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BIOCHEMISTARY
PROJECT
TOPICS : GLYCOGENESIS
SUBMITTED BY : HARIOM
GOUR
The synthesis of glycogen from glucose is
called glycogenesis.
Glycogenesis take place in the cytosol
and requires ATP and UTP.
It is stored mainly in liver and muscle.
The liver content of glycogen is greater
than that of muscle.
Small amount of glycogen are also present
in other tissue like RBC, WBC, Kidney and
Brain.
Uterus also store glycogen during
pregnancy to nourish the embryo.
 Glycogen is the form energy storage in
the body.
They also know as animal starch.
Glycogen is multi branched polysaccharide
of glucose.
 Since the muscle mass of the body is
considerably greater than that of the liver, about
three-quarters of total body glycogen is in
muscle.
 Glycogen is present in the cytosol in the form of
granules ranging in diameter from 10 to 40 nm.
• Glucose unit linked by linearly by alpha (1-4)
Glycosidic bonds from one glucose to the next.
• Branches are linked to the chains from which they
are branching off alpha(1-6)glycosidic bonds
between the 1st glucose of the new branch and a
glucose on the stem chain.
• In glycogen, the branches occur at intervals of 8-10
glucose units
 The main function of glycogen is as secondary
long-term energy storage molecules.
 The function of liver glycogen is to maintain the
blood glucose level, particularly between meals.
 Liver glycogen stores increase in a well-fed state
which are depleted during fasting.
 Muscle glycogen serves as a fuel reserve for the
supply of ATP during muscle contraction.
1.Glycogenesis 2.Glycogenolysis
Activation
Initiation
Elongation
Glycogen Branching
Glucose is converted into glucose-6-phosphate by the action
of enzyme glucokinase (liver) or hexokinase(muscles), with
conversion of ATP to ADP.
Glucose-6-phosphate is converted into glucose-1-
phosphate by the action of enzyme phosphoglucomutase.
•Glucose 1-phosphate reacts with uridine triphosphate (UTP) to
form the active nucleotide uridine diphosphate glucose
(UDPGlc) and pyrophosphate.
• The reaction is catalyzed by UDP Glc pyrophosphorylase.
•UDP-glucose, the glucose donor in the biosynthesis of glycogen, is an
activated form of glucose.
• Synthesis of glycogen from glucose is carried out by the enzyme glycogen
synthase.
• This enzyme utilizes UDP-glucose as one substrate and the non-reducing
end of glycogen as another.
 Glucose+ATP glucose-1-phosphate+ADP
 Glucose-6phosphate glucose-1-phosphate
 Glucose-1-phosphate+UTP UDP-glucose+PPi
 PPi + H2O 2Pi
 UDP-glucose+(glycogen)n (glycogen)n+1+UDP
 UDP+ATP UTP+ ADP
Thus, two ATP is utilized, one is required for
the phosphorylation of glucose while the other is
needed for conversion of UDP to UTP.
Von gierke disease
Pompe disease
Cori’s disease
Her’s disease
glycogenesis

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glycogenesis

  • 2. The synthesis of glycogen from glucose is called glycogenesis. Glycogenesis take place in the cytosol and requires ATP and UTP. It is stored mainly in liver and muscle. The liver content of glycogen is greater than that of muscle.
  • 3. Small amount of glycogen are also present in other tissue like RBC, WBC, Kidney and Brain. Uterus also store glycogen during pregnancy to nourish the embryo.  Glycogen is the form energy storage in the body. They also know as animal starch. Glycogen is multi branched polysaccharide of glucose.
  • 4.  Since the muscle mass of the body is considerably greater than that of the liver, about three-quarters of total body glycogen is in muscle.  Glycogen is present in the cytosol in the form of granules ranging in diameter from 10 to 40 nm.
  • 5. • Glucose unit linked by linearly by alpha (1-4) Glycosidic bonds from one glucose to the next. • Branches are linked to the chains from which they are branching off alpha(1-6)glycosidic bonds between the 1st glucose of the new branch and a glucose on the stem chain. • In glycogen, the branches occur at intervals of 8-10 glucose units
  • 6.  The main function of glycogen is as secondary long-term energy storage molecules.  The function of liver glycogen is to maintain the blood glucose level, particularly between meals.  Liver glycogen stores increase in a well-fed state which are depleted during fasting.  Muscle glycogen serves as a fuel reserve for the supply of ATP during muscle contraction.
  • 7.
  • 10. Glucose is converted into glucose-6-phosphate by the action of enzyme glucokinase (liver) or hexokinase(muscles), with conversion of ATP to ADP.
  • 11. Glucose-6-phosphate is converted into glucose-1- phosphate by the action of enzyme phosphoglucomutase.
  • 12. •Glucose 1-phosphate reacts with uridine triphosphate (UTP) to form the active nucleotide uridine diphosphate glucose (UDPGlc) and pyrophosphate. • The reaction is catalyzed by UDP Glc pyrophosphorylase.
  • 13. •UDP-glucose, the glucose donor in the biosynthesis of glycogen, is an activated form of glucose. • Synthesis of glycogen from glucose is carried out by the enzyme glycogen synthase. • This enzyme utilizes UDP-glucose as one substrate and the non-reducing end of glycogen as another.
  • 14.  Glucose+ATP glucose-1-phosphate+ADP  Glucose-6phosphate glucose-1-phosphate  Glucose-1-phosphate+UTP UDP-glucose+PPi  PPi + H2O 2Pi  UDP-glucose+(glycogen)n (glycogen)n+1+UDP  UDP+ATP UTP+ ADP Thus, two ATP is utilized, one is required for the phosphorylation of glucose while the other is needed for conversion of UDP to UTP.
  • 15. Von gierke disease Pompe disease Cori’s disease Her’s disease