Team:CIDEB-UANL Mexico/labwork conclusions

From 2014hs.igem.org

(Difference between revisions)
Line 333: Line 333:
<p>From the results obtained we can conclude that:</p>
<p>From the results obtained we can conclude that:</p>
-
<p>1) The NhaS module did work as expected by giving to the bacteria the ability to survive in a medium with high sodium concentrations. The concentrations where the bacteria survived were from 1% up to 15% of NaCl in the medium. Some bacteria appeared to be red reporting that the NhaS gen is active, but some of them appeared to be white although they survived in the medium, indicating too that the NhaS gene was activated and working properly.</p>
+
<p>1) The NhaS module did work as expected by giving to the bacteria the ability to survive in a medium with high sodium concentrations. The concentrations where the bacteria survived were from 1% up to 15% of NaCl in the medium. Some bacteria appeared to be red reporting that the NhaS gen is active, but some of them appeared to be white although they survived in the medium, indicating too that the NhaS gene was activated and working properly. The reason that appeared red and white colonies was due to a mutation in the RBS region or in at the beginning of the RFP region.</p>
-
<p>2)In the Aroma module tests, the medium with 10mM of salicylic acid was the one that produced the most intense odor and if the quantity is increased to 30m the odor is not reported. This indicates that the plasmid was actually in the bacteria and that the riboswitch actually worked at 35°C.  In the case of the plaque that had the odor even if it was incubate at 29 ºC, it is concluded that this happened because the riboswitch is very sensitive to heat, and it was activated during the little time at which it was outside the incubator. </p>
+
<p>2) In the Aroma module tests, the medium with 10mM of salicylic acid was the one that produced the most intense odor and if the quantity is increased to 30m the odor is not reported. This indicates that the plasmid was actually in the bacteria and that the riboswitch actually worked at 35°C.  In the case of the plaque that had the odor even if it was incubate at 29 ºC, it is concluded that this happened because the riboswitch is very sensitive to heat, and it was activated during the little time at which it was outside the incubator. </p>
<div style="text-align: right;"><a href="https://2014hs.igem.org/Team:CIDEB-UANL_Mexico/labwork_conclusions#"><font color="blue">Return to the Top</font></a></p></div>
<div style="text-align: right;"><a href="https://2014hs.igem.org/Team:CIDEB-UANL_Mexico/labwork_conclusions#"><font color="blue">Return to the Top</font></a></p></div>

Revision as of 03:18, 15 June 2014

iGEM CIDEB 2014 - Project

Conclusions

From the results obtained we can conclude that:

1) The NhaS module did work as expected by giving to the bacteria the ability to survive in a medium with high sodium concentrations. The concentrations where the bacteria survived were from 1% up to 15% of NaCl in the medium. Some bacteria appeared to be red reporting that the NhaS gen is active, but some of them appeared to be white although they survived in the medium, indicating too that the NhaS gene was activated and working properly. The reason that appeared red and white colonies was due to a mutation in the RBS region or in at the beginning of the RFP region.

2) In the Aroma module tests, the medium with 10mM of salicylic acid was the one that produced the most intense odor and if the quantity is increased to 30m the odor is not reported. This indicates that the plasmid was actually in the bacteria and that the riboswitch actually worked at 35°C. In the case of the plaque that had the odor even if it was incubate at 29 ºC, it is concluded that this happened because the riboswitch is very sensitive to heat, and it was activated during the little time at which it was outside the incubator.

iGEM CIDEB 2014 - Footer