Glycogen Flashcards
Glycogen
1) a glucose polymer (up to 100,000 molecules of glucose/ molecule of glycogen)
2) Homopolysaccharide (because only made of glucose)
Backbone of glycogen
D-glucose are linked together by O-glycosidic bonds
Glycosidic bond
A bond linking a sugar with another molecule (in glycogen, this other molecule is another glucose)
(O-, N- and P- glycosidic bond)
α1->4 intra-chain bond vs α1->6 inter-chain bond
Reduinng sugar characteristics:
1) are sugars capable of acting as a reducing agent since they still have a free aldehyde or ketone group.
2) needs to have an hemiacetal or hemiketal group.
Reducing agent
A compound who gives electrons to an oxidizing agent.
Reducing Sugar quality
If the anomeric carbon (alpha or beta involved in the bond) is part of an hemiacetal or hemiketal, the corresponding carbohydrate has the possibility of being converted to its linear form and thus, displays an aldehyde or ketone group
Hemiacetal
A carbon which is part of an ether bond (R-O-R’) but is also attached to an alcohol (OH) is called an hemiacetal. Hemiacetal are derived from aldehyde (e.g. glucose).
Hemiketal
Carbon which is part of an ether bond (R-O-R’) but is also attached to an alcohol (OH). Hemiketal are derived from ketone (e.g. fructose).
Anomeric Carbon
A carbon at the center of an hemiacetal or hemiketal functional group
Picture explanation of hemiacetal and anomeric carbons
Both bottom are hemiacetal (one on right is beta bond because OH farther away from CH2OH whereas Beta is )H closer to CH2OH)
- Carbon in bottom can be reduced back to linear form with anomeric carbon at top of picture
Explanaition of reducing ends
On one side of a sugar there is a reducing end and a non-reducing end = the black circle (top = anomeric carbon) forms a o-glycosidic bond and is not available to be reduced, but on the green end it can be reduced since its available and a reducing end
In sucrose on the bottom, both reducing ends (circled in black = anomeric carbon) are involved in o-glycosidic bond meaning that neither can be reduced as they are both occupied
Glycogen structure (reducing vs non-reducing ends)
1) One reducing end by glycogen molecule
**Technically not true, because the first glucose is bonded to a protein (glycogenin) so it is not available to be reduced
2) All other ends are called non-reducing end
Why are we generating glycogen
One molecule of glycogen displays a third of the osmotic pressure when compared to the number of glucose monomers constituting this glycogen molecule. If glucose molecules were stocked unchanged in the cell, the cell would be highly osmotic, so water would permeate into the cell, and pumping out the excess water would be too costly in energy, the cells would just burst open.
This allows the cell to keep a negative concentration gradient of glucose between the interior and the exterior of the cell, therefore facilitating glucose entry into the cell (trick the cell to think there is no glucose inside but it is in fact glycogen).
Why does glycogen have this chain-like shape
These branches allow a greater number of non-reducing ends. These non-reducing ends are the site of glycogen metabolism (catabolism and anabolism), so the more non-reducing ends there are, the quicker the glycogen is metabolized (more efficient for glycogen breakdown because breakdown can be occurring at multiple ends at the same time)