Difference between revisions of "Team:Goettingen/Parts"
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<p>Basic parts are functional DNA units that cannot be divided into smaller parts. A construct of multiple basic parts is called a composite part. Here, the functionality of a basic part was increased through the implementation of different functional sites. The parts of our team are listed and shortly described in the following table: </p> | <p>Basic parts are functional DNA units that cannot be divided into smaller parts. A construct of multiple basic parts is called a composite part. Here, the functionality of a basic part was increased through the implementation of different functional sites. The parts of our team are listed and shortly described in the following table: </p> | ||
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| − | + | <p>Furthermore, we have characterized an existing part. We have selected the part <a href="http://parts.igem.org/Part:BBa_E2050" target="_blank">BBa_E2050 (mERP)</a>, which we have used for transformation of different <em>B. subtilis</em> strains. Because the plasmid pSB1C3 does not contain an origin of replication for <em>B. subtilis</em>, we have cloned the fluorophore gene using the plasmid pAC7 and transformed the <em>E. coli</em> strain DH5α with the resulting plasmids. The fluorophore gene was also fused to a self-made promoter, which is characterized by a good consensus sequence for the housekeeping sigma factor A and a perfect ribosome binding site (RBS) of <em>B. subtilis</em>. Further information can be found on the parts registry sites. Some of the constructed <em>B. subtilis</em> strains were used for the competition experiments (please check out the Results section). </p> | |
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| − | <p>Furthermore, we have characterized an existing part. We have selected the part <a href="http://parts.igem.org/Part:BBa_E2050" target="_blank">BBa_E2050 (mERP)</a>, which we have used for transformation of different <em>B. subtilis</em> strains. Because the plasmid pSB1C3 does not contain an origin of replication for <em>B. subtilis</em>, we have cloned the fluorophore gene using the plasmid pAC7 and transformed the <em>E. coli</em> DH5α with the resulting plasmids. The fluorophore gene was also fused to a self-made promoter, which is characterized by a good consensus sequence for the housekeeping sigma factor A and a perfect ribosome binding site (RBS) of <em>B. subtilis</em>. Further information can be found on the parts registry sites. Some of the constructed <em>B. subtilis</em> strains were used for the competition experiments (please check out the Results section). </p> | + | |
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Latest revision as of 17:15, 17 October 2018
Team Göttingen
iGEM 2018
Glyphosate on my plate?
| E-mail: | igem2018@gwdg.de |
|---|---|
| Adress: | c/o iGEM 2018 |
| Department of General Microbiology | |
| Grisebachstraße 8 | |
| 37077 Göttingen | |
| Germany |
We are especially grateful to our numerous sponsors on gofundme, who supported our project and made it possible.
Every public donor, who helped us to achieve our goals got a special place on our bacterial wall of fame and a handdrawn microbe to show our appreciation. A link to that wall can be found here:
Parts
Connecting global research
Our contribution to a huge parts collection.
The concept of iGEM is based on the exchange of internationally provided DNA sequences. These sequences are called Biobricks and are collected in a big database, which grows steadily as iGEM progresses. In this way, teams all over the globe can benefit from the part collection and improve the work that was done previously by other teams, to drive the research further.
Basic parts and composite parts
Basic parts are functional DNA units that cannot be divided into smaller parts. A construct of multiple basic parts is called a composite part. Here, the functionality of a basic part was increased through the implementation of different functional sites. The parts of our team are listed and shortly described in the following table:
Furthermore, we have characterized an existing part. We have selected the part BBa_E2050 (mERP), which we have used for transformation of different B. subtilis strains. Because the plasmid pSB1C3 does not contain an origin of replication for B. subtilis, we have cloned the fluorophore gene using the plasmid pAC7 and transformed the E. coli strain DH5α with the resulting plasmids. The fluorophore gene was also fused to a self-made promoter, which is characterized by a good consensus sequence for the housekeeping sigma factor A and a perfect ribosome binding site (RBS) of B. subtilis. Further information can be found on the parts registry sites. Some of the constructed B. subtilis strains were used for the competition experiments (please check out the Results section).