9.5 Glycogenesis and Glycogenolysis Flashcards

1
Q

Glycogen

A
  • branched polymer of glucose, represents a storage form of
    glucose.
  • Glycogen synthesis and degradation occur primarily in liver and skeletal muscle, although other tissues store smaller quantities
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2
Q

How is glycogen stored in the cytoplasm?

A
  • As granules
  • Each granule has a central protein core with polyglucose chains radiating outward to form a sphere
  • If the chains are branched, the
    glucose density is highest at the periphery of the granule, allowing more rapid release of glucose on demand
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3
Q

Difference between glycogen in the liver and in skeletal muscle?

A
  • Liver glycogen is broken down to maintain a constant level of glucose in the blood
  • Muscle glycogen is broken down to provide glucose to the muscle during vigorous exercise.
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4
Q

Glycogenesis

A
  • the synthesis of glycogen granules
  • begins with a core
    protein called glycogenin
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5
Q

Glycogen Synthase

A
  • the rate-limiting enzyme of glycogen synthesis and
    forms the α-1,4 glycosidic bond found in the linear glucose chains of the granule
  • stimulated by glucose 6-phosphate and insulin. It is inhibited by epinephrine and glucagon through a protein kinase cascade that phosphorylates and inactivates the enzyme
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6
Q

Branching enzyme

A
  • responsible for introducing α-1,6-linked branches into
    the granule as it grows
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7
Q

How is a branch created?

A
  • Hydrolyzes one of the α-1,4 bonds to release a block of oligoglucose (a few glucose molecules bonded together in a chain), which is then moved and added in a slightly different location.
  • Forms an α-1,6 bond to create a branch

-Mnemonic: α-1,4 keeps the same branch moving “4ward”; α-1,6 (one-six) “puts a branch in the mix.”

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8
Q

Glycogenolysis

A
  • the process of breaking down
    glycogen
  • rate-limiting enzyme of glycogenolysis
  • The glucose 1-phosphate formed by glycogen phosphorylase is converted to glucose 6-phosphate by the same mutase used in glycogen synthesis
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9
Q

How is glycogen phosphorylase activated in liver vs skeletal muscle?

A
  • Glycogen phosphorylase is activated by glucagon in the liver, so that glucose can be
    provided for the rest of the body.
  • In skeletal muscle, it is activated by AMP and epinephrine, which signal that the muscle is active and requires more glucose.
  • It is inhibited by ATP.
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10
Q

Glycogen Phosphorylase

A
  • breaks α-1,4 glycosidic bonds, releasing glucose 1- phosphate from the periphery of the granule. It cannot break α-1,6 bonds and therefore stops when it nears the outermost branch points
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11
Q

Debranching enzyme

A
  • a two-enzyme complex that deconstructs the branches in glycogen that have been exposed by glycogen phosphorylase
  • Debranching enzyme is actually made up of two enzymes with different functions: one moves the terminal end of a glycogen chain to the branch point (α-1,4:α-1,4 transferase), and one removes the glucose monomer actually present at the branch point (α-1,6 glucosidase).
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12
Q

Debranching Enzyme Pathway

A
  • Breaks an α-1,4 bond adjacent to the branch point and moves the small oligoglucose chain that is released to the exposed end of the other chain.
  • Forms a new α-1,4 bond.
  • Hydrolyzes the α-1,6 bond, releasing the single residue at the branch point as free glucose. This represents the only free glucose produced directly in glycogenolysis (as opposed to the glucose produced from glucose 1 phosphate, which must be converted by a mutase to glucose 6-phosphate before it can be converted to glucose via the enzyme glucose-6-phosphatase).
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13
Q

Isoforms

A
  • slightly different versions of the same protein; in the case of glycogen enzymes, there are often different isoforms of the enzymes in the liver and muscle.
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