RP1: Rate of enzyme controlled reaction

    Cards (12)

    • Factors which affect enzyme controlled reactions

      Temperature, pH , enzyme concentartion and substrate concentartion
    • Hazard, risk and precaution from broken glass
      Cuts from sharp object
      Keep away from edge of desk
      Low
    • Hazard, risk and precaution from water bath/ hot liquids

      Scalding
      Use tongs/ eye protection
      Low- run under cold water
    • Hazard, risk and precaution from enzymes

      Allergies
      Avoid contact with skin/eyes
      Goggles
      Low
    • Conclusion of practical if temperature
      • As the temperature increases from 10°C,​ kinetic energy increases​​ so more enzyme-substrate complexes ​​form. This means that the rate of reaction increases​​ up to the optimum temperature.
      • At temperatures beyond the optimum, ​bonds​​ in the enzyme ​tertiary structure break​​, which changes the shape of the​ active site​​This means that the substrate and enzyme are no longer ​complementary​​.
    • Explain why the student did not add a buffer to the pH solution

      As measuring change in pH in experiment
    • Two variables the student controlled in experiment while investigating the effect of lipase concentration on the hydrolysis of lipids
      Temperature
      Volume of suspension of lipids
    • Give one other suitable control for experiment
      Boiled lipase solution
    • Explain results shown in graph of lipase experiment

      Fatty acids produced.
      Curve levels off as all of substrate is used up
    • The student repeated the lipase experiment with a higher concentartion of lipase solution. Explain results you would expect to find

      Faster fall in pH and levels off at same point
      More E-S complexes formed
      Same amount of fatty acides produced
    • Explain why cats were used in investigation as model organisms
      Mammals so likely to have same physiology as humans
      Can use a large number
      Small enough to keep in lab
    • How is a control set up when measuring enzyme activity?

      Replace enzyme solution with distilled water or boiled enzyme solution
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