BackChapter 5: Carbohydrates – Structure, Function, and Biological Roles
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Chapter 5: Carbohydrates
Overview
Carbohydrates are one of the four major classes of biological macromolecules, alongside proteins, lipids, and nucleic acids. They are composed of sugars and their polymers, serving diverse roles in living organisms.
Four macromolecules of life: proteins, carbohydrates, lipids, nucleic acids.
Carbohydrates = sugars and their polymers.
Functions:
Energy storage
Structural support
Cell identity (recognition/signaling)
Precursors for larger molecules (e.g., nucleic acids)
Monosaccharides (Simple Sugars)
Monosaccharides are the simplest carbohydrates, consisting of single sugar units. They serve as building blocks for more complex carbohydrates.
General formula:
Most common: glucose
Classification:
Number of carbons: trioses (3C), pentoses (5C, e.g., ribose), hexoses (6C, e.g., glucose)
Carbonyl group position:
Aldose: carbonyl at end (aldehyde)
Ketose: carbonyl in middle (ketone)
Hydroxyl group arrangement: OH groups can differ in orientation, leading to functional differences (e.g., glucose vs galactose)
Form: linear (rare in solution) or ring (common in aqueous solutions)
α-glucose vs β-glucose: differ in orientation of the OH on C-1
Disaccharides
Disaccharides are carbohydrates composed of two monosaccharide units joined by a covalent bond called a glycosidic linkage, formed via condensation (dehydration) reactions.
Formed by: condensation (dehydration) reaction
Covalent bond: glycosidic linkage (joins OH groups)
Example: maltose = glucose + glucose (α-1,4 bond)
α vs β glycosidic linkages:
α linkages = storage polysaccharides (e.g., starch, glycogen)
β linkages = structural polysaccharides (e.g., cellulose, chitin)
Disaccharide | Monomers | Bond Type |
|---|---|---|
Sucrose | Glucose + Fructose | α-1,2 |
Lactose | Glucose + Galactose | β-1,4 |
Maltose | Glucose + Glucose | α-1,4 |
Polysaccharides (Carbohydrate Polymers)
Polysaccharides are large carbohydrate polymers formed by linking monosaccharide units via glycosidic bonds. Their properties depend on monomer type and bond position/orientation.
Made by: dehydration reactions, linked via glycosidic bonds
Properties depend on:
Monomer type
Bond position/orientation
Storage Polysaccharides
Starch (plants):
α-glucose monomers
Stored in plastids (e.g., chloroplasts)
Two forms:
Amylose: unbranched, α-1,4 bonds
Amylopectin: branched (α-1,6 every ~30 units)
Glycogen (animals):
Stored in liver and muscle
Highly branched (α-1,6 every ~10 units)
Broken down during exercise into glucose
Structural Polysaccharides
Cellulose (plants):
β-glucose monomers
Straight chains; parallel strands linked by H-bonds → microfibrils (rigidity)
Chitin (fungi cell walls, arthropod exoskeletons):
β-glucose derivative (N-acetylglucosamine, NAG)
Provides stiffness and protection
Peptidoglycan (bacterial cell walls):
Alternating monosaccharides with β linkages
Cross-linked by short peptides for extra strength and elasticity
Polysaccharide | Monomer | Bond Type | Function |
|---|---|---|---|
Starch | α-glucose | α-1,4; α-1,6 | Energy storage (plants) |
Glycogen | α-glucose | α-1,4; α-1,6 | Energy storage (animals) |
Cellulose | β-glucose | β-1,4 | Structural (plants) |
Chitin | N-acetylglucosamine | β-1,4 | Structural (fungi, arthropods) |
Peptidoglycan | Modified sugars | β-1,4 + peptide cross-links | Structural (bacteria) |
Carbohydrates in Cell Identity
Carbohydrates attached to proteins (glycoproteins) on the cell surface act as cell identity markers, playing crucial roles in cell-cell recognition and signaling.
Glycoproteins: carbohydrates attached to proteins
Located on cell surface: act as cell identity markers
Functions:
Cell-cell recognition (distinguishing self vs foreign cells)
Cell-cell signaling (communication)
Each cell has a unique glycoprotein “signature”
Carbohydrates in Energy Storage
Carbohydrates are vital for energy storage in cells, with their energy derived from the chemical bonds between carbon and hydrogen atoms.
Photosynthesis:
Carbs store energy in C-H and C-C bonds: high potential energy because electrons are shared equally
Compare bonds:
C-H, C-C = high energy
C-O = low energy (O is electronegative, electrons shared unequally)
Fats store ~2x more energy/gram than carbs (more C-H, fewer C-O)
Enzymes for Carbohydrate Breakdown
Specific enzymes catalyze the hydrolysis of glycosidic bonds in carbohydrates, enabling their digestion and utilization.
Phosphorylase: breaks α-glycosidic bonds in glycogen → glucose
Amylase: breaks α-glycosidic bonds in starch (in saliva & pancreas)