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GLYCOGEN
METABOLISM
BY
K.DHARSHINI
I PHARM d
RVS
RVS COLLEGE OF PHARMACEUTICAL SCIENCES
SULUR, COIMBATORE, TAMIL NADU, INDIA.
GLYCOGEN
Glycogen is
generally a
polymer of glucose
This slide share deals with :
1. Glycogenesis
2. Glycogenolysis
3. Regulation of
glycogenesis and
Glycogenolysis
STRUCTURE
OF GLYCOGEN
Representation of the bonds
present in glycogen (*follow the
colors)
GLUCOSYL
RESIDUE(glucose
monomer)
NON-REDUCING
END
2. GLYCOGENIN
(protein core)
GLYCOGENESIS
• Step1:Synthesisofuridinediphosphateglucose
• Step2:Synthesisofaprimertoinitiateglycogen
synthesis
• Step3:Elongationofglycogenchains
• Step4:Formationofbranches
• Step5:Repetitionofstep3and4isdonetoforma
glycogenpolymer
MAJOR STEPS INVOLVED IN GLYCOGENESIS:
STEP 1:
• The enzymes hexokinase and glucokinase convert glucose to glucose 6
phosphate
• Phosphoglucomutase catalyses the Conversion of glucose 6 phosphate to
glucose 1 phosphate
• Uridine di phosphate glucose ( UDGP) is synthesized from glucose1 phosphate
and utp by udp glucose pyrophosphorylase
STEP 2 :
• A small fragment of pre-existing glycogen must act as a primer to initiate
glycogen synthesis
• the enzyme glycogen initiator synthase transfers the first molecule of glucose to
glycogenin
• Then glycogenin itself takes up a few glucose residues to form a Fragment of
primer
STEP 3 :
• Glycogen synthase is responsible for the formation of 1,4 glycosidic linkages
• This enzyme transfers the glucose from UDPG to the non –reducing end of glycogen to form alpha 1,4
linkages
STEP 4 :
• The formation of branches is brought by the action of a branching enzyme,
• Namely glucosyl alpha 4,6 transferase
• This enzyme transfers a small fragment of 5 to 8 glucose residues from the non reducing end of
glycogen chain to another glucose residue where it is linked with alpha 1,6 bond
• This leads to the formation of a new non reducing end besides the existing one
• Glycogen is further elongated and branched by the enzymes glycogen synthase and glucosyl 4-6
transferase
P
A
T
H
W
A
Y
The overall reaction of the glycogen synthesis for the
addition of each glucose residue
(GLUCOSE) n +GLUCOSE +2ATP
 (GLUCOSE) n+1 +2ADP +Pi
GLYCOGENOLYSIS
MAJOR STEPS INVOLVED IN GLYCOGENOLYSIS :
• Step1:Shorteningofchains
• Step2:Removalofbranches
• Step3:Conversionofglucose1phosphatetoglucose6
phosphateviaenzymephosphoglucomutase
Step 1 :
• The alpha 1,4 glycosidic bonds Are cleaved sequentially by the enzyme glycogen phosphorylase
to yield glucose 1-phosphate (phosphorolysis)
• The glycogen so formed is known as limit dextrin
• Glycogen phosphorylase possesses a molecule of pyridoxal phosphate
Step 2 :
• The branches of glycogen are cleaved by two enzyme activities present on a single polypeptide
called debranching enzyme
• Glucosyl 4:4 transferase removes a fragment of 3 or 4 glucose residues attached at a branch and
transfers them to another chain
• Here one alpha 1,4 cleaved and the same alpha 1,4 bond is made but the places are different
• Amylo alpha 1,6 glucosidase breaks the alpha 1,6 bond
• The remaining molecule of glycogenis again available for the action of phosphorylase and
debranching enzyme to repeat the reactions
Step 3 :
• Through the combined action of glycogen phosphorylase and debranching
enzyme glucose 1 phosphate and free glucose In a ratio of 8:1 are produced
• Glucose 1 phosphate is converted to glucose 6 phosphate by the enzyme
phosphoglucomutase
• The fate of glucose 6 phosphate depends on the tissue
• The liver, kidney ,and intestine contain the enzyme glucose 6 phosphatase
that cleaves glucose 6 phosphate to glucose
P
A
T
H
W
A
Y
The liver is the major
glycogen storage organ to
provide glucose into the
circulation to be utilized by
various tissue
REGULATION OF
GLYCOGENESIS
AND
GLYCOGENOLYSIS
Dephosphorylation
(Snthase Phosphatase)
Synthase d
Synthase
I
• Glycogen synthase is present in muscle and liver in two interconvertible form
• Synthase d is the dependent form and inactive form of the enzyme
• Synthase I is the independent form And active form of the enenzyme
• Synthase I is converted into synthase d by phosphorylation
• Synthase d is converted to synthase I by the enzyme synthase phosphatase by
dephosphorylation
Phosphorylation
GLYCOGEN SYNTHASE
OR GLUCOSYL TRANSFERSAE
PHOSPHORYLASE
Active
Phosphorylase
A
Inactive
Phosphorylase
B
• Phosphorylase exist in two forms
• The active phosphorylase a splits glucose 1 phosphate units from
glycogen
• The inactivated form is activated in presence of atp by a specific
phosphorylase kinase which is in turn stimulated by cyclic AMP
A good coordination and regulation of glycogen synthesis and it’s
degradation are essential to maintain the blood glucose levels. Glycogenesis
and Glycogenolysis are respectively controlled by glycogen synthase and
glycogen phosphorylase. regulation of these enzymes is accomplished by
three mechanisms
• ALLOSTERIC REGULATION
• HORMONAL REGULATION
• INFLUENCE OF CALCIUM
RECOLLECTION
WALL
ACKNOWLEDGEMENT
SINCERE THANKS TO
1. MR. S. S. Rajendran M. Pharm for his constant
support and supervision
2. The Library faculties of RVS COPS, Coimbatore, India
for their help with the requirements
3. Heart felt thanks to all professors and parents for
their cooperation regarding this slide share
The End

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Glycogen Metabolism and Regulation

  • 1. GLYCOGEN METABOLISM BY K.DHARSHINI I PHARM d RVS RVS COLLEGE OF PHARMACEUTICAL SCIENCES SULUR, COIMBATORE, TAMIL NADU, INDIA.
  • 2. GLYCOGEN Glycogen is generally a polymer of glucose This slide share deals with : 1. Glycogenesis 2. Glycogenolysis 3. Regulation of glycogenesis and Glycogenolysis
  • 3. STRUCTURE OF GLYCOGEN Representation of the bonds present in glycogen (*follow the colors)
  • 6. • Step1:Synthesisofuridinediphosphateglucose • Step2:Synthesisofaprimertoinitiateglycogen synthesis • Step3:Elongationofglycogenchains • Step4:Formationofbranches • Step5:Repetitionofstep3and4isdonetoforma glycogenpolymer MAJOR STEPS INVOLVED IN GLYCOGENESIS:
  • 7. STEP 1: • The enzymes hexokinase and glucokinase convert glucose to glucose 6 phosphate • Phosphoglucomutase catalyses the Conversion of glucose 6 phosphate to glucose 1 phosphate • Uridine di phosphate glucose ( UDGP) is synthesized from glucose1 phosphate and utp by udp glucose pyrophosphorylase STEP 2 : • A small fragment of pre-existing glycogen must act as a primer to initiate glycogen synthesis • the enzyme glycogen initiator synthase transfers the first molecule of glucose to glycogenin • Then glycogenin itself takes up a few glucose residues to form a Fragment of primer
  • 8. STEP 3 : • Glycogen synthase is responsible for the formation of 1,4 glycosidic linkages • This enzyme transfers the glucose from UDPG to the non –reducing end of glycogen to form alpha 1,4 linkages STEP 4 : • The formation of branches is brought by the action of a branching enzyme, • Namely glucosyl alpha 4,6 transferase • This enzyme transfers a small fragment of 5 to 8 glucose residues from the non reducing end of glycogen chain to another glucose residue where it is linked with alpha 1,6 bond • This leads to the formation of a new non reducing end besides the existing one • Glycogen is further elongated and branched by the enzymes glycogen synthase and glucosyl 4-6 transferase
  • 10. The overall reaction of the glycogen synthesis for the addition of each glucose residue (GLUCOSE) n +GLUCOSE +2ATP  (GLUCOSE) n+1 +2ADP +Pi
  • 12. MAJOR STEPS INVOLVED IN GLYCOGENOLYSIS : • Step1:Shorteningofchains • Step2:Removalofbranches • Step3:Conversionofglucose1phosphatetoglucose6 phosphateviaenzymephosphoglucomutase
  • 13. Step 1 : • The alpha 1,4 glycosidic bonds Are cleaved sequentially by the enzyme glycogen phosphorylase to yield glucose 1-phosphate (phosphorolysis) • The glycogen so formed is known as limit dextrin • Glycogen phosphorylase possesses a molecule of pyridoxal phosphate Step 2 : • The branches of glycogen are cleaved by two enzyme activities present on a single polypeptide called debranching enzyme • Glucosyl 4:4 transferase removes a fragment of 3 or 4 glucose residues attached at a branch and transfers them to another chain • Here one alpha 1,4 cleaved and the same alpha 1,4 bond is made but the places are different • Amylo alpha 1,6 glucosidase breaks the alpha 1,6 bond • The remaining molecule of glycogenis again available for the action of phosphorylase and debranching enzyme to repeat the reactions
  • 14. Step 3 : • Through the combined action of glycogen phosphorylase and debranching enzyme glucose 1 phosphate and free glucose In a ratio of 8:1 are produced • Glucose 1 phosphate is converted to glucose 6 phosphate by the enzyme phosphoglucomutase • The fate of glucose 6 phosphate depends on the tissue • The liver, kidney ,and intestine contain the enzyme glucose 6 phosphatase that cleaves glucose 6 phosphate to glucose
  • 16. The liver is the major glycogen storage organ to provide glucose into the circulation to be utilized by various tissue
  • 18. Dephosphorylation (Snthase Phosphatase) Synthase d Synthase I • Glycogen synthase is present in muscle and liver in two interconvertible form • Synthase d is the dependent form and inactive form of the enzyme • Synthase I is the independent form And active form of the enenzyme • Synthase I is converted into synthase d by phosphorylation • Synthase d is converted to synthase I by the enzyme synthase phosphatase by dephosphorylation Phosphorylation GLYCOGEN SYNTHASE OR GLUCOSYL TRANSFERSAE
  • 19. PHOSPHORYLASE Active Phosphorylase A Inactive Phosphorylase B • Phosphorylase exist in two forms • The active phosphorylase a splits glucose 1 phosphate units from glycogen • The inactivated form is activated in presence of atp by a specific phosphorylase kinase which is in turn stimulated by cyclic AMP
  • 20. A good coordination and regulation of glycogen synthesis and it’s degradation are essential to maintain the blood glucose levels. Glycogenesis and Glycogenolysis are respectively controlled by glycogen synthase and glycogen phosphorylase. regulation of these enzymes is accomplished by three mechanisms • ALLOSTERIC REGULATION • HORMONAL REGULATION • INFLUENCE OF CALCIUM
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  • 23. ACKNOWLEDGEMENT SINCERE THANKS TO 1. MR. S. S. Rajendran M. Pharm for his constant support and supervision 2. The Library faculties of RVS COPS, Coimbatore, India for their help with the requirements 3. Heart felt thanks to all professors and parents for their cooperation regarding this slide share