Difference between revisions of "Team:UFSCar-Brasil/achievements.html"
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<h3 class="ui header" id="overview">Overview</h3> | <h3 class="ui header" id="overview">Overview</h3> | ||
− | <p> | + | <p> During laboratory activities realized by UFSCar-Brasil team, was obtained different results for the proposed project, as well as the contribution with new biobricks for registry and new protocols for scientific community use in forward projects. |
− | + | Based on molecular biology, bioinformatics and microbiology techniques, our Team could propose protocols and biobricks, which assist obtaining protein of difficult expression through the UspA promoter, as well as maintaining bacterial viability at room temperature by plasmolysis induced polyethylene glycol. Thus, we believe that with the expansion of synthetic biology to market manufactures, our protocols represent an important tool in enabling bacteria genetically engineered shelf products.</p> | |
+ | <p>Another important point refer to the following project's module, characterized by overexpression of chaperones during cell growth and the utilization of a biosafety method as Killswitch; Developed by UFSCar-Brazil team, these modules can also represent important tools that envisaged the viability and theoretical basis of the project. | ||
+ | We believe that, although many structural and funding problems, attach ourselves to the iGEM spirit and we achieved great achievements, and through impressive results in the laboratory, which are described below, contribute to the development of synthetic biology.</p> | ||
</div> | </div> | ||
Revision as of 11:16, 18 September 2015
Overview
During laboratory activities realized by UFSCar-Brasil team, was obtained different results for the proposed project, as well as the contribution with new biobricks for registry and new protocols for scientific community use in forward projects. Based on molecular biology, bioinformatics and microbiology techniques, our Team could propose protocols and biobricks, which assist obtaining protein of difficult expression through the UspA promoter, as well as maintaining bacterial viability at room temperature by plasmolysis induced polyethylene glycol. Thus, we believe that with the expansion of synthetic biology to market manufactures, our protocols represent an important tool in enabling bacteria genetically engineered shelf products.
Another important point refer to the following project's module, characterized by overexpression of chaperones during cell growth and the utilization of a biosafety method as Killswitch; Developed by UFSCar-Brazil team, these modules can also represent important tools that envisaged the viability and theoretical basis of the project. We believe that, although many structural and funding problems, attach ourselves to the iGEM spirit and we achieved great achievements, and through impressive results in the laboratory, which are described below, contribute to the development of synthetic biology.
Parts
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Result
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Judging Criteria
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