BackOrganic Compounds: Structure and Function in Biology
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Organic Compounds
Introduction
Organic compounds are molecules primarily composed of carbon atoms bonded with hydrogen, oxygen, nitrogen, and other elements. They form the basis of all living organisms and are essential for life’s structure and function. The four major classes of organic compounds in biology are carbohydrates, lipids, proteins, and nucleic acids.
Polymers and Monomers
Definition and Relationship
Monomers: Small, repeating units that serve as the building blocks of polymers. Example: glucose, amino acids.
Polymers: Large molecules formed by joining many monomers together through covalent bonds. Example: starch, proteins.
Mono means "one"; poly means "many".
Polymerization and Depolymerization
Dehydration Synthesis (Condensation Reaction): Process by which monomers are joined to form polymers, releasing water as a byproduct.
Hydrolysis: Process by which polymers are broken down into monomers by the addition of water.
Dehydration Synthesis | Hydrolysis |
|---|---|
Make polymers | Breakdown polymers |
Monomers → Polymers | Polymers → Monomers |
Carbohydrates
Overview
Carbohydrates are organic molecules that serve as fuel and building material for cells. They include simple sugars and complex polymers.
General formula: Ratio of 1 carbon : 2 hydrogen : 1 oxygen ()
Monosaccharide → Disaccharide → Polysaccharide
Monosaccharides: Monomers (e.g., glucose, ribose)
Functions of Polysaccharides
Storage: Plants store energy as starch; animals as glycogen.
Structure: Plants use cellulose for cell walls; arthropods use chitin for exoskeletons.
Additional info: The difference between storage and structural polysaccharides is due to the position and orientation of glycosidic linkages.
Classification of Monosaccharides
Aldoses (Aldehyde sugars): e.g., Glyceraldehyde, Ribose, Glucose, Galactose
Ketoses (Ketone sugars): e.g., Dihydroxyacetone, Ribulose, Fructose
Trioses: 3-carbon sugars ()
Pentoses: 5-carbon sugars ()
Hexoses: 6-carbon sugars ()
Type | Example | Structure |
|---|---|---|
Aldose (Triose) | Glyceraldehyde | CHO-(CHOH)-CH2OH |
Ketose (Triose) | Dihydroxyacetone | CH2OH-CO-(CHOH)-CH2OH |
Aldose (Pentose) | Ribose | CHO-(CHOH)4-CH2OH |
Ketose (Pentose) | Ribulose | CH2OH-CO-(CHOH)3-CH2OH |
Aldose (Hexose) | Glucose, Galactose | CHO-(CHOH)5-CH2OH |
Ketose (Hexose) | Fructose | CH2OH-CO-(CHOH)4-CH2OH |
Linear and Ring Forms of Glucose
Monosaccharides such as glucose can exist in both linear and ring forms. In aqueous solutions, the ring form is predominant.
Linear form: Open-chain structure
Ring form: Cyclization occurs between the carbonyl group and a hydroxyl group
Carbohydrate Synthesis: Formation of Disaccharides
Glycosidic linkage: Covalent bond formed between two monosaccharides by a dehydration reaction.
Maltose: Formed from two glucose molecules ()
Sucrose: Formed from glucose and fructose ()
Example equation:
Storage and Structural Polysaccharides
Starch: Storage polysaccharide in plants; composed of amylose and amylopectin.
Glycogen: Storage polysaccharide in animals; highly branched.
Cellulose: Structural polysaccharide in plant cell walls; composed of β-glucose monomers.
Chitin: Structural polysaccharide in arthropod exoskeletons; contains nitrogen.
Polysaccharide | Function | Monomer | Linkage | Digestibility |
|---|---|---|---|---|
Starch | Storage (plants) | α-glucose | 1-4 α linkages | Digestible by humans |
Glycogen | Storage (animals) | α-glucose | Highly branched 1-4, 1-6 α linkages | Digestible by humans |
Cellulose | Structure (plants) | β-glucose | 1-4 β linkages | Not digestible by humans |
Chitin | Structure (arthropods) | Modified β-glucose (with N-acetyl group) | β linkages | Not digestible by humans |
Summary
Carbohydrates are essential for energy storage and structural integrity in living organisms.
Monosaccharides are the building blocks; polysaccharides are the functional macromolecules.
Glycosidic linkages and the arrangement of monomers determine the properties and digestibility of polysaccharides.