Carbohydrates: Definition, Functions & Examples (DP IB Biology)
Revision Note
Monosaccharides
The monomers of carbohydrates are monosaccharides
Two monosaccharides can join to form a disaccharide
Many monosaccharides join to form a polysaccharide
Monosaccharides can join together via condensation reactions
The new chemical bond that forms between two monosaccharides is known as a glycosidic bond
Monosaccharides have the general formula CnH2nOn
Where 'n' is the number of carbon atoms in the molecule
Note that this formula only applies to monosaccharides
Monosaccharide properties include:
Colourless crystalline molecules
Soluble in water
There are different types of monosaccharide formed from molecules with varying numbers of carbon atoms, for example:
Triose molecules contain 3 carbon atoms, e.g. glyceraldehyde
Pentose molecules contain 5 carbon atoms, e.g. ribose
Hexose molecules contain 6 carbon atoms, e.g. glucose
Ribose and glucose structure diagrams
Pentose sugars, such as ribose (top), can be recognised by their five-point carbon rings and hexose sugars, such as glucose (bottom) by their six-point carbon rings
Glucose
The most well-known carbohydrate monomer is glucose
Glucose has the molecular formula C6H12O6
Glucose is the most common monosaccharide and is of central importance to most forms of life
Glucose is the main substrate used in respiration, releasing energy for the production of ATP
Glucose is produced during photosynthesis
Glucose exists in two structurally different forms, alpha (α) glucose and beta (β) glucose, these structures are known as the isomers of glucose
This structural variety results in different functions between carbohydrates
This seemingly minor example of isomerism has far-reaching consequences on the functions of the polymers
Glucose structure diagrams
The straight chain structure of glucose can form rings of alpha glucose. Glucose also forms rings of beta glucose.
Different polysaccharides are formed from the two isomers of glucose
Starch and glycogen are made from molecules of alpha glucose
Cellulose is made from molecules of beta glucose
Properties of glucose
Glucose has several properties that are essential to its function in living organisms
Stable structure due to the presence of covalent bonds which are strong and hard to break
Soluble in water due to its polar nature
Easily transportable due to its water solubility
A source of chemical energy when its covalent bonds are broken
Examiner Tips and Tricks
You should be able to recognise ring structures of hexose and pentose monosaccharides, and use glucose as an example of a hexose monosaccharide
Polysaccharides: Energy Storage
The function of carbohydrates
Carbohydrates function as essential energy storage molecules and as structural molecules
Starch and glycogen are effective storage polysaccharides because they are:
Compact
Large quantities can be stored in a small space
Insoluble
This is essential because soluble molecules will dissolve in cell cytoplasm, lowering the water potential and causing water to move into cells
If too much water enters an animal cell it will burst
Cellulose is a structural polysaccharide because it is:
Strong and durable
Insoluble and slightly elastic
Chemically inert; few organisms possess enzymes that can hydrolyse it
Polysaccharide function diagram
The different structures of starch, glycogen and cellulose allow each polysaccharide to perform different functions
Starch
Starch is the storage polysaccharide of plants
Starch is stored as granules in chloroplasts
It is made of alpha glucose monomers
Starch is constructed from two different polysaccharides:
Amylose (10 - 30 % of starch)
Unbranched helix-shaped chain with 1,4 glycosidic bonds between α-glucose molecules
The helix shape enables it to be more compact and thus it is more resistant to digestion
Amylopectin (70 - 90 % of starch)
Contains 1,4 glycosidic bonds between α-glucose molecules as well as 1, 6 glycosidic bonds, creating a branched molecule
The branches result in many terminal glucose molecules that can be easily hydrolysed for use during cellular respiration, or added to for storage
Amylose and amylopectin structure diagrams
Amylose (top) and amylopectin (bottom); the two polysaccharides that form starch in plant cells
Glycogen
Glycogen is the storage polysaccharide of animals and fungi
The monomer of glycogen is alpha glucose, joined by 1,4- and 1,6 glycosidic bonds
Glycogen is more branched than amylopectin, providing more free ends where glucose molecules can be removed by hydrolysis
This means that glycogen can be broken down quickly, supplying the higher metabolic needs of animal cells
Liver and muscles cells contain glycogen as visible granules, enabling high rates of cellular respiration
Glycogen structure diagram
Glycogen is a highly branched storage molecule present in animals and fungi
The Structure of Cellulose
Cellulose is a structural carbohydrate found in the cell walls of plants
Molecules of cellulose are straight and unbranched
Cellulose is a polymer of β-glucose monomers
β-glucose differs very slightly in structure to α-glucose; the hydroxyl group on carbon 1 sits above the carbon ring in β-glucose, whereas it sits below the ring in α-glucose
It means that in order to form a glycosidic bond with a molecule of β-glucose, every alternate molecule of β-glucose in the chain must invert itself, or flip upside down
Beta glucose in cellulose diagram
Every other molecule of beta glucose needs to flip upside down in order for glycosidic bonds to form in cellulose
The alternating pattern of the monomers in cellulose allows hydrogen bonding to occur between strands of β-glucose monomers, adding strength to the polymer
Hydrogen bonds link several molecules of cellulose to form microfibrils
Hydrogen bonding in cellulose diagram
Cellulose molecules are linked by hydrogen bonds
Cellulose function diagram
Cellulose molecules are joined by hydrogen bonds to form microfibrils; this gives cellulose its structural strength
Polysaccharide structure summary table
Feature | Starch | Glycogen | Cellulose | |
---|---|---|---|---|
Amylose | Amylopectin | |||
Monomer | α-glucose | α-glucose | α-glucose | β-glucose |
Branches | No | Yes (approximately every 20 monomers) | Yes (approximately every 10 monomers) | No |
Helix shape | Yes | No | No | No |
Glycosidic bonds | 1, 4 | 1, 4 and 1, 6 | 1, 4 and 1, 6 | 1, 4 |
Present in cell type | Plant | Plant | Animal | Plant |
You've read 0 of your 5 free revision notes this week
Sign up now. It’s free!
Did this page help you?