BackModule 3 Molecules of Life: Structure and Function of Biological Macromolecules
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Molecules of Life
Key Terms and Definitions
Organic compound: A chemical compound containing carbon atoms bonded to hydrogen, often with other elements such as oxygen, nitrogen, sulfur, or phosphorus.
Functional group: A specific group of atoms within a molecule responsible for characteristic chemical reactions.
Hydroxyl group (-OH): A polar functional group found in alcohols; increases solubility in water.
Phosphate group (-PO4): A functional group important in energy transfer (e.g., ATP).
Methyl group (-CH3): A nonpolar group that can affect gene expression and molecular shape.
Carboxyl group (-COOH): A functional group found in organic acids; acts as an acid by donating H+.
Amino group (-NH2): A functional group that acts as a base; found in amino acids.
Sulfhydryl (thiol) group (-SH): Important for stabilizing protein structure via disulfide bonds.
Monomer: A small molecule that can join with others to form a polymer.
Polymer: A large molecule made of repeating monomer units.
Dehydration synthesis (condensation): A reaction that joins two molecules by removing a water molecule.
Hydrolysis: A reaction that breaks a bond in a molecule by adding water.
Carbohydrate: Organic molecules composed of carbon, hydrogen, and oxygen; main energy source for cells.
Monosaccharide: Simple sugar; monomer of carbohydrates (e.g., glucose).
Disaccharide: Two monosaccharides joined by a glycosidic bond (e.g., sucrose).
Polysaccharide: Large carbohydrate made of many monosaccharides (e.g., starch, cellulose).
Glycogen: Animal storage form of glucose; highly branched polysaccharide.
Starch: Plant storage form of glucose; less branched than glycogen.
Cellulose: Structural polysaccharide in plant cell walls; unbranched and forms fibers.
Lipid: Hydrophobic organic molecule, including fats, oils, and sterols.
Fatty acid: Long hydrocarbon chain with a carboxyl group; building block of lipids.
Fat: Triglyceride; energy storage molecule in animals.
Oil: Liquid fat at room temperature; usually from plants.
Sterol (Steroid): Lipid with four fused rings; includes cholesterol and hormones.
Triglyceride: Lipid made of three fatty acids and one glycerol.
Saturated fat: Fatty acid chains with no double bonds; solid at room temperature.
Unsaturated fat: Fatty acid chains with one or more double bonds; liquid at room temperature.
Amino acid: Monomer of proteins; contains amino, carboxyl, and R group.
Peptide bond: Covalent bond joining amino acids in a protein.
R group: Side chain of an amino acid; determines its properties.
Polypeptide: Chain of amino acids linked by peptide bonds.
Protein: Functional biological molecule made of one or more polypeptides.
Primary structure: Linear sequence of amino acids in a protein.
Secondary structure: Local folding (e.g., alpha helix, beta sheet) stabilized by hydrogen bonds.
Tertiary structure: Overall 3D shape of a polypeptide; stabilized by various bonds and interactions.
Quaternary structure: Association of multiple polypeptide chains in a protein.
Denaturation: Loss of protein structure (and function) due to environmental changes.
Nucleotide: Monomer of nucleic acids; consists of a sugar, phosphate, and nitrogenous base.
Nitrogenous base: Component of nucleotides; includes adenine, thymine, cytosine, guanine, uracil.
DNA (Deoxyribonucleic acid): Double-stranded nucleic acid; stores genetic information.
RNA (Ribonucleic acid): Single-stranded nucleic acid; involved in protein synthesis.
Deoxyribose: Five-carbon sugar in DNA.
Ribose: Five-carbon sugar in RNA.
Double helix: Structure of DNA; two strands coiled around each other.
Antiparallel: Orientation of DNA strands running in opposite directions.
Sugar-phosphate backbone: Repeating pattern of sugar and phosphate in nucleic acids.
Complementary base pairing: Specific pairing of bases (A-T/U, G-C) in DNA/RNA.
Importance of Carbon in Organic Compounds
Carbon is central to organic chemistry because it can form four covalent bonds, allowing for a diversity of stable, complex molecules. Its ability to bond with itself and other elements leads to a variety of molecular structures, including chains, rings, and branches.
Functional Groups in Organic Molecules
Functional groups determine the chemical reactivity and properties of organic molecules.
Common functional groups include hydroxyl, carboxyl, amino, phosphate, methyl, and sulfhydryl.
For example, the carboxyl group acts as an acid, while the amino group acts as a base.
Monomers and Polymers
Monomers are the building blocks of polymers.
Examples: Glucose (monomer of starch), amino acids (monomers of proteins), nucleotides (monomers of nucleic acids).
Polymers are large molecules made by linking monomers through covalent bonds.
Condensation (Dehydration Synthesis) and Hydrolysis
Dehydration synthesis: Joins two monomers by removing a water molecule.
Hydrolysis: Breaks a polymer into monomers by adding water.
Equation for Dehydration Synthesis:
Equation for Hydrolysis:
Carbohydrates: Structure and Function
General formula:
Major uses: Energy source (glucose), energy storage (starch, glycogen), structural support (cellulose).
Types of Carbohydrates
Monosaccharides: Simple sugars (e.g., glucose, fructose).
Disaccharides: Two monosaccharides joined (e.g., sucrose = glucose + fructose).
Polysaccharides: Many monosaccharides linked (e.g., starch, glycogen, cellulose).
Properties of Glycogen, Starch, and Cellulose
Glycogen: Highly branched; energy storage in animals.
Starch: Moderately branched; energy storage in plants.
Cellulose: Unbranched; structural component in plant cell walls; not digestible by humans.
Lipids: Structure and Function
Composed mainly of hydrocarbons; hydrophobic due to nonpolar C-H bonds.
Major types: Fats, oils, phospholipids, sterols.
Functions: Energy storage, membrane structure, signaling molecules.
Saturated vs. Unsaturated Fats
Saturated fats: No double bonds; straight chains; solid at room temperature (e.g., butter).
Unsaturated fats: One or more double bonds; kinked chains; liquid at room temperature (e.g., olive oil).
Double bonds in unsaturated fats prevent tight packing, lowering melting point.
Amino Acids and Proteins
General structure: Central carbon, amino group, carboxyl group, hydrogen, and R group (side chain).
R group chemistry determines the properties (e.g., polar, nonpolar, acidic, basic) of each amino acid.
Peptide bond: Covalent bond between amino group of one amino acid and carboxyl group of another.
Levels of Protein Structure
Primary: Sequence of amino acids.
Secondary: Local folding (alpha helix, beta sheet) via hydrogen bonds.
Tertiary: 3D shape stabilized by interactions (hydrogen bonds, ionic bonds, disulfide bridges, hydrophobic interactions).
Quaternary: Association of multiple polypeptide chains.
Protein Denaturation
Loss of structure and function due to heat, pH changes, or chemicals.
Example: Cooking an egg denatures egg white proteins.
Nucleic Acids: DNA and RNA
Nucleotide structure: Phosphate group, five-carbon sugar (deoxyribose or ribose), nitrogenous base.
DNA nucleotides: Deoxyribose sugar; bases A, T, G, C.
RNA nucleotides: Ribose sugar; bases A, U, G, C.
Structure of DNA
Double helix with antiparallel strands.
Sugar-phosphate backbone on the outside; bases paired inside (A-T, G-C) via hydrogen bonds.
Functions of Nucleic Acids and Nucleotides
DNA: Stores genetic information.
RNA: Involved in protein synthesis and gene regulation.
Nucleotides: Also function as energy carriers (e.g., ATP) and signaling molecules.
Table: Comparison of DNA and RNA
Feature | DNA | RNA |
|---|---|---|
Sugar | Deoxyribose | Ribose |
Strands | Double-stranded | Single-stranded |
Nitrogenous Bases | A, T, G, C | A, U, G, C |
Function | Genetic information storage | Protein synthesis, gene regulation |
Example: ATP (adenosine triphosphate) is a nucleotide that stores and transfers energy in cells.
Additional info: This guide expands on the objectives by providing definitions, explanations, and examples for each key concept, ensuring a comprehensive overview suitable for exam preparation.