Biologicalcatalysts that increase the rate of metabolic reactions in living organisms
Carbohydrates
Made of carbon, oxygen and hydrogen
Are polymers that break down into simplesugars
Molecules of repeating single sugars called saccharides (glucose)
Proteins
Made of carbon, oxygen, hydrogen, sulfur, nitrogen and phosphorous
Are polymers (long chain molecules) that are broken down into its monomers (smaller basic units): aminoacids
Large molecules made up of aminoacids
Lipids
Lipids (fats and oils) are made of carbon, oxygen and hydrogen
They are large polymers that are broken down into 3 fatty acids molecules and a glycerol molecule (smaller basic units)
Glycogen
A large carbohydrate made from many glucose molecules joined together. Serves as an energy store in animals
Starch
A large carbohydrate molecule made up of many glucose molecules. An energy storage molecule in plants
Active site
Part of the enzyme that is complementary to the shape of the substrate. The shape of the active site may change if the enzyme is exposed to high temperatures or extremes of pH
Iodine test for starch:
Add orange-brown iodine solution to the food sample
If there is starch present the colour will change from orange-brown to blue-black
Benedict's test for sugars:
Add blue Benedict's solution to the food sample
Heat the sample for 5 minutes at 70 degrees Celcius
If there is sugar present the colour will change from blue to green to yellow to red depending how much sugar there is in the sample (red would have the highest concentration)
Sudan III test for lipids:
Add red Sudan III stain solution to the food sample
Shake the tube gently
If there are lipids present a brightredlayer will form at the top of the liquid
Biuret test for proteins:
Add blue Biuret solution to the food sample
Shake the tube
If there is protein present the colour will change from blue to purple
Test for fats:
Add 2cm^3 of ethanol to the test solution
Add 2cm^3 of distilledwater
If there is fat present the solution will go from colourless to forming a milky white emulsion
Enzymes are biologicalcatalysts, They are protein molecules and the shape of the enzyme is vital to its function. Each enzyme has its own uniquely shaped activesite where the substrate binds
Lock and key hypothesis:
The shape of the substrate is complementary to the shape of the activesite so when they bind it forms an enzyme-substratecomplex
Once bound (now enzyme-productcomplex), the reaction takes place and the products and enzyme are released from the surface of the activesite
Effect of temperature on enzyme function
The optimum temp is around 37 degrees Celcius (body temperature)
The rate of reaction increases with an increase in temperature up to this optimum, but above this temperature it rapidly decreases and eventually the reaction stops
When the temperature becomes too hot, the bonds in the structure will break
This changes the shape of the activesite, so the substrate can no longer fit in
The enzyme is said to be denatured and can no longer work
Practical: investigate how enzyme activity can be affected by changes in temperature
Starch solution is heated to set a temperature
Amylase is added
Iodine is added after a minute
Measure the time it takes until the iodine stops turning blue-black (this means that starch is not present as amylase has broken the starch down into glucose)
Repeat the test with different temperatures
Effect of pH on enzyme function
The optimum pH for most enzymes is 7, but some that are produced in acidic conditions, such as the stomach, have a lower optimum pH
If the pH is too high or too low, the forces that hold the amino acid chains that make up the protein will be affected
This will change the shape of the activesite, so the substrate can no longer fit in
The enzyme is said to be denatured and can no longer work
Catalyst
A substance which increases the speed of a reaction, without being changed or used up in the reaction