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Report on cell membrane
Report on cell membrane
Question about cell membrane
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The beet Lab experiment was tested to examine bio-membranes and the amount of betacyanin extracted from the beets. The betacyanin is a reddish color because it transmits wavelengths in red color and absorbs most other colors. The membrane is composed of a phospholipid bilayer with proteins embedded in it. The phospholipid bilayer forms a barrier that is impermeable to many substances like large hydrophilic molecules. The cells of beets are red and have large vacuoles that play a big role for the reddish pigment. This experiment aimed to answer the question, “How do cell membranes work?” The hypothesis we aim to test is: Cell membranes work as a fluid mosaic bilayer of phospholipids with many embedded proteins. We predicted that the 50% Acetone will break down the most betacyanin. Our hypothesis was proven wrong by our data collected. We could test our predictions by doing the experiment multiple times and compare the …show more content…
results to each others. Materials and Methods In this lab, we examined the properties of bio membranes. We used a “Spec 20” to measure the amount of betacyanin in the solutions. The Spec 20 reports two types of measurements which are percent transmittance and absorbance. We cut the beet cores using a metal rod, rinsed them in the sink to eliminate human error, placed them in the freezer, and water bath multiple times. The beet cores were cut into small pieces, so that one piece can be dropped into a small test tube that had different solvents in each tube. Also, they were cut the same size, so the data would be as accurate as possible. We worked as a team and had two group members working with the solvents and two others working with the temperatures. The cell membranes were messed with by using hot and cold temperatures to look at the differences of betacyanin extracted. The different temperatures were -20C, 4C, 37, and 22C. The solvents were 1% Acetone, Saline, 50% Acetone, 50% Methanol and 1% Methanol. The test tubes put into the freezer sat there for 20 minutes and the other test tubes were put into the hot bath for another 20 minutes. Results We predicted that the 50% Methanol would break down the most betacyanin in the beet. In our results, the most absorbed was from the 50% Methanol. The least absorbed was the 11% Acetone. The table below shows our results. 11% Acetone 0.089 50% Acetone 0.145 1% Methanol 0.235 50% Methanol 0.370 Saline 0.170 The other experiment we tested was putting the test tubes in the freezer for 20 minutes.
The least absorbed was the 4 Celsius with only 0.040 absorbed. The most absorbed was -20 Celsius with 0.219 absorbed.
Treatments Absorbance
-20 C 0.219
4 C 0.040
22 C 0.080
37 C 0.125
The mean for the temperatures is 0.116 and the solvents is 20. We predicted the 37 Celsius would be the most absorbed, but it was the -20 Celsius which can be seen in the graph above.
Discussion
The data we gathered was tested to be as accurate as possible. Our prediction on the solvents did not support our data that we collected. The cause of this could be due to human error when washing the beets or the cutting of the beets. The beets were not perfectly cut the same size, so some beet pieces were bigger than others which can affect the final the final result. We followed each step and followed the time limits cautiously. I can say if we were to redo the experiment our results would be similar because we would attempt to do the experiment as close as we did the first
time.
the replicate shows the same trend as the first experiment. I used a measuring cylinder and a beaker to measure out the amounts of water; however these did not seem to affect the quality of my results. To increase the accuracy of my results I could have perhaps used a burette. Even though I did the best I could to keep the experiment accurate, I did. some places there were mistakes that unintentionally occurred.
For the lab experiment for testing the stability of beet cell membranes using pH, many materials were used as follows. Obtaining a beet we punch out cores, using a cork borer. After washing the cores we put each one inside a separate test tube, and added a different pH solution in each one. After 3 minutes in these exposure solutions, we took the beet out with a dissecting needle. Then transferred each beet to a separate test tube containing deionized water. After 20 minutes in these diffusion solutions, we took the beets out with a dissecting needle and discard it. We then stirred each solution in the test tube with a stirring rod, and transferred it to a cuvette. A spectrophotometer was then calibrated, and used to measure the absorbance of each exposure solution, and diffusion solution.
plasma membranes, meaning animals and plants contain lipids. In this paper I will display and
The sugar beet currently grown is far removed from the garden plant. Later the root became a popular vegetable, especially the red type of beet known as beetroot. In the second half of the eighteenth century the chemist Marggraf demonstrated that the sweet tasting crystals obtained from juice of beets and sugar cane were similar, this was the first step in developing beets into an industrial crop for extraction of sugar. Before that time nobody paid much attention to what gave the roots their sweetness. Beets with higher levels of sucrose were selected from a white fodder beet variety. The White Silesian variety is still considered to be the primary source of sugar beet germplasm grown today (Fischer 1989).
* Size of potatoes * Diameter of each potato tube * Time in sugar solution We need to make sure in both experiments the fair test lists are used and the procedures are carried out. This needs to be done otherwise my results will not be accurate and will look odd. Method: Firstly we got out all our equipment.
“The plasma membrane is the edge of life, the boundary that separates the living cell from its nonliving surroundings. The plasma membrane is a remarkable film, so thin that you would have to stack 8,000 of these membranes to equal the thickness of the page you are reading. Yet the plasma membrane can regulate the traffic of chemicals into and out of the cell. The key to how a membrane works is its structure” (Simon, 02/2012, p. 60).
The ice treated beets absorbed the refined water for 20 minutes. While sitting tight for test tubes 5 and 6 to cool, we started the hot medications. We removed the beet segment from tube 1 and inundated it in a recepticle of heated water at 70 degrees Celsius. Following 1 minute in the high temp water shower, the beat was come back to test tube 1 and 10.0 mL of refined water was included. Subsequently we chilled off the high temp water shower to 55 degrees Celsius and submerged the beet from the tube 2 for 1 minute. We restored the beet from test tube 2 and included 10 mL of refined water at room temperature. The high temp dilute shower was then cooled to 40 degrees Celsius and test tube three was submerged in the shower for one moment. When we completed we restored the beet to test tube three and included 10 mL of refined water. At last, we cooled the high temp water shower to 20 degrees Celsius and included test tube four for one moment and after that additional 10 mL of refined water to the test tube. The treated beets in tube 1-4 were permitted to absorb the refined water at room temperature for 20
As soon as the sample of beetroot is placed into the distilled water diffusion occurs naturally, which is the net movement of molecules. from a region of high concentration (beetroot sample) to a region of low concentration (beetroot sample low concentration (distilled water). From 40°C upwards there is a sudden increase in absorbency, this is. because the optimum temperature at which enzymes and cells can work at is 37°C and as soon as you go above this temperature it will cause the enzymes and cells to denature and cease from working effectively. Even if you then lower the temperature again the cell will not regain.
As the temperature increases the transmission reading on the colorimeter decreases. From information that I had already gathered I knew it would be around the 60°C mark to 65°C, hence which I decided to add a test at 63°C. This would help me
the water baths I think were accurate enough but having two thermometers in each bath maybe would have helped to hold the temperature readings more accurately. We were not given any instructions either to shake or not to shake the test tubes with the coloured solutions before inserting them in the spectrophotometer to read the absorbance. By shaking each test tube a certain number of times before putting it in the spectrophotometer could have improved the accuracy of the absorbance of the solutions.
...eadings. The absorbance readings for test tube 5, were always further away from the expected values than test tube 1. This is because the NaOH was not added to each tube at a time, but in sequential order with the test tube numbers. This allowed the reaction in test tube 5 to proceed longer than in test tube 1, allowing more product to be produced, giving a higher absorbance reading than expected. In fact, this trend was shown in all the test tubes. In increasing order of test tube numbers, every absorbance was more off than expected.
consistent with the same reaction rate throughout the experiment. The average rate of reaction for the endotherms was 7.90 mL/sec and the endotherm had a higher standard deviation which shows it less reliable since the data points are spread unevenly. The standard
Our task was to investigate what the optimum ratio of solute to solvent that will produce the maximum cooling/heating effect?
Overall I think I carried out the experiment in a precise way and I took my time trying to make all my measurements as accurate as possible so that my data is reliable. Next time I will do more tests instead of just 3 so I have more results and so I could get a more accurate average. I will also do the experiment with more fruit juices to see if there are other fruits with a higher content of vitamin C. I will do an experiment to see if there is a difference in Vitamin C levels between fresh juice and store bought juice. I can also test different brands of juice to see if they have different levels of vitamin C.
There is also the potential of human error within this experiment for example finding the meniscus is important to get an accurate amount using the graduated pipettes and burettes. There is a possibility that at one point in the experiment a chemical was measured inaccurately affecting the results. To resolve this, the experiment should have been repeated three times.