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
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
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.
4
Q
Glycogenesis
A
- the synthesis of glycogen granules
- begins with a core
protein called glycogenin
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
6
Q
Branching enzyme
A
- responsible for introducing α-1,6-linked branches into
the granule as it grows
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.”
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
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.
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
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).
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).
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.