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Macromolecules
Chapter 5
All are polymers
Monomer – subunit of polymer
Macromolecule – large organic polymer
Those found in living systems:
Carbohydrates
Lipids
Proteins
Nucleic acids
MUST KNOW for each group
• Monomers
• Type of bond or linkage between monomers
• Examples – in living systems
• Functions – in living systems
Carbohydrates
• C, H, O
• Monomer= Monosaccharide (like glucose)
Lipids
• C, H, O
• Monomer = glycerol and fatty acids
Proteins
• C, H, O, N
• Monomer = Amino Acid
Nucleic Acid
• C, H, O, N, P
• Monomer = Nucleotide
Polymerization reactions
• Condensation (dehydration synthesis)
– Monomers join covalently
– Removal of water molecule
– One monomer loses –0H
– One loses –H
– These join to form water
– Requires energy and catalysts (enzymes)
• Hydrolysis– Breaks covalent bond by addition of water
– Digestive enzymes catalyze hydrolysis
• 40-50 common monomers (unity)
• Arranged in different ways (diversity)
Compare dehydration synthesis with hydrolysis
Carbohydrates
• Monomers – monosaccharide (usually multiples of CH2O like C6H12O6)
–Glucose, fructose, galactose–Glucose most common
• Stores energy in chemical bonds
Dihydroxyacetone
Ribulose
Ket
oses
Ald
oses
Fructose
Glyceraldehyde
Ribose
Glucose Galactose
Hexoses (C6H12O6)Pentoses (C5H10O5)Trioses (C3H6O3)
(a) Linear and ring forms (b) Abbreviated ring structure
Disaccharide
• double sugar (2 monosaccharides)
• Dehydration synthesis –> formula ?
• Glycosidic linkage formed-covalent bond forms by dehydration syn.
• Glucose + glucose = maltose
• Glucose + galactose = lactose
• Glucose + fructose = sucrose
Dehydration Synthesis
(b) Dehydration reaction in the synthesis of sucrose
Glucose Fructose Sucrose
MaltoseGlucoseGlucose
(a) Dehydration reaction in the synthesis of maltose
1–4glycosidic
linkage
1–2glycosidic
linkage
Dehydration synthesis
Polysaccharides
• 100 to 1000 monosaccharides• Functions:• Storage polysaccharides:
– Starch – plants • Stored in plastids (amyloplast)
– Amylose – simplest starch– Animals have enzymes to hydrolyze starch
Amylopectin
• Glycogen – animal storage polysaccharide– Stored in muscles and liver of vertebrates– Provides energy to humans for about a day
Glycogen
• Structural polysaccharides– Cellulose – plant cell wall
• Most abundant organic compound on Earth
– Differs from starch in glycosidic linkage
– Cannot be digested by most organisms
– Exceptions-cows, termites have microorganisms that digest cellulose
Starch and cellulose-how are they different?
• Based on –OH attached to no. 1 carbon
• Starch = alpha configuration, often helical
• Cellulose = beta configuration, straight (glucose “upside down”)
Chitin – structural polysaccharide in animals
• Polymer of amino sugars (has a nitrogen group)
• Exoskeleton of arthropods (insects, spiders, crustaceans, etc.)
• Cell walls of some fungi• Surgical thread
Lipids
• Hydrophobic• Diverse group, not considered
polymers• 1. FATS
– Monomers: one glycerol + 3 fatty acids• Triglyceride or triacylglycerol
– Dehydration synthesis (condensation)– Ester linkage –> 3 H2O molecules
ExplainEster linkage
Characteristics of fats
• Insoluble in water– b/c C-H bonds nonpolar
• Variation due to fatty acid composition– Vary in length
– Vary in number and location of double bonds
Compare fatty acids
Compare saturated and unsaturated fats
• Double bonds ?• At room temperature?• Examples?• Artificial hydrogenation
– Converting unsaturated fatty acids to saturated by adding what?
– peanut butter– Prevents lipids from separating out in liquid
form
Function of fats
• Energy storage – 1g of fat stores twice as much energy as 1g polysaccharide– More compact fuel reservoir
• Cushions vital organs
• Insulates against heat loss
Phospholipid
• Monomers: one glycerol, 2 fatty acids, one phosphate group
• Phosphate negatively charged
• Fatty acid tail – hydrophobic
• Phosphate head – hydrophilic
Phospholipid
Phospholipid and self-assembly into bilayer
Functions
• Cell membranes– Form a bilayer
• Hydrophilic heads to exterior
• Hydrophobic tails to interior
Steroids
• Lipids with 4 fused carbon rings
• Cholesterol – important steroid
– Precursor to sex hormones and bile acids
– Component of cell membranes
– Can contribute to atherosclerosis