Transcript
Lab 4: Diffusion and Osmosis
The cell membrane plays the dual roles of protecting the living cell by acting as a barrier to the outside world, yet at the same time it must allow the passage of food and waste products into and out of the cell for metabolism to proceed. How does the cell carry out these seemingly paradoxical roles? To understand this process you
need to understand the makeup of the cell membrane and an important phenomenon known as diffusion.
Diffusion is the movement of a substance from an area of high concentration to an area of low concentration due to random molecular motion. All atoms and molecules possess kinetic energy, which is the energy of movement. It is this kinetic energy that makes each atom or molecule vibrate and move around. (In fact, you can quantify the kinetic energy of the atoms/molecules in a substance by measuring its temperature.) The moving atoms bounce off each other, like bumper cars in a carnival ride. The movement of particles due to this energy is called Brownian motion. As these atoms/molecules bounce off each other, the result is the movement of these particles from an area of high concentration to an area of low concentration. THIS is diffusion. The rate of diffusion is influenced by both temperature (how fast the particles move) and size (how big they are).
Part 1: Brownian Motion
In this part of the lab, you will use a microscope to observe Brownian motion in carmine red powder, which is a dye obtained from the pulverized guts of female cochineal beetles.
Materials
Glass slide Toothpick Carmine red powder Coverslip Tap water
Procedure
1. Obtain a microscope slide and place a drop of tap water on it.
2. Using a toothpick, carefully add a very miniscule quantity of carmine red powder to the drop of water and add a coverslip.
3. Observe under scanning, low, and then high power.
Lab Questions
1. Describe the activity of the carmine red particles in water.
They are vibrating like bumper cars.
2. If the slide were warmed up, would the rate of motion of the molecules speed up, slow down, or remain the same? Why?
The motion would speed up because as the temperature increased the kinetic energy would also increase.
Part 2: Diffusion across a semipermeable membrane
Because of its structure, the cell membrane is a semipermeable membrane. This means that SOME substances can easily diffuse through it, like oxygen, or carbon dioxide. Other substances, like glucose or sodium ions, are unable to pass through the cell membrane unless they are specifically transported via proteins embedded in the membrane itself. Whether or not a substance is able to diffuse through a cell membrane depends on the characteristics of the substance and characteristics of the membrane. In this lab, we will make dialysis tubing “cells” and explore the effect of size on a molecule’s ability to diffuse through a “cell membrane”.
The following information might be useful in understanding and interpreting your results in this lab:
Phenolphthalein
Atomic formula: C H O
Iodine
Atomic formula: I or I
Starch
Atomic formula: (C H O )
Sodium Hydroxide
Atomic formula: NaOH
20 14 4
2 6 10 5 n
Atomic mass: 318.32 g/mol
Color in acidic soln : Clear
Color in basic soln: Pink
Atomic mass: 126 g/mol
Atomic mass: HUGE! Color in Iodine: Bluish
Atomic mass: 40.1 g/mol
Acid/Base: Base
Materials
2 pieces of dialysis tubing
Thread
Phenolphthalein
Iodine
Wax pencil
2 beakers
NaOH
Starch solution
Pipettor
Pipette
Procedure
1. Using a wax pencil, label one beaker #1. Label the other beaker #2.
2. Fill beaker #1 with 300 ml of tap water, then add 10 drops of 1 M NaOH. Do not spill the NaOH- it is
very caustic!
3. Fill beaker #2 with 300 ml of tap water, then add iodine drops drop by drop until the solution is
bright yellow.
4. Now prepare your 2 dialysis tubing “bags”. Seal one end of each dialysis tube by carefully folding the end “hotdog style” 2 times, then “hamburger style” 1 time. Tie the folded portion of the tube securely with string. It is critical that your tubing is tightly sealed, to prevent leaks.
5. Add 10 ml of water and three drops of phenolphthalein to one of your dialysis tube bags. Seal the other end of the bag by carefully folding and tying as before.
6. Thoroughly rinse the bag containing phenolphthalein, then place it in into the beaker containing the
NaOH.
7. Add 10 ml of starch solution to the other dialysis tube. Again seal the bag tightly and rinse as above.
Place this bag containing the starch solution into BEAKER #2.
8. Let diffusion occur between the bags and the solutions in the beakers.
9. After 10 minutes, observe the color changes in the two bags and the external solutions. Draw a picture of each system below.
66802031559500
365760024828500
469900023123660043656252518935Iodine
00Iodine
128082321231920010814052520729Sodium hydroxide
00Sodium hydroxide
43653211645616Starch
00Starch
10680701709420Phenolphthalein
00Phenolphthalein
Data
Record the colors (below) and label contents inside and outside the bags (above):
Beaker #1
Beaker #2
Initial
Final
Initial
Final
Color inside bag
clear
dark pink
clear
dark blue
Color outside bag
(in beaker)
clear
mostly clear; some pink
yellow
yellow
Lab Questions
1. Which substance diffused across the membrane in beaker #1? How do you know?
Sodium hydroxide! The first clue is that when Phenol mixes with a base such as sodium hydroxide it turns pink and after about 20 minutes the solution inside the dialysis bag turned dark pink. The second clue is that sodium hydroxide is a smaller molecule, 40 g/mol as compared to 318 g/mol for phenol. Therefore, it is more likely the sodium hydroxide could pass through the semipermeable membrane before the phenol would.
2. Which substance diffused across the membrane in beaker #2? How do you know?
Iodine! The first clue is that when starch mixes with iodine it turns dark blue and after about 20 minutes the solution inside the dialysis bag turned dark blue. The second clue is that iodine is a smaller molecule, 126 g/mol as compared to HUGE for starch. Therefore, it is more likely the iodine could pass through the semipermeable membrane before the starch would.
3. Why might some ions and molecules pass through the dialysis bag while others might not?
The semipermeable membrane of the dialysis bag has certain size holes that will let molecules that are smaller than the holes pass through, but molecules bigger than the holes will not fit through.
Part 3: Osmosis and the Cell Membrane
Osmosis is the movement of water across a semipermeable membrane (such as the cell membrane). The tonicity of a solution involves comparing the concentration of a cell’s cytoplasm to the concentration of its environment. Ultimately, the tonicity of a solution can be determined by examining the effect a solution has on a cell within the solution.
By definition, a hypertonic solution is one that causes a cell to shrink. Though it certainly is more complex
than this, for our purposes in this class, we can assume that a hypertonic solution is MORE CONCENTRATED
with solutes than the cytoplasm. This will cause water from the cytoplasm to leave the cell, causing the cell to
shrink. If a cell shrinks when placed in a solution, then the solution is hypertonic to the cell.
If a solution is hypotonic to a cell, then the cell will swell when placed in the hypotonic solution. In this case, you can imagine that the solution is LESS CONCENTRATED than the cell’s cytoplasm, causing water from the solution to flow INTO the cell. The cell swells!
Finally, an isotonic solution is one that causes no change in the cell. You can imagine that the solution and the cell have equal concentrations, so there is no net movement of water molecules into or out of the cell.
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In this exercise, you will observe osmosis by exposing a plant cell to salt water.
Prediction
What do you think will happen to the cell in this environment? Draw a picture of your hypothesis.
Materials
Elodea leaf Microscope slide Coverslip 5% NaCl solution
Procedure
1. Remove a leaf from an Elodea plant using the forceps.
2. Make a wet mount of the leaf. Use the pond water to make your wet mount.
3. Observe the Elodea cells under the compound microscope at high power (400 X) and draw a typical cell below.
4. Next, add several drops of 5% salt solution to the edge of the coverslip to allow the salt to diffuse under the coverslip. Observe what happens to the cells (this may require you to search around along the edges of the leaf). Look for cells that have been visibly altered.
Results
Draw a typical cell in both pond and salt water and label the cell membrane and the cell wall in both drawings below.
2325370122555Cell wall
00Cell wall
1057275119380Cell membrane
00Cell membrane
23972081150450054273454445Cell wall
00Cell wall
41592501270Cell membrane
00Cell membrane
14351002749800
577596043180004623435431800037242752413000048831524320500
Cell in Pond Water Cell in Salt Water
Lab Questions
1. What do you see occurring to the cell membrane when the cell was exposed to salt water? Why does this happen?
The cell membrane shrivels. The extracellular fluid has a higher concentration of salt and a lower concentration of water than the fluid inside the cell. Therefore, the water must move from higher concentration inside the cell to lower concentration outside the cell, causing the cell membrane to shrivel.
2. Describe the terms hypertonic, hypotonic and isotonic.
Read above!
3. How would your observations change if NaCl could easily pass through the cell membrane and into the cell?
If the sodium chloride could easily pass through the membrane then the salt would move into the cell until the inside and outside have equal salt concentrations. Therefore, the water would also have equal concentrations and there would be no net movement of water. The solutions inside and outside the cell would be isotonic.
Part 4: Experimental design
You and your group will design an experiment to determine the relative molecular weights of methylene blue and potassium permanganate. You may use a petri dish of agar, which is a jello-like medium made from a polysaccharide found in the cell walls of red algae. You will also have access to a cork borer and a small plastic ruler.
Materials
1 petri dish of agar Methylene blue Potassium permanganate Other?
Hypothesis
If potassium permanganate has a lower molecular weight than methlylene blue, and therefore is a smaller molecule than methlylene blue, potassium permanganate should diffuse farther through the agar in the same amount of time.
Experimental design
29019508890000
414528011430Potassium permanganate
00Potassium permanganate
266368734565Methylene blue
00Methylene blue
Data
Conclusions
Further questions/other comments