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Biomolecules: Structure and Function of Carbohydrates and Lipids

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Biomolecules

Introduction

Biomolecules are essential components of cells, playing critical roles in structure, function, and energy storage. The four main classes are carbohydrates, lipids, proteins, and nucleic acids. Each class is composed of specific monomers: carbohydrates (sugars), lipids (fatty acids and glycerol), proteins (amino acids), and nucleic acids (nucleotides).

Carbohydrates

Monosaccharides

Monosaccharides are the simplest carbohydrates, serving as monomers for disaccharides and polysaccharides. They are classified by the number of carbon atoms: trioses (3C), pentoses (5C), hexoses (6C), etc. Their general formula is $(CH_2O)_n$.

  • Structure: Contains a carbonyl group (C=O) and multiple hydroxyl groups (-OH). Can be an aldose (aldehyde group) or ketose (ketone group).

  • Function: Main energy source due to many C-H bonds; also serve as building blocks for larger molecules.

No. of C atoms

General Name

Chemical Formula

Examples

Functions

3

Triose sugar

C3H6O3

Glyceraldehyde

Intermediate in respiration/photosynthesis

5

Pentose sugar

C5H10O5

Ribose, Deoxyribose

RNA, DNA, ATP components

6

Hexose sugar

C6H12O6

Glucose, Fructose, Galactose

Main energy source, components of disaccharides

Structures of aldoses and ketoses

Properties of Monosaccharides

  • Physical: Sweet, soluble, crystalline.

  • Chemical: All are reducing sugars (can reduce Cu2+ to Cu+ in Benedict's test).

Benedict's Test: Used to detect reducing sugars. The color change from blue to orange-red indicates increasing concentration of reducing sugar.

Benedict's test color scale

Oxidation of glucose in Benedict's test involves the conversion of the open-chain form of glucose to gluconate, with Cu2+ reduced to Cu+.

Oxidation of glucose in Benedict's test

Isomerism in Monosaccharides

Glucose exists in equilibrium between open-chain and ring forms. The ring structure can be either α-glucose or β-glucose, differing in the position of the hydroxyl group on carbon-1.

Open chain and ring forms of glucose α-glucose and β-glucose structures

  • α-glucose: OH group on C1 is below the ring.

  • β-glucose: OH group on C1 is above the ring.

Disaccharides

Disaccharides are formed by condensation reactions between two monosaccharides, creating a glycosidic bond and releasing water. The bond type depends on the participating carbons.

  • Maltose: α-1,4-glycosidic bond (glucose + glucose)

  • Sucrose: α-1,2-glycosidic bond (glucose + fructose)

  • Lactose: β-1,4-glycosidic bond (glucose + galactose)

Formation of glycosidic bonds in disaccharides Formation of maltose Formation of sucrose Formation of lactose

  • Physical properties: Sweet, soluble, crystalline.

  • Chemical properties: Most are reducing sugars except sucrose.

Hydrolysis: Glycosidic bonds can be broken by acid or enzyme hydrolysis, yielding monosaccharides.

Polysaccharides

Polysaccharides are polymers of monosaccharides linked by glycosidic bonds. They can be storage (starch, glycogen) or structural (cellulose).

Starch

Starch is a plant storage polysaccharide composed of α-glucose monomers. It consists of two components:

  • Amylose: Unbranched, α-1,4-glycosidic bonds, helical structure.

  • Amylopectin: Branched, α-1,4 and α-1,6-glycosidic bonds.

Amylose structure Amylopectin structure Amylose and amylopectin comparison Amylose and amylopectin glycosidic bonds

Amylose coils into a helical structure stabilized by hydrogen bonds.

Helical structure of amylose Amylose molecular model

Amylopectin is highly branched, allowing rapid hydrolysis and compact storage.

Starch grains accumulate in chloroplasts of plant cells.

Starch grains in chloroplast

Glycogen

Glycogen is the main storage polysaccharide in animals, structurally similar to amylopectin but with more extensive branching.

Glycogen granules in animal cells Branching in glycogen Glycogen structure: reducing and non-reducing ends Highly branched glycogen molecule

  • Allows rapid mobilization of glucose units for energy.

  • Stored in liver and muscle cells.

Cellulose

Cellulose is a structural polysaccharide in plant cell walls, composed of β-glucose monomers linked by β-1,4-glycosidic bonds. Adjacent glucose molecules are rotated 180°, forming straight, unbranched chains.

Comparison of starch and cellulose structure Cellulose structure: β-1,4-glycosidic bonds

  • Chains run parallel, forming microfibrils via extensive hydrogen bonding.

  • High tensile strength and permeability due to macrofibril arrangement.

Cellulose chains forming microfibrils Cellulose microfibrils in plant cell wall

Lipids

Triglycerides

Triglycerides are the most common lipids, formed by condensation of three fatty acids and one glycerol molecule, creating three ester bonds and releasing three water molecules.

  • Fatty acids: Long hydrocarbon chains with a carboxyl group. Can be saturated (no double bonds) or unsaturated (one or more double bonds).

  • Glycerol: A three-carbon alcohol with three hydroxyl groups.

Saturated and unsaturated fatty acids Triglyceride structure and packing Glycerol structure Formation of triglyceride by esterification Triglyceride molecular model

  • Physical properties: Fats (solid at room temp) have saturated fatty acids; oils (liquid at room temp) have unsaturated fatty acids.

  • Solubility: Insoluble in water, soluble in organic solvents.

  • Function: Energy storage, heat insulation, protection, buoyancy.

Phospholipids

Phospholipids are major components of cell membranes, consisting of one glycerol, two fatty acids, and one phosphate group. They are amphipathic, with a hydrophilic head and hydrophobic tails.

Phospholipid structure Phosphatidylcholine molecular model

  • Form bilayers in aqueous environments, creating cell membranes.

  • Can form micelles for fat transport.

Steroids and Sterols

Steroids are lipids with a four-ring carbon skeleton. Cholesterol is a key sterol in animals, serving as a precursor for steroid hormones and regulating membrane fluidity.

  • Insoluble in water, transported as lipoproteins.

  • LDL and HDL are types of lipoproteins with different effects on cardiovascular health.

*Additional info: The notes above expand on the original content with academic context, including definitions, examples, and structural explanations. All included images are directly relevant to the explanations provided and reinforce key concepts in carbohydrate and lipid structure and function.*

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