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G. D. RUNGTA COLLEGE OF SCIENCE & TECHNOLOGY, KOHKA, BHILAI.
BY:-
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Dr. ARUNIMA KARKUN
ASST. PROFESSOR
CLASSIFICATION OF POLYSACCHARIDES, GLUCONEOGENESIS
GLYCOGENOLYSIS
 INTRODUCTION
 WHAT ARE POLYSACCHARIDES?
 GENERAL CHARACTERSTICS OF
POLYSACCHARIDES
 CLASSIFICATION OF POLYSACCHARIDES
1. Homopolysaccharides
2. Heteropolysaccharides
 ROLE OF POLYSACCHARIDES
 GLUCONEOGENESIS
 GLYCOGENOLYSIS
 SUMMARY
 REFERENCES
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CLASSIFICATION OF POLYSACCHARIDES
 All organisms utilize carbohydrates  important
biomolecules.
 Nutrition: “carbos” are more than just starch and sugar.
 The term carbohydrate is derived from the french word:
“hydrate de carbone.”
 compounds composed of C, H, and O.
 empirical formula: (CH2O)n.
 Defination:- carbohydrate defined as
polyhydroxyaldehyde or ketone which produce
them on hydrolysis.
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CLASSIFICATION OF POLYSACCHARIDES
 FUNCTION OF CARBOHYDRATES
 Most abundant dietary source of energy (4 cal/g) for all organisms.
 Participate in the structure of cell membrane & cellular functions.
 Structural components of many organisms, include the fiber (cellulose) of
Plants, exoskeleton of some insects.
 Storage of energy to meet the immediate energy demands of the body.
 CLASSIFICATION OF CARBOHYDRATES
I. MONOSACCHARIDES- glucose, fructose.
I. OLIGOSACCHARIDES
• Di, tri, tetra, penta, upto 9 or 10
• Most important are the disaccharides-lactose, sucrose.
II. POLYSACCHARIDES OR GLYCANS
• Homopolysaccharides-starch, glycogen, cellulose
• Heteropolysaccharides
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CONT.
CLASSIFICATION OF POLYSACCHARIDES
 Generally called glycans.
 Contains a number of monosaccharide units linked by
glycosidic bonds.
 CHARACTERISTICS:
 Polymers (MW from 200,000).
 White and amorphous products (glassy)
 Not sweet.
 Not reducing; do not give the typical aldose or
ketose reactions).
 Form colloidal solutions or suspensions.
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POLYSACCHARIDES
CLASSIFICATION OF POLYSACCHARIDES
POLYSACCHARIDES
HOMOPOLYSACCHARIDES HETROPOLYSACCHARIDES
CLASSIFICATION OF POLYSACCHARIDES
Divided into two broad groups:
(i) Homopolysaccharides-
 Contains only one type of monomer.
 On hydrolysis, they yield only one type of monosaccharide.
Examples: Starch, cellulose, glycogen
(ii) Heteropolysaccharides-
 Contain two or more types of monomers.
 On hydrolysis, they yield mixture of monosaccharides.
Examples: hyaluronic acid, chondriotin sulphate, heparin,
and mureins.
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Fig. no 1
CLASSIFICATION OF POLYSACCHARIDES
1. STARCH
• Two forms: amylose , amylopectin.
• 1,4-a-D-glucopyranose polymer.
• Function: plant glucose/energy storage.
• Hydrolysis  glucopyranose.
• Easily digested by mammals.
• Natural starches contain 10-20% amylose and 80-90%
amylopectin.
a. Amylose - unbranched α (1-4 )
• 200 to 20 000 glucose units.
• Water soluble(15-20%).
• Stained blue by iodine.
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Homopolysaccharides-
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CLASSIFICATION OF POLYSACCHARIDES
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b. Amylopectin - branched
α (1-4 ) + α (1-6 )
 Up to million glucose
units.
 Water insoluble
amylopectin(80-
82%).
 Stained red-brown by
iodine.
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STRUCTURE NO .1
STRUCTURE NO .2
CONT.
CLASSIFICATION OF POLYSACCHARIDES
2. GLYCOGEN
 The glucose storage polymer in animals, is similar in
structure to amylopectin
 But glycogen has more a(16) branches.
 The highly branched structure permits rapid glucose
release from glycogen stores, e.g., in muscle during
exercise.
 The ability to rapidly mobilize glucose is more essential
to animals than to plants
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S H O
OH
H
OHH
OH
CH2OH
H
O H
H
OHH
OH
CH2OH
H
O
HH H O
O
H
OHH
OH
CH2
H
H H O
H
OHH
OH
CH2OH
H
OH
HH O
O
H
OHH
OH
CH2OH
H
O
H
O
1 4
6
H O
H
OHH
OH
CH2OH
H
H H O
H
OHH
OH
CH2OH
H
H
O
1
OH
3
4
5
2
glycogen
CONT.
STRUCTURE NO .3
CLASSIFICATION OF POLYSACCHARIDES
3. CELLULOSE - nonbranched ß (1-4 )
• Insoluble, chemically very resistant.
• Major structural material of plants, wood, cotton.
• It is a major constituent of fiber.
• Cellulose is totally absent in animal.
• Composed of ß - D-glucose units linked by ß (1-4 ) glycosidic
bonds.
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STRUCTURE NO . 4
CONT.
CLASSIFICATION OF POLYSACCHARIDES
4.CHITIN
N-acetyl-D-glukosamine a ( 1-4 )
• Structural polysaccharide of exoskeleton of invertebrates (in complex with proteins
and/or CaCO3)
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D-galakturonic acid a (1-4)
• Methylesters
often side chains containing other
monosaccharides.
• Present in small fruits, plants.
STRUCTURE NO.5
.
STRUCTURE NO..6
CONT
CLASSIFICATION OF POLYSACCHARIDES
2.HETEROPOLYSACCHARIDES
 It is composed of a mixture of monosaccharides.
 On hydrolysis, they yield a mixture of monosaccharides.
 HETEROPOLYSACCHARIDES - are further
classified into two types:
A. NEUTRAL SUGARS.
B. MUCOPOLYSACCHARIDES .
A. NEUTRAL SUGARS.
 This group Includes some hemicellulose, some gums,
mucilages & pectic substances.
 Give more than one type of sugar units on hydrolysis &
sometimes non-sugar components .
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CLASSIFICATION OF POLYSACCHARIDES
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B. MUCOPOLYSACCHARIDES .
 Mucopolysaccharides are heteroglycans made up of
polysaccharides made up of repeating units of sugar
derivatives, namely amino sugars & uronic sugar.
 Commonly known as Glycosaminoglycans (GAG).
 Mucopolysaccharides are essential components of tissue
structure.
 Some Mucopolysaccharides are found in combination with
proteins to form Mucoproteins or mucoids or proteoglycans .
 Mucopolysaccharides include hyaluronic acid ,heparin ,
dermatan sulfate, keratan sulfate.
CLASSIFICATION OF POLYSACCHARIDES
1.HYALURONATE (Hyaluronan) or Hyluronic acid.
 It is a glycosaminoglycan with a repeating
disaccharide consisting of 2 glucose derivatives, glucuronate
(glucuronic acid) & N-acetyl-glucosamine.
 The glycosidic linkages are ß (1-3) & ß (1-4).
 Hyaluronidase is an enzyme present in high concentration in
testes, seminal fluid, in certain snake & insects that breaks ß(1-
4) linkages.
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H O
H
H
OHH
OH
COO
H
H O
OH H
H
NHCOCH3H
CH2OH
H
OO
D-glucuronate
O
1
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4
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6
1
23
4
5
6
N-acetyl-D-glucosamine
hyaluronate
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MUCOPOLYSACCHARIDES
STRUCTURE NO..7
CLASSIFICATION OF POLYSACCHARIDES
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2. KERATAN SULFATE
 It is a heterogeneous GAG with a variable sulfate content, besides small
amounts of mannose, fructose, sialic acid etc.
 It is essentially consists of alternating units of D- galactosamine and
N-acetylglucasamine .
 They are present in cartilage, bone, cornea, nail, hoofs, claws.
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STRUCTURE NO.8
CONT.
CLASSIFICATION OF POLYSACCHARIDES
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3.HEPARIN
 Heparin is an anticoagulant (prevents blood clotting) that occurs in blood,
lung, liver, kidney, spleen etc.
 Made in mast cell & released into the blood.
 Heparin is composed of alternating units of N-sulfo D-glucosamine 6-
sulfate & glucoronate 2-sulfate,
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STRUCTURE NO.9
CONT.
CLASSIFICATION OF POLYSACCHARIDES
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 ROLE OF POLYSACCHARIDES
TABLE NO .1
GLUCONEOGENESIS
 Definition: the biosynthesis of glucose primarily from pyruvate and its
precursors.
 The major substrates/precursors for gluconeogenesis are lactate, pyruvate,
glucogenic amino acid, propionate & glycerol.
 The liver is the major location for gluconeogenesis (about 1kg glucose
synthesized everyday).
 Gluconeogenesis occurs mainly in the Cytosol, although some precursors are
produced in the Mitochondria.
 This is essential cycle for the survival of humans and other animals.
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GLUCONEOGENESIS
 Gluconeogenesis closely resembles the reversed pathway of glycolysis,
although it is not the complete reversal of glycolysis.
 Essentially, 3(out of 10) reactions of glycolysis are irreversible.
 The 7 reactions are common for both glycolysis & Gluconeogenesis.
 The 3 irreversible steps of glycolysis are catalysed by the enzymes, namely
hexokinase , phosphofructokinase and pyruvate kinase.
 These 3 stages- bypassed by alternate enzymes specific to Gluconeogenesis
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GLUCONEOGENESIS
21CYCLE NO.1
CONT.
GLUCONEOGENESIS
 These 3 stages- bypassed by alternate enzymes specific to Gluconeogenesis are below:-
1. Conversion of pyruvate to phosphophenol-pyruvate:
 This takes place in two steps –
a) Pruvate carboxylase is a biotin-dependent mitochondrial enzyme that converts
Pruvate to oxaloacetate in presence of ATP & CO2.
b) In the cytosol, phosphoenolpyruvate carboxykinase converts oxaloacetate to
phosphoenolpyruvate.
2. Conversion of fructose 1,6-biphosphate to fructose 6-phosphate:
 Phosphophenolpyruvate undergoes the reversal of glycolysis until fructose
1,6-biphosphate is produced.
3. Conversion of Glucose 6-phosphate to Glucose:
 Glucose 6-phosphate catalyses the conversion of Glucose 6-phosphate to
Glucose.
 Glycolysis & Gluconeogenesis are both spontaneous.
 If both pathways were simultaneously active in a cell, it would constitute a
"futile cycle" that would waste energy .
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GLUCONEOGENESIS
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SEQEUENTIAL REACTIONS OF GLUCONEOGENESIS
CHART NO.2
CONT.
GLUCONEOGENESIS
 Overall summary of Gluconeogenesis for the conversion of
pyruvate to glucose is shown below:-
Glycolysis:
glucose + 2 NAD+ + 2 ADP + 2 Pi 
2 pyruvate + 2 NADH + 2 ATP.
Gluconeogenesis:
2 pyruvate + 2 NADH + 4 ATP + 2 GTP +2H+ 
glucose + 2 NAD+ + 4 ADP + 2 GDP + 6 Pi +6H +
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GLUCONEOGENESIS
IMPORTANCE OF GLUCONEOGENESIS :-
 Brain, central nervous system, erythrocytes, testes & kidney medulla are
dependent on glucose for continuous supply of energy.
 In fasting even more than a day gluconeogenesis must occur to meet the basal
requirements of the body.
 Glucose is the only source that supplies energy to the skeletal muscle , under
anaerobic conditions.
 Certain metabolites produced in the tissues accumulate in the blood e.g
lactate ,glycerol etc gluconeogenesis effectively clears them from blood.
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GLYCOGENOLYSIS
 DEFINATION:-The degradation of stored glycogen in the liver and
muscle constitutes GLYCOGENOLYSIS.
 The pathways for the synthesis and degradation of glycogen are not possible
are not reversible.
 An independent set of enzymes present in the cytosol carry out glycogenolysis.
 Glycogen is degraded by breaking α-1,4- & α-1,6-glycosidic bonds.
 A good coordination & regulation of glycogen synthesis & its degradation are
essential to maintain the blood glucose levels.
 Glycogenesis & glycogenolysis are , respectively, controlled by the enzymes
glycogen synthase & glycogen phosphorylase.
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GLYCOGENOLYSIS
2.ACTION OF GLYCOGEN PHOSPHORYLASE:-
 The α-1,4-glycosidic bonds are cleaved sequentially by the enzyme glycogen to
yield glucose 1-phosphate.This process is called phosphorolysis.
 The glycogen so formed is known as limit dextin which cannot be further
degraded by phosphorylase.
2. ACTION OF DEBRANCHING ENZYME:
 The branches of glycogen are cleaved by two enzyme activities present on a single
polypeptide called debranching enzyme, hence it is a bifunctional enzyme.
 Amylo α-1,4-glycosidase breaks the α-1,6-bond at the branch with a single glucose
residue and release a free glucose.
3.FORMATION OF GLUCOSE 6-PHOSPHATE AND GLUCOSE:
 Through the combined action of glycogen phosphorylase and debranching enzyme
glucose 1-phosphate & free glucose in a ratio of 8:1 are produced .
 Glucose 1-phosphate is converted to glucose 6-phosphate by the enzyme
phosphoglucomutase.
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GLYCOGENOLYSIS
28CYCLE NO.2
*
GLYCOGENOLYSIS
 Glycogen is the storage form of glucose.
 The degradation of glycogen (glycogenolysis) in muscle
meets the immediate fuel requirements.
 On the other hand the liver glycogen maintains the blood
glucose level.
 Enzymes defects in synthesis or the degradation of glycogen
leads to storage disorders.
 Von Gierke’s disease is due to the defect in the enzyme
glucose 6- phosphatase .
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SUMMARY
 Carbohydrates are the polyhydroxyaldhyde or ketones or compounds which
produce them on hydrolysis .
 Carbohydrates are broadly classified into three groups:-
MONOSACCHARIDES,OLIGOSACCHARIDES,POLYSACCHARIDES.
 Polysaccharides are the polymers of monosaccharides on their derivative, held
together by glycosidic bonds.
 Polysaccharides are broadly classified into two groups:-
(A)Hompolysaccharides (B)Heteropolysaccharides
 The biosynthesis of glucose primarily from pyruvate and its precursors is
known as gluconeogenesis.
 The degradation of stored glycogen in the liver and muscle constitutes
glycogenolysis.
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CLASSIFICATION OF POLYSACCHARIDES , GLUCONEOGENESIS,
GLYCOGENOLYSIS
 Polysaccharides play important role in structure & storage for plants.
 Polysaccharides are also help in cell envelope development in bacteria.
 Polysaccharides provides exoskeleton in spiders & insects.
 In fasting even more than a day gluconeogenesis must occur to meet the
basal requirements of the body.
 Glucose is the only source that supplies energy to the skeletal muscle ,
under anaerobic conditions.
 Certain metabolites produced in the tissues accumulate in the blood e.g
lactate ,glycerol etc gluconeogenesis effectively clears them from blood.
 Glycogenolysis supplies energy to muscles & other body parts.
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CLASSIFICATION OF POLYSACCHARIDES , GLUCONEOGENESIS,
GLYCOGENOLYSIS
ALBERT L. LEHNINGER YEAR -2005 BIOCHEMISTRY,
2ND EDITION, FREEMAN
PUBLICATION.
L. NELSON & M. COX YEAR -2009 PRINCIPLES OF
BIOCHEMISTRY, 5TH
EDITION,STUTTGAT
PUBLICATION.
J. L. JAIN YEAR -2010 PRINCIPLES OF
BIOCHEMISTRY,
6TH EDITION,S.CHAND
PUBLICATION.
U.SATYANARAYANA ,
U.CHAKRAPANI
YEAR -2010 BIOCHEMISTRY,
6TH EDITION,UPPALA
PUBLICATION.
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OTHER SOURCES- WEB LINKS
33

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Classification of polysaccharides, gluconeogenesis and glucogenolysis.

  • 1. G. D. RUNGTA COLLEGE OF SCIENCE & TECHNOLOGY, KOHKA, BHILAI. BY:- 1 Dr. ARUNIMA KARKUN ASST. PROFESSOR
  • 2. CLASSIFICATION OF POLYSACCHARIDES, GLUCONEOGENESIS GLYCOGENOLYSIS  INTRODUCTION  WHAT ARE POLYSACCHARIDES?  GENERAL CHARACTERSTICS OF POLYSACCHARIDES  CLASSIFICATION OF POLYSACCHARIDES 1. Homopolysaccharides 2. Heteropolysaccharides  ROLE OF POLYSACCHARIDES  GLUCONEOGENESIS  GLYCOGENOLYSIS  SUMMARY  REFERENCES S Y N O P S I S 2
  • 3. CLASSIFICATION OF POLYSACCHARIDES  All organisms utilize carbohydrates  important biomolecules.  Nutrition: “carbos” are more than just starch and sugar.  The term carbohydrate is derived from the french word: “hydrate de carbone.”  compounds composed of C, H, and O.  empirical formula: (CH2O)n.  Defination:- carbohydrate defined as polyhydroxyaldehyde or ketone which produce them on hydrolysis. 3 I N T R O D U C T I O N
  • 4. CLASSIFICATION OF POLYSACCHARIDES  FUNCTION OF CARBOHYDRATES  Most abundant dietary source of energy (4 cal/g) for all organisms.  Participate in the structure of cell membrane & cellular functions.  Structural components of many organisms, include the fiber (cellulose) of Plants, exoskeleton of some insects.  Storage of energy to meet the immediate energy demands of the body.  CLASSIFICATION OF CARBOHYDRATES I. MONOSACCHARIDES- glucose, fructose. I. OLIGOSACCHARIDES • Di, tri, tetra, penta, upto 9 or 10 • Most important are the disaccharides-lactose, sucrose. II. POLYSACCHARIDES OR GLYCANS • Homopolysaccharides-starch, glycogen, cellulose • Heteropolysaccharides 4 I N T R O D U C T I O N CONT.
  • 5. CLASSIFICATION OF POLYSACCHARIDES  Generally called glycans.  Contains a number of monosaccharide units linked by glycosidic bonds.  CHARACTERISTICS:  Polymers (MW from 200,000).  White and amorphous products (glassy)  Not sweet.  Not reducing; do not give the typical aldose or ketose reactions).  Form colloidal solutions or suspensions. 5 W H A T A R E P O L Y S A C C H A R I D E S ? POLYSACCHARIDES
  • 7. CLASSIFICATION OF POLYSACCHARIDES Divided into two broad groups: (i) Homopolysaccharides-  Contains only one type of monomer.  On hydrolysis, they yield only one type of monosaccharide. Examples: Starch, cellulose, glycogen (ii) Heteropolysaccharides-  Contain two or more types of monomers.  On hydrolysis, they yield mixture of monosaccharides. Examples: hyaluronic acid, chondriotin sulphate, heparin, and mureins. 7 C L A S S I F I C A T I O N Fig. no 1
  • 8. CLASSIFICATION OF POLYSACCHARIDES 1. STARCH • Two forms: amylose , amylopectin. • 1,4-a-D-glucopyranose polymer. • Function: plant glucose/energy storage. • Hydrolysis  glucopyranose. • Easily digested by mammals. • Natural starches contain 10-20% amylose and 80-90% amylopectin. a. Amylose - unbranched α (1-4 ) • 200 to 20 000 glucose units. • Water soluble(15-20%). • Stained blue by iodine. 8 Homopolysaccharides- E X A M P L E S
  • 9. CLASSIFICATION OF POLYSACCHARIDES 9 b. Amylopectin - branched α (1-4 ) + α (1-6 )  Up to million glucose units.  Water insoluble amylopectin(80- 82%).  Stained red-brown by iodine. E X A M P L E S - STRUCTURE NO .1 STRUCTURE NO .2 CONT.
  • 10. CLASSIFICATION OF POLYSACCHARIDES 2. GLYCOGEN  The glucose storage polymer in animals, is similar in structure to amylopectin  But glycogen has more a(16) branches.  The highly branched structure permits rapid glucose release from glycogen stores, e.g., in muscle during exercise.  The ability to rapidly mobilize glucose is more essential to animals than to plants 10 E X A M P L E S H O OH H OHH OH CH2OH H O H H OHH OH CH2OH H O HH H O O H OHH OH CH2 H H H O H OHH OH CH2OH H OH HH O O H OHH OH CH2OH H O H O 1 4 6 H O H OHH OH CH2OH H H H O H OHH OH CH2OH H H O 1 OH 3 4 5 2 glycogen CONT. STRUCTURE NO .3
  • 11. CLASSIFICATION OF POLYSACCHARIDES 3. CELLULOSE - nonbranched ß (1-4 ) • Insoluble, chemically very resistant. • Major structural material of plants, wood, cotton. • It is a major constituent of fiber. • Cellulose is totally absent in animal. • Composed of ß - D-glucose units linked by ß (1-4 ) glycosidic bonds. 11 E X A M P L E S STRUCTURE NO . 4 CONT.
  • 12. CLASSIFICATION OF POLYSACCHARIDES 4.CHITIN N-acetyl-D-glukosamine a ( 1-4 ) • Structural polysaccharide of exoskeleton of invertebrates (in complex with proteins and/or CaCO3) 12 E X A M P L E S 5. PECTIN D-galakturonic acid a (1-4) • Methylesters often side chains containing other monosaccharides. • Present in small fruits, plants. STRUCTURE NO.5 . STRUCTURE NO..6 CONT
  • 13. CLASSIFICATION OF POLYSACCHARIDES 2.HETEROPOLYSACCHARIDES  It is composed of a mixture of monosaccharides.  On hydrolysis, they yield a mixture of monosaccharides.  HETEROPOLYSACCHARIDES - are further classified into two types: A. NEUTRAL SUGARS. B. MUCOPOLYSACCHARIDES . A. NEUTRAL SUGARS.  This group Includes some hemicellulose, some gums, mucilages & pectic substances.  Give more than one type of sugar units on hydrolysis & sometimes non-sugar components . 13
  • 14. CLASSIFICATION OF POLYSACCHARIDES 14 B. MUCOPOLYSACCHARIDES .  Mucopolysaccharides are heteroglycans made up of polysaccharides made up of repeating units of sugar derivatives, namely amino sugars & uronic sugar.  Commonly known as Glycosaminoglycans (GAG).  Mucopolysaccharides are essential components of tissue structure.  Some Mucopolysaccharides are found in combination with proteins to form Mucoproteins or mucoids or proteoglycans .  Mucopolysaccharides include hyaluronic acid ,heparin , dermatan sulfate, keratan sulfate.
  • 15. CLASSIFICATION OF POLYSACCHARIDES 1.HYALURONATE (Hyaluronan) or Hyluronic acid.  It is a glycosaminoglycan with a repeating disaccharide consisting of 2 glucose derivatives, glucuronate (glucuronic acid) & N-acetyl-glucosamine.  The glycosidic linkages are ß (1-3) & ß (1-4).  Hyaluronidase is an enzyme present in high concentration in testes, seminal fluid, in certain snake & insects that breaks ß(1- 4) linkages. 15 H O H H OHH OH COO H H O OH H H NHCOCH3H CH2OH H OO D-glucuronate O 1 23 4 5 6 1 23 4 5 6 N-acetyl-D-glucosamine hyaluronate E X A M P L E S MUCOPOLYSACCHARIDES STRUCTURE NO..7
  • 16. CLASSIFICATION OF POLYSACCHARIDES 16 2. KERATAN SULFATE  It is a heterogeneous GAG with a variable sulfate content, besides small amounts of mannose, fructose, sialic acid etc.  It is essentially consists of alternating units of D- galactosamine and N-acetylglucasamine .  They are present in cartilage, bone, cornea, nail, hoofs, claws. E X A M P L E S STRUCTURE NO.8 CONT.
  • 17. CLASSIFICATION OF POLYSACCHARIDES 17 3.HEPARIN  Heparin is an anticoagulant (prevents blood clotting) that occurs in blood, lung, liver, kidney, spleen etc.  Made in mast cell & released into the blood.  Heparin is composed of alternating units of N-sulfo D-glucosamine 6- sulfate & glucoronate 2-sulfate, E X A M P L E S STRUCTURE NO.9 CONT.
  • 18. CLASSIFICATION OF POLYSACCHARIDES 18  ROLE OF POLYSACCHARIDES TABLE NO .1
  • 19. GLUCONEOGENESIS  Definition: the biosynthesis of glucose primarily from pyruvate and its precursors.  The major substrates/precursors for gluconeogenesis are lactate, pyruvate, glucogenic amino acid, propionate & glycerol.  The liver is the major location for gluconeogenesis (about 1kg glucose synthesized everyday).  Gluconeogenesis occurs mainly in the Cytosol, although some precursors are produced in the Mitochondria.  This is essential cycle for the survival of humans and other animals. 19 I N T R O D U C T I O N
  • 20. GLUCONEOGENESIS  Gluconeogenesis closely resembles the reversed pathway of glycolysis, although it is not the complete reversal of glycolysis.  Essentially, 3(out of 10) reactions of glycolysis are irreversible.  The 7 reactions are common for both glycolysis & Gluconeogenesis.  The 3 irreversible steps of glycolysis are catalysed by the enzymes, namely hexokinase , phosphofructokinase and pyruvate kinase.  These 3 stages- bypassed by alternate enzymes specific to Gluconeogenesis 20 I N T R O D U C T I O N
  • 22. GLUCONEOGENESIS  These 3 stages- bypassed by alternate enzymes specific to Gluconeogenesis are below:- 1. Conversion of pyruvate to phosphophenol-pyruvate:  This takes place in two steps – a) Pruvate carboxylase is a biotin-dependent mitochondrial enzyme that converts Pruvate to oxaloacetate in presence of ATP & CO2. b) In the cytosol, phosphoenolpyruvate carboxykinase converts oxaloacetate to phosphoenolpyruvate. 2. Conversion of fructose 1,6-biphosphate to fructose 6-phosphate:  Phosphophenolpyruvate undergoes the reversal of glycolysis until fructose 1,6-biphosphate is produced. 3. Conversion of Glucose 6-phosphate to Glucose:  Glucose 6-phosphate catalyses the conversion of Glucose 6-phosphate to Glucose.  Glycolysis & Gluconeogenesis are both spontaneous.  If both pathways were simultaneously active in a cell, it would constitute a "futile cycle" that would waste energy . 22 R E A C T I O N S
  • 23. GLUCONEOGENESIS 23 SEQEUENTIAL REACTIONS OF GLUCONEOGENESIS CHART NO.2 CONT.
  • 24. GLUCONEOGENESIS  Overall summary of Gluconeogenesis for the conversion of pyruvate to glucose is shown below:- Glycolysis: glucose + 2 NAD+ + 2 ADP + 2 Pi  2 pyruvate + 2 NADH + 2 ATP. Gluconeogenesis: 2 pyruvate + 2 NADH + 4 ATP + 2 GTP +2H+  glucose + 2 NAD+ + 4 ADP + 2 GDP + 6 Pi +6H + 24 O V E R A L L S U M M A R Y
  • 25. GLUCONEOGENESIS IMPORTANCE OF GLUCONEOGENESIS :-  Brain, central nervous system, erythrocytes, testes & kidney medulla are dependent on glucose for continuous supply of energy.  In fasting even more than a day gluconeogenesis must occur to meet the basal requirements of the body.  Glucose is the only source that supplies energy to the skeletal muscle , under anaerobic conditions.  Certain metabolites produced in the tissues accumulate in the blood e.g lactate ,glycerol etc gluconeogenesis effectively clears them from blood. 25 I M P O R T A N C E
  • 26. GLYCOGENOLYSIS  DEFINATION:-The degradation of stored glycogen in the liver and muscle constitutes GLYCOGENOLYSIS.  The pathways for the synthesis and degradation of glycogen are not possible are not reversible.  An independent set of enzymes present in the cytosol carry out glycogenolysis.  Glycogen is degraded by breaking α-1,4- & α-1,6-glycosidic bonds.  A good coordination & regulation of glycogen synthesis & its degradation are essential to maintain the blood glucose levels.  Glycogenesis & glycogenolysis are , respectively, controlled by the enzymes glycogen synthase & glycogen phosphorylase. 26 I N T R O D U C T I O N
  • 27. GLYCOGENOLYSIS 2.ACTION OF GLYCOGEN PHOSPHORYLASE:-  The α-1,4-glycosidic bonds are cleaved sequentially by the enzyme glycogen to yield glucose 1-phosphate.This process is called phosphorolysis.  The glycogen so formed is known as limit dextin which cannot be further degraded by phosphorylase. 2. ACTION OF DEBRANCHING ENZYME:  The branches of glycogen are cleaved by two enzyme activities present on a single polypeptide called debranching enzyme, hence it is a bifunctional enzyme.  Amylo α-1,4-glycosidase breaks the α-1,6-bond at the branch with a single glucose residue and release a free glucose. 3.FORMATION OF GLUCOSE 6-PHOSPHATE AND GLUCOSE:  Through the combined action of glycogen phosphorylase and debranching enzyme glucose 1-phosphate & free glucose in a ratio of 8:1 are produced .  Glucose 1-phosphate is converted to glucose 6-phosphate by the enzyme phosphoglucomutase. 27 R E A C T I O N S
  • 29. GLYCOGENOLYSIS  Glycogen is the storage form of glucose.  The degradation of glycogen (glycogenolysis) in muscle meets the immediate fuel requirements.  On the other hand the liver glycogen maintains the blood glucose level.  Enzymes defects in synthesis or the degradation of glycogen leads to storage disorders.  Von Gierke’s disease is due to the defect in the enzyme glucose 6- phosphatase . 29 I M P O R T A N C E
  • 30. SUMMARY  Carbohydrates are the polyhydroxyaldhyde or ketones or compounds which produce them on hydrolysis .  Carbohydrates are broadly classified into three groups:- MONOSACCHARIDES,OLIGOSACCHARIDES,POLYSACCHARIDES.  Polysaccharides are the polymers of monosaccharides on their derivative, held together by glycosidic bonds.  Polysaccharides are broadly classified into two groups:- (A)Hompolysaccharides (B)Heteropolysaccharides  The biosynthesis of glucose primarily from pyruvate and its precursors is known as gluconeogenesis.  The degradation of stored glycogen in the liver and muscle constitutes glycogenolysis. 30 S U M M A R Y
  • 31. CLASSIFICATION OF POLYSACCHARIDES , GLUCONEOGENESIS, GLYCOGENOLYSIS  Polysaccharides play important role in structure & storage for plants.  Polysaccharides are also help in cell envelope development in bacteria.  Polysaccharides provides exoskeleton in spiders & insects.  In fasting even more than a day gluconeogenesis must occur to meet the basal requirements of the body.  Glucose is the only source that supplies energy to the skeletal muscle , under anaerobic conditions.  Certain metabolites produced in the tissues accumulate in the blood e.g lactate ,glycerol etc gluconeogenesis effectively clears them from blood.  Glycogenolysis supplies energy to muscles & other body parts. 31 C O N C L U S I O N
  • 32. CLASSIFICATION OF POLYSACCHARIDES , GLUCONEOGENESIS, GLYCOGENOLYSIS ALBERT L. LEHNINGER YEAR -2005 BIOCHEMISTRY, 2ND EDITION, FREEMAN PUBLICATION. L. NELSON & M. COX YEAR -2009 PRINCIPLES OF BIOCHEMISTRY, 5TH EDITION,STUTTGAT PUBLICATION. J. L. JAIN YEAR -2010 PRINCIPLES OF BIOCHEMISTRY, 6TH EDITION,S.CHAND PUBLICATION. U.SATYANARAYANA , U.CHAKRAPANI YEAR -2010 BIOCHEMISTRY, 6TH EDITION,UPPALA PUBLICATION. 32 R E F E R E N C E S OTHER SOURCES- WEB LINKS
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