Course Content
Rural Sociology & Educational Psychology 2 (2+0)
0/17
B.Sc. Ag. I Semester
    About Lesson
    Oligosaccharides and Polysaccharides; Carbohydrates are classified into monosaccharides, oligosaccharides, and polysaccharides based on the number of sugar units they contain.
    • Oligosaccharides

    Definition: Oligosaccharides are carbohydrates that consist of 2 to 10 monosaccharide units linked by glycosidic bonds. They are soluble in water, sweet in taste, and crystalline in nature.

    General Formula: (C6H10O5)n where n = 2 to 10.

    Classification of Oligosaccharides: Oligosaccharides are classified based on the number of monosaccharide units:

    • Disaccharides (2 sugar units) – e.g., Sucrose, Lactose, Maltose
    • Trisaccharides (3 sugar units) – e.g., Raffinose
    • Tetrasaccharides (4 sugar units) – e.g., Stachyose

     

    Types of Oligosaccharides

    • Disaccharides (n = 2): Disaccharides are the most common oligosaccharides. They are formed by the condensation of two monosaccharides through a glycosidic bond (removal of water).

    Disaccharide

    Composition

    Glycosidic Bond

    Source

    Sucrose

    Glucose + Fructose

    α(1→2)

    Sugarcane, Sugar beet

    Lactose

    Glucose + Galactose

    β(1→4)

    Milk

    Maltose

    Glucose + Glucose

    α(1→4)

    Malt, Starch hydrolysis

    • Sucrose: Non-reducing sugar (No free aldehyde or ketone group).
    • Lactose and Maltose: Reducing sugars (Free aldehyde/ketone group).

     

    • Trisaccharides (n = 3); Trisaccharides contain three monosaccharide units. Example: Raffinose → Galactose + Glucose + Fructose (found in beans, cabbage).
    • Tetrasaccharides (n = 4): Tetrasaccharides contain four monosaccharide units. Example: Stachyose → Two Galactose + Glucose + Fructose (found in legumes).

     

    Functions of Oligosaccharides

    1. Energy Source – Easily hydrolyzed into monosaccharides for energy production.
    2. Prebiotics – Some oligosaccharides (e.g., raffinose) act as prebiotics, supporting gut health.
    3. Glycoproteins & Glycolipids – Found in cell membranes, involved in cell recognition and signaling.
    4. Milk Oligosaccharides – Important for infant gut health (e.g., human milk oligosaccharides).

     

    1. Polysaccharides

    Definition: Polysaccharides are complex carbohydrates made up of more than 10 monosaccharide units, linked by glycosidic bonds. They are insoluble in water, tasteless, and non-reducing.

    General Formula: (C6H10O5)n  where n = hundreds to thousands.

     

    Classification of Polysaccharides: Polysaccharides can be classified based on their composition and function.

    i) Based on Composition

    • Homopolysaccharides – Contain only one type of monosaccharide. Example: Starch, Glycogen, Cellulose, Chitin.
    • Heteropolysaccharides – Contain two or more types of monosaccharides. Example: Hyaluronic acid, Heparin, Agar, Peptidoglycan.

     

    ii) Based on Function

    • Storage Polysaccharides – Energy storage in plants and animals. Examples: Starch (plants), Glycogen (animals).
    • Structural Polysaccharides – Provide structural support to plants and animals. Examples: Cellulose (plants), Chitin (exoskeleton of insects, fungi).

     

    Types of Polysaccharides

    1. Storage Polysaccharides

    (a) Starch (Plant Storage Polysaccharide)

    • Made of: Amylose + Amylopectin.
    • Source: Cereals, tubers, grains.
    • Function: Stores energy in plants.

    Component

    Structure

    Glycosidic Bond

    Properties

    Amylose

    Linear, unbranched

    α(1→4)

    Helical, water-insoluble

    Amylopectin

    Branched

    α(1→4) & α(1→6)

    Water-soluble

    • Iodine Test for Starch → Blue-black color indicates the presence of starch.

     

    (b) Glycogen (Animal Storage Polysaccharide)

    • Structure: Highly branched polymer of glucose (like amylopectin but more branched).
    • Glycosidic Bond: α(1→4) in chains, α(1→6) at branching points.
    • Location: Liver and muscles.
    • Function: Energy storage in animals.

     

    1. Structural Polysaccharides

    (a) Cellulose (Plant Structural Polysaccharide)

    • Structure: Linear polymer of β-D-glucose.
    • Glycosidic Bond: β(1→4) (forms rigid fibers).
    • Function: Provides mechanical strength to plant cell walls.
    • Digestion: Humans cannot digest cellulose due to lack of cellulase enzyme.
    • Uses: Paper, textiles, cotton.

     

    (b) Chitin (Animal Structural Polysaccharide)

    • Structure: Linear polymer of N-acetylglucosamine (NAG).
    • Glycosidic Bond: β(1→4).
    • Location: Exoskeleton of insects, fungi cell walls.
    • Function: Provides strength and protection.
    • Uses: Surgical threads, biodegradable plastics.

     

    1. Heteropolysaccharides (Mixed Monosaccharides)

    (a) Hyaluronic Acid

    • Composition: Glucuronic acid + N-acetylglucosamine.
    • Function: Present in connective tissue, synovial fluid, maintains lubrication.

    (b) Heparin

    • Composition: Glucosamine + Iduronic acid + Sulfate groups.
    • Function: Anticoagulant, prevents blood clotting.

    (c) Peptidoglycan (Murein)

    • Composition: N-acetylglucosamine (NAG) + N-acetylmuramic acid (NAM).
    • Function: Bacterial cell wall component, provides rigidity.

     

    Summary Table

    Polysaccharide

    Composition

    Function

    Glycosidic Bond

    Starch

    Glucose (Amylose + Amylopectin)

    Energy storage in plants

    α(1→4), α(1→6)

    Glycogen

    Glucose

    Energy storage in animals

    α(1→4), α(1→6)

    Cellulose

    Glucose

    Structural (plants)

    β(1→4)

    Chitin

    N-Acetylglucosamine

    Structural (insects, fungi)

    β(1→4)

    Hyaluronic Acid

    Glucuronic acid + NAG

    Lubrication

    β(1→3), β(1→4)

    Peptidoglycan

    NAG + NAM

    Bacterial cell wall

    β(1→4)

     

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