 cuvettes or test tubes. Note that
each tube contains .0025 × .008 moles, or 20 micromole, of DOPA.
- Add 0.5 mL of undiluted enzyme extract to one of the tubes containing
the 8 mM DOPA. Mix by inversion, place into the spectrophotometer, and
immediately begin timing the reaction. Carefully measure the time required
for the conversion of 8 micromoles of DOPA. Note that since the cuvette
will contain a volume of 3.0 mL, the concentration when 8 micromoles
are converted will be 8/3.0 or 2.67 mM dopachrome. Use the data from
the standard curve to determine the absorbance equal to 2.67 mM
dopachrome. This absorbance value will be the end point for the reaction.
The absorbance equal to 3.33 mM dopachrome = _______
- As the reaction takes place within the spectrophotometer, the absorbance
will increase as dopachrome is formed. When the absorbance reaches the
value above, note the elapsed time from the mixing of the enzyme extract
with the 10 mM DOPA. Express the time as a decimal rather than minutes
and seconds. The time should be between 3 and 5 minutes. If the end point
is reached before 3 minutes, repeat step 8, but using the next dilution of
enzyme (i.e., the 1/10 after the undiluted, the 1/100 after the 1/10 and the
1/1000 after the 1/100).
The rate of activity = ________________ micromoles/minute/0.5 mL of
diluted extract. The dilution factor (inverse of dilution, 1,10,100, or 1000)
The activity of the undiluted enzyme is ____________ micromoles/
minute/0.5 mL or _____________ micromoles/minute/1.0 mL of extract.
- For the enzyme dilution that reaches the end point between 3 and 5
minutes, calculate the velocity of reaction. Divide the amount of product
formed (10 micromoles) by the time required to reach the end point.