4.2.2.1 Human Digestive System Flashcards
Carbohydrates—sugar
Role in body, biochemical test, positive/negative result
Role in body: glucose used for respiration, a process that releases energy
Biochemical test:
Benedict’s solution
BOIL the solution
Semi quantitative
Test result:
Will change blue—>green—>yellow—>red
Carbohydrates—starch
Monomer, role in body, biochemical test, test result
Monomer:
Simple sugars (e.g maltose)
role in body:
Broken down into glucose to release energy
biochemical test:
Iodine SOLUTION
test result:
Positive—blue black
Negative—orange brown
Lipids (fats and oils)
Monomer, role in body, biochemical test, test result
Monomer:
3 fatty acids, 1 glycerol monomer
role in body:
Insulation
Long term energy store
Protects organs
biochemical test:
Use Sudan III
Add equal parts of food and water
Add Sudan III and shake tube
test result:
Positive—red layer forms on surface
Negative—no layer
Proteins
Monomer, role in body, biochemical test, test result
Monomer:
Amino acids
role in body:
Growth and repair
biochemical test:
Biuret solution
test result:
Positive—lilac
Negative—blue
BI: RP4 food tests
Risk assessment
Safety goggles should be worn when carrying out the tests
Wash off spills on skin immediately
Sudan 3 contains ethanol—high flammable. Keep solution away from make flames
Biuret solution contains copper sulphate—poisonous, and sodium hydroxides—caustic
Take care with boiling water
BI: RP4
Apparatus
food to be tested
• a pestle and mortar
• a stirring rod
• filter funnel and filter paper
• 2 x beaker, 250 ml
• test tubes
• Benedict’s solution, iodine solution, sudan Ill solution, biuret solution
• water bath
BI: RP4
Testing for sugars
- Fill a test tube about a quarter full with some of the filtered food solution.
- Add 5 drops of Benedict’s solution to the solution in the test tube.
- Put the test tube into a water bath set at 65°C for five minutes.
- Note any colour change.
If a reducing sugar (such as glucose) is present, the solution will turn from blue to green, yellow, or brick-red. The colour depends on the sugar concentration.
BI: RP4
Testing for starch
- Take 5 ml of the filtered food solution put it into a clean test tube.
- Add a few drops of iodine solution and note any colour change.
If starch is present, the iodine solution will change from an orange/brown to a blue/ black colour.
BI: RP4
Testing for lipids
- Half fill a test tube with some of the unfiltered food solution.
- Add 3 drops of Sudan Ill stain to the solution in the test tube. Shake gently to mix.
If fat is present: a red-stained oil layer will separate out and float on the water surface.
BI: RP4
Testing proteins
- Put 2 cm of the filtered food solution into a test tube.
- Add 2 cm’ of Buret solution to the solution in the test tube. Shake gently to mix and note any colour change.
Proteins will turn the solution from blue to lilac or purple.
Enzymes
Are a group of large proteins that act as biological catalysts
Speed up the rate of chemical reactions—lower the activation energy—without being used up
Enzymes lock and key
Enzymes with a specifically shaped active site and a substrate that is complementary in shape to the enzyme’s active site bind together.
Forms an ENZYMME-SUBSTRATE COMPLEX—this lowers the activation energy and the bonds in the substrate get broken
Reaction is complete and products are released from the active site
The enzyme remains unchanged
Factors affecting enzymes activity—temperature
When temp too low:
Enzymes and substrates—less kinetic energy so don’t collide very often—>so fewer enzyme substrate complexes form, rate of reaction is slow
When temp at optimum:
Enzymes and substrates—more kinetic energy so collide very often—>so many enzyme substrate complexes form, rate of reaction is at its fastest
When temp too high:
Have of active site changes so substrate = no longer complementary and cannot bind to the enzyme
Enzyme = denatured
Rate of reaction slows and then stops
Factors affecting enzyme activity: pH
Basically like temp
But enzymes will denature if too high AND if too low
BI: RP5
Place a few drops of iodine solution into each depression on the spotting tile.
2. Number two test tubes, and add:
• 2 cm buffer pH solution to tube 1 (your teacher will tell you which pH)
• 2 cm amylase solution to tube 1
• 2 cm starch solution to tube 2.
3. Place them into a water bath set at 30 °C and leave them for 5 minutes.
4. Add the starch to the amylase/buffer solution.
5. Start the stop clock and leave it on throughout the test.
6. Mix gently using the pipette and immediately remove one drop of the mixture.
7. Place this drop in the first depression of the spotting tile with the iodine solution. The iodine solution should turn blue-black
8. Use the pipette to remove one drop of the mixture every 30 seconds. Put each drop into the iodine solution in the next depression on the spotting tile. Rinse the pipette with water after each drop. Continue until the iodine solution and the amylase/buffer/starch mixture remain orange, or until you have no wells of iodine left.
9. Record the time taken for the amylase to digest all the starch.