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LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION
Chapter 5
The Structure and Function of Large Biological Molecules
Lectures by Erin Barley Kathleen Fitzpatrick
© 2011 Pearson Education, Inc.
Overview: The Molecules of Life
• All living things are made up of fourclasses of large biological molecules: carbohydrates, lipids, proteins, and nucleic acids • Macromolecules are large molecules composed of thousands of covalently connected atoms • Molecular structure and function are inseparable
© 2011 Pearson Education, Inc.
Concept 5.1: Macromolecules are polymers, built from monomers
• A polymer is a long molecule consisting of many similar building blocks• These small building-block molecules are buildingcalled monomers • Three of the four classes of life’s organic molecules are polymers
– Carbohydrates – Proteins – Nucleic acids
© 2011 Pearson Education, Inc.
The Synthesis and Breakdown of Polymers
• A dehydration reaction occurs when two monomers bond together through the loss of a water molecule • Polymers are disassembled to monomersby hydrolysis, hydrolysis, a reaction that is essentially the reverse of the dehydration reaction
Animation: Polymers
© 2011 Pearson Education, Inc.
Figure 5.2a
(a) Dehydration reaction: synthesizing a polymer
1 2 3
Short polymer Dehydration removes a water molecule, forming a new bond.
Unlinked monomer
1
2
3
4
Longer polymer
Figure 5.2b
(b) Hydrolysis:breaking down a polymer
1 2 3 4
Hydrolysis adds a water molecule, breaking a bond.
1
2
3
The Diversity of Polymers
• Each cell has thousands of different macromolecules • Macromolecules vary among cells of an organism, vary more within a species, and vary even more between species • An immense variety of polymers can be built from a small set of monomers
HO
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Concept 5.2: Carbohydrates serve as fuel and building material
• Carbohydrates include sugars and the polymers of sugars • The simplest carbohydrates are monosaccharides, or single sugars • Carbohydrate macromolecules are polysaccharides, polymers composed of many sugar building blocks
© 2011 Pearson Education, Inc.
Sugars
• Monosaccharides have molecular formulas that areusually multiples of CH2O • Glucose (C6H12O6) is the most common monosaccharide • Monosaccharides are classified by
– The location of the carbonyl group (as aldose or ketose) – The number of carbons in the carbon skeleton
© 2011 Pearson Education, Inc.
Figure 5.3
Aldoses (Aldehyde Sugars)
Ketoses (Ketone Sugars)
Trioses: 3-carbon sugars (C3H6O3)
GlyceraldehydeDihydroxyacetone
Pentoses: 5-carbon sugars (C5H10O5)
Ribose
Ribulose
Hexoses: 6-carbon sugars (C6H12O6)
Glucose
Galactose
Fructose
Figure 5.3a
Aldose (Aldehyde Sugar)
Ketose (Ketone Sugar)
Trioses: 3-carbon sugars (C3H6O3)
Glyceraldehyde
Dihydroxyacetone
Figure 5.3b
Aldose (Aldehyde Sugar)
Ketose (Ketone Sugar)
Pentoses: 5-carbon sugars (C5H10O5)
RiboseRibulose
Figure 5.3c
Aldose (Aldehyde Sugar)
Ketose (Ketone Sugar)
Hexoses: 6-carbon sugars (C6H12O6)
Glucose
Galactose
Fructose
• Though often drawn as linear skeletons, in aqueous solutions many sugars form rings • Monosaccharides serve as a major fuel for cells and as raw material for building molecules
© 2011 Pearson Education, Inc.
Figure 5.4
1 2 3 4 5 6 46 5 1 3 2 4
6 5 1 3 2
(a) Linear and ring forms
6 5 4 3 2 1
(b) Abbreviated ring structure
• A disaccharide is formed when a dehydration reaction joins two monosaccharides • This covalent bond is called a glycosidic linkage
Animation: Disaccharide
© 2011 Pearson Education, Inc.
Figure 5.5
1–4 glycosidic 1 linkage 4
Glucose
Glucose
Maltose
(a) Dehydration...
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