monomers are the smaller units which polymers are made from. Monomers are usually based around carbon
monomers join by condensation reactions to form polymers. Polymers are broken down by hydrolysis reactions
monosaccharides, aminoacid and nucleotides are all examples of monomers
Condensation reactions:
a condensation reaction joins 2 molecules together with the formation of a chemical bond and releases 1 molecule of water for each bond formed between the monomers
Hydrolysis reactions:
a hydrolysis reaction breaks a chemical bond between 2 molecules, and this uses up 1 water molecule for every bond broken
Carbohydrates:
all carbohydrates are composed of carbon, hydrogen and oxygen
carbohydrates are divided into monosaccharides, disaccharides and polysaccharides
Monosaccharides:
these are monomers of which other larger carbohydrates are composed of
monosaccharides are soluble and sweet and have the general formula (CH2O)n
glucose is a hexose because it has 6 carbon atoms (C6H12O6)
other monosaccharides are pentoses (ribose in RNA or deoxyribose in DNA) or trioses
Glucose, Galactose and Fructose:
glucose is a product of photosynthesis and a major substrate of respiration
glucose has 2 isomers; alpha-glucose and beta-glucose. In a-glucose the OH is below the H and in b-glucose the OH is above the H
glucose, galactose (found in milk sugar) and fructose (found in fruits and most plants) are common hexose monosaccharides (6 carbons)
Disaccharides:
two monosaccharides linked together forms a disaccharide
alpha glucose + alpha glucose = maltose
glucose + fructose = sucrose
glucose + galactose = lactose
when 2 monosaccharides join together, a water molecule is removed (condensation reaction). A glycosidic bond is formed
Testing for sugars:
to test for reducing sugars (glucose, maltose, lactose):
add Benedict's reagent (blue)
heat to 90°C in a water bath
if a reducing sugar is present the sample will turn from blue to green to yellow to brick red (depending on the concentration)
Testing for non-reducing sugars:
to test for non-reducing sugars (sucrose) heat the sample with Benedict's - if there's no change then there are no reducing sugars present
heat a fresh sample with acid (hydrochloric) to hydrolyse it into it's monosaccharides
then neutralise with an alkali (sodium hydroxide)
now redo the Benedict's test
Problems with the Benedict's test:
it is non-specific - it doesn't tell you the type of sugar present
Benedict's is qualitative - it cannot tell you the exact value for the concentration of sugars present
highly subjective - colours may be perceived differently
Polysaccharides:
polysaccharides are long chains (polymers) of monosaccharides joined with glycosidic bonds. They are formed by condensation reactions. The important polysaccharides are starch, cellulose and glycogen
because they are long molecules polysaccharides are often insoluble. This means that they are very suitable for storage
polysaccharides are broken down in hydrolysis reactions into monosaccharides or disaccharides which can then be used by the organism/cell
Starch:
starch is a storage polysaccharide that is found as granules or grains in plant cells, usually concentrated in the seeds as an energy store or in storage organs, such as potato tubers. the main role of starch is energy storage
starch is made up of long chains of alpha-glucose - it has coiled sections and branched sections. Coiling occurs due to many alpha 1,4 glycosidic bonds. Branching occurs due to both alpha 1,4 and alpha 1,6 glycosidic bonds
Features of starch:
polymer of a-glucose - provides glucose for respiration
helical/coiled - compact; lots of alpha-glucose can be tightly packed into a cell allowing more to be stored
branched - glycosidic bonds are easily hydrolysed by enzymes to release glucose for respiration
insoluble - osmotically inactive/ doesn't affect water potential
large - cannot diffuse out of cell membrane
chemically inert - doesn't become involved in chemical reactions
To test for starch:
add iodine dissolved in potassium iodide solution
if starch is present, the iodine will turn from orange/brown to blue-black
Glycogen:
glycogen is found in animal cells (mainly muscle and liver cells) . Glycogen is similar to starch; it is an energy storage molecule, it is made from long chains of alpha glucose molecules, joined together by glycosidic bonds
it has coiled sections and branched sections, however it is more highly branched than starch and is made up of shorter chains compared to amylopectin. Because it's made of shorter chains, it's more easily hydrolysed
Features of glycogen:
polymer of a-glucose - provides glucose for respiration
helical/coiled - compact; lots of alpha-glucose can be tightly-packed into a cell allowing more to be stored
branched - glycosidic bonds are easily hydrolysed to release glucose. This happens even quicker in glycogen which is essential for the relatively higher metabolic rate of animals
insoluble - osmotically inactive / does not affect water potential
large - cannot diffuse across the cell membrane
chemically inert - doesn't become involved in chemical reactions
Cellulose:
cellulose is a polymer of many beta glucoses joined together by glycosidic bonds. This provides differences in it's structure compared to starch and glycogen
cellulose is a major component of plant cell walls and provides strength and support
Cellulose and hydrogen bonding:
cellulose forms straight, unbranched chains that run parallel to eachother, allowing hydrogen bonding to occur between the chains
cellulose molecules are grouped to form microfibrils
as there are so many hydrogen bonds, they are collectively strong, therefore the chains are held tightly providing high tensile strength. This makes the cell wall rigid, so prevents osmotic lysis
Features of cellulose:
made of long straight unbranched chains of b-glucose / hydrogen bonding forms between parallel chains / forms microfibrils and macrofibrils - provides rigidity, strength and support to the plant cells, which prevents osmotic lysis (too much water moving in and the cell bursting)