The Chemical Building Blocks of Life. Chapter 3

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Transcription:

The Chemical Building Blocks of Life Chapter 3

Biological Molecules Biological molecules consist primarily of -carbon bonded to carbon, or -carbon bonded to other molecules. Carbon can form up to 4 covalent bonds. Carbon may be bonded to functional groups with specific properties. 2

3

Biological Molecules Isomers are molecules with the same chemical formula. -structural isomers -stereoisomers Chiral molecules are mirror-images of each other. 4

Biological Molecules 5

Biological Molecules Biological molecules are typically large molecules constructed from smaller subunits. Monomer: single subunit (mono = 1; -mer = unit) Polymer: many units (poly = many) 6

Biological Molecules dehydration synthesis: formation of large molecules by the removal of water -monomers are joined to form polymers hydrolysis: breakdown of large molecules by the addition of water -polymers are broken down to monomers 7

Biological Molecules 8

Carbohydrates Molecules with a 1:2:1 ratio of carbon, hydrogen, oxygen -empirical formula: (CH 2 O) n -examples: sugars, starch, glucose C H covalent bonds hold much energy Carbohydrates are good energy storage molecules. 9

Carbohydrates Glucose -a monosaccharide single sugar -contains 6 carbons -very important in energy storage -fructose is a structural isomer of glucose -galactose is a stereoisomer of glucose 10

Carbohydrates 11

Carbohydrates 12

Carbohydrates Disaccharides -2 monosaccharides linked together by dehydration synthesis -used for sugar transport or energy storage -examples: sucrose, lactose, maltose 13

Carbohydrates 14

Carbohydrates Polysaccharides -long chains of sugars -used for energy storage -plants use starch; animals use glycogen -used for structural support -plants use cellulose; animals use chitin 15

Carbohydrates 16

Carbohydrates 17

Carbohydrates 18

Carbohydrates 19

Carbohydrates 20

Carbohydrates 21

Nucleic Acids Two types: DNA and RNA Functions: specialized for the storage, transmission, and use of genetic information 22

Nucleic Acids Nucleic acids are polymers of nucleotides. -nucleotides: sugar + phosphate + nitrogenous base -sugar is deoxyribose in DNA or ribose in RNA -Nitrogenous bases include -purines: adenine and guanine -pyrimidines: thymine, cytosine, uracil 23

Nucleic Acids 24

Nucleic Acids 25

Nucleic Acids 26

Nucleic Acids DNA -nucleotides connected by phosphodiester bonds - double helix: 2 polynucleotide strands connected by hydrogen bonds -polynucleotide strands are complementary -genetic information is carried in the sequence of nucleotides 27

Nucleic Acids 28

Nucleic Acids RNA -contains ribose instead of deoxyribose -contains uracil instead of thymine -single polynucleotide strand -functions: -read the genetic information in DNA -direct the synthesis of proteins 29

Nucleic Acids 30

Nucleic Acids Other nucleotides -ATP: adenosine triphosphate -primary energy currency of the cell -NAD + and FAD: electron carriers for many cellular reactions 31

Proteins Protein functions include: 1. enzyme catalysts 2. defense 3. transport 4. support 5. motion 6. regulation 7. storage 32

Proteins Proteins are polymers of amino acids. Amino acids -20 different amino acids -joined by dehydration synthesis -peptide bonds form between adjacent amino acids 33

Proteins 34

Proteins Amino acid structure -central carbon atom surrounded by -amino group -carboxyl group -single hydrogen -variable R group 35

Proteins The structure of the R group dictates the chemical properties of the amino acid. Amino acids can be classified as: 1. nonpolar 2. polar 3. charged 4. aromatic 5. special function 36

Proteins The shape of a protein determines its function. -primary structure sequence of amino acids -secondary structure interaction of groups in the peptide backbone -α helix -β sheet 37

Proteins 38

Proteins 39

Proteins 40

Proteins Protein structure (continued) -tertiary structure folded shape of the polypeptide chain -quaternary structure interactions between multiple polypeptide subunits Protein folding is aided by chaperone proteins. 41

Proteins 42

Proteins Motifs are common elements of secondary structure seen in many polypeptides. Domains are functional regions of a polypeptide. 43

Proteins 44

Proteins Denaturation is a change in the shape of a protein, usually causing loss of function. -may involve complete unfolding -caused by changes in the protein s environment -ph -temperature -salt concentration 45

Proteins 46

Lipids Lipids are a group of molecules that are insoluble in water. A high proportion of nonpolar C H bonds causes the molecule to be hydrophobic. Two main categories: -fats (triglycerides) -phospholipids 47

Lipids Triglycerides (fats) -composed of 1 glycerol + 3 fatty acids Fatty acids are long hydrocarbon chains which may be -saturated -unsaturated -polyunsaturated 48

Lipids 49

Lipids 50

Lipids Triglycerides -an excellent molecule for energy storage -store twice as much energy as carbohydrates -animal fats are usually saturated fats and are solid at room temperature -plant fats (oils) are usually unsaturated and are liquid at room temperature 51

Lipids Phospholipids -composed of: -1 glycerol -2 fatty acids -a phosphate group Phospholipids contain polar heads and nonpolar tails. 52

Lipids 53

Lipids Phospholipids spontaneously form micelles or lipid bilayers. These structures cluster the hydrophobic regions of the phospholipid toward the inside and leave the hydrophilic regions exposed to the water environment. Lipid bilayers are the basis of biological membranes. 54

Lipids 55

Lipids 56