lecture 16 - introduction to the structure and function of carbohydrates Flashcards
What are the functions of carbohydrates?
As monosaccharides and disaccharides they are…..
–used as energy stores, fuels and metabolic intermediates
–important in the structural backbone of DNA and RNA
As polysaccharides they are….. –structural elements cell walls- plants and bacteria extracellular matrix connective tissue lubrication of skeletal joints –linked to proteins and lipids cell-cell recognition cell adhesion intracellular localisation tags on glycoproteins determine metabolic fate of glycoconjugates e.g. Starch, Glycogen, Cellulose
What is the general formula for carbohydrates?
CnH2nOn
What are aldoses and ketoses?
Monosaccharides that contain an aldehyde group are called aldoses, whereas those containing a
ketone group are ketoses. Monosaccharides are also classified by the number of carbon atoms as
trioses, tetroses, pentoses, hexoses, etc.
What kind of isomerism is seen in carbohydrates?
Carbohydrates, along with many other natural substances, exhibit a type of isomerism in which two
isomers are mirror images of each other. The two isomers are called enantiomers. The prefixes Dand
L- are used to distinguish between enantiomers (e.g. D-glyceraldehyde versus L-glyceraldehyde;
D-galactose versus L-galactose). Most natural monosaccharides belong to the D-family
How do you determine if a carbohydrate is a D or L isomer?
using penultimate carbon (chiral carbon)
D isomer has OH group on right hand side
What are epimers?
Isomers that differ only in the configuration around one chiral carbon atom
What are heteropolysaccharides and homopolysaccharides?
Homopolysaccharides - only 1 type of monomer
Heteropolysaccharides - multiple types of monomer
Describe the structure of glycogen
1-4 glycosidic bonds between alpha glucose monomers
alpha 1-6 branching every 8-12 residues
stored as granules in liver cell
the non-reducing ends are where glycogen is cleaved
the reducing ends have a free hydroxyl group where glucose can bind
Describe the structure of starch
amylose - 1-4 glycosidic bonds between alpha glucose monomers
amylopectin- 1-4 glycosidic bonds between alpha glucose monomers
alpha 1-6 branching every 24-30 residues
major fuel store in plant cells
very long polymers of glucose synthesised in chloroplast
can be stored in cytoplasm or chloroplast
What is the difference between alpha and beta isomers?
alpha sugars have the C1 OH group below the plane of the ring
beta sugars have the C1 OH group above the plane of the ring