Chapter 28 Nucleosides, Nucleotides, and Nucleic Acids

1. Chapter 28Nucleosides, Nucleotides,and Nucleic Acids

2. 28.1Pyrimidines and Purines

3. Pyrimidines and Purines • In order to understand the structure and properties of DNA and RNA, we need to look at their structural components. • We begin with certain heterocyclic aromatic compounds called pyrimidines and purines.

4. 6 6 7 5 1 5 N N 1 N 8 4 2 2 9 N H 4 N N 3 3 Pyrimidines and Purines • Pyrimidine and purine are the names of the parent compounds of two types of nitrogen-containing heterocyclic aromatic compounds. Pyrimidine Purine

5. H NH2 H N N N H H2N H N H N N H Pyrimidines and Purines • Amino-substituted derivatives of pyrimidine and purine have the structures expected from their names. 4-Aminopyrimidine 6-Aminopurine

6. H H H H N N HO H O H N N H Pyrimidines and Purines • But hydroxy-substituted pyrimidines and purines exist in keto, rather than enol, forms. enol keto

7. O OH H N N N H N H N H N N H N H H keto Pyrimidines and Purines • But hydroxy-substituted pyrimidines and purines exist in keto, rather than enol, forms. enol

8. O O CH3 HN HN O O NH NH Important Pyrimidines • Pyrimidines that occur in DNA are cytosine and thymine. Cytosine and uracil are the pyrimidines in RNA. NH2 HN O NH Uracil Thymine Cytosine

9. NH2 O N N HN N NH NH H2N N N Important Purines • Adenine and guanine are the principal purines of both DNA and RNA. Adenine Guanine

10. O O CH3 CH3 H3C N N N HN N O O N N N CH3 CH3 Caffeine Theobromine Caffeine and Theobromine • Caffeine (coffee) and theobromine (coffee and tea) are naturally occurring purines.

11. 28.2Nucleosides

12. Nucleosides • The classical structural definition is that a nucleoside is a pyrimidine or purine N-glycoside of D-ribofuranose or 2-deoxy-D-ribofuranose. • Informal use has extended this definition to apply to purine or pyrimidine N-glycosides of almost any carbohydrate. • The purine or pyrimidine part of a nucleoside is referred to as a purine or pyrimidine base.

13. NH2 N N O HOCH2 O HO OH Table 28.2 • Pyrimidine nucleosides Cytidine Cytidine occurs in RNA; its 2-deoxy analog occurs in DNA

14. O H3C NH O N HOCH2 O HO Table 28.2 • Pyrimidine nucleosides Thymidine Thymidine occurs in DNA

15. O NH O N HOCH2 O HO OH Table 28.2 • Pyrimidine nucleosides Uridine Uridine occurs in RNA

16. NH2 N N N N HOCH2 O HO OH Table 28.2 • Purine nucleosides Adenosine Adenosine occurs in RNA; its 2-deoxy analog occurs in DNA

17. O N NH N NH2 N HOCH2 O HO OH Table 28.2 • Purine nucleosides Guanosine Guanosine occurs in RNA; its 2-deoxy analog occurs in DNA

18. 28.3Nucleotides • Nucleotides are phosphoric acid esters of nucleosides.

19. NH2 O N OCH2 HO N P 5' HO N N O 1' 4' 3' 2' HO OH Adenosine 5'-Monophosphate (AMP) • Adenosine 5'-monophosphate (AMP) is also called 5'-adenylic acid.

20. NH2 N N O O N N OCH2 HO O P P O HO HO HO OH Adenosine Diphosphate (ADP)

21. NH2 N N O O O N N HO OCH2 P O O P P O HO HO HO HO OH Adenosine Triphosphate (ATP) • ATP is an important molecule in several biochemical processes including:energy storage (Sections 28.4-28.5)phosphorylation

22. HOCH2 O O HO HO ATP + HO HO HO HO OH OH O (HO)2POCH2 ADP + ATP and Phosphorylation hexokinase This is the first step in the metabolism of glucose.

23. NH2 N N N N CH2 O O O OH P O HO cAMP and cGMP • Cyclic AMP and cyclic GMP are "second messengers" in many biological processes. Hormones (the "first messengers") stimulate the formation of cAMP and cGMP. Cyclic adenosine monophosphate (cAMP)

24. O N NH N NH2 N CH2 O O OH O P O HO cAMP and cGMP • Cyclic AMP and cyclic GMP are "second messengers" in many biological processes. Hormones (the "first messengers") stimulate the formation of cAMP and cGMP. Cyclic guanosine monophosphate (cGMP)

25. 28.4Bioenergetics

26. Bioenergetics • Bioenergetics is the thermodynamics of biological processes. • Emphasis is on free energy changes (DG) • when DG is negative, reaction is spontaneous in the direction written • when DG is 0, reaction is at equilibrium • when DG is positive, reaction is not spontaneous in direction written

27. mA(aq) nB(aq) Standard Free Energy (DG°) • Sign and magnitude of DG depends on what the reactants and products are and their concentrations. • In order to focus on reactants and products, define a standard state. • The standard concentration is 1 M (for a reaction in homogeneous solution). • DG in the standard state is called the standard free-energy change and given the symbol DG°.

28. mA(aq) nB(aq) Standard Free Energy (DG°) • Exergonic: An exergonic reaction is one for which the sign of DG° is negative. • Endergonic: An exergonic reaction is one for which the sign of DG° is positive.

29. mA(aq) nB(aq) Standard Free Energy (DG°) • It is useful to define a special standard state for biological reactions. • This special standard state is one for which the pH = 7. • The free-energy change for a process under these conditions is symbolized as DG°'.

30. 28.5ATP and Bioenergetics

31. Hydrolysis of ATP ATP + H2O ADP + HPO42– • G°' for hydrolysis of ATP to ADP is –31 kJ/mol • Relative to ADP + HPO42–, ATP is a "high-energy" compound. • When coupled to some other process, the conversion of ATP to ADP can provide the free energy to transform an endergonic process to an exergonic one.

32. –OCCH2CH2CHCO– + NH4+ +NH3 O O O O H2NCCH2CH2CHCO– + H2O +NH3 Glutamic Acid to Glutamine DG°' = +14 kJ Reaction is endergonic

33. DG°' = –17 kJ O O O O H2NCCH2CH2CHCO– + HPO42– + ADP +NH3 Glutamic Acid to Glutamine –OCCH2CH2CHCO– + NH4+ + ATP +NH3 Reaction becomes exergonicwhen coupled to the hydrolysisof ATP

34. O O O O O P OCCH2CH2CHCO– + ADP –O –O +NH3 Glutamic Acid to Glutamine –OCCH2CH2CHCO– + ATP +NH3 Mechanism involvesphosphorylation of glutamic acid

35. H2NCCH2CH2CHCO– + HPO42– +NH3 O O O O O P OCCH2CH2CHCO– + NH3 –O –O +NH3 Glutamic Acid to Glutamine followed by reaction of phosphorylated glutamic acid with ammonia