Unit 1: Biochemistry - Comprehensive Study Notes
1.3 Introduction to Macromolecules
Dehydration Synthesis (Condensation): join monomers by covalent bonds; removal of H from one monomer and OH from another; results in loss of a water molecule; forms a covalent bond and polymerizes monomers
Polymerization is the joining of many monomers into polymers
Hydrolysis: cleave covalent bonds by adding water; water splits a polymer into monomers
In biological reactions, enzymes catalyze specific hydrolysis or dehydration steps
1.3 Macromolecule Formation & Hydrolysis (Figure-based prompts)
Example: formation of a peptide bond between amino acids via dehydration synthesis
In peptide bond formation, a water molecule is released (H from one amino acid and OH from another)
The resulting bond is a covalent peptide bond
1.3 Biomolecules Overview
Monomers and Polymers by category:
Carbohydrates: Monosaccharides
P
** Monosaccharides
Lipids: Fatty acids + glycerol
Proteins: Amino acids
Nucleic Acids: Nucleotides
All biomolecules have functional roles (energy, storage, structure, catalysis, information storage, etc.)
1.4 Carbohydrates
Functions: energy source; structural support
Monomer: Monosaccharide; Polymer: Polysaccharide
Bonds: Glycosidic bonds; CH2O ratio 1:2:1
Important examples: glycogen, starch (energy storage); cellulose (structure in plants); chitin (fungi/exoskeletons); peptidoglycan (bacteria)
Monosaccharide isomers: glucose, galactose, fructose share formula C6H12O6 but differ structurally
Disaccharides: two monosaccharides joined by glycosidic bond via dehydration synthesis
Oligosaccharides: 3–10 monosaccharides; found in glycoproteins/glycolipids; important for cell recognition; often not digested by stomach acid; fermented in the gut to short-chain fatty acids
Polysaccharides: starch, glycogen, cellulose; starch/glycogen are energy storage; cellulose is structural; other polysaccharides include chitin and peptidoglycan
Digestive differences: humans digest starch with amylase; cellulose requires cellulase (not produced by humans)
Key AP-style Qs emphasize that structure and branching affect properties and digestibility
1.4 Carbohydrates – Monosaccharides & Disaccharides
Glucose formula: C6H12O6; glucose, fructose, galactose are isomers
Disaccharides formed by dehydration synthesis (glycosidic bonds)
Oligosaccharides: 3–10 units; often linked to proteins/lipids (glycoproteins/glycolipids) for cell recognition
Cellulose vs. starch: different glycosidic linkages ( in starch; in cellulose) explain digestibility differences
1.4 Cellulose & Starch
Humans can digest starch (amylose; linkages) but not cellulose ( linkages) due to enzyme specificity (amylase vs cellulase)
Cellulose passes as dietary fiber; important for colon health
RCQ prompts discuss how polymer structure influences digestibility
1.4 Carbohydrates – Polysaccharides
Polysaccharides serve as energy storage (starch in plants; glycogen in animals) and structural support (cellulose in plants; chitin in some fungi and in exoskeletons)
Other structural polysaccharide: peptidoglycan in bacterial cell walls
Important note: substantial variety in structure but general purpose across categories
1.4 Quick AP-style Questions on Carbohydrates
Statements about structure: monosaccharides vs. polysaccharides; linkage types; hydrogen bonding; and disaccharide structure
1.4 Carbohydrates: Glucose & Isomers
Glucose, fructose, galactose all C6H12O6 but with different structural formulas
Isomerism different properties despite same formula
1.5 Lipids
Lipids are composed mainly of fatty acids (long hydrocarbon chains) with elements C, H, O
Generally nonpolar and hydrophobic
Bond formation: ester bond forms when a fatty acid bonds with glycerol or another alcohol, releasing H2O
Major classes: fats/oils (triglycerides), phospholipids, steroids, waxes, vitamins (lipophilic examples: A, D, E, K)
1.5 Lipid Structure – Fatty Acids
Fatty acids: long hydrocarbon chain ending in –COOH (carboxyl group)
Hydrocarbon tails are nonpolar; carboxyl group is polar/acidic
1.5 Saturated vs. Unsaturated Lipids
Saturated fatty acids: only single bonds between carbons; typically solid at room temperature
Unsaturated fatty acids: include one or more double bonds causing kinks; typically liquid at room temperature
More double bonds more unsaturated more liquid at room temperature
1.5 Lipids – AP-style Question (Solid at room temperature)
Linoleic acid (with double bonds) vs. Palmitic acid (saturated, no double bonds)
Correct reasoning: absence of double bonds in palmitic allows closer packing and solid at room temperature; double bonds in linoleic introduce kinks preventing tight packing
1.5 Lipids – Functions
Fats: energy storage and insulation
Steroids (e.g., cholesterol): hormones; modulate membrane fluidity
Phospholipids: form lipid bilayers; amphipathic (polar heads, nonpolar tails)
Waxes: protective barriers; dehydration prevention
1.5 Lipids – Phospholipids (Structure & Membranes)
Glycerol + two fatty acids + phosphate group
Amphipathic: polar head (glycerol + phosphate) and nonpolar tails
Phospholipid bilayer forms cell membranes; outer and internal membranes of organelles
The phosphate group provides a negative charge, contributing to membrane properties
1.5 Lipids – Membrane Stability & Saturation in Thermophiles (AP-style)
Predictions: more saturated fatty acids increase membrane stability at high temperatures due to tighter packing; less fluidity is beneficial for stability in heat
1.5 Lipids – Steroids & Vitamins
Steroids: four fused carbon rings; regulate growth, development, metabolism, homeostasis
Cholesterol: modulates membrane fluidity; provides structural stability
Vitamins: lipid-soluble vitamins (A, D, E, K) functioning as coenzyme precursors; fat-soluble
Water-soluble vitamins (B and C) differ in solubility and storage
1.5 Lipids – Waxes & Soaps
Waxes formed by dehydration synthesis between fatty acids and alcohols
Soap: amphipathic molecules with hydrophobic tails and hydrophilic heads; they emulsify oils/dirt; disrupt lipid membranes of microbes