A. Structure and Function 1. Carbon a. Forms four (4) covalent bonds linked together in chains or rings Forms skeleton of basic biochemicals b.

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1 Biochemistry

2 2 A. Structure and Function 1. arbon a. Forms four (4) covalent bonds linked together in chains or rings Forms skeleton of basic biochemicals b. in three dimensions (3D) Diagrams in 2D may appear as 90 o angles Actual angle in 3D is o Tetrahedryl shape c.,,,

3 2. Functional Groups 3 ydroxyl Polar Alcohols and sugars arboxyl (Acid), Polar & acidic rganic acids, fatty acids, and amino acids

4 2. Functional Groups 4 Methyl 3 Nonpolar & hydrophobic Side chains, lipids Amino (Amine) N 2, N 3 + Polar & basic Amino acids; proteins

5 2. Functional Groups 5 Phosphate Polar & acidic DNA, RNA, ATP, and phospholipids 2 P 4, P 4, P 2-4

6 B. Macromolecules 6 Four Major lasses Fuels: arbohydrates and Lipids similar in all organisms sequence not coded by DNA Information: Proteins and Nucleic Acids distinctive in each organism unit sequence coded by DNA

7 1. arbohydrates 7 Fuel and Building Material Suffix -ose Size of carbon skeleton varies from 3 to 7 lassification # of arbon Example Triose 3 Glyceraldehyde Pentose 5 Ribose exose 6 Glucose

8 a. Monosaccharides 8 = simple sugars (one sweet) - (hydroxyl) attached to all but one remaining bonded to an oxygen = (carbonyl) 2:1 ratio of hydrogen to oxygen Glucose ( )

9 a. Monosaccharides 9 Soluble in water Taste sweet Many form rings in solution Galactose ( ) Deoxyribose ( ) 2 2

10 a. Monosaccharides 10 Many monosaccharides are isomers Same molecular formula Different structural formulas With different physical properties ( ) ( ) ( ) 2 Galactose 2 Glucose 2 2 Fructose

11 ondensation of Maltose 11 Dehydration Synthesis

12 ydrolysis of Maltose 12 Water is split (hydrolysis) Reverse reaction of condensation The metabolism of digestion ydrolysis

13 b. Disaccharides 13 = double sugars (two sweets) 2 monosaccharides joined by dehydration synthesis (condensation) Sucrose is a disaccharide of glucose & fructose 2 Glucose Fructose 2 2 Sucrose & Water 2

14 b. Disaccharides 14 Water is removed from the monosaccharides (dehydration) A disaccharide is produced (synthesis) 2:1 ratio of hydrogen to oxygen remains Part of the metabolism in many plants sucrose = table sugar (pure cane sugar) 2 2 2

15 c. Polysaccharides 15 = polymers of monosaccharides = complex carbohydrates formed by condensation polymerization glucose molecules linked by dehydration synthesis 4 basic types storage structure plants animals

16 c. Polysaccharides 16 4 basic types storage structure plants Starches animals Starches helical glucose polymer Amylose: 1, 4 linkages

17 17 4 basic types storage structure plants Starches animals Starches helical glucose polymer Amylose: 1, 4 linkages Amylpectin: 1, 4 with 1, 6 branching

18 c. Polysaccharides 18 4 basic types storage structure plants Starches ellulose animals ellulose linear glucose polymer 1, 4 and 4, 6 linkages plant cell walls fiber and wood

19 c. Polysaccharides 19 4 basic types storage structure plants Starches ellulose animals Glycogen Glycogen large glucose polymer 1, 4 and 4, 6 linkages extensively branched stored in liver and muscle tissue

20 c. Polysaccharides 20 4 basic types storage structure plants Starches ellulose animals Glycogen hitin hitin structural polymer of amino sugar similar to glucose arthropod exoskeletons fungi cell walls

21 21 Plant Starch (Amylose) Actually forms a spiral 2 Glucose Polymerization of glucose to form starch

22 Starch

23 ellulose Structure

24 ellulose 24

25 hitin N 2 3 N 2 N 2 N 2 N 3 3 3

26 hitin 26

27 2. Lipids 27 ydrophobic Molecules Nonpolar; mostly and Diverse a) Triglycerides b) Phospholipids c) Steroids

28 a. Triglycerides 28 Three fatty acids and a glycerol Glycerol has 3 carbons each with an group Each fatty acid has a group These condense to form triglyceride and three 2 (by dehydration synthesis)

29 Fatty Acids 29 Determines properties of fat ydrocarbon chain with a Most fats = 3 FAs + glycerol Glycerol: 3-carbon alcohol 3 s attract the of FAs Saturated - No = double bonds Unsaturated - ne or more = double bonds

30 3 chains may be the same or may differ a. Triglycerides 30 Variations are in the fatty acid composition: length of chain number and location of = bonds

31 31 Triglyceride Triglyceride (Fat) Formation Add 3 Fatty Acids Glycerol 3 Waters Remove These Waters

32 a. Triglycerides 32 Saturated Fats No = double bonds Maximum number of hydrogen Usually solid Beef Fat Animal sources

33 a. Triglycerides 33 Unsaturated Fats (ils) ne or more = double bonds Tails kink Linseed il Usually liquid Plant sources

34 b. Phospholipids 34 Two fatty acids, a polar head, and a glycerol Like a triglyceride 1 fatty acid swapped for polar phosphate Soap-like properties ydrophobic and ydrophilic ends omponent of ell Membranes

35 b. Phospholipids 35 Polar ead Glycerol Fatty Acid Tails ydrophilic ydrophobic

36 c. Fat-like Substances 36 omplex ring forms arotenoids holesterol Natural substance Found in cell surfaces

37 Steroids (holesterol derivatives) 37 holesterol Estradiol Testosterone

38 3. Proteins 38 Polymers of amino acids Molecular tools for multiple roles Enzymes i.e. amylase, catalase ormones i.e. insulin, glucagon arriers i.e. hemoglobin, cytochromes Structure i.e. collagen, myosin

39 a. Amino Acids 39 Small molecules 20 kinds 1 carboxyl group 1 amino group N 2 1 hydrogen atom 1 variable "R" group determines uniqueness Joined by peptide bonds to form polypeptide Different sequence makes different protein

40 a. Amino Acids 40 Amino Group arboxylic Acid Group R entral arbon R Group (20 variations)

41 d. Fibrous Protein 41 ollagen consists of three chains wrapped as a triple helix Fibrous structural, extended water insoluble

42 Pepsin d. Globular Protein digestive enzyme hydrolysis of peptide bonds 42 Globular non-structural compact, sherical

43 d. Protein Denaturation 43 Loss of function Process of unfolding or grossly changing the tertiary structure of a protein. igh temps Extreme p Salts

44 Amino Acids: Phenylalanine Structure 44 Amine Group arboxylic Acid Group Alpha arbon Phenylalanine R Group

45 Amino Acids: Leucine Structure 45 Amine Group arboxylic Acid Group Leucine R Group

46 Amino Acids: ysteine Structure 46 Amine Group arboxylic Acid Group ysteine R Group

47 b. Peptide Bond Phenylalanine Leucine 47 By ondensation between & N 2

48 b. Dipeptide Peptide Bond 48 Water

49 c. Structural omplexity 49 Primary: AA sequence, disulfide bridges Secondary: oiling of the chain helices or pleated sheets Tertiary: folding and rotating Quaternary: Two or more polypeptides chains

50 c. Structural omplexity Primary Tertiary (Sequence) (Folding) 50 Quaternary (Layering) Secondary (oiling)

51 helices or pleated sheets 51 Secondary Structures Insulin two chains a helix in the green chain two short helices in blue Fibronectin a cell adhesion protein consists entirely of beta-sheets

52 4. Nucleic Acids 52 Information polymers ondensation of nucleotides Phosphate of one nucleotide to Sugar of next nucleotide

53 a. Nucleotides 53 Each nucleotide is made of three parts a pentose (ribose or deoxyribose) a phosphate group ( P 4 ) a nitrogenous base (5 types source of variation)

54 54 a. Nucleotides N 2 Phosphate Group P 2 N N N N Deoxyribose or Ribose Nitrogenous Base (1 of 5) Pentose Sugar

55 a. Nucleotides 55 May make RNA or DNA Some are energy carriers (ATP, NAD) Some are chemical messengers (camp)

56 Nucleic Acid Molecule Nucleotides can be joined together into a chain 56 Result is a nucleic acid Nucleotide polymer DNA or RNA onnected by sugarphosphate backbone

57 yclic AMP: (Adenosine Monophosphate) N 2 57 Used for intracellular communication 2 N N N N Ribose P

58 ATP: (Adenosine Triphosphate) 58 Used for energy transfer N 2 from one molecule to another P P P 2 N N N N Deoxyribose or Ribose

59 59 oenzyme Structure N 2 P 2 N N N N Deoxyribose or Ribose

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