1. The Metabolic Pathway of Shikimic Acid Aromatic Amino Acids Phenolic Compounds Jan Michael O. Santos Philippine Normal University College of Science Department of Physical Sciences

2. Outline of Discussion 1. Shikimic Acid Pathway a.Origin of Shikimic Acid b.Starting Material c.Enzymes d.Pathway- Mechanism e.Product

3. 2. Aromatic Amino Acids a.What are the Aromatic Amino Acids b.Starting Material c.Enzymes d.Pathway- Mechanism e.Products

4. 3. Phenolic Compounds a.What are Phenolic Compounds b.Starting Material c.Enzymes d.Pathway- Mechanism e.Products

5. DEFINITION OF TERMS 1.Shikimic acid or shikimate: is an important biochemical metabolite in plants and microorganisms. 2.Aromatic compound: is a hydrocarbon with alternating double bonds and single bonds between carbon atoms 3.Amino acids: are molecules containing an amine group, a carboxylic acid group and a side chain (specific)

6. 4. Phenolic Compounds: are a large and diverse group of molecules, which includes many families of aromatic secondary metabolite in plants. 5. Enzymes: are group of molecules that serve as a catalyst with a high degree of specificity for a certain substrate or class of substrates. It can only act on one substrate or on a family of structurally similar substrates.

7. MAJOR ENZYMES 1.Synthase: Joints two molecules together w/o hydrolyzing a pyrophosphate bond. 2.Dehydratase: Removes water to create a double bond 3.Dehydrogenase: Removes hydrogen atom from its substrate 4.Kinase: Transfer a phosphate group from a high-energy phosphate compound such as ATP to its substrate.

8. SHIKIMIC ACID

9. Where this came from? Shikimi Illicium anisatum

10. Shikimic acid is a precursor for: 1.Aromatic amino acids phenylalanine and tyrosine 2.Indole, and indole derivatives and a.a.a tryptophan 3. Alkaloids 4.Phenylpropanoids, flavonoids, tannins, and lignins.

11. FORMATION OF SHIKIMIC ACID Starting materials 1 st : Pyruvate to Phospoenolpyruvate

12. FORMATION OF SHIKIMIC ACID 2 nd : Erthryrose-4-phosphate

13. FORMATION OF SHIKIMIC ACID Analyze this reaction, what are the other materials involve?

14. FORMATION OF SHIKIMIC ACID 3-deoxy-D-arabinoheptulosonate 7- phosphate (DAHP) synthase is the first enzyme in a series of metabolic reactions known as the shikimate pathway. Since it is the first enzyme in the shikimate pathway, it controls the amount of carbon entering the pathway.

15. FORMATION OF SHIKIMIC ACID

16. H+ erythrose-4-phosphate phosphoenol pyruvate H+ shikimic acid NADPH H+ FORMATION OF SHIKIMIC ACID B:

17. FORMATION OF SHIKIMIC ACID 3-dehydroquinate synthase is the second enzyme of the shikimate pathway. It catalyzes the elimination of phosphate from DAHP to generate 3-dehydroquinate (DHQ).

18. FORMATION OF SHIKIMIC ACID

20. 3-Dehydroquinate Dehydratase (DHQD) catalyzes the third step of the shikimate pathway, dehydration of 3-dehydroquinate to 3-dehydroshikimate.

21. FORMATION OF SHIKIMIC ACID

23. Shikimate-5-Dehydrogenase (SDH) The fourth step of the shikimate pathway is the reduction of DHS to shikimate. the reaction is catalyzed by an NADP-dependent shikimate dehydrogenase (SHD)

24. FORMATION OF SHIKIMIC ACID

26. Shikimate Kinase (SK)- In the fifth step of the shikimate pathway, shikimate kinase catalyzes the specific phosphorylation of the 3-hydroxyl group of D-shikimate to yield shikimate 3-phosphate using ATP as a co- subtrate

27. FORMATION OF SHIKIMIC ACID

29. 5-Enolpyruvylshikimate 3-Phosphate Synthase (EPSPS) is the sixth enzyme of the shikimate pathway. It catalyzes the reversible formation of 5-enolpyruvyl-shikimate-3- phosphate (EPSP) from shikimate 3- phosphate and PEP.

30. FORMATION OF SHIKIMIC ACID

32. Chorismate Synthase (CS) The seventh and final step in the main trunk of the shikimate pathway is the trans-1,4 elimination of phosphate from EPSP to yield chorismate

33. FORMATION OF SHIKIMIC ACID In this reaction, the second of the three double bonds of the benzene ring is introduced. The reaction is catalyzed by chorismate synthase and requires reduced flavin for activity even though the overall reaction is redox neutral.

34. FORMATION OF SHIKIMIC ACID

36. SHIKIMIC ACID TO AROMATIC ACID The seven-step shikimate pathway links the metabolism of carbohydrates to the biosynthesis of aromatic amino acids and many aromatic secondary metabolites, including tetrahydrofolate and ubiquinone.

38. Aromatic Amino Acids

39. 1. What are aromatic amino acids? Aromatic Amino Acids are amino acids that include an aromatic ring. Example includes: Phenylalanine, Tryptophan, Histidine, Tyrosine (but only F, W, Y can be synthesized by Shikimate pathway)

40. The Aromatic Family  In plants and microorganism: Phe, Tyr, and Trp  Precursors are: PEP ERYTHROSE-4-PHOSPHATE CHORISMATE

41. The Starting Material CHORISMATE

42. Enzymes Isomerase is an enzyme that catalyzes the structural rearrangement of isomers. Mutase: catalyzes the shifting of a functional group from one position to another within the same molecule. Transferase: catalyzes the transfer of a functional group (methyl or phosphate)from one molecule to another

43. The Pathway

44. The Mechanisms From Chorismate to Prephenate

45. The Mechanisms What is Claisen Rearrangement? Claisen Rearrangement is a powerful carbon-carbon bond- forming chemical reaction discovered by Rainer Ludwig Claisen.

46. In NMR spectrum (chair conformation)

47. Chair and Boat Conformation

48. OVER-ALL STRUCTURE CHORISMATEPREPHENATE

49. Phenylalanine Biosynthesis

50. Prephenate dehyrdatase to Phenylpyruvate

51. The Mechanism Phenylpyruvate to Phenylalanine Phenylalanine aminotransferase catalyze this reaction

52. The Mechanisms Prephenate to Phenylpyurvate to Phenylalanine

53. SOURCES OF ESSENTIAL AMINO ACIDS Phenylalanine

54. Tyrosine Biosynthesis

55. The Mechanism Prephenate to p-Hydroxyphenylpyruvate Prephenate dehydrogenase catalyzed this reaction.

56. The Mechanism p-Hydroxyphenylpyruvate to Tyrosine Tyrosine aminotransferase catalyzed this reaction

57. SOURCES OF ESSENTIAL AMINO ACIDS Tyrosine

58. OVER-ALL PATHWAY

59. Tryptophan Biosynthesis

60. The Mechanism This reaction is catalyzed by athranilate synthase

61. The Mechanism This reaction is catalyzed by athranilate phosphoribosyl transferase

62. The Mechanism This reaction is catalyzed by phosphoribosyl athranilate isomerase.

63. The Mechanism This reaction is catalyzed by indole-3- glucerol phosphate synthase.

64. This reaction is catalyzed by tryptrophan synthase

65. OVER-ALL PATHWAY

66. SOURCES OF ESSENTIAL AMINO ACIDS Tryptophan

67. SOURCES OF ESSENTIAL AMINO ACIDS Phenylalanine

68. SOURCES OF ESSENTIAL AMINO ACIDS Tyrosine

69. SOURCES OF ESSENTIAL AMINO ACIDS Tryptophan

70. AMINO ACID DEGRADATION INTERMEDIATES CO 2 Pyruvate Acetyl-CoA Acetoacetate Citrate Isocitrate  -ketoglutarate Succinyl-CoA Fumarate Oxaloacetate Citric Acid Cycle CO 2 Glucose AlaSer CysThr* GlyTrp* Ile* Leu Lys Thr* Leu Trp* Lys Tyr* Phe* Asn Asp Phe* Tyr* Ile* Met Val ArgHis GluPro Gln Glucogenic Ketogenic * Both Glucogenic and Ketogenic Purely Ketogenic

72. PHENOLICS These are the class of natural occuring compound with one or more phenolic compounds or benzene ring with –OH group. Quercetin, a typical flavonoid, is a natural phenol

73. BIOSYNTHESIS OF PHENOLICS Most of the natural phenols are derived from secondary plant metabolism of the shikimic acid pathway, malic acid pathway or both.

75. APPLICATIONS One very good example are HORSE GRAMS- a kind of beans

76. SOURCES OF PHENOLIC ACIDS Horse Grams/ beans has the following kinds of phenolic acids: Protocatechuic acid Caffeic Acid p-coumaric acid

77. Thank You for Listening!