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Team:Macquarie Australia/Results
From 2013.igem.org
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<center><font size=4>Promoter Ligation</font size></center> | <center><font size=4>Promoter Ligation</font size></center> | ||
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| - | Promoter was ligated onto the genes and plated up on LB + CAM plates, we observed a lot of colony growth. | + | 1st Attempt at ligation: |
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| + | Promoter was ligated onto the genes and plated up on LB + CAM plates, we observed a lot of colony growth. | ||
We inoculated LB + CAM broth with a colony from the corresponding plate. A variety of growth was | We inoculated LB + CAM broth with a colony from the corresponding plate. A variety of growth was | ||
observed, a few plates corresponding to a certain genes had a lot more colonies than others, this | observed, a few plates corresponding to a certain genes had a lot more colonies than others, this | ||
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the image description showing the order of genes on the agar. | the image description showing the order of genes on the agar. | ||
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<img src="https://static.igem.org/mediawiki/2013/c/cd/Didn%27t_work_.jpg" align="right" height="127" width="267"> | <img src="https://static.igem.org/mediawiki/2013/c/cd/Didn%27t_work_.jpg" align="right" height="127" width="267"> | ||
| - | PCR: | + | PCR of 1st attempt: |
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The PCR showed that the ligation was not successful, we derived the reason of this problem to either an improper clean up and therefore self ligation or improper restriction enzyme digest. | The PCR showed that the ligation was not successful, we derived the reason of this problem to either an improper clean up and therefore self ligation or improper restriction enzyme digest. | ||
Revision as of 06:42, 27 September 2013
Results and Characterisation
This page aims to provide a summary of our most important successful results, which have provided large strides towards the development of goal; Chlorophyll synthesis within E. coli. An in-depth view of our results can be found in our Notebook
Primary Results
[Description]
Sequencing Results
Sequencing results obtained from our successful ligation of gBlock fragments
| BioBricks | Amino Acid Match | Match Percentage |
|---|---|---|
| POR | 317/319 | 99% |
| ChlG | 320/320 | 100% |
| ChlP | 421/427 | 99% |
| ChlM | 278/280 | 99% |
| YCF | 130/130 | 100% |
| CTH1 | 372/374 | 99% |
| ChlI1 | 353/353 | 100% |
| DVR1 | 299/300 | 99% |
| Plastocyanin | 97/97 | 100% |
| Gun4 | 216/216 | 100% |
Characterisation
1st Attempt at ligation:
Promoter was ligated onto the genes and plated up on LB + CAM plates, we observed a lot of colony growth. We inoculated LB + CAM broth with a colony from the corresponding plate. A variety of growth was observed, a few plates corresponding to a certain genes had a lot more colonies than others, this can be observed from the image with the description order of genes. More colonies corresponding to a gene displayed more colony growth than others which can be observed from the image description showing the order of genes on the agar.
PCR of 1st attempt:
The PCR showed that the ligation was not successful, we derived the reason of this problem to either an improper clean up and therefore self ligation or improper restriction enzyme digest.
