Required practical 1 Flashcards
Investigation into the effect of a named variable on the rate of an enzyme-controlled reaction.
Give examples of variables that could affect the rate of an enzyme controlled reaction
● Enzyme concentration / volume
● Substrate concentration / volume
● Temperature of solution
● pH of solution
● Inhibitor concentration
Any one of these can be the independent variable
and need to be varied (eg. by preparing a dilution
series of varying concentrations). All others (except
inhibitors) would be control variables so would
need to be kept constant.
Describe how temperature can be
controlled. (2)
● Use a thermostatically controlled water bath
● Monitor using a thermometer at regular intervals
and add hot / cold water if temperature fluctuates
Describe how pH can be controlled. (2)
● Use a buffer solution
● Monitor using a pH meter at regular intervals
Why were enzyme & substrate solutions left in
water baths for 10 mins before mixing? (1)
● So solutions equilibrate / reach the temperature of
the water bath
Describe a control experiment. (2)
● Use denatured enzymes (eg. by boiling)
● Everything else same as experiment, eg. same conc.
/ volume of substrate (at start) and enzyme, same
type / volume of buffer solution, same temperature
Describe how the rate of an enzyme-controlled reaction can be measured
● Measure time taken for reaction to reach a set point,
eg. concentration / volume / mass / colour of
substrate or product
○ Rate of reaction = 1 / time; example units = s
-1
● Measure concentration / volume / mass / colour of
substrate or product at regular intervals (or using a
continuous data logger) throughout reaction
○ Plot on a graph with time on the x axis and
whatever is being measured on the y axis
○ Draw a tangent at t = 0 (or any other time for
rate at a particular point)
○ Initial rate of reaction = change in y / change in
x; example units = cm3 s
-1
Suggest a safety risk and explain
how to reduce this risk. (2)
● Handling enzymes may cause an allergic reaction
● Avoid contact with skin by wearing gloves and eye protection
Explain why using a colorimeter to
measure colour change is better
than comparison to colour
standards. (2)
Not subjective
● More accurate
Explain a procedure that could be
used to stop each reaction. (1)
● Boil / add strong acid / alkali → denature enzyme
● Put in ice → lower kinetic energy so no enzyme-substrate
complexes form
● Add high concentration of inhibitor → no enzyme-substrate
complexes form
Describe how processed data can be presented as a graph
- Label x-axis with ‘[named independent variable] / [units]’ and y-axis with ‘rate of reaction / [units]’
- Plot a linear scale on each axis that will allow the graph to occupy over half available space
- Mark data points with crosses
- Join data points by straight lines if intermediate values are not known
OR draw a line / curve of best fit if there is a clear trend
Explain why the rate of reaction decreases over time throughout each
experiment
● Initial rate is highest as substrate concentration not limiting / many
enzyme-substrate complexes form
● Reaction slows as substrate used up and often stops as there is no substrate left