Team:Bielefeld-CeBiTec/HumanPractice/ScholarAcademy

From 2014.igem.org

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This year, the third CeBiTec Pupils Academy took place at the Centre for Biotechnology (CeBiTec) in Bielefeld. This project is established by the CeBiTec in cooperation with the “Familie-Osthushenrich”-Foundation and the district council of Detmold. It gives 20 young, aspiring pupils a widespread insight look in synthetic biology and iGEM. Besides they received a first overview of the day-to-day life of a student. <br>
This year, the third CeBiTec Pupils Academy took place at the Centre for Biotechnology (CeBiTec) in Bielefeld. This project is established by the CeBiTec in cooperation with the “Familie-Osthushenrich”-Foundation and the district council of Detmold. It gives 20 young, aspiring pupils a widespread insight look in synthetic biology and iGEM. Besides they received a first overview of the day-to-day life of a student. <br>
We prepared four basic biotechnological experiments. Before the experimental part started, we presented the theoretical foundations and our project to them. <br>
We prepared four basic biotechnological experiments. Before the experimental part started, we presented the theoretical foundations and our project to them. <br>
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The experiments were devided in two parts. In the first section the pupils executed a transformation of mixed plasmids in <i>E. coli</i> DH5&alpha; via electroporation and by heat shock. The mix contains pSB1C3::RFP and cp46::GFP. pSB1C3::RFP carries a chloramphenicol resistance and cp46::GFP carries a kanamycin resistance. Because the transformed bacteria were plated on LB-plates without antibiotic, as well as with chloramphenicol or kanamycin, only respective bacteria were growing.  On the day of the analysis of the results the pupils should decide which antibiotic resistance is located on the same plasmid with which reporter gene.<br>
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The experiments were divided in two parts. In the first section the pupils executed a transformation of mixed plasmids in <i>E. coli</i> DH5&alpha; via electroporation and by heat shock. The mix contains pSB1C3::RFP and cp46::GFP. pSB1C3::RFP carries a chloramphenicol resistance and cp46::GFP carries a kanamycin resistance. Because the transformed bacteria were plated on LB-plates without antibiotic, as well as with chloramphenicol or kanamycin, only respective bacteria were growing.  On the day of the analysis of the results the pupils should decide which antibiotic resistance is located on the same plasmid with which reporter gene.<br>
In the second part the pupils had the opportunity to isolate plasmids from a liquid culture with a miniprep-kit. For the experiments they had a script. Working along this they had the chance to think about the transformation methods and the ingredients of the used plasmid miniprep-kit and to ask as much as they wanted. <br>
In the second part the pupils had the opportunity to isolate plasmids from a liquid culture with a miniprep-kit. For the experiments they had a script. Working along this they had the chance to think about the transformation methods and the ingredients of the used plasmid miniprep-kit and to ask as much as they wanted. <br>
In addition to present our project to them, we took an advisory role for all questions around studying. Therefore a get-together-dinner was organized. <br>
In addition to present our project to them, we took an advisory role for all questions around studying. Therefore a get-together-dinner was organized. <br>

Revision as of 16:55, 30 August 2014


Pupils Academy

This year, the third CeBiTec Pupils Academy took place at the Centre for Biotechnology (CeBiTec) in Bielefeld. This project is established by the CeBiTec in cooperation with the “Familie-Osthushenrich”-Foundation and the district council of Detmold. It gives 20 young, aspiring pupils a widespread insight look in synthetic biology and iGEM. Besides they received a first overview of the day-to-day life of a student.
We prepared four basic biotechnological experiments. Before the experimental part started, we presented the theoretical foundations and our project to them.
The experiments were divided in two parts. In the first section the pupils executed a transformation of mixed plasmids in E. coli DH5α via electroporation and by heat shock. The mix contains pSB1C3::RFP and cp46::GFP. pSB1C3::RFP carries a chloramphenicol resistance and cp46::GFP carries a kanamycin resistance. Because the transformed bacteria were plated on LB-plates without antibiotic, as well as with chloramphenicol or kanamycin, only respective bacteria were growing. On the day of the analysis of the results the pupils should decide which antibiotic resistance is located on the same plasmid with which reporter gene.
In the second part the pupils had the opportunity to isolate plasmids from a liquid culture with a miniprep-kit. For the experiments they had a script. Working along this they had the chance to think about the transformation methods and the ingredients of the used plasmid miniprep-kit and to ask as much as they wanted.
In addition to present our project to them, we took an advisory role for all questions around studying. Therefore a get-together-dinner was organized.
For us, the best thing was to get in touch with the motivated pupils and to inspire them for the concept of iGEM. It was interesting to realize how important such a competition is for the right choice of the study in the area of biotechnology or bioinformatics. Because with iGEM you can carry out a project of your choice. This is a major advantage for a biotechnological study.
All in all we had lots of fun to take care of the pupils. We got the impression that we organized an interesting and funny week to the pupils. The discussions with them and their questions about synthetic biology and our project gave us the chance to refine the way we communicate science in the iGEM competition.

We thank the organization-team for their support and the opportunity to be part of the third Students Academy