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Life, 6th Edition

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Title: Life, 6th Edition


1
CHAPTER 3Macromolecules Their Chemistry and
Biology
2
Chapter 3 Macromolecules Their Chemistry and
Biology
  • Macromolecules Giant Polymers
  • Condensation Reactions
  • Proteins Polymers of Amino Acids
  • Carbohydrates Sugars and Sugar Polymers

3
Chapter 3 Macromolecules Their Chemistry and
Biology
  • Nucleic Acids Informational Macromolecules
  • Lipids Water-Insoluble Molecules
  • The Interactions of Macromolecules

4
Macromolecules Giant Polymers
  • Macromolecules are formed by covalent bonds
    between monomers and include polysaccharides,
    proteins, and nucleic acids.
  • Review Figure 3.1 and Table 3.1
  • 4

5
3.1
figure 03-01.jpg
  • Figure 3.1

6
Table 3.1
table 03-01.jpg
  • Table 3.1

7
Macromolecules Giant Polymers
  • Macromolecules have specific three-dimensional
    shapes.
  • Different functional groups give local sites on
    macromolecules specific properties.
  • 7

8
Condensation Reactions
  • Monomers are joined by condensation reactions.
  • Hydrolysis reactions break polymers into
    monomers.
  • Review Figure 3.2
  • 8

9
3.2
figure 03-02.jpg
  • Figure 3.2

10
Proteins Polymers of Amino Acids
  • Functions of proteins include support,
    protection, catalysis, transport, defense,
    regulation, and movement.
  • They sometimes require an attached prosthetic
    group.
  • 10

11
Proteins Polymers of Amino Acids
  • Twenty amino acids are found in proteins.
  • Each consists of an amino group, a carboxyl
    group, a hydrogen, and a side chain bonded to the
    a carbon atom.
  • Review Table 3.2
  • 11

12
Table 3.2 Part 1
table 03-02a.jpg
  • Table 3.2 Part 1

13
Table 3.2 Part 2
table 03-02bc.jpg
  • Table 3.2 Part 2

14
Table 3.2 Part 3
table 03-02d.jpg
  • Table 3.2 Part 3

15
Proteins Polymers of Amino Acids
  • Side chains of amino acids may be charged, polar,
    or hydrophobic.
  • SH groups can form disulfide bridges.
  • Review Table 3.2 and Figure 3.3
  • 15

16
3.3
figure 03-03.jpg
  • Figure 3.3

17
Proteins Polymers of Amino Acids
  • Amino acids are covalently bonded together by
    peptide linkages.
  • Review Figure 3.4
  • 17

18
3.4
figure 03-04.jpg
  • Figure 3.4

19
Proteins Polymers of Amino Acids
  • Polypeptide chains of proteins are folded into
    specific three-dimensional shapes.
  • Primary, secondary, tertiary, and quaternary
    structures are possible.
  • 19

20
Proteins Polymers of Amino Acids
  • The primary structure of a protein is the
    sequence of amino acids bonded by peptide
    linkages.
  • Review Figure 3.5
  • 20

21
Proteins Polymers of Amino Acids
  • Secondary structures are maintained by hydrogen
    bonds between atoms of the amino acid residues.
  • Review Figure 3.5
  • 23

22
3.5 Part 1
figure 03-05a.jpg
  • Figure 3.5 Part 1

23
Proteins Polymers of Amino Acids
  • The tertiary structure is generated by bending
    and folding of the polypeptide chain.
  • Review Figures 3.5
  • 24

24
Proteins Polymers of Amino Acids
  • The quaternary structure is the arrangement of
    polypeptides in a single functional unit
    consisting of more than one polypeptide subunit.
  • Review Figures 3.5, 3.7
  • 25

25
3.5 Part 2
figure 03-05b.jpg
  • Figure 3.5 Part 2

26
3.7
figure 03-07.jpg
  • Figure 3.7

27
Proteins Polymers of Amino Acids
  • Weak chemical interactions are important in the
    binding of proteins to other molecules.
  • Review Figure 3.8
  • 27

28
3.8
figure 03-08.jpg
  • Figure 3.8

29
Proteins Polymers of Amino Acids
  • Proteins denatured by heat, acid, or chemicals
    lose tertiary and secondary structure and
    biological function.
  • Review Figure 3.9
  • 29

30
3.9
figure 03-09.jpg
  • Figure 3.9

31
Proteins Polymers of Amino Acids
  • Chaperonins assist protein folding by preventing
    binding to inappropriate ligands.
  • Review Figure 3.10
  • 31

32
3.10
figure 03-10.jpg
  • Figure 3.10

33
Carbohydrates Sugars and Sugar Polymers
  • All carbohydrates contain carbon bonded to H and
    OH groups.
  • 33

34
Carbohydrates Sugars and Sugar Polymers
  • Hexoses are monosaccharides that contain six
    carbon atoms.
  • Review Figures 3.11, 3.12
  • 34

35
3.11
figure 03-11.jpg
  • Figure 3.11

36
3.12 Part 1
figure 03-12a.jpg
  • Figure 3.12 Part 1

37
3.12 Part 2
figure 03-12b.jpg
  • Figure 3.12 Part 2

38
Carbohydrates Sugars and Sugar Polymers
  • The pentoses are five-carbon monosaccharides.
  • Review Figure 3.12
  • 38

39
Carbohydrates Sugars and Sugar Polymers
  • Glycosidic linkages may have either a or b
    orientation in space.
  • They covalently link monosaccharides into larger
    units.
  • Review Figures 3.13, 3.14
  • 39

40
3.13
figure 03-13.jpg
  • Figure 3.13

41
3.14 Part 1
figure 03-14a.jpg
  • Figure 3.14 Part 1

42
3.14 Part 2
figure 03-14b.jpg
  • Figure 3.14 Part 2

43
Carbohydrates Sugars and Sugar Polymers
  • Cellulose, a polymer, is formed by glucose units
    linked by ß-glycosidic linkages between carbons 1
    and 4.
  • Review Figure 3.14
  • 43

44
Carbohydrates Sugars and Sugar Polymers
  • Starches are formed by a-glycosidic linkages
    between carbons 1 and 4 and are distinguished by
    amount of branching through glycosidic bonds at
    carbon 6.
  • Review Figure 3.14
  • 44

45
Carbohydrates Sugars and Sugar Polymers
  • Glycogen contains a-1,4 glycosidic linkages and
    is highly branched.
  • Review Figure 3.14
  • 45

46
Carbohydrates Sugars and Sugar Polymers
  • Chemically modified monosaccharides include the
    sugar phosphates and amino sugars.
  • A derivative of the amino sugar glucosamine
    polymerizes to form the polysaccharide chitin.
  • Review Figure 3.15
  • 46

47
3.15
figure 03-15.jpg
  • Figure 3.15

48
Nucleic Acids Informational Macromolecules
  • In cells, DNA is the hereditary material. DNA and
    RNA play roles in protein formation.
  • 48

49
Nucleic Acids Informational Macromolecules
  • Nucleic acids are polymers of nucleotides
    consisting of a phosphate group, a sugar, and a
    nitrogen-containing base.
  • The DNA bases are adenine, guanine, cytosine, and
    thymine.
  • In RNA uracil substitutes for thymine.
  • Review Figure 3.16 and Table 3.3
  • 49

50
3.16
figure 03-16.jpg
  • Figure 3.16

51
Table 3.3
table 03-03.jpg
  • Table 3.3

52
Nucleic Acids Informational Macromolecules
  • In the nucleic acids, bases extend from a
    sugarphosphate backbone.
  • DNA and RNA information resides in their base
    sequences.
  • 52

53
Nucleic Acids Informational Macromolecules
  • RNA is single-stranded.
  • DNA is a double-stranded helix with
    complementary, hydrogen-bonded base pairing
    between adenine and thymine and guanine and
    cytosine.
  • The two strands run in opposite directions.
  • Review Figures 3.17, 3.18
  • 53

54
3.17 Part 1
figure 03-17a.jpg
  • Figure 3.17 Part 1

55
3.17 Part 2
figure 03-17b.jpg
  • Figure 3.17 Part 2

56
3.18
figure 03-18.jpg
  • Figure 3.18

57
Nucleic Acids Informational Macromolecules
  • Comparing the DNA base sequences of different
    living species provides information on
    evolutionary relatedness.
  • 57

58
Lipids Water-Insoluble Molecules
  • Lipids can form gigantic structures, but these
    aggregations are not chemically macromolecules
    because individual units are not linked by
    covalent bonds.
  • 58

59
Lipids Water-Insoluble Molecules
  • Fats and oils are composed of three fatty acids
    covalently bonded to a glycerol molecule by ester
    linkages.
  • Review Figure 3.19
  • 59

60
3.19
figure 03-19.jpg
  • Figure 3.19

61
Lipids Water-Insoluble Molecules
  • Saturated fatty acids have a hydrocarbon chain
    with no double bonds.
  • The hydrocarbon chains of unsaturated fatty acids
    have one or more double bonds that bend the
    chain, making close packing less possible.
  • Review Figure 3.20
  • 61

62
3.20
figure 03-20.jpg
  • Figure 3.20

63
Lipids Water-Insoluble Molecules
  • Phospholipids have a hydrophobic hydrocarbon
    tail and a hydrophilic phosphate head.
  • Review Figure 3.21
  • 63

64
3.21
figure 03-21.jpg
  • Figure 3.21

65
Lipids Water-Insoluble Molecules
  • In water, the interactions of the hydrophobic
    tails and hydrophilic heads generate a
    phospholipid bilayer two molecules thick.
  • The head groups are directed outward, interacting
    with surrounding water.
  • Tails are packed in the interior.
  • Review Figure 3.22
  • 65

66
3.22
figure 03-22.jpg
  • Figure 3.22

67
Lipids Water-Insoluble Molecules
  • Carotenoids trap light energy in green plants.
    ß-Carotene can be split to form vitamin A, a
    lipid vitamin.
  • Review Figure 3.23
  • 67

68
3.23
figure 03-23.jpg
  • Figure 3.23

69
Lipids Water-Insoluble Molecules
  • Some steroids function as hormones.
  • Cholesterol is synthesized by the liver and has a
    role in some cell membranes, and in the digestion
    of other fats.
  • Review Figure 3.24
  • 69

70
3.24
figure 03-24.jpg
  • Figure 3.24

71
Lipids Water-Insoluble Molecules
  • Vitamins, required for normal functioning, must
    be acquired from the diet.
  • 71

72
The Interactions of Macromolecules
  • Both covalent and noncovalent linkages are found
    between the various classes of macromolecules.
  • 72

73
The Interactions of Macromolecules
  • Glycoproteins contain an oligosaccharide label
    that directs the protein to the proper cell
    destination.
  • The carbohydrate groups of glycolipids are on the
    cells outer surface, serving as recognition
    signals.
  • 73

74
The Interactions of Macromolecules
  • Hydrophobic interactions bind cholesterol to the
    protein that transports it in the blood.
  • 74
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