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Polysaccharides

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Title: Polysaccharides


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Polysaccharides
  • www.themegallery.com

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By Dr. Batoul Izzularab
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Polysaccharides
  • Polysaccharides are long carbohydrate molecules
    of monosaccharide units joined together by
    glycosidic bonds. They range in structure from
    linear to highly branched.
  • When all the monosaccharides in a polysaccharide
    are the same type, the polysaccharide is called a
    homopolysaccharide or homoglycan, but when more
    than one type of monosaccharide is present they
    are called heteropolysaccharides or heteroglycans.

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General properties of polysaccharides
  • They are formed from great number of
    monosaccharide units (more than ten unit)
    attached together by glucosidic bond.
  • They are high molecular weight compound
  • All give positive molish test
  • All are nonreducing sugar
  • All are optically active compound
  • All are negative for ozazone test

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General properties of polysaccharides
  • All formed colloid solution i.e. insoluble in
    water , on hydrolysis they give a great number of
    monosaccharide unit
  • They form specific color with iodine e.g. starch
    gives blue color with iodine
  • Beside they are important nutritive mitral , they
    are important in manufacture of
  • Textile
  • Artificial silk
  • Paper

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Homopolysaccharide
  • Starch
  •  It is a homopolymer of glucose forming an a-
    glucosidic chain, called glucosan or glucan
  • It is the most important dietary carbohydrate in
    cereals, potatoes, legumes and other vegetables.
  • Starch never present in animals tissue

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Starch
  • Starch granules is formed of amylose (13-20)
    which has nonbranching helical structure , and
    amylopectin (80-85) , which consists of branched
    chains composed of 24-30 glucose residues united
    by a1?4 linkages in the chain and by a1?6
    linkages at the branched points

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Starch
  • Amylose (13-20)
  • The amylose represents the inner part of starch
    granules.
  • It has a non-branching helical coil structure,
    containing only a1?4 glycosidic link.
  • It gives deep blue color with iodine.

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Starch
  • Amylose
  • Amylose a1?4 linkage

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Starch
  • Amylopectin (80-85)
  • This represents the outer layer of starch
    granules.
  • It is a branched chain structure, containing both
    ? 1?4 glycosidic link (Straight chain and
    ?1-6bond (branch point)
  • Each chain of amylopectin in composed of 25-30
    glucose units linked together by ?1-6 bond at the
    branch points.
  • Amylopectin gives red color with iodine

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Starch
  • Amylopectin
  • Amylopectin a1?6 linkages

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Starch
  • Acid hydrolysis of starch produces great number
    of glucose units
  • Enzymatic hydrolysis of starch by salivary
    amylase
  •  
  • Starch ?amylodextrin ?achrodextrin ?maltose 

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Dextrin
  • Dextrins are produced during enzymatic hydrolysis
    of starch by salivary amylase and pancreatic
    amylase.
  • They are -like starch- formed of glucose units
    attached together by ?1-4 and ? 1-6 glycosidic
    bonds.
  • Their structure is simpler than starch.

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Dextrin
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Glycogen
  • Glycogen is the store of carbohydrates in animal
    life called "Animal starch".
  • It is present mainly in the liver and muscles and
    gives red color with iodine.
  • Chemically, it a highly branched chain
    homopolysaccharide.

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Glycogen
  • Each chain is composed of 12-14 glucose units
    linked by ?1-4glycosidic link in the straight
    chain and ?1-6 link in the branch points. It
    resembles the amylopectin part of starch.
  • Glycogen store in liver which function as a
    source of blood glucose maintenance during
    starvation and in between meals

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Glycogen
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Cellulose 
  • It is a long straight non-branching chains of
    glucose units) ?-D-glucose), attached by?1-4
    glycosidic link.
  • The straight chains are cross linked by
    hydrogen bonds.
  • It is the chief constituent of the frame work of
    plants e.g. leaved vegetables, cotton, woodetc

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Cellulose
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Cellulose
  • Properties
  • Non-reducing homopolysaccharide.
  • Gives no color with iodine.
  • Not digested in the human GIT, because of the
    absence of hydrolytic enzymes that attack ?-link.

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Cellulose
  • Its presence in the diet is important, because it
    cannot be digested, so it forms the main bulk of
    stool, stimulating the intestinal movements, and
    preventing constipation.
  • Cellulose is digested in the GIT of herbivores,
    thus acting as source of energy. The GIT of these
    animals contains microorganisms that produce
    cellulase enzyme

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Inulin
  • Inulin is a fructosan, formed of ?-fructose units
    attached by ?1-2 glycosidic link.
  • It is present in plants e.g. root of dahlias,
    artichokes and other plants.
  • It is not digested or metabolized by human GIT.
  • Inulin clearance is one of the important
    physiological diagnostic tests for investigation
    and measurement of glomerular filtration rate
    (GFR) of the kidney.

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Inulin
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Chitin
  • Chitin forms of the shells of crustaceans and
    exoskeleton of insects.
  • It is formed of repeated N-acetylglucosamine units

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Heteropolysaccharides
  • Heteropolysaccharides are polysaccharides on
    hydrolysis give rise into different type of
    monosaccharide unit i.e. different of
    monosaccharide units
  • Agar Agar
  • Derived from certain sea weeds. It is used as
    culture media for bacterial growth. The main
    sugar unit is galactose.

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Pectins
  • These are Heteropolysaccharides containing
    arabinose, galactose, and galacturonic acid.
  • They are present in fruits, like orange, lemons,
    apricotsetc.
  • Pectins have gellation properties, hence used for
    treatment of infantile diarrhea.

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Glycosaminoglycans (GAG), (mucopolysaccharides(
  • Glycosaminoglycans are Heteropolysaccharides
    which are present abundantly in the human body.

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Glycosaminoglycans (GAG), (mucopolysaccharides(
  • They are characterized by
  • Chemically, they are formed mostly of repeated
    disaccharides units that contain
  • amino sugar (N-acetyl glucosamine or N-acetyl
    galactosamine)
  • uronic acid (glucuronic acid or its 5 epimer
    iduronic acid

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Glycosaminoglycans (GAG), (mucopolysaccharides(
  • Most are present extracellulary except heparin.
  • mostly they act as structural components of the
    connective tissue e.g. collagen, bones, elastin,
    etc
  • They can also act as lubricants, because they
    have the property of holding water e.g. synovial
    fluid and vitreous humor of the eye.

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Glycosaminoglycans (GAG), (mucopolysaccharides(
  • Types
  • GAGs are either sulfate free (Hyaluronic acid) or
    sulfate containing as chondroitin sulfate,
    heparin, heparan sulfate, keratan sulfate and
    dermatan sulfate.
  •  

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Hyaluronic Acid
  • Structure
  • Repeated disaccharide units, composed of
    glucuronic acid and N-acetyl glucosamine.
  •  

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Hyaluronic Acid
  • Site
  • Present in
  • Synovial fluid.
  • Vitreous humor of the eye.
  • Skin and loose connective tissue.
  • Cartilage
  • Embyronic tissue.

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Hyaluronic Acid
  • Functions
  • Gel made of hyaluronic acid has good resistance
    to compression, thus it acts as lubricant and
    shock absorber in the synovial fluid.
  • It makes extra cellular matrix loose, because of
    its ability to attract water.
  • It forms an important part of cementing ground
    substance.

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Hyaluronidase Enzyme
  • This enzyme hydrolyses hyaluronic acid, thus
    allowing invasive agents to penetrate the tissue.
  • It is secreted by certain bacteria to help their
    invasion to tissue.
  • Secreted by Cercaria (infective stage of
    bilharziasis) to help penteration of skin.

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Chondroitin Sulfate
  • Structure
  • Repeated disaccharide units composed of
    Glucuronic acid and N-acetyl galactosamine
    sulfate. The sulfate group is either attached to
    carbon 4 forming chondroitin -4- sulfate or
    carbon 6 forming chondroitin -6- sulfate.
  •  

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Chondroitin Sulfate
  • Site
  • Cartilage, tendons, ligaments, bones.
  • Aorta, skin, cornea.
  • Functions
  • It has a role in binding collagen of cartilage
    and holding its fibers together. Compressibility
    of cartilage in weight bearing is due to
    chondroitin sulfate.

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Heparin
  • Structure
  • Disaccharide repeated units of
  • Iduronic acid with sulfate on C2
  • Glucosamine with sulfate on C3 and C6.

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Heparin
  • Site
  • In the mast cells (intracellular compound (
  • Function
  • Anticoagulant
  • Stimulates the release of lipoprotein lipase
    enzyme that hydrolyses the absorbed fats.

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Heparan Sulfate
  • It is like heparin in structure, but it
  • (1) contains fewer sulfate groups and
  • (2) Some glucosamines are acetylated.
  • Function
  • It is an extra cellular compounds, entering in
    the structure of receptors on cell surface.
  • It participates in cell adhesion and cell-cell
    interaction.

40
Keratan Sulfate
  • Structure
  • The disaccharide unit is composed of
  • (1) Galactose with sulfate on C6 and
  • (2 (N-acetyl glucosamine with sulfate on C6. No
    uronic acid
  • Site Cornea and cartilage .It plays a role in
    corneal transparency.
  •  

41
Dermatan Sulfate
  • Structure
  • Disacchride units composed of
  • L-Iduronic acid
  • N-acetyl galactosamine with sulfate on C6.
  • It is widely distributed in animal tissue,
    resembling chondroitin sulfate and Heparan
    sulfate.
  • It has anti thrombotic properties similar to
    heparin.
  •  

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Proteoglycans and Glycoproteins
  • Both are proteins containing carbohydrates but
    they contain different sugars, have different
    structures perform different functions and
    present in different sites.

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Proteoglycans
  • When proteins are attached to glycosaminoglycans
    (mucopolysaccharides), the compound is called
    Proteoglycans.
  • They serve as ground substance associated with
    structural elements of tissue e.g. bones,
    cartilage, elastin, collogen etc.
  • The glycosaminoglycans are present as long
    unbranched chains around a protein core.

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Proteoglycans
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Glycoproteins (Mucoproteins)
  • These occur in many different situations in
    fluids and tissues, including cell membranes.
  • They have protein core to which are attached
    carbohydrate chains which are
  • short, composed of 2-15 sugar units, or often
    oligosaccharide units, and
  • branched.

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Glycoproteins (Mucoproteins
  • Sugar present in glycoproteins include
  • Hexoses Galactose and mannose.
  • Pentoses Arabinose and xylose.
  • Melthyl pentose (L-fucose
  • Sialic acid.
  • Acetyl hexosamines, N-acetyl glucosamines and
    N-acetyl galactosamines.
  • They contain no glucose, no uronic acid or
    sulfate group.

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Glycoproteins (Mucoproteins
  • Functions
  • Components of extra cellular matrix.
  • Act as biological lubricants in mucin of the GIT,
    respiratory tract and urogenital tract
  • Components of cell membrane as
  • Blood group antigens, A, B, AB.
  • Cell surface recognition receptors

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Glycoproteins (Mucoproteins
  • Functions
  • Certain hormones are glycoproteins as Thyroid
    stimulating hormone (TSH) and human chorionic
    gonadotrophin HCG.
  • Some enzymes are glycoproteins
  • The immunologic components e.g.
    Immunoglobulins,complement factors, interferon
    ...etc are glycoproteins

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Thank You!
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