Difference between revisions of "Team:Tuebingen/schoolclassatlab"

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<img id="schoollab" style="max-height: 200px; display: block; margin-left: auto; margin-right: auto;" src="https://static.igem.org/mediawiki/2015/5/57/Team_Tuebingen_SchoolPic1_300pxheight.jpg"/>
 
<img id="schoollab" style="max-height: 200px; display: block; margin-left: auto; margin-right: auto;" src="https://static.igem.org/mediawiki/2015/5/57/Team_Tuebingen_SchoolPic1_300pxheight.jpg"/>
  
<p>The field of synthetic biology is often dealt with in the media and in many cases, the possible consequences of genetically modified organisms (GMOs) in food are discussed highly controversial. A main reason for the high emotionality regarding this topic is the fact that knowledge about genetics and general methods used in gene technology and ecology is  rare in public. On September 17th, we therefore invited 40 pupils in their final high-school year from the Mildred Scheel Schule Böblingen to our institute, in order to introduce this controversially discussed topic with them. Our intention was to convey the theoretical as well as the practical background of synthetic biology by talking about gene technology, presenting our iGEM project, and performing daily used gene technology methods with them.
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<p>The field of synthetic biology is often dealt with in the media and often the possible consequences of genetically modified organisms (GMOs) in food is discussed highly controversial. One main reason for the high controversy is the lack of communication between researchers and the public. On September 17th, we invited 40 pupils in their final high-school year from the Mildred Scheel Schule Böblingen to our institute. Our aim was to introduce the practical and theoretical background of synthetic biology, our work and discuss related topics. In the practical part of the school@lab day we teached some widely used methods like  PCR and restriction digestion.  
 
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We performed an experiment to prove the existence of the cry1Ab gene that codes for a delta-endotoxin in the genome of genetically modified corn. These cry-toxins are pore-forming toxins that are naturally produced by Bacillus thuringiensis. Their incorporation in the encoding gene of corn genome helps to perish a corn parasite (the European corn borer) during corn cultivation because of the insecticidal effects of cry-toxins.
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We performed an experiment to prove the existence of CRY1Ab, a corn gene that encodes for a delta-endotoxin. These CRY-toxins form pores, which are naturally produced by Bacillus thuringiensis. Their incorporation into the corn genome helps to perish the European corn borer, a corn parasite, during corn cultivation as these CRY-toxins have a insecticidal effect. <img id="schoollab" style="max-height:200px; display: block; margin-left: auto; margin-right: auto;" src="https://static.igem.org/mediawiki/2015/f/fc/Team_Tuebingen_SchoolPic2_300pxheight.jpg"/>
<img id="schoollab" style="max-height:200px; display: block; margin-left: auto; margin-right: auto;" src="https://static.igem.org/mediawiki/2015/f/fc/Team_Tuebingen_SchoolPic2_300pxheight.jpg"/>
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The day started with an introduction to synthetic biology and frequently used methods followed by the practical part. During a lunch break, we give an insight into the implications of GMOs and gene technology in general, followed by a vivid discussion. The practical part began with a DNA extraction from food samples which were used for a polymerase chain reaction (PCR). The PCR products were finally separated via agarose gel electrophoresis to check if the cry1Ab gene was present in their own maize samples. Another approach to show the pupils basic methods of gene technology was a restriction digest. The pupils were given one of five different plasmids, which they should identify by a restriction digest.   <br>
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In the theoretical part we gave an overview to synthetic biology and introduced widely used methods. We tried to demonstrate insights into the implications of GMOs and gene technology in general. In the practical part we extracted  DNA from food samples, which were used for PCR (Polymerase Chain Reaction). The PCR products were then separated via agarose gel electrophoresis to check on CRY1Ab. Restriction digestion was used to identify one out of five given plasmids. <br>
 
<img id="schoollab" style="max-height:200px; display: block; margin-left:auto; margin-right:auto;" src="https://static.igem.org/mediawiki/2015/9/93/Team_Tuebingen_SchoolPic3_300pxheight.jpg"/>
 
<img id="schoollab" style="max-height:200px; display: block; margin-left:auto; margin-right:auto;" src="https://static.igem.org/mediawiki/2015/9/93/Team_Tuebingen_SchoolPic3_300pxheight.jpg"/>
 
This little exercise on the interpretation of scientific data, and the test on the cry1A(b)-gene were well received by the pupils as they were able to figure out what it is like to analyze their own results and draw conclusions from that. We discussed together what might have gone wrong and what information they got from the  corn samples.They were excited to learn methods like PCR and gel electrophoresis, because such experiments are usually not carried out in school. Especially the loading of an agarose gel was very fascinating for them and led to a lot of questions concerning the theoretical background.
 
This little exercise on the interpretation of scientific data, and the test on the cry1A(b)-gene were well received by the pupils as they were able to figure out what it is like to analyze their own results and draw conclusions from that. We discussed together what might have gone wrong and what information they got from the  corn samples.They were excited to learn methods like PCR and gel electrophoresis, because such experiments are usually not carried out in school. Especially the loading of an agarose gel was very fascinating for them and led to a lot of questions concerning the theoretical background.
 
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All in all, we hope that the pupils enjoyed this excursion to the field of synthetic biology and got a profound first impression, so that they are motivated to form a well-founded opinion about different forms of gene technology and maybe go into gene technology themselves after they finish school.
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The pupils learned how to interpret scientific data and test for CRY1Ab was used to teach analysis of their own results and draw conclusions from it. We discussed possible errors and what information they obtained from the corn samples. The pupils were excited to learn new methods as such experiments are usually not carried out in school. The experiments led to a lot of questions concerning the theoretical background and resulted in a vivid discussion.
 
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Revision as of 20:54, 18 September 2015

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The field of synthetic biology is often dealt with in the media and often the possible consequences of genetically modified organisms (GMOs) in food is discussed highly controversial. One main reason for the high controversy is the lack of communication between researchers and the public. On September 17th, we invited 40 pupils in their final high-school year from the Mildred Scheel Schule Böblingen to our institute. Our aim was to introduce the practical and theoretical background of synthetic biology, our work and discuss related topics. In the practical part of the school@lab day we teached some widely used methods like PCR and restriction digestion.


We performed an experiment to prove the existence of CRY1Ab, a corn gene that encodes for a delta-endotoxin. These CRY-toxins form pores, which are naturally produced by Bacillus thuringiensis. Their incorporation into the corn genome helps to perish the European corn borer, a corn parasite, during corn cultivation as these CRY-toxins have a insecticidal effect.


In the theoretical part we gave an overview to synthetic biology and introduced widely used methods. We tried to demonstrate insights into the implications of GMOs and gene technology in general. In the practical part we extracted DNA from food samples, which were used for PCR (Polymerase Chain Reaction). The PCR products were then separated via agarose gel electrophoresis to check on CRY1Ab. Restriction digestion was used to identify one out of five given plasmids.
This little exercise on the interpretation of scientific data, and the test on the cry1A(b)-gene were well received by the pupils as they were able to figure out what it is like to analyze their own results and draw conclusions from that. We discussed together what might have gone wrong and what information they got from the corn samples.They were excited to learn methods like PCR and gel electrophoresis, because such experiments are usually not carried out in school. Especially the loading of an agarose gel was very fascinating for them and led to a lot of questions concerning the theoretical background.

The pupils learned how to interpret scientific data and test for CRY1Ab was used to teach analysis of their own results and draw conclusions from it. We discussed possible errors and what information they obtained from the corn samples. The pupils were excited to learn new methods as such experiments are usually not carried out in school. The experiments led to a lot of questions concerning the theoretical background and resulted in a vivid discussion.