SUGARS AND POLYSACCHARIDES Flashcards
What are carbohydrates?
- Consists of carbon, hydrogen and oxygen in a ratio of 1:2:1
- Major source of energy from diets
What are proteins?
- Coded by precise DNA sequences
- Approx 20 amino acids (building blocks)
- Standard peptide link (except for proline)
- Tightly folded structures
- Well defined
What are polysaccharides?
A large molecule made of many smaller monosaccharides. Monosaccharides are simple sugars, like glucose. Special enzymes bind these small monomers together creating large sugar polymers, or polysaccharides. A polysaccharide is also called a glycan.
- Synthesized by enzymes without a template
- Various links (alpha 1,4/1,6, beta 1.4)
- Range of structures: rod, coil, amorphous
- Poorly defined
- Starch, glycogen and cellulose
What are monosaccharides?
A monosaccharide is the most basic form of carbohydrates. Monosaccharides can by combined through glycosidic bonds to form larger carbohydrates, known as oligosaccharides or polysaccharides.
- Contains 3 (trisose) to 7 (heptose) carbon atoms (CH2O)n
- Aldehydes (HC=O) or ketoses (C=0)
What are enantiomers?
They are mirror images of a chiral molecule
- AKA optical isomers
- Glucose can be found in nature as either D-Glucose or L-Glucose. The main difference between D and L Glucose is that D-Glucose rotates plane polarized light clockwise whereas L-Glucose rotates plane polarized light anticlockwise
- D-glucose can be digested
- L-glucose cannot be digested
Why is L-glucose a laxative?
The sugar is not digested so it remains in the gut lumen. The sugar, because of osmosis, draws water in from the surrounding tissue. This extra water then causes the laxative effect.
How are cyclic structures formed?
Monosaccharides with 5-6 carbon atoms form cyclic structures
- The hydroxyl group on C5 reacts with the aldehyde or ketose group
- Cyclization of glucose produces a new asymmetric centre at C1: Anomeric carbon (C1)
- The 2 stereo-isomers are called anomers α and β
- Different anomers of the same sugar are recognised by different enzymes
- Important for glycosidic bond formation and hydrolysis
- In solution, equilibrium exists between straight chain and two cyclic forms, cyclic forms are locked and less amenable to modifications
What is a glycosidic bond?
A glycosidic bond is a type of covalent bond that joins a carbohydrate molecule to another group which may or may not be another carbohydrate
- Bonds formed between 2 OH groups on different sugars leads to a loss of water
- Catalyzed by specific glycosyltransferases
What are oligosaccharides?
Contains 3-10 monosaccharides
-Heparin, blood group antigens
What does a 1,4 link mean?
The bond connects carbon atom number 1 in one glucose to carbon atom number 4 in another glucose
Difference between alpha and beta glycosidic bonds
ALPHA: GLYCOGEN
-The hydroxyl group attached to carbon number 1 is below the plane of the cyclic ring
BETA: CELLULOSE
- The hydroxyl group attached to carbon number 1 is above the lane of the ring
- Hydrogen molecules between adjacent cellulose molecules allow them to form strong fibres
*Amylase in the digestive tract hydrolyses the ALPHA glycosidic bond but is inactive against BETA glycosidic bonds
Where are 1,6 links present?
At branching points
What is glycogen?
Glycogen is a multibranched polysaccharide of glucose that serves as a form of energy storage in animals, fungi, and bacteria.
- Main storage form of glucose in the body
- A core protein of glycogenin surrounded by branches of glucose units
- Insulin acts on hepatocytes to stimulate glycogen synthase
- Glucose molecules are added to the chains of glycogen as long as both insulin and glucose levels remain high
What breaks down glycogen when it is needed for energy?
Glycogen phosphorylase
What are modified sugars?
Monosaccharides can be modified to acquire new characteristics and properties
-Modifications are made by replacing the OH group with Phosphates (PO4) to give phosphorylated sugars for energy, amine (NH2) groups to produce amino sugars, sulphate (SO4) groups to give sulfated sugars, lipid groups to give glycolipids and the removal of O to give deoxy sugars