BackBio 100 LEC Chapter 5 Part 1 UPDATED
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Bio 100 LEC Chapter 5 Part 1
Chapter 5: The Structure and Function of Large Biological Molecules
Introduction
This chapter explores the categories, properties, and functions of large biological molecules, focusing on their structural diversity and biological roles. Understanding these molecules is fundamental to cell biology, metabolism, and genetics.
Macromolecules and Polymers
Concept 5.1: Macromolecules are Polymers, Built from Monomers
Macromolecules are large biological molecules capable of forming polymers, which are long chains made from repeating subunits called monomers. The diversity in arrangement and organization of monomers leads to a wide variety of polymers with distinct properties.
Macromolecules: Carbohydrates, proteins, and nucleic acids are true macromolecules because they form polymers.
Monomers: The simplest subunit; the nature of the monomer dictates the properties of the resulting polymer.
Polymerization: The process of joining monomers to form polymers.

Synthesis and Breakdown of Polymers
Polymers are synthesized and broken down by specific chemical reactions:
Dehydration Reaction (Condensation): Joins monomers by removing a water molecule, forming a covalent bond.
Hydrolysis: Breaks polymers into monomers by adding a water molecule.
Enzymes: Biological catalysts that facilitate these reactions.
Equation for Dehydration Reaction:
Equation for Hydrolysis:

Diversity of Polymers
Variation Among Biological Molecules
The abundance and types of large biological molecules vary between cells and species. Polymers may serve structural or energy storage functions, and their stability and breakdown are essential for cellular processes.
Structural Polymers: Provide integrity and support (e.g., cellulose).
Energy Storage Polymers: Built to be broken down for energy (e.g., starch, glycogen).

Carbohydrates
Concept 5.2: Carbohydrates Serve as Fuel and Building Material
Carbohydrates are macromolecules composed of carbon, hydrogen, and oxygen, typically in a 1:2:1 ratio. They include sugars and their polymers, serving as energy sources and structural materials.
Monosaccharides: Simple sugars (e.g., glucose, fructose) with formulas usually multiples of CH2O.
Classification: Based on carbonyl group location (aldose or ketose) and number of carbons (triose, pentose, hexose).
Energy Storage: Abundant C-H bonds make carbohydrates ideal for energy storage, released during oxidation.

Linear and Ring Forms of Glucose
Glucose can exist in both linear and ring forms, especially in aqueous environments. The ring form is predominant in cells and can be either alpha or beta, depending on the orientation of the hydroxyl group at carbon 1.
Alpha Glucose: Hydroxyl group below the plane of the ring.
Beta Glucose: Hydroxyl group above the plane of the ring.

Formation of Disaccharides
Monosaccharides can be joined to form disaccharides (two sugars) or oligosaccharides (a few sugars). The joining occurs via dehydration reactions, resulting in glycosidic linkages.
Maltose: Formed from two glucose molecules via a 1-4 glycosidic linkage.
Sucrose: Formed from glucose and fructose via a 1-2 glycosidic linkage.

Polysaccharides: Starch, Glycogen, and Cellulose
Polysaccharides are polymers of monosaccharides linked by glycosidic bonds. Their structure and function depend on the type of monomer and linkage.
Starch: Energy storage in plants; composed of alpha glucose monomers. Includes amylose (unbranched) and amylopectin (branched).
Glycogen: Energy storage in animals; highly branched polymer of glucose, stored in liver and muscle.
Cellulose: Structural component of plant cell walls; composed of beta glucose monomers, forming rigid, linear rods aggregated into microfibrils.



Alpha and Beta Linkages in Polysaccharides
The orientation of glucose monomers (alpha or beta) determines the type of glycosidic linkage and the properties of the polysaccharide. Alpha linkages are digestible by human enzymes, while beta linkages are not.
Starch: 1-4 alpha linkages.
Cellulose: 1-4 beta linkages.

Digestive Differences: Humans vs. Herbivores
Humans can digest starch (alpha linkages) but not cellulose (beta linkages), which passes as insoluble fiber. Herbivores, such as cows, rely on symbiotic microbes to hydrolyze cellulose and access its nutrients.
Mutualism: Microbes benefit from the environment, herbivores gain nutrients.
Nutritional Implications: Cellulose aids in digestive tract health for humans, but is not a nutrient source.

Lipids
Concept 5.3: Lipids are a Diverse Group of Hydrophobic Molecules
Lipids are large biological molecules that are not true polymers. They are defined by their insolubility in water and consist mainly of hydrocarbon regions. Lipids include fats, phospholipids, and steroids, each with distinct roles.
Fats and Oils: Energy storage and thermal insulation.
Phospholipids: Structural role in cell membranes.
Steroids: Regulation, hormones, and vitamins.

Fats: Structure and Function
Fats (triacylglycerols) are formed from glycerol and fatty acids via dehydration synthesis, resulting in ester linkages. Fats are used for long-term energy storage, cushioning, and insulation.
Glycerol: Three-carbon alcohol with hydroxyl groups.
Fatty Acid: Carboxyl group attached to a hydrocarbon chain.
Triglyceride: Glycerol bound to three fatty acids.

Saturated and Unsaturated Fats
The properties of fats depend on the presence or absence of double bonds in fatty acids:
Saturated Fats: No double bonds; tightly packed; solid at room temperature (e.g., animal fats).
Unsaturated Fats: One or more cis double bonds; kinks prevent tight packing; liquid at room temperature (e.g., oils).

Trans Fats
Trans fats are artificially created by manipulating unsaturated fats to have trans double bonds, resulting in a more compact structure. Trans fats are linked to increased risk of cardiovascular disease.
Cis vs. Trans: Cis double bonds cause kinks; trans double bonds allow tighter packing.
Health Implications: Trans fats are more harmful than saturated fats.

Phospholipids
Phospholipids consist of a glycerol backbone, two fatty acid tails, and a phosphate group attached to a polar molecule. They are amphipathic, with hydrophilic heads and hydrophobic tails, and spontaneously form bilayers in aqueous environments, creating cell membranes.
Hydrophilic Head: Glycerol, phosphate, and polar group.
Hydrophobic Tails: Hydrocarbon chains.
Bilayer Formation: Hydrophobic tails face inward, hydrophilic heads face outward.

Steroids
Steroids are lipids with a four-ring hydrocarbon skeleton. Sterols are steroids with hydroxyl groups. Cholesterol is a key steroid in animal cell membranes and a precursor for other steroids like testosterone and estrogen.
Structure: Four fused rings with attached functional groups.
Function: Membrane component, hormone precursor.
Health Implications: Cholesterol levels are linked to cardiovascular health.

Additional info: Enzyme specificity, functional group chemistry, and the role of polymers in cellular metabolism will be discussed in later chapters. This guide provides foundational knowledge for understanding biological macromolecules and their functions.