Betacyanin Release from Damaged Beet Cell Membranes
Betacyanin Release from Damaged Beet Cell Membranes

Betacyanin Release from Damaged Beet Cell Membranes

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Introduction

A red pigment called Betacyanin located in the vacuole of the beet cells is released when the membrane is damaged (Danyk, 2013). The membrane is necessary for sustainability of the cell’s life, it separates the cell from the outside environment, and is responsible for diffusion, exocytosis and endocytosis, and transport.

It can be damaged by stress such as changes in the phospholipid bilayer (Reece et al, 2011). Changes to the hydrophilic bilayer causes breakdown of the components of the cell membrane, phosphate and glycerol. Determining the Betacyanin leakage will illustrate the damage caused to the membrane. The beet cells are being exposed to different temperatures and their Betacyanin concentrations are being analysed. This test is being done to see if extreme high and low temperatures cause more damage to the cell m

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embrane than moderate temperatures.

Methods

  • Preparation of Beet Cells: A cork borer was used to remove five beet cylinders, and they were cut to fifteen millimeter length. They were then rinsed in cool water to remove the Betacyanin from damaged cells that were damaged when the cylinders were made (Danyk, 2013).
  • Applying Stress to the Membrane: Five test tubes were used. Two tubes contained beet samples and were placed in the freezer (-5°C) and in a refrigerator (5°C) for 15 minutes. The third beet sample was placed in a cup of 70° C water for 3 minutes. The fourth beet was placed in 40° C water for 3 minutes. A fifth beet was placed in 25° C water for 3 minutes. After the beets have been placed in their temperature environments for the desired time, they were placed in the appropriate test tubes filled with
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milliliters of distilled water at room temperature for 15 minutes. The beets were then removed from the test tubes.

  • Evaluation of Membrane Stress: The test tubes were arranged from lightest to darkest and analyzed using a spectrophotometer. The absorbency was prepared and set at 460 nm. The absorbency was measured and is a direct measure of the Betacyanin concentration and membrane damage. The Betacyanin concentration was calculated by dividing the absorbency reading by 0. 0084 to get the concentration in micrometers (Danyk, 2013).
  • Results

    The data showed a trend that temperature in extreme values increases the Betacyanin concentration. The beet cells exposed to the -5°C and 70°C temperatures show the greatest amounts of Betacyanin leakage, compared to the other temperatures (5°C, 25°C, 45°C) (Refer to Attachment 1: Figure 1).

    Discussion

    High and low temperatures and damage and destroy a cell membrane. The results show this expectation because the beet cells released more Betacyanin at high and low temperatures which suggests more damage to the cells. Our results illustrate the integrity of a membrane is important for the proper function of the cell. Damage was caused at high and low temperatures but very little was caused at the intermediate temperatures. At hot temperatures the proteins denature and molecules in the cell move faster. At cold temperatures the water freezes, expands, and ruptures the membrane. A mean concentration was calculated from the class, using 5 individual tests.

    Literature Cited

    1. Danyk, H. 2013. Biology 1010: The Cellular Basis of Life Laboratory Manual. University of Lethbridge.
    2. Reece, J. B. L. A. Urry, M. L. Cain, S. A. Wasserman, P. V. Minorsky and R. B. Jackson. 2011. Campbell Biology, Ninth Edition. Person Benjamin Cummings, San

    Francisco, CA.

     

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