Difference between revisions of "Team:NTU-Singapore/Results"
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After that we carried out another test to confirm our results more carefully. From the results it was shown that mutant 8M1 of the lactate permease was found to have a consistent growth enhancement for our chassis. However, for our lactate dehydrogenase, none was found to have better expression than the wild type. | After that we carried out another test to confirm our results more carefully. From the results it was shown that mutant 8M1 of the lactate permease was found to have a consistent growth enhancement for our chassis. However, for our lactate dehydrogenase, none was found to have better expression than the wild type. | ||
− | <div align="centre"><img class="" src="https://static.igem.org/mediawiki/2015/d/db/SH7_mutants.png" width="600px" height="450px"></div | + | <div align="centre"><img class="" src="https://static.igem.org/mediawiki/2015/d/db/SH7_mutants.png" width="600px" height="450px"></div> |
<p style="text-align:center; font-size: 19px; color: black"> | <p style="text-align:center; font-size: 19px; color: black"> | ||
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− | <div align="centre"><img class="" src="https://static.igem.org/mediawiki/2015/7/78/SH8_mutants.png" width="600px" height="450px"></div | + | <div align="centre"><img class="" src="https://static.igem.org/mediawiki/2015/7/78/SH8_mutants.png" width="600px" height="450px"></div><p style="text-align:center; font-size: 19px; color: black"> |
Growth of Shewanella oneidensis MR1 over expressing lactate permease. | Growth of Shewanella oneidensis MR1 over expressing lactate permease. | ||
</p></p> | </p></p> |
Revision as of 19:42, 18 September 2015
Our Results
Ribosomal Binding Site
Growth Curve
As the measurements are carried out in six batches, the growth of mutants of the same batch are similar but differed a little among batches. This implies that GFP expression does not have any significant effect on the bacteris's growth.
1AT denotes A of base pair 1 is changed to T, the same is applied for other notations of RBS mutants.
GFP Readings
The GFP fluorescence readings of mutants shows interesting results. Although the growth curve is similar among mutants, fluorescence intensities varied among the mutants. In summary, it was found that substitution mutations occurring to the AGGAG sequence within BBa_R0034, AAAGAGGAGAAA, showed a decreased GFP expression while others showed increased GFP output. Especially for mutations to base pair 7, GFP expression is near total-depression.
After normalising the GFP fluorescence readings with the OD600 at T=8, the ratio of the normalised fluorescence of the mutants to wild type RBS is computed and plotted as shown.
We also spotted the mutants on an LB agar plate to have a qualitative view of the GFP brightness. The culture is diluted to OD600 = 0.4 then 3uL of the culture is spotted on to the agar. Brightness of these spots parallels the results in the above graph. For example, 7GA, 8AG and 9GA is the brightest among the mutations on their respective base pairs while 12AC and 11AC are the darkest.