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Role of cell membrane essay
Cell membrane in physiology
Cell membrane in physiology
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How Temperature Effects the Movement of Pigment Through Cell Membranes
Abstract
The experiment below displays the effects of temperature on the
pigment in uncooked beetroot cells. The pigment in beetroot cells lies
within the cell vacuole and is called anthocyanin, each vacuole is
surrounded by a tonoplast membrane and outside it, the cytoplasm is
surrounded by the plasma membrane, therefore the foundation of this
experiment lies with the temperature at which the membranes will
rupture and therefore leak the pigment. To do this a series of
uncooked beetroot cylinders will be exposed to different temperatures
and then to distilled water at room temperature (24ºC). The colour of
the distilled water is the variable here which will show us, using a
colorimeter what temperature the membranes splits using the
transmission of the water (light passing directly through and the
absorbency (light getting absorbed by the anthocyanin molecules).
Introduction
Within the cells of a beetroot plant, a pigment is held within the
vacuole of a beetroot cell, this pigment gives the beetroot its
red/purple colour. If a cell is damaged or ruptured in a beetroot and
the cell surface membrane ruptures, the pigment 'drains' from the
cells like a dye. It is this distinction that can be employed to test
which conditions may affect the integrity of the cell surface
membrane. The pigments are actually betalain pigments, named after the
red beetroot (beta vulgaris) it breaks down at about 60ºC. They
replace anthocyanins in plants. Unlike anthocyanins, betalains are not
pH indicators, i.e. they do not change colour when the pH is lowered.
Beetroot pigments are unstable at high temperatures, but the chemistry
depends on a number of variables. Including the pH and composition of
the solution, oxygen concentration and how long the solution is
heated. However for the cell membranes an increase in temperature
weakens the structure, just as the decrease in temperature decreases
membrane fluidity until death, the increase in temperature does
likewise until the membrane ruptures by the phospholipids breaking
down to produce holes in the membrane, this is what will release the
The Effect of Temperature on an Enzyme's Ability to Break Down Fat Aim: To investigate the effect of temperature on an enzyme’s (lipase) ability to break down fat. Hypothesis: The graph below shows the rate increasing as the enzymes get closer to their optimum temperature (around 35 degrees Celsius) from room temperature. The enzyme particles are moving quicker because the temperature increases so more collisions and reactions occur between the enzymes and the substrate molecules. After this the graph shows the rate decreasing as the enzymes are past their optimum temperature (higher than). They are getting exposed to temperatures that are too hot and so the proteins are being destroyed.
Experiment #3: The purpose of this experiment to test the chromatography of plant pigments the alcohol test strip test will be used.
Homeostasis is essential to the cell’s survival. The cell membrane is responsible for homeostasis. The membrane has a selective permeability which means what moves in and out of the cell is regulated. Amino acids, sugars, oxygen, sodium, and potassium are examples of substances that enter the cell. Waste products and carbon dioxide are removed from the cell.
When molecules bump into each other, the kinetic energy that they have can be converted into chemical potential energy of the molecules. If the potential energy of the molecule becomes great enough, the activation energy of a reaction can be archived and a change in chemical state will result. Thus the greater the kinetic energy of the molecules in a system, the greater the resulting chemical potential energy. As the temperature of a system is increased it is possible that more molecules per unit time will reach the activation energy (2). Therefore the rate of reaction will increase. On the other hand if the temperature reaches a certain amount the enzyme might denature and therefore no longer able to carry out the reaction.
The objective of this study was to determine how temperature affects the activity level of the Cepaea nemoralis. Both experiments showed the same relative trend of increased movement in a warm environment as opposed to decreased movement in a cold environment. Both trials had a much greater mean distance travelled over one minute in the warm environment than they did in the cold environment. However, many snails displayed no activity in the cold environment by retracting into their shells and whenever fresh hot water was added to the hot treatment to keep the temperature stable, the snails would get agitated and begin to crawl up the walls of the glass bowl. Generally, the 30 degrees Celsius temperature increased the locomotion of the snails, and the 5 degrees Celsius restricted its ability to move. In a study, it was concluded that muscle contraction is inhibited by low temperatures, therefore we predicted that the C. nemoralis would move much quicker when exposed to high temperatures than it would when exposed to lower temperatures (Holewijn & Heus, 1992). Our results were consistent with our prediction because in both trials, the C. nemoralis on average had a higher mean distance travelled in the hot treatment than in the cold treatment.
We initially cut six uniform barrels of beet utilizing a cork borer. We ensured that the majority of the barrels were a similar size. Next, we put the chambers of beet tissue hotel in a beaker and flushed them with tap water for two minutes keeping in mind the end goal to wash the betacyanin from the harmed cells at first glance. They were washed similarly, and a while later we disposed of the shaded flush water. Delicately, we put each of the beets into various, dry test tubes. While moving the beets we were mindful so as to make an effort not to cut, squash, or generally harm them. At long last we marked the test tubes 1-6. We utilized cold and hot medicines for various test tubes. For the cool treatment, we put 2 tubes in ice (5 and 6).
Above in table 4.1 the results are shown. Test tube 2 was the only tube that had a change in color. The reason that test tube 2 was the only one that changed in color was because a reaction that was produced by catechol oxidase. Tube 2 was the only tube that had potato extract and catechol this is why the reaction occurred. The potato extract and catechol was not present at the same time in the other tubes and that is the reason they had no change.
This indicated that the effect of high temperature on the activity of peroxidase was irreversible and so if the optimum temperature was restored the enzyme activity will not increase again because denaturation resulted in a permanent change in the shape of the active site of the peroxidase enzyme. In conclusion, the results of this experiment supported the hypothesis that enzymes including peroxidase enzyme are sensitive to temperature changes[George
They are connected in series by an electron transport chain and they differ in the organization of light harvesting systems and pigment compositions. The two pigments found in the photosystems of green algae are chlorophylls and carotenoids (Green and Durnford, 1996). Chlorophyll is the principal pigment that functions to trap light energy and it is present in two forms; chlorophyll a (Chl a) and chlorophyll b (Chl b), and they can be distinguished based on their absorption spectra. Chl a has an absorption maxima of 659 nm and 429 nm while Chl b has an absorption maxima of 642 nm and 455 nm (Zscheile and Comar, 1941). The presence of two pigments with differing absorption maxima functions to broaden the range of light that can be absorbed and used for photosynthesis. Carotenoids are also present in the photosystems and in addition to serving as light harvesting apparatus, the carotenoids are involved in energy dissipation in the presence of excess light (Santabarbara et al.,
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.
Photosynthesis is a widely studied topic among the world of science due to its importance for life and its many uses. Photosynthetic pigments reflect and absorb different wavelengths of visible light based off their polarity. In this experiment, we studied photosynthetic pigments, first, by determining polarity and then, by measuring the amount of light of a given wavelength that a pigment absorbs. We used two methods in this experiment, chromatography and spectrophotometry. For the first portion of our experiment we determined the distance each pigment migrated, their R_f values, and their polarity. Our predications based off polarity, lead to our hypothesis
The Prediction is that as the temperature rises as does the permeability of the cell membrane, as the permeability and the temperature increase so does the amount of pigment being released.
The research of pigments has performed an important part in the junction of progress, genes, and developing chemistry. Pigmentation's application as a visible phenotypic marker has resulted in over 100 years of intense research of cover shade stresses in lab rats, thereby creating an impressive record of applicant genes and an knowing of the developing systems accountable for the phenotypic results.
The purpose of this experiment was to determine the amount of all-trans-lycopene present in a can of tomato paste in order to determine the quality of the tomato paste. This was achieved by proper separation of lycopene from the other pigments in the tomato paste through column chromatography. The column was able to achieve proper separation given the high polarity of the packing, alumina. Given alumina’s high polarity, the pigments present in the tomato paste with a greater polarity would travel more slowly through the column than the molecules with a lower polarity. Due to the fact that each pigment presented as a different color, in addition to variations in polarity, the separation of lycopene was made possible. The yellow band, composed of carotenes, traveled the quickest through the column, suggesting it was the least polar pigment present. If it were more polar, it
Reptiles have this famous ability to gather of disperse colored pigments inside their cells. The colors can also be mixed by putting a yellow pigment over a blue one to create a green color. Sometimes changes arise by tiny packets of the dark dye melanin, for example, it can be spread throughout other cells to lighten the skin. One research shows that if they altered the crystal packing themselves by putting the cells in salty water to suck the fluid out of them, they would reproduce a color change. For chameleons, there is an extra layer in their cells that reflect near- infrared wavelengths that help them stay cool in the