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Biological Molecules: Structure, Function, and Types

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Biological Molecules

Introduction to Organic Molecules

Aside from water, most biologically important molecules contain carbon. These organic molecules are essential for life and are characterized by the presence of carbon atoms bonded in various configurations. The versatility of carbon allows for the formation of a wide variety of complex molecules necessary for biological processes.

  • Organic molecules: Molecules containing carbon (excluding certain simple carbon compounds like CO2, CO, graphite, diamonds, and coal).

  • Living organisms can synthesize organic molecules.

  • Carbon atoms have a valence of 4, allowing them to form up to four covalent bonds with other atoms.

  • This bonding versatility enables the formation of diverse molecular structures.

Functional Groups in Organic Molecules

Functional groups are specific groups of atoms attached to the carbon skeleton of organic molecules. They confer distinct chemical and physical properties and are often the sites of chemical reactivity.

  • Functional groups behave consistently across different molecules.

  • They determine the chemical properties and reactivity of organic molecules.

There are seven general functional groups commonly found in biological molecules:

Functional Group

Structure

Properties

Example(s)

Hydroxyl

-OH

Polar; involved in condensation and hydrolysis reactions

Alcohols (e.g., ethanol)

Carbonyl

-C=O

Polar; forms aldehydes (terminal) or ketones (internal)

Glucose (aldehyde), acetone (ketone)

Carboxyl

-COOH

Polar; acidic (can donate a proton); involved in peptide bonds

Amino acids, fatty acids

Amino

-NH2

Polar; acts as a weak base; involved in peptide bonds

Amino acids

Sulfhydryl

-SH

Nonpolar; stabilizes protein structure

Cysteine (amino acid)

Phosphate

-PO4

Polar; acidic; links nucleotides; important in energy transfer

ATP, DNA, RNA

Methyl

-CH3

Nonpolar; increases hydrophobicity

Methylated DNA

Synthesizing Organic Molecules: Monomers and Polymers

Monomers and Polymers

Biological macromolecules are often constructed from smaller subunits called monomers. When monomers are linked together, they form polymers, which are long chains of repeating units.

  • Monomer: A small molecule that can join with others to form a polymer.

  • Polymer: A large molecule composed of repeating monomer units.

Dehydration Synthesis and Hydrolysis

  • Dehydration synthesis (condensation reaction): The process by which two monomers are covalently bonded together with the removal of a water molecule.

  • One monomer loses a hydroxyl group (-OH), and the other loses a hydrogen atom (-H).

  • Hydrolysis: The process of breaking a covalent bond between two monomers by adding a water molecule.

  • One monomer gains a hydroxyl group (-OH), and the other gains a hydrogen atom (-H).

Example: The formation of a peptide bond between two amino acids involves dehydration synthesis, while the breakdown of a disaccharide into monosaccharides involves hydrolysis.

Classes of Biological Macromolecules

Overview of Macromolecule Classes

There are four major classes of biological macromolecules, each with distinct monomers, polymers, and functions.

Macromolecule Class

Monomer

Polymer

Examples

Carbohydrates

Monosaccharides

Disaccharides, Polysaccharides

Glucose, Sucrose, Starch, Glycogen, Cellulose

Lipids

Fatty acids, Glycerol

Triglycerides, Phospholipids, Steroids

Oils, Fats, Waxes, Cholesterol

Proteins

Amino acids

Polypeptides

Keratin, Silk

Nucleic Acids

Nucleotides

DNA, RNA

DNA, RNA

Carbohydrates

Structure and Function

Carbohydrates are organic molecules composed of carbon, hydrogen, and oxygen, typically in the ratio CH2O. They serve as fuel and building material for cells.

  • Monomers: Monosaccharides (simple sugars), e.g., glucose.

  • Disaccharides: Two monosaccharides joined by a glycosidic linkage (covalent bond formed by dehydration synthesis).

  • Polysaccharides: Polymers of many monosaccharides, used for energy storage and structural support.

Monosaccharides

  • General formula: (CH2O)n

  • Each carbon (except one) has a hydroxyl group; one carbon has a carbonyl group.

  • In aqueous solutions, monosaccharides with five or more carbons form ring structures.

  • Glucose is the most common monosaccharide and a primary energy source for cells.

  • Produced by photosynthetic organisms from CO2, H2O, and light.

Disaccharides

Disaccharides are formed by joining two monosaccharides via a glycosidic linkage.

Disaccharide

Monomers

Common Use

Maltose

Glucose + Glucose

Important in beer brewing

Lactose

Glucose + Galactose

Sugar present in milk

Sucrose

Glucose + Fructose

Table sugar; most common disaccharide

Polysaccharides

  • Polysaccharides are large macromolecules composed of hundreds or thousands of monosaccharides.

  • Formed by enzyme-mediated condensation reactions.

  • Serve two main biological functions:

    • Energy storage: Starch (plants), Glycogen (animals)

    • Structural support: Cellulose (plants), Chitin (fungi and arthropods)

  • Starch: Glucose polymer used for energy storage in plants.

  • Glycogen: Glucose polymer used for energy storage in animals, stored in muscle and liver cells.

  • Stored polysaccharides can be hydrolyzed to release glucose as needed.

Example: When energy is required, glycogen in animal liver cells is broken down via hydrolysis to release glucose into the bloodstream.

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