Professional Documents
Culture Documents
Faculty of Sciences
Department of Biology
BIOL 202
Date: 11/11/2014
* Endocytosis: the phenomenon where the cells takes in large particles and
ingests them. A type of endocytosis is phagocytosis. This is when a cell takes
in and digest an object.
* Membrane carrier proteins: - Facilitated diffusion (down the gradient, from
high to low concentration, and no energy required).
- Protein channels( passage of insoluble to
lipid molecules through the membrane, no energy required)
- Active transport( down and up the gradient,
and require energy), ex: sodium-potassium pump.
We were not able to see the particles of neither the water nor the carmine
dye moving.
1- We can obviously see that the carmine dye powder is insoluble in water
(Tiny bits of the powder are suspended in the water.
2-We were able to see the red granules vibrating or " jiggling".
In this picture, we can see that the potassium permanganate is mixed with
the hot water better than with the cold water. In the hot water we almost
have 1 color in all the tube, while in the cold water, the potassium
permanganate is taking more time to mix with all the regions of the water in
the tube.
Therefore, we can conclude that when the temperature augments, the rate
of diffusion augments.
* Post-Lab Questions:
7- After three minutes, the diffusion in the tube with hot water is the
greatest.
8- The temperature of the tube with greatest diffusion increases the
molecular motion of the water and potassium permanganate.
9- Yes, the tube with least diffusion will eventually reach the same state as
the tube with greatest diffusion because the temperature only makes the
rate of diffusion faster.
1- We cut 9 potato cylinders using the "Cork Borer" and placed them on a
Petri dish cover. Then, we evened them out using the knife and a ruler.
2- We took the measurements of each potato cylinder ( using a ruler) and
recorded them. Then, we took the cylinders to the balance and measured
each cylinder's weigh and recorded them. 3- We took 3 petri dishes and filled
each one of them with a solution ( hypotonic, hypertonic, and isotonic), and
we labeled them.
4- Then we placed 3 potato cylinders in each of the 3 petri dishes and
labeled their places.
5-We waited 20 minutes for them to equilibrate.
6- After 20 minutes of waiting, we threw away the solutions and we wiped
the cylinders with a paper towel, then, we took the weigh and length of each
one of them and recorded them.
Results and Discussion
Solution
Length (cm)
Before
After
20% NaCl
(hyperton
ic)
0.9%
NaCl
(Isotonic)
Distilled
Water
(Hypotoni
c)
Weight (g)
Before
0.62 0.61
13
68
0.60
67
0.61
33
0.59
86
After
0.61
09
0.56
98
0.59
29
0.53
54
0.59
41
0.63
46
0.60
87
0.67
54
0.62
29
0.59
75
0.68
71
0.71
23
0.68
09
Post-Lab Questions
13) changes in length of the potato cylinders are due to the moving of
water molecules into and out of the cell by osmosis, although each
molecule moves randomly, the water molecules as a whole move in
the net direction of into or out of the cell
14) 20% NaCl solution was hypertonic
15)in the isotonic solution there would be no net movement of the
water molecules because the solute concentration on the inside of the
potato is the same as that on the outside of the potato (0.9% NaCl)
dialysis tube
parafilm
starch solution
glucose solution
benedicts reagent
iodine solution
droppers
methods:
1)
first we obtained a test tube and filled it half way up with water
2)
then we obtained a strip of dialysis tubing and we tied a knot at one of
the ends of the dialysis tube, then pulled on the knot a little bit to make sure
that it was water tight,
3)
we then opened the other end of the dialysis tube and, using the
dropper, we filled half of the dialysis tube with starch solution and the, using
a different dropper other half with glucose solution
4)
we then closed the dialysis tubing and bent the closed part of the
dialysis tubing over the edge of the tubing
5)
we rinsed the dialysis tube and then we put the dialysis tube into the
test tube that was half filled with water, and then we bent the top of the
dialysis tube over the edge of the test tube and applied parafilm to the test
tube and securely wrapped and twisted the dialysis tube around the test
tube and secured it in the test tube
6)
we then filled up the rest of the test tube with distilled water
7)
8)
remove the parafilm and take out the dialysis tubing and separate the
liquid in the dialysis tube into two separate test tubes using a dropper
9)
label the first test tube one and the other test tube 2
10) do the same thing with the water, divide the liquid into two test tubes
and label the first one one, and the second one second,
11) test the number one solutions against benedicts reagent, by adding
benedicts reagent and putting the test tube into a water bath at 60 degrees
celsius for 10 minutes
12) test the number two test tubes with iodine solution (test for the
presence of starch)
13)
Post-lab questions
10) yes the glucose diffused out of the tubing , because the result for the
liquid in the test tube when tested against benedicts reagent we got a
mustard yellow precipitate
11) no the starch did not diffuse out of the test tube because the result for
the number two test tube gave a yellow solution on addition of iodine
solution
12) glucose molecules are smaller than starch molecules, which makes sense
because starch is a polymer of glucose
-
20%nacl solution
Methods
1) the microscope was prepared and all we had to do was observed