1. HOW ENZYMES FUNCTION © 2012 Pearson Education, Inc.

2. What do we already know about enzymes Enzymes are biological catalysts MOST enzymes are proteins (some are made of RNA called ribozymes…) Suffix –ase Speed up Chemical Reactions

3. Why are enzymes so important??

4. How do enzymes lower the activation energy of a chemical reaction? They physically position their substrates in orientations that increase the likelihood of chemical bonds being broken or formed. They do NOT participate in the reaction, they set the stage for it!

5. What is the induced fit model of enzyme activity? If this were the chemical reaction that catalase is responsible for…

6. Figure 5.14_s1 1 Enzyme (sucrase) Active site Enzyme available with empty active site

7. Figure 5.14_s2 2 1 Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit

8. Figure 5.14_s3 32 1 Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit Substrate is converted to products H2OH2O

9. Figure 5.14_s4 4 32 1 Products are released Fructose Glucose Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit Substrate is converted to products H2OH2O

10. Some enzymes need a little help in order to function properly…Cofactors and Coenzymes

11. Some environmental factors can impact the levels of enzyme activity…Some of these factors modify the SHAPE of the enzyme, where as others limit the number of ENZYME-SUBSTRATE interactions that can take place….What are some of these factors? pH Temperature Enzyme Concentration Substrate Concentration

12. How can we measure enzyme activity?  Appearance of a Product  Disappearance of a substrate  Indirect Ways: Ex: Color Change, Change in Temp, Bubble formation

13. Figure 5.UN02 ATP cycle ATP ADP P Energy from exergonic reactions Energy for endergonic reactions Quick Review of Exergonic and Endergonic Reactions

14. Why do you think it is important that enzyme activity is tightly regulated?

15. What are some ways in which enzyme activity can be regulated?  Gene Expression Regulation – Do not produce the enzyme unless it is needed! –Example: Digestive Enzymes  Competitive Inhibition  Noncompetitive Inhibition

16. Figure 5.15A Substrate Enzyme Allosteric site Active site Normal binding of substrate Competitive inhibitor Noncompetitive inhibitor Enzyme inhibition

17.  Competitive inhibitors © 2012 Pearson Education, Inc.

18.  Noncompetitive inhibitors (Allosteric Regulation) © 2012 Pearson Education, Inc.

19. Feedback Inhibition*** - Is this competitive or noncompetitive inhibition?

20.  The product of a metabolic pathway (multi-step enzyme catalyzed) may act as an inhibitor of one of the enzymes in the pathway. © 2012 Pearson Education, Inc.

21. Figure 5.15B Feedback inhibition Starting molecule Product Enzyme 1 Enzyme 2 Enzyme 3 Reaction 1 Reaction 2 Reaction 3 A B C D

23. What is activation energy?  The energy barrier that must be overcome before a chemical reaction can begin © 2012 Pearson Education, Inc.

24. Figure 5.13A_1 Activation energy barrier Reactant Products Without enzyme Energy

25. How do cells overcome the energy barrier in order for a reaction to occur?  The use of ENZYMES!!!! (Catalysts) © 2012 Pearson Education, Inc.

26. Figure 5.13A Activation energy barrier Reactant Products Without enzyme With enzyme Reactant Products Enzyme Activation energy barrier reduced by enzyme Energy

27. Figure 5.13Q Reactants Products Energy Progress of the reaction a b c Which line represents an enzyme-catalyzed reaction?

28. What are some key features of enzyme activity?  biological catalysts that lower the E A needed for a reaction to begin,  increase the rate of a reaction without being consumed by the reaction, and  are usually proteins, although some RNA molecules can function as enzymes (ribozymes). © 2012 Pearson Education, Inc.

29. Animation: How Enzymes Work Right click on animation / Click play

30. Enzymes are very selective and specific in their activity…  The specific reactant that an enzyme acts on is called the enzyme’s substrate.  A substrate fits into a region of the enzyme called the active site.  Enzymes are specific because their active site fits only specific substrate molecules.  Tertiary structure accounts for the specificity © 2012 Pearson Education, Inc.

31. 5.14 A specific enzyme catalyzes each cellular reaction  The following figure illustrates the catalytic cycle of an enzyme. © 2012 Pearson Education, Inc.

32. Figure 5.14_s1 1 Enzyme (sucrase) Active site Enzyme available with empty active site

33. Figure 5.14_s2 2 1 Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit

34. Figure 5.14_s3 32 1 Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit Substrate is converted to products H2OH2O

35. Figure 5.14_s4 4 32 1 Products are released Fructose Glucose Enzyme (sucrase) Active site Enzyme available with empty active site Substrate (sucrose) Substrate binds to enzyme with induced fit Substrate is converted to products H2OH2O

37. They physically position their substrates (reactants) in orientations that increase the likelihood of chemical bonds being broken or formed. They do NOT participate in the reaction, they set the stage for it! 5 How do enzymes help to lower the activation energy needed for a reaction to occur?

38. Explain the role of cofactors and coenzymes  Groups of atoms that bind to the enzyme for proper functioning  Organic coenzymes (vitamins) or inorganic co-factors (minerals)  Ex: DNA interaction enzymes require Zinc 2+  Ex: NAD and FAD carry electrons

39. Common Cofactors and Coenzymes

40. Table 5.UN05

41. How does substrate concentration affect enzyme activity?  Enzyme rate will increase and then remain constant (assuming constant amount of enzyme)

42. How does enzyme concentration affect enzyme activity?  Assuming that there is always substrate available…enzyme rate will increase!

43. How does temperature affect enzyme activity?  Temperature affects molecular motion.  Optimum temperature = maximum rate of activity  Below = slow movement  Above = denaturation

44. How does pH affect enzyme activity?  Optimum pH varies  Denaturation occurs both above and below optimum

45. Why is it important that metabolic pathways (enzyme activity) are regulated? Thousands of chemical reactions are occurring in cells simultaneously. Regulation of enzymes and thus reaction rates helps maintain internal homeostasis.

46. Figure 5.15A Substrate Enzyme Allosteric site Active site Normal binding of substrate Competitive inhibitor Noncompetitive inhibitor Enzyme inhibition

47.  Competitive inhibitors –block substrates from entering the active site and –reduce an enzyme’s productivity. © 2012 Pearson Education, Inc.

48.  Noncompetitive inhibitors (Allosteric Regulation) –bind to the enzyme somewhere other than the active site, –change the shape of the active site, and –prevent the substrate from binding. © 2012 Pearson Education, Inc.

50. 5.15 Enzyme inhibitors can regulate enzyme activity in a cell  In some reactions, the product may act as an inhibitor of one of the enzymes in the pathway that produced it. This is called feedback inhibition.  Can be positive or negative feedback © 2012 Pearson Education, Inc.

52. Figure 5.15B Feedback inhibition Starting molecule Product Enzyme 1 Enzyme 2 Enzyme 3 Reaction 1 Reaction 2 Reaction 3 A B C D