Team:Calgary/Project/DataPage

From 2012.igem.org

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<p><b><a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K902000">BBa_K902000</a></b> and <b><a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K902004">BBa_K902004,</a></b>: two novel hydrolase enzymes were submitted to the registry for the hydrolysis of two different sugar conjugated electroactive compounds.  Used in conjunction with the existing lacZ part in the registry (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_I732005">BBa_I732005,</a>), this allows for the electrochemical detection of three compounds with a single electrode.  A uidA inducible generator (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_k902002">BBa_k902002,</a>) was submitted and characterized electrochemically.  This data can be found on our <a href="http://2012.igem.org/Team:Calgary/Project/FRED/Reporting">electroreporting page</a>.
<p><b><a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K902000">BBa_K902000</a></b> and <b><a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K902004">BBa_K902004,</a></b>: two novel hydrolase enzymes were submitted to the registry for the hydrolysis of two different sugar conjugated electroactive compounds.  Used in conjunction with the existing lacZ part in the registry (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_I732005">BBa_I732005,</a>), this allows for the electrochemical detection of three compounds with a single electrode.  A uidA inducible generator (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_k902002">BBa_k902002,</a>) was submitted and characterized electrochemically.  This data can be found on our <a href="http://2012.igem.org/Team:Calgary/Project/FRED/Reporting">electroreporting page</a>.
   
   
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<p><b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>,<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902023">BBa_K902023</a></b> and<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902074">BBa_K902074</a></b>: three novel riboswitchs were submtted along with two associated promoters (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) and <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) and an inducible/repressible promoter <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902065">BBa_K902065</a></b>) were submitted to the registry.  One of these riboswitches (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) was tested with GFP using this construct, (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902014">BBa_K902014</a></b>), with its promoter and GFP using this construct (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902017">BBa_K902017</a></b>) and with its promoter and the S7 kill gene using this construct (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902018">BBa_K902018</a></b>).  This data can be found on our killswitch (<b><a href="http://2012.igem.org/Team:Calgary/Project/HumanPractices/Killswitch/Regulation">regulation</a></b>) page.
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<p><b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>,<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902023">BBa_K902023</a></b> and <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902074">BBa_K902074</a></b>: three novel riboswitchs were submtted along with two associated promoters (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) and <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) and an inducible/repressible promoter <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902065">BBa_K902065</a></b>) were submitted to the registry.  One of these riboswitches (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902008">BBa_K902008</a></b>) was tested with GFP using this construct, (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902014">BBa_K902014</a></b>), with its promoter and GFP using this construct (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902017">BBa_K902017</a></b>) and with its promoter and the S7 kill gene using this construct (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902018">BBa_K902018</a></b>).  This data can be found on our killswitch (<b><a href="http://2012.igem.org/Team:Calgary/Project/HumanPractices/Killswitch/Regulation">regulation</a></b>) page.
<p>Submitted genes for denitorgenation an desulphurization.  A novel oxidoreductase part <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902058">BBa_K902058</a></b>  was also submitted and characterized for use in the desulphurization project.  This data can be found on our uprading <b><a href="http://2012.igem.org/Team:Calgary/Project/OSCAR/Desulfurization">desulfurization</a></b> page.</p>
<p>Submitted genes for denitorgenation an desulphurization.  A novel oxidoreductase part <b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K902058">BBa_K902058</a></b>  was also submitted and characterized for use in the desulphurization project.  This data can be found on our uprading <b><a href="http://2012.igem.org/Team:Calgary/Project/OSCAR/Desulfurization">desulfurization</a></b> page.</p>

Revision as of 19:58, 3 October 2012

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Detect and Destroy: Data Page

Design

Figure 1. The Calgary team has developed a duel system for the detection of toxic components in tailing ponds as well as the remediation of these compounds. Tailing ponds are large bodies of water containing waste products produced from the extraction of bitumen in the oils ands. Our biosensor involved the identification of a toxin promoter through a transposon screen. An electrochemical detector was implemented with a multiple output system allowing for the detection of multiple compounds simultaneously. This promoter/detector system was then complimented with the production of a biosensor prototype involving both a physical device and a software program for easy data analysis. Rather than just sensing toxins in the tailings ponds, our major objective were to detoxify the tailings through the reduction of toxins such as carboxylic acids (mainly naphthenic acids) and catechol, turning them into useable hydrocarbons. Purification of these hydrocarbons would contribute to an added economic and industrial benefit. In order to house this system, we also aimed to design a bioreactor for our bacteria as well as optimize product output through a flux-variability based model. Finally, in order to create higher quality hydrocarbons, we explored desulphurization and denitrogenation pathways in order to upgrade our fuel. To do this in a safe and environmentally sound way, we designed not only structural containment mechanisms, but also genetic containment mechanisms through novel inducible ribo-killswitches.

Major Accomplishments

Characterization of new parts submitted to the Registry

BBa_K902000 and BBa_K902004,: two novel hydrolase enzymes were submitted to the registry for the hydrolysis of two different sugar conjugated electroactive compounds. Used in conjunction with the existing lacZ part in the registry (BBa_I732005,), this allows for the electrochemical detection of three compounds with a single electrode. A uidA inducible generator (BBa_k902002,) was submitted and characterized electrochemically. This data can be found on our electroreporting page.

BBa_K902008,BBa_K902023 and BBa_K902074: three novel riboswitchs were submtted along with two associated promoters (BBa_K902008) and BBa_K902008) and an inducible/repressible promoter BBa_K902065) were submitted to the registry. One of these riboswitches (BBa_K902008) was tested with GFP using this construct, (BBa_K902014), with its promoter and GFP using this construct (BBa_K902017) and with its promoter and the S7 kill gene using this construct (BBa_K902018). This data can be found on our killswitch (regulation) page.

Submitted genes for denitorgenation an desulphurization. A novel oxidoreductase part BBa_K902058 was also submitted and characterized for use in the desulphurization project. This data can be found on our uprading desulfurization page.

Further characterization of parts already present within the registry

Decatecholization - Optimized an existing biobrick for the production of xylE (catechol dioxygenase) for the degradation of catechol using a constitutive promoter. Other OSCAR parts?!?!?!?

Parts Already In the Registry

Optimized the Petrobrick (BBa_590025) to be able to convert naphthenic acids into alkane and alkene compounds.

Additional Work and Characterizations

Developed a program using MATLAB for the optimization of metabolic pathways in synthetic biology metabolic networks. The program allows you to build an artificial synthetic biology network in E. coli and predicts substrates that should be fed to the organism to increase production of the compound. This was characterized and validated in the wetlab with the Petrobrick.

Developed hardware and software for the development of a biosensor using an electrochemical sensor. The software is available on our wiki. (Robert can you help me flush this out a bit, or one of the engineers?