Difference between revisions of "Team:IIT Delhi/results"

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The assimilatory Nitrite Reductase gene under the control of a strong Promoter Anderson J23104 with a Ribosome Binding Site was cloned onto the pSB1A3 plasmid backbone. This gene catalyses the conversion of Nitrite (NO2 -) to Ammonium (NH4 +).
 
The assimilatory Nitrite Reductase gene under the control of a strong Promoter Anderson J23104 with a Ribosome Binding Site was cloned onto the pSB1A3 plasmid backbone. This gene catalyses the conversion of Nitrite (NO2 -) to Ammonium (NH4 +).
  
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<a href="http://parts.igem.org/Part:BBa_K1866001" target="_blank"> Part:BBa_K1866001</a>
 
<a href="http://parts.igem.org/Part:BBa_K1866001" target="_blank"> Part:BBa_K1866001</a>
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This part consists of NosZ gene and a sequence encoding for Super Yellow Fluorescence Protein downstream to it.
 
This part consists of NosZ gene and a sequence encoding for Super Yellow Fluorescence Protein downstream to it.
 
NosZ gene product catalyses the conversion of Nitrous Oxide (N2O) to molecular Nitrogen gas in a process called denitrification.
 
NosZ gene product catalyses the conversion of Nitrous Oxide (N2O) to molecular Nitrogen gas in a process called denitrification.
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<a href="http://parts.igem.org/Part:BBa_K1866002" target="_blank"> Part:BBa_K1866002</a>
  
 
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Promoter+RibosomeBindingSite+NrfA+SYFP
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This part has the Super Yellow Fluorescence Protein tagged to the NrfA gene product from our biobrick BBa_K186600
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<a href="http://parts.igem.org/Part:BBa_K1866003" target="_blank"> Part:BBa_K1866003</a>
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Promoter+RibosomeBindingSite+Sqr gene
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This part consists of the Sulfide Quinone Reductase Sqr gene under the control of a strong promoter with a Ribosome Binding Site. The Sqr gene catalyses the conversion of hydrogen Sulfide gas to elemental Sulfur.
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<a href="http://parts.igem.org/Part:BBa_K1866004" target="_blank"> Part:BBa_K1866004</a>
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Promoter+RibosomeBindingSite+NosZ+SuperYellowFluorescenceProtein
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This part consists of the gene NosZ that encodes for an enzyme named Dissimilatory Nitrous Oxide Reductase.
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This enzyme catalyses the conversion of Nitrous Oxide, a greenhouse gas to Nitrogen gas. The NosZ gene is cloned under the control of a strong Promoter with a Ribosome Binding Site for optimum expression.
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This part also consists of a Super Yellow Fluorescence Protein tag to check the expression of the NosZ gene.
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</h2>
 
</h2>

Revision as of 19:43, 18 September 2015

Parts Submitted

Part:BBa_K1866000
Promoter+RibosomeBindingSite+NrfA
The assimilatory Nitrite Reductase gene under the control of a strong Promoter Anderson J23104 with a Ribosome Binding Site was cloned onto the pSB1A3 plasmid backbone. This gene catalyses the conversion of Nitrite (NO2 -) to Ammonium (NH4 +).

Part:BBa_K1866001
NosZ gene+SuperYellowFluorescenceProtein
This part consists of NosZ gene and a sequence encoding for Super Yellow Fluorescence Protein downstream to it. NosZ gene product catalyses the conversion of Nitrous Oxide (N2O) to molecular Nitrogen gas in a process called denitrification.

Part:BBa_K1866002
Promoter+RibosomeBindingSite+NrfA+SYFP
This part has the Super Yellow Fluorescence Protein tagged to the NrfA gene product from our biobrick BBa_K186600

Part:BBa_K1866003
Promoter+RibosomeBindingSite+Sqr gene
This part consists of the Sulfide Quinone Reductase Sqr gene under the control of a strong promoter with a Ribosome Binding Site. The Sqr gene catalyses the conversion of hydrogen Sulfide gas to elemental Sulfur.

Part:BBa_K1866004
Promoter+RibosomeBindingSite+NosZ+SuperYellowFluorescenceProtein
This part consists of the gene NosZ that encodes for an enzyme named Dissimilatory Nitrous Oxide Reductase. This enzyme catalyses the conversion of Nitrous Oxide, a greenhouse gas to Nitrogen gas. The NosZ gene is cloned under the control of a strong Promoter with a Ribosome Binding Site for optimum expression. This part also consists of a Super Yellow Fluorescence Protein tag to check the expression of the NosZ gene.



Criteria Fulfilled


For Bronze:
  • We registered for iGEM, and are going to attend the Giant Jamboree.
  • We have completed the Judging Form.
  • We have created and shared a description of the team's project using the iGEM wiki, and documented the team's parts using the Registry of Standard Biological Parts.
  • We are going to present a poster and a talk at the iGEM Jamboree.
  • We have created a page on our team wiki with a clear attribution of each aspect of our project, following all the necessary criteria as per the instructions.
  • We have document a new standard BioBrick Part, which is central to our project and are going to submit this part to the iGEM Registry, adhering to the iGEM Registry guidelines.


    • For Silver:
  • We have experimentally validated that our BioBrick Part as well as the device (of our own design and construction) works as per the expectations. Apart from that, we also documented the characterization of this part in the Main Page section of the Registry.
  • We submitted this new part to the iGEM Parts Registry.
  • Our team has identified the issue of Pollution in general. We have investigated the effect it has through numerous surveys carried out in different parts of Delhi. We are implementing our prototype in project "Aanch" of Enactus. And finally, we have published a documentation on Pollution to make people aware of the seriousness of the issue.


    • For Gold:
  • We are mentoring the iGEM IIT Kharagpur team, participating for the first time in the Giant Jamboree Competition.
  • We have improved the characterization of our previously existing BioBrick Part.
  • We have designed a functional prototype of our project.
  • And finally, we integrated the issues raised during the surveys, through necessary changes in our design.

    		•

    Acknowledgement

    A few months back, it was a dream. Today, it’s a reality. The transition didn't come by our efforts alone. There are people who didn’t hesitate to spend their valuable time on us. And we certainly do owe a lot to them.
    We are sincerely thankful to Prof. Shaikh Ziauddin Ahammad and Dr. Stefan Oehler from the Department of Biochemical Engineering and Biotechnology for their constant support. We are grateful to Prof. Biswajit Kundu and Prof. James Gomes from the Kusuma School of Biological Sciences for their valuable advices which helped us a lot to strategise our work plan.
    We are thankful to Prof. Anurag Sharma, Dean, IIT Delhi, for allowing us to use the UG lab (Biotech) and Prof. P.V.M Rao for letting us the access to Workshop, IIT Delhi. We are also thankful to Garima Goyal (Protein Engineering Lab) and Anamika (RNA 2 Lab) for allowing us to access to their labs.
    We are also thankful to the Rishabh Mathur, Mayank Sahu, Shashank Yadav and Rishabh Verma, previous members of iGEM IIT Delhi, for their valuable advices at different points of time.