Team:Brown/Project/Analysis

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(Optical Density)
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Initially we introduced arabinose to the culture of cells and allowed the cultures to sit at room temperature for several hours and measured the optical density before and after the cells lysed.  0.2% arabinose by mass was added to the cultures.
Initially we introduced arabinose to the culture of cells and allowed the cultures to sit at room temperature for several hours and measured the optical density before and after the cells lysed.  0.2% arabinose by mass was added to the cultures.
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[[Image:Od-before-after-cell-lysis.jpg|left|thumb|480px|This data indicates that significant lysis occurs over a period of a few hours, confirming that the lysis cassette functions as predicted.]]
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[[Image:Control-vs-test-lysed-cells.jpg|right|thumb|405px|This image illustrates the change in cell density of a culture with cells induced to lyse. Notice the clarity of the solution in the tube on the right (test with ara) compared to that of the tube on the left (control).]]
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    <td><div align="center">[[Image:Od-before-after-cell-lysis.jpg|left|thumb|480px|This data indicates that significant lysis occurs over a period of a few hours, confirming that the lysis cassette functions as predicted.]]</div></td>
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    <td><div align="center">[[Image:Control-vs-test-lysed-cells.jpg|right|thumb|400px|The culture on the left has no Arabinose added and the cells did not lyse. The tube on the right had 0.2% Arabinose by mass added and the cells lysed.]]</div></td>
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Revision as of 06:44, 29 October 2008



Contents

Optical Density

In order to test the mechanism of the SRRz lysis cassette, we took optical density measurements as cell lysis occurred. The construct we used for testing was contained on the pVJ4 plasmid. This plasmid was obtained from the Mekalanos lab at HMS and contained the SRRz gene cassette in a pBAD18 plasmid.

Initially we introduced arabinose to the culture of cells and allowed the cultures to sit at room temperature for several hours and measured the optical density before and after the cells lysed. 0.2% arabinose by mass was added to the cultures.

This data indicates that significant lysis occurs over a period of a few hours, confirming that the lysis cassette functions as predicted.
The culture on the left has no Arabinose added and the cells did not lyse. The tube on the right had 0.2% Arabinose by mass added and the cells lysed.






Next, we wanted to test the amount of time required for lysis to occur. We added 0.2% by volume of an arabinose stock solution to cell cultures and measured the optical densities of the cultures at certain distinct time points. The following graphs exhibit optical density trends during gene expression and resulting cell lysis and cell wall degradation. The first graph shows a test measuring optical density and correlates that data to a predicted change in resistance that should occur as the cells lyse. The second graph shows another test of change in optical density over time.


Optical Density WRT Time
Optical Density WRT Time



Optical density of the cell cultures significantly dropped between 1 and 2 hours after induction, signifying the expression of the lysis gene cassette. Notice that optical density increases slightly within the first hour of the test, due to continued cell growth before the lytic event. The predicted change in resistance reflects this period of cell growth.

NaCl Testing

  • Multiple "Salt Tests" were performed to determine the exact sensitivity of our apparatus.

Salt concentrations originally tested are listed below. Further tests are to be run where the greatest resistance jump occurred to determine the exact concentration needed to see a significant resistance decrease due to cell lysis.

  • Molarity (M):
  1. .000005 2 .00001 3 .00005 4 .0001 5 .0005 6 .001 7 .005 8 .01 9 .05 10 .1

Resistance Testing

  • This test was done with 50X concentrated pVJ4 E. coli bacteria resuspended in M9 Minimal Media. Cultures were left overnight.

Conductivity Testing

Conductance.png

  • Different from expected resistance measurements, the conductivity of the lysed solutions greatly increased. Initial conductivity tests were run one after the other due to the limited availability of conductivity probes. Team Toxipop now has access to two probes.