Team:TU-Munich/HumanPractice/Education

From 2013.igem.org

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== Introducing Synthetic Biology Kits at educational institutions ==
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== Introducing Synthetic Biology Kits at Educational Institutions ==
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[[File:TUM13_School_puote.png|center|900px]]
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 +
What is better than teaching one class about SynBio?<br>
 +
Enabling many teachers to complete this task!
 +
 +
<div class="quote">
 +
"If you want to build a ship, do not drum up people together to collect wood and do not assign them tasks and work, but rather teach them to long for the endless immensity of the sea."
 +
<div class="author">- Antoine de Saint-Exupéry</div>
 +
</div>
==Introduction==
==Introduction==
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[[File:TUM13_Schulkits.jpg|thumb|right|400px|Prepared School-Kits, ready for delivery!]]
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[[File:TUM13_Schulkits.jpg|thumb|right|400px|'''Figure 1:''' Prepared Educational-Kits, ready for delivery!]]
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Corresponding to this famous statement in pedagogics, the TU Munich iGEM Team of 2013 realized the importance to inspire and teach disciples in educational institutions to long for the endless immensity of Synthetic Biology. We want to make it possible for disciples to take their first steps in the enormously evolving field of Synthetic Biology and let them take a breath of this subject, which will change the world in the near future due to its unlimited fields of application.
+
Following this famous statement in pedagogics, we realized the importance to inspire and teach students in educational institutions to long for the endless immenseness of Synthetic Biology. We want to make it possible for disciples to take their first steps in the enormously evolving field of Synthetic Biology and let them take a breath of this subject, which will change the world in the near future due to its unlimited fields of application.
-
The idea is to send an "Educational-Kit" with all required reagents and lab-protocols, based on the experiments we designed, to educational institutions which are interested in inspiring young prospective people to think about a promising career in science. Our experiments are styled constitutive, based on every previously performed experiment, so every disciple, independent of training level, is able to understand and take notice of the resulting phenomena which Synthetic Biology makes possible.
+
The idea is to send an "Educational-Kit" with all required reagents and lab-protocols to educational institutions. Based on the experiments we designed we'd like to inspire young prospective people to think about a promising career in science. Our experiments are styled constitutive, based on every previously performed experiment, so every student, independent of training level, is able to understand and take notice of the resulting phenomena enabled by Synthetic Biology.
==The Educational-Kit==
==The Educational-Kit==
-
The reagents, which are necessary for the realization of the experiments are all found in the kit, except for competent cells, which have to be stored at -20°C. It was set much value on the autonomous preparation of the final reagents, which have to be used, so nearly all reagents will be send in their blank shape. The aim, the iGEM Team of the TU Munich 2013 is pursuiting, is that the disciples should learn as many steps as possible in the realization of the designed experiments. Following reagents are existent in the kit:  
+
The reagents, which are necessary for the realization of the experiments are all found in the kit, except for competent cells, which have to be stored at -20°C. It was set much value on the autonomous preparation of the final reagents, so nearly all reagents will be sent in their blank shape. Our aim is teaching the students all, or at least most, of the necessary steps of the designed experiments during the execution. The kit consists of the following reagents:
{|cellspacing="0" border="1" right  
{|cellspacing="0" border="1" right  
 +
|+ '''Table 1:''' Contents of the educational kit
! align="center";| Reagent
! align="center";| Reagent
! align="center";| Amount of the Reagent
! align="center";| Amount of the Reagent
Line 25: Line 32:
|-
|-
|LB-Medium
|LB-Medium
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|Reagents for about 3 L are in the kit
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| align=right | Reagents for about 3 L are in the kit
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|Yes
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| align=center | Yes
|-
|-
|"Banana-Odor"-Plasmid
|"Banana-Odor"-Plasmid
-
|100 µl (10 ng/µl)
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| align=right | 100 µl (10 ng/µl)
-
|Yes
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| align=center | Yes
|-
|-
|"RFP-Generator"-Plasmid
|"RFP-Generator"-Plasmid
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|100 µl (10 ng/µl)
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| align=right | 100 µl (10 ng/µl)
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|Yes
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| align=center | Yes
|-
|-
|"Luciferase"-Plasmid
|"Luciferase"-Plasmid
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|100 µl (10 ng/µl)
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| align=right | 100 µl (10 ng/µl)
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|Yes
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| align=center | Yes
|-
|-
|Isoamylalcohol (>98 %)
|Isoamylalcohol (>98 %)
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|10 ml
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| align=right | 10 ml
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|Yes
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| align=center | Yes
|-
|-
|Agar plates (Resistance: Kanamycin)
|Agar plates (Resistance: Kanamycin)
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|4 Plates
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| align=right | 4 Plates
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|Yes
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| align=center | Yes
|-
|-
|Agar plates (Resistance: Chloramphenicol)
|Agar plates (Resistance: Chloramphenicol)
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|2
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| align=right | 2
-
|Yes
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| align=center | Yes
|-
|-
|L-Arabinose (500 mM)
|L-Arabinose (500 mM)
-
|3.76 g (50 ml)
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| align=right | 3.76 g (50 ml)
-
|Yes
+
| align=center | Yes
|-
|-
|Kanamycin
|Kanamycin
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|25 ml
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| align=right | 25 ml
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|Yes
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| align=center | Yes
|-
|-
|Chloramphenicol
|Chloramphenicol
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|25 ml
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| align=right | 25 ml
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|Yes
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| align=center | Yes
|-
|-
|Competent Cells  
|Competent Cells  
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|6 Tubes (Aliquotvolume: 150 µl)
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| align=right | 6 Tubes (Aliquotvolume: 150 µl)
-
|No
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| align=center | No
|-
|-
|}  
|}  
-
As you may have noticed, we provide three different plasmids, which are used seperately in each designed experiment. After these experiments have been performed, disciples experienced the whole way from transformation, over cultivating cells, inducing the production of proteins and in the end demonstrate the conversion of a substrate by the produced enzyme.  
+
As you may have noticed, we provide three different plasmids, which are used separately in each designed experiment. After the experiments have been performed, disciples should have experienced the whole way from transformation, over cultivating cells, inducing the production of proteins. In the end they should also have observed the conversion of a substrate by the produced enzyme.
-
<br>
+
-
<br>
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<br>
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==Experiment Number 1==
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==Experiment Number 1: Bacteria in Red==
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[[File:TUM13_RFP_Generator.jpg|thumb|right|400px|Results of Experiment Number 1]]
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[[File:TUM13_RFP_Generator.jpg|thumb|right|400px|'''Figure 2:''' Results of Experiment Number 1]]
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The aim of the first experiment is to transform the [http://parts.igem.org/Part:BBa_K801100 "RFP-Generator"-Plasmid] into ''Escherichia coli'', which contains genes coding for Chloramphenicol resistance plus a red fluorophor, and to plate them on Chloramphenicol-Agarplates. The Agarplates, provided with the antibiotica Chloramphenicol, make a selection process possible, whose aim is to kill all bacteria which have not incorporated the "RFP-Generator"-Plasmid. The expression rate of the red fluorophor is controlled by a constitutive promotor, so the Red fluorescent Protein is expressed continuously. After just about one day of incubation time, the disciples are able to notice a change in colour of the bacteria from ocher to red.
+
The aim of the first experiment is to transform the [http://parts.igem.org/Part:BBa_K801100 "RFP-Generator"-Plasmid] into ''Escherichia coli'', which contains genes, coding for Chloramphenicol resistance, plus a red fluorophor. Then they should be plated on Chloramphenicol-Agarplates. The Agarplates, provided with the antibiotica Chloramphenicol, trigger a selection process, whose aim is to kill all bacteria which have not incorporated the "RFP-Generator"-Plasmid. The expression rate of the red fluorophor is controlled by a constitutive promoter, so the '''R'''ed '''F'''luorescent '''P'''rotein is expressed continuously. After just about one day of incubation time, the students can notice a change in color of the bacteria from ocher to red with the naked eye.
-
The Biobrick we used to realize this experiment was firstly designed by the [https://2010.igem.org/Team:Groningen iGEM Team of Groningen in 2010] to simplify the cloning step by detecting internalized plasmids, which self-circularized without integration of the desired insert. Bacteria, which internalize self-circularized Plasmids will produce red colonies, so these undesired bacterial colonies can be avoided in the next steps of the experiment, to be sure to use the right construct.  
+
The Biobrick we used to realize this experiment was firstly designed by the [https://2010.igem.org/Team:Groningen iGEM Team of Groningen in 2010] to simplify the cloning step by detecting internalized plasmids, which self-circularized without integration of the desired insert. Bacteria, which internalize self-circularized Plasmids will produce red colonies, so these undesired bacterial colonies can be avoided in the next steps of the experiment, to be sure of using the right construct.
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
+
-
==Experiment Number 2==
+
==Experiment Number 2: Glowing Bacteria Lamp==
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[[File:TUM13_Luciferase.jpg|thumb|right|300px|Structure of the Luciferase]]
+
[[File:TUM13_Luciferase.jpg|thumb|right|300px|'''Figure 3:''' Structure of the Luciferase]]
-
In the second experiment disciples should perform the transformation, learned in experiment one, with the "Luciferase"-Plasmid which encodes genes for Kanamycin resistance and a protein-fluorophor called Luciferase. Another very important point is that the Luciferasegene is subordinated to a L-Arabinose Operon. After the transformation of the DNA-Plasmid has taken place, discicples should learn how to cultivate bacteria in liquid LB-Medium and how to induce protein expression by using L-Arabinose as an inductor of the L-Arabinose promotor. The glow of the Luciferase can be observed after just a couple of hours.  
+
In the second experiment students should perform the transformation, which they learned in experiment one, with the "Luciferase"-Plasmid. The Plasmid encodes genes for Kanamycin resistance and a lux - gene cassette containing a protein-fluorophor called Luciferase. Another very important point is that the lux-gene is subordinated to a L-Arabinose Operon. After the transformation of the DNA-Plasmid has taken place, students should learn how to cultivate bacteria in liquid LB-Medium and how to induce protein expression by using L-Arabinose as an inductor of the L-Arabinose promoter. The glow of the Luciferase can already be observed after a few hours.
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
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==Experiment Number 3==
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==Experiment Number 3: Banana Odor Generator==
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[[File:SchmolkerMollath.png|thumb|right|400px|Results of Experiment three]]
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[[File:SchmolkerMollath.png|thumb|right|400px|'''Figure 4:''' Results of Experiment three]]
-
In the third experiment, all aspects learned in the previous experiments come together. These aspects are necessary to understand the following approaches. The [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] encodes an enzyme called Alcohol-Acetyltransferase I. This enzyme is able to convers Isoamylalcohol into Isoamylacetat, which spreads the odor of banana. Additionally there is found a resistance gene for Kanamycin and an inducible L-Arabinose promotor, which controls the expressions rate of the Alcohol-Acetyltransferase I enzyme. The disciples should transform the [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] into ''Escherichia coli'', cultivate the successfully transformed bacteria in a bigger scale and in the end, induce the protein expression by using L-Arabinose. In the last step, the disciples should add the substrate Isoamylalcohol to the cell culture, so the produced enzyme can transform it into Isoamylacetat.  
+
In the third experiment, all aspects learned in the previous experiments come together. The [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] encodes an enzyme called Alcohol-Acetyltransferase I. This enzyme is able to convert Isoamylalcohol into Isoamylacetat, which spreads the odor of banana. Additionally the plasmid harbors a resistance gene for Kanamycin and an inducible L-Arabinose promoter, which controls the expressions rate of the Alcohol-Acetyltransferase I enzyme. The students should transform the [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] into ''Escherichia coli'', cultivate the successfully transformed bacteria in a larger scale and in the end, induce the protein expression by using L-Arabinose. In the last step, the students should add the substrate Isoamylalcohol to the cell culture, so the produced enzyme can transform it into Isoamylacetat.  
-
The Biobrick, which spreads the odor of banana, after transforming its substrate, was firstly established by the [http://openwetware.org/wiki/IGEM:MIT/2006 iGEM Team of the Massachusetts Institute of Technology in 2006]. Their aim was mainly to produce different compounds in ''Escherichia coli'' that smell fragrant. Another very interesting application of the "Banana-Odor" Biobrick is pursued by the [https://2013.igem.org/Team:Queens_Canada/Project/Repel iGEM Team of Queens in 2013]. This team tries to neutralize foot odour by creating a skin creme containing bacteria with a genetical engineered metabolic pathway to neutralize the volatile compounds that cause these smells. This pathway begins with the uptake of isovaleric acid, a known mosquito semiochemical that is present is foot odour, and converts it into banana smell. By establishing this skin creme, it should be possible to prevent people from being attacked by mosquitos and saved from typical alienable diseases mosquitos spread.  
+
The Biobrick, which spreads the odor of banana, after transforming its substrate, was first established by the [http://openwetware.org/wiki/IGEM:MIT/2006 iGEM Team of the Massachusetts Institute of Technology in 2006]. Their aim was to produce different compounds in ''Escherichia coli'' that smell fragrant. Another very interesting application of the "Banana-Odor" Biobrick is pursued by the [https://2013.igem.org/Team:Queens_Canada/Project/Repel iGEM Team of Queens in 2013]. This team tries to neutralize foot odor by creating a skin creme containing bacteria with a genetically engineered metabolic pathway to neutralize the volatile compounds that cause these smells. This pathway begins with the uptake of isovaleric acid, a known mosquito semiochemical that is present in foot odor, and converts it into banana smell. By establishing this skin creme, it should be possible to prevent people from being attacked by mosquitos and saved from typical alienable diseases mosquitos spread.
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
+
-
<br>
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==Target Audience==
==Target Audience==
-
Our target audience have been secondary schools, which focus a biotechnical educational pathway, so all students have access to the required laboratory equipment for the experiments. Before sending the kits to the schools, we tested them in detail - with success. All schools we contacted, to spread our Synthetic Biology kits, are very enthusiastic concerning our idea of supporting young prospective scientists, so they are very excited to receive and use our kit!
+
The target audience for our kit are secondary schools with focus on a biotechnological educational pathway, so all students have access to the required laboratory equipment for the experiments. Before sending the kits to the schools, we tested them in detail - with success. All schools we contacted to spread our Synthetic Biology kits are very enthusiastic concerning our idea of supporting young prospective scientists, so they are very excited to receive and use our kit!
-
==Availability of the School-kit==
+
==Availability of the Educational-kits==
-
We appreciate other interested schools in trying our “School kits”. Do not be ashamed of contacting us, so we can supply you with our forward-looking Synthetic Biology “School-kit”!
+
We appreciate other interested schools in trying out our “Educational-kits”. Do not hesitate contacting us. We are happy to supply you with our forward-looking Synthetic Biology “Educational-kit”!
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<br>
+
 
 +
You can '''send requests''' to: igem@wzw.tum.de
 +
 
 +
Due to the World Championship Jamboree of iGEM, we offer the description of our "Educational Kit" directly to everyone, who is interested in it! Just click on the download-Button to get it! This decision supports the open-source idea which is intrinsic to iGEM as well as our team, to facilitate the education of every pupil, prospective scientist and scientists.
 +
 
 +
[[media:Educational_kit.pdf|'''Get your Educational kit!''']]
 +
 
 +
We are very sad to tell you that our "Educational Kit" is just available in german language, because our target audience have been german secondary schools with a focus on a biotechnological educational pathway. However, we´re working on a translated version.
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<html><ul class="bxslider"> <!-- das muss so hässlich sein, damit kein absatz eingefügt wird -->
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<li><img src="https://static.igem.org/mediawiki/2013/2/2e/Educational_Kit_1.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/f/fd/Educational_Kit_2.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/5/5b/Educational_Kit_3.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/6/66/Educational_Kit_4.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/c/c9/Educational_Kit_5.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/4/49/Educational_Kit_6.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/9/9d/Educational_Kit_7.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/2/2c/Educational_Kit_8.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/b/b7/Educational_Kit_9.png" /></li>
 +
<li><img src="https://static.igem.org/mediawiki/2013/a/ae/Educational_Kit_10.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/2/2c/Educational_Kit_11.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/0/04/Educational_Kit_12.png" /></li>
 +
<li><img src="https://static.igem.org/mediawiki/2013/c/c6/Educational_Kit_13.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/8/83/Educational_Kit_14.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/7/77/Educational_Kit_15.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/4/49/Educational_Kit_16.png" /></li>
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<li><img src="https://static.igem.org/mediawiki/2013/d/d9/Educational_Kit_17.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/9/96/Educational_Kit_18.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/6/6c/Educational_Kit_19.png" /></li>
 +
<li><img src="https://static.igem.org/mediawiki/2013/7/70/Educational_Kit_20.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/c/cd/Educational_Kit_21.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/5/5e/Educational_Kit_22.png" /></li>
 +
<li><img src="https://static.igem.org/mediawiki/2013/b/ba/Educational_Kit_23.png" /></li>
 +
        <li><img src="https://static.igem.org/mediawiki/2013/d/d1/Educational_Kit_24.png" /></li>
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        <li><img src="https://static.igem.org/mediawiki/2013/3/3e/Educational_Kit_25.png" /></li>
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</ul>
 +
</html>
==References==
==References==
<!-- Kopiervorlagen -->
<!-- Kopiervorlagen -->
-
[[http://www.ncbi.nlm.nih.gov/pubmed/6327079 Edens et al., 1984]]
 
-
#[[http://www.ncbi.nlm.nih.gov/pubmed/6327079 Edens et al., 1984]] Edens, L., Bom, I., Ledeboer, A. M., Maat, J., Toonen, M. Y., Visser, C., and Verrips, C. T. (1984). Synthesis and processing of the plant protein thaumatin in yeast. ''Cell'', 37(2):629–33.
 
-
<!-- Ab hier richtige Referenzen einfügen -->
 
-
#
 
 +
[[https://2010.igem.org/Team:Groningen iGEM Team Groningen 2010]] <br>
 +
 +
[[http://www.ncbi.nlm.nih.gov/pubmed/22368493 Close D et al., 2012]] Close D, Xu T, Smartt A, Rogers A, Crossley R, Price S, Ripp S, Sayler G (2012). The evolution of the bacterial luciferase gene cassette (lux) as a real-time bioreporter. ''Sensors'', 12(1):732-52. <br>
 +
 +
[[http://openwetware.org/wiki/IGEM:MIT/2006 iGEM Team Massachusetts Institute of Technology 2006]] <br>
 +
[[https://2013.igem.org/Team:Queens_Canada/Project/Repel iGEM Team Queens 2013]] <br>
<!-- End of content -->
<!-- End of content -->

Latest revision as of 12:59, 30 December 2013


Introducing Synthetic Biology Kits at Educational Institutions

What is better than teaching one class about SynBio?
Enabling many teachers to complete this task!

"If you want to build a ship, do not drum up people together to collect wood and do not assign them tasks and work, but rather teach them to long for the endless immensity of the sea."

- Antoine de Saint-Exupéry

Introduction

Figure 1: Prepared Educational-Kits, ready for delivery!

Following this famous statement in pedagogics, we realized the importance to inspire and teach students in educational institutions to long for the endless immenseness of Synthetic Biology. We want to make it possible for disciples to take their first steps in the enormously evolving field of Synthetic Biology and let them take a breath of this subject, which will change the world in the near future due to its unlimited fields of application.

The idea is to send an "Educational-Kit" with all required reagents and lab-protocols to educational institutions. Based on the experiments we designed we'd like to inspire young prospective people to think about a promising career in science. Our experiments are styled constitutive, based on every previously performed experiment, so every student, independent of training level, is able to understand and take notice of the resulting phenomena enabled by Synthetic Biology.

The Educational-Kit

The reagents, which are necessary for the realization of the experiments are all found in the kit, except for competent cells, which have to be stored at -20°C. It was set much value on the autonomous preparation of the final reagents, so nearly all reagents will be sent in their blank shape. Our aim is teaching the students all, or at least most, of the necessary steps of the designed experiments during the execution. The kit consists of the following reagents:

Table 1: Contents of the educational kit
Reagent Amount of the Reagent Is it existent in the kit?
LB-Medium Reagents for about 3 L are in the kit Yes
"Banana-Odor"-Plasmid 100 µl (10 ng/µl) Yes
"RFP-Generator"-Plasmid 100 µl (10 ng/µl) Yes
"Luciferase"-Plasmid 100 µl (10 ng/µl) Yes
Isoamylalcohol (>98 %) 10 ml Yes
Agar plates (Resistance: Kanamycin) 4 Plates Yes
Agar plates (Resistance: Chloramphenicol) 2 Yes
L-Arabinose (500 mM) 3.76 g (50 ml) Yes
Kanamycin 25 ml Yes
Chloramphenicol 25 ml Yes
Competent Cells 6 Tubes (Aliquotvolume: 150 µl) No

As you may have noticed, we provide three different plasmids, which are used separately in each designed experiment. After the experiments have been performed, disciples should have experienced the whole way from transformation, over cultivating cells, inducing the production of proteins. In the end they should also have observed the conversion of a substrate by the produced enzyme.

Experiment Number 1: Bacteria in Red

Figure 2: Results of Experiment Number 1

The aim of the first experiment is to transform the [http://parts.igem.org/Part:BBa_K801100 "RFP-Generator"-Plasmid] into Escherichia coli, which contains genes, coding for Chloramphenicol resistance, plus a red fluorophor. Then they should be plated on Chloramphenicol-Agarplates. The Agarplates, provided with the antibiotica Chloramphenicol, trigger a selection process, whose aim is to kill all bacteria which have not incorporated the "RFP-Generator"-Plasmid. The expression rate of the red fluorophor is controlled by a constitutive promoter, so the Red Fluorescent Protein is expressed continuously. After just about one day of incubation time, the students can notice a change in color of the bacteria from ocher to red with the naked eye.

The Biobrick we used to realize this experiment was firstly designed by the iGEM Team of Groningen in 2010 to simplify the cloning step by detecting internalized plasmids, which self-circularized without integration of the desired insert. Bacteria, which internalize self-circularized Plasmids will produce red colonies, so these undesired bacterial colonies can be avoided in the next steps of the experiment, to be sure of using the right construct.

Experiment Number 2: Glowing Bacteria Lamp

Figure 3: Structure of the Luciferase

In the second experiment students should perform the transformation, which they learned in experiment one, with the "Luciferase"-Plasmid. The Plasmid encodes genes for Kanamycin resistance and a lux - gene cassette containing a protein-fluorophor called Luciferase. Another very important point is that the lux-gene is subordinated to a L-Arabinose Operon. After the transformation of the DNA-Plasmid has taken place, students should learn how to cultivate bacteria in liquid LB-Medium and how to induce protein expression by using L-Arabinose as an inductor of the L-Arabinose promoter. The glow of the Luciferase can already be observed after a few hours.

Experiment Number 3: Banana Odor Generator

Figure 4: Results of Experiment three

In the third experiment, all aspects learned in the previous experiments come together. The [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] encodes an enzyme called Alcohol-Acetyltransferase I. This enzyme is able to convert Isoamylalcohol into Isoamylacetat, which spreads the odor of banana. Additionally the plasmid harbors a resistance gene for Kanamycin and an inducible L-Arabinose promoter, which controls the expressions rate of the Alcohol-Acetyltransferase I enzyme. The students should transform the [http://parts.igem.org/Part:BBa_J45014 "Banana-Odor"-Plasmid] into Escherichia coli, cultivate the successfully transformed bacteria in a larger scale and in the end, induce the protein expression by using L-Arabinose. In the last step, the students should add the substrate Isoamylalcohol to the cell culture, so the produced enzyme can transform it into Isoamylacetat.

The Biobrick, which spreads the odor of banana, after transforming its substrate, was first established by the [http://openwetware.org/wiki/IGEM:MIT/2006 iGEM Team of the Massachusetts Institute of Technology in 2006]. Their aim was to produce different compounds in Escherichia coli that smell fragrant. Another very interesting application of the "Banana-Odor" Biobrick is pursued by the iGEM Team of Queens in 2013. This team tries to neutralize foot odor by creating a skin creme containing bacteria with a genetically engineered metabolic pathway to neutralize the volatile compounds that cause these smells. This pathway begins with the uptake of isovaleric acid, a known mosquito semiochemical that is present in foot odor, and converts it into banana smell. By establishing this skin creme, it should be possible to prevent people from being attacked by mosquitos and saved from typical alienable diseases mosquitos spread.

Target Audience

The target audience for our kit are secondary schools with focus on a biotechnological educational pathway, so all students have access to the required laboratory equipment for the experiments. Before sending the kits to the schools, we tested them in detail - with success. All schools we contacted to spread our Synthetic Biology kits are very enthusiastic concerning our idea of supporting young prospective scientists, so they are very excited to receive and use our kit!

Availability of the Educational-kits

We appreciate other interested schools in trying out our “Educational-kits”. Do not hesitate contacting us. We are happy to supply you with our forward-looking Synthetic Biology “Educational-kit”!

You can send requests to: igem@wzw.tum.de

Due to the World Championship Jamboree of iGEM, we offer the description of our "Educational Kit" directly to everyone, who is interested in it! Just click on the download-Button to get it! This decision supports the open-source idea which is intrinsic to iGEM as well as our team, to facilitate the education of every pupil, prospective scientist and scientists.

Get your Educational kit!

We are very sad to tell you that our "Educational Kit" is just available in german language, because our target audience have been german secondary schools with a focus on a biotechnological educational pathway. However, we´re working on a translated version.

References

[iGEM Team Groningen 2010]

http://www.ncbi.nlm.nih.gov/pubmed/22368493 Close D et al., 2012 Close D, Xu T, Smartt A, Rogers A, Crossley R, Price S, Ripp S, Sayler G (2012). The evolution of the bacterial luciferase gene cassette (lux) as a real-time bioreporter. Sensors, 12(1):732-52.

http://openwetware.org/wiki/IGEM:MIT/2006 iGEM Team Massachusetts Institute of Technology 2006

[iGEM Team Queens 2013]

Retrieved from "http://2013.igem.org/Team:TU-Munich/HumanPractice/Education"