Materials
Internet access
Molecular model kit (optional)
Introduction
1. Research the macromolecules listed in Table 1.
2. Complete the information for each macromolecule. The following Web site will be helpful: http://faculty.clintoncc.suny.edu/faculty/Michael.Gregory/files/Bio%20100/Bio%20100%20Lectures/Biochemistry/biochemi.htm.
Table 1
Type of Macromolecule
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Elements
(C, H, O, N, S, P)
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Monomer
(examples)
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Polymer
(examples)
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Functions
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Carbohydrate
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Lipid
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Protein
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Nucleic acid
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Observations
1. What elements are present in the macromolecules in the table?
2. Which elements are present in all four types?
3. Draw an atomic model for carbon.
4. Draw a Lewis diagram for carbon.
5. What is it about the electron structure of carbon that makes it so flexible in making different biomolecules?
6. What are the monomer units of a protein called?
7. Using the text or Web site listed above, draw a general structure of an amino acid (or use a molecular model kit to make a model of it), and use the drawing or model to show how a peptide bond forms.
Part 2. Fats and Carbs (Lipids and Carbohydrates): Good Guys with a Bad Rep
A. A Simple Test for Fats
(Note: Start this at beginning of class to allow adequate time for slow heating.)
Materials
Vegetables or fruits, diced or cut in very small pieces
Flour or bread (whole grain and white; crumbs are best)
Oil (1 mL)
Nuts — any kind, ground or chopped
Bacon, cut into small pieces
Hotdog or hamburger, cut into small pieces
Snack foods — crackers, chips, cheese doodles, or similar foods, crushed
Heat source — microwave, hot plate, hot water bath, or heating pad
Brown butcher paper or brown grocery sack
Paper plate or water-proof container
Procedure
1. Cut a 4 x 4 inch square from the butcher paper for each sample.
2. Place a small amount of a sample on a square.
3. Fold or wrap the samples as tightly as possible, and place them on a paper plate. If you are using a hot water bath, place the plate in a water-proof container.
4. Heat the samples during the remainder of the period.
5. Remove heat source, and open the squares.
6. Record in Table 2 which samples left a translucent spot (grease spot, indicating presence of fat/oil) on the paper.
Table 2
Sample Name
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Grease Spot
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No Grease Spot
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Function of Lipids
(see Table 1)
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Observations
1. Which sample seems to contain the most fat/oil? Which contains the least or none at all?
2. Did any samples give surprising results?
3. Judging from the Function of Lipids column, are lipids important in our diets, or are they not really necessary?
4. Do we need lipids/fats in our diets?
B. Two Simple Tests for Carbohydrates
Materials
Sugar
Molasses
Honey
Cornstarch
Potatoes
Vegetables or fruits, diced or cut in very small pieces
Flour or bread (whole grain and white; crumbs are best)
Nuts, bacon, hotdog, or hamburger, chopped cut into small pieces
Snack foods — crackers, chips, cheese doodles, or similar foods
Benedict’s solution
Iodine
Test tubes or micro well plates
Beakers to hold test tubes
Heat source — hot water bath, heater, heating pad, or microwave
Pipettes
Procedure
Benedict’s test for simple (reducing) sugars
1. Make a solution (add small amount of water and stir) in a test tube of the substance to be tested, and pipette approximately 2–3 mL Benedict’s solution into the tube.
2. Alternatively, pipette 2–3 mL Benedict’s solution into a tube onto a small chunk of fruit, vegetable, bread, snack food, meat, nut, etc.
3. Heat the tube gently in a hot water bath for about 2 minutes. A color change from blue to green to yellow/orange/red indicates the presence of a simple (reducing) sugar.
4. Record results in Table 3.
Iodine test for starch
1. Add 1–5 drops of iodine solution directly to the sample solid food or solution.
2. The result is almost instantaneous, but allow iodine to soak into solids. A color change from orange to blue-black shows the presence of starch.
3. Record results in Table 3.
Table 3
Sample Name
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Positive
Benedict’s Test
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Positive
Iodine Test
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Presence of Carbohydrates
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Function of Carbohydrates
(from Table 1)
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Observations
1. What is the difference in the Benedict’s test and the Iodine test?
2. Are the lipid/fat and carbohydrate tests qualitative or quantitative?
3. Judging from the Function of Carbohydrates column, are carbohydrates important in our diets, or are they not necessary? Why, or why not?
Part 3. Proteins, Amino Acids, and Enzymes: The Effect of Heat and Acid on the Enzyme Peroxidase Introduction
Proteins are macromolecules essential to life. In addition to their locomotor and structural functions, their activity as enzymes in regulating biochemical reactions is important. In this lesson, you will examine two factors affecting the rate at which a common enzymatic reaction occurs. These two factors are heat and change in pH to an acidic environment.
Hydrogen peroxide is produced as a “waste product” in eukaryotic cells. It is a metabolic poison (toxin), which needs to be decomposed fairly quickly to maintain health. Peroxidase is an enzyme found in many living organisms that decomposes (breaks down) hydrogen peroxide into oxygen and water. This process is easily studied in potatoes. If peroxidase is present and functioning properly, there will be decomposition (gas evolution) clearly obvious in the tubes. In the presence of heat or acid, which denatures (breaks apart the bonds) the protein (the enzyme peroxidase), there will be no decomposition.
Materials
Hot water bath
Potato cubes (1 to 2 cubic centimeters)
3 percent hydrogen peroxide solution
Pipette
Test tubes
Citric or acetic acid solution — lemon juice or vinegar
Procedure
1. Prepare for this lab by cutting out 6 potatoes into cubes of approximately the same size. The fresher they are, the better for this investigation; however, the cubes may be stored in cool water. Prepare the 6 cubes and 6 test tubes (half full) according to the guidelines in Table 4.
Table 4
Tube
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Test Tube Fluid
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Potato Cube Preparation
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Observations
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Was peroxidase present?
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1
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Water
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Boiled for 5 min., cooled, rinsed
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2
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Peroxide
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Boiled for 5 min., cooled, rinsed
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3
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Water
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Soaked in acid for 10 min., rinsed
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4
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Peroxide
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Soaked in acid for 10 min., rinsed
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5
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Water
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None
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6
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Peroxide
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None
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Observations
1. Write the chemical equation for the enzymatic decomposition of hydrogen peroxide. Include the enzyme peroxidase.
2. In the above equation, which is the substrate?
3. What is the function of an enzyme?
4. What happened to the enzyme in the boiling water?
5. What happened to the enzyme in the acid solution?
6. Which tube(s) was/were the control?
7. Write a hypothesis for this experiment.
Introduction
DNA contains the genetic instructions for everything a particular cell does, and all living things contain DNA. It is possible to separate DNA from split peas and other vegetables in order to see, feel, and smell DNA.
Materials
Dried split peas
Salt
Liquid detergent
Meat tenderizer
Rubbing or ethyl alcohol
Cold water
Test tubes
Strainer
Blender
Toothpicks
Procedure
1. Predict how you think the DNA will look. Record your prediction as Observation 1.
2. Measure 2/3 cup of dried split peas. Add about 1/8 teaspoon of salt and 1-1/3 cups of cold water. Mix the ingredients in a blender on high speed for 15 seconds.
3. Pour the pea mixture through a strainer into another container. Add about 2 tablespoons of liquid detergent to the mixture. Let it sit for 5 to 10 minutes.
4. Pour the mixture into 3 test tubes or smaller containers so that each is 1/3 full. Then add a pinch of meat tenderizer to each container and stir gently.
5. Tilt each test tube and slowly pour rubbing alcohol (70–95 percent isopropyl or ethyl alcohol) down the inside wall of the tube so that it forms a layer on top of the mixture. Keep pouring in alcohol until the tube contains about the same amount of alcohol as it does pea mixture.
6. In a few minutes, the DNA will rise into the alcohol layer from the pea mixture layer. You can use a toothpick to pull the DNA out.
Observations
1. Predict how you think the split pea DNA will look.
2. Describe the DNA: What is its texture? Does it have an odor?
3. Does the DNA look different from what you expected? If so, how?
Sample Released SOL Test Items
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