Team:Frankfurt

From 2012.igem.org

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<big> <span style="color:#00008B"> '''Welcome to our page and greetings from the Goethe University Frankfurt am Main. We are pleased about your visit of our website. You will find more details about our project using the menu above. We appreciate your critic and comments.''' </span> </big>
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= Steviomyces - it's gonna be sweet =
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== Project Description ==
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<html><div class="thumb tright"><div class="thumbinner" style="width:400px;"><img src="https://lh3.googleusercontent.com/-jAqJRiiSCAU/UGN9LJDLPII/AAAAAAAAABU/yAT7wg2OJcY/s400/iGEM_NOS14.jpg" /><div class="thumbcaption">iGEM at the Night of Science - it's gonna be sweet. You can see the stevia plant, a self-made stevia cake and german stevia götterspeise. There is also some commercial stevia chocolate available</div></div></div></html>
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Therefore, we aim to develop biobricked pathway expressing all necessary genes for rebaudioside A production in common baker's yeast ''Saccharomyces cerevisae'', a well known, safe organism used in food production for millenia.
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As a precursor for the diterpene steviol is geranylgeranyl pyrophosphate (GGPP), an intermediate of the mevalonate pathway and the steroid metabolism, we plan to overexpress certain key enzymes of this pathway in order to create a favorable amount of educts for steviol biosynthesis, as literature research hinted at this particular bottleneck.
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Furthermore, we aim to clone, biobrick and express the enzymes for a bifunctional cyclase from ''Gibberella fujikuroi'' catalyzing a two step cyclisation from GGPP to ''ent''-kaurene, the ''ent''-kaurene oxidase, as well from ''Gibberella fujikuroi'', catalyzing the reaction from ''ent''-kaurene to ''ent''-kaurenoic acid, and a ''ent''-kaurenoic acid hydroxylase from ''Stevia rebaudiana'', catalyzing the final step producing steviol.
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Finally, we will try to introduce certain uracil-glycosil transferases (UGTs) from ''Stevia rebaudiana'', catalyzing various glycosilation reactions necessary to produce rebaudiosides. As one UGT believed to be necessary for rebaudioside A production is not yet known, we might conduct experiments to find this particular UGT or a viable substitute.
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Basing upon a microorganism producing stevia sweetener, other problems such as purification and product recovery might be improved biotechnologically. Furthermore, the biobricks for stevia production can be used in other organisms and for other applications.
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== Aims and Achievements of our Project==
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In our participation in the 2012 iGEM Competition we were able to successfully test the gen assembly method via gap repair cloning and construct a plasmid for increased Geranylgeranyl Pyrophosphate production and transformed it into yeast. We presented our idears to the general, professional and university public and discussed them both with regard to technical, social and ethical implications. Last but not least we were able to gain financial, technical and administrative support and overcame the obstacles to create an iGEM Team for the first time at our institution. We are planning to establish the iGEM competition as an fixed part of the educational proposals at the Goethe University.
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<br>Regrettably we were not able to conduct many biochemical trials to investigate the function of our gen cassette. We are going to concetrate on those biochemical methods in the next years competition. For that purpose we will try to analyze the metabolome of our modified pathways and do protein assays. Additionally we want to create the final steps to Steviol in yeast and also give some attention in the production of different Diterpene compounts.
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{| width="100%" align="center"
!align="center"|[[Image:Frankfurt_logo.png|50px|right]]
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!align="center"|[[Team:Frankfurt|Home]]
!align="center"|[[Team:Frankfurt|Home]]
!align="center"|[[Team:Frankfurt/Team|Team]]
!align="center"|[[Team:Frankfurt/Team|Team]]
!align="center"|[[Team:Frankfurt/Project|Project]]
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!align="center"|[[Team:Frankfurt/Organisms|Organisms]]
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!align="center"|[[Team:Frankfurt/New Yeast RFC|New Yeast RFC]]
!align="center"|[[Team:Frankfurt/Notebook|Notebook]]
!align="center"|[[Team:Frankfurt/Notebook|Notebook]]
!align="center"|[[Team:Frankfurt/Parts|Registered Parts]]
!align="center"|[[Team:Frankfurt/Parts|Registered Parts]]
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!align="center"|[http://igem.org/Team.cgi?year=2012&team_name=Frankfurt Official Team Profile]
!align="center"|[http://igem.org/Team.cgi?year=2012&team_name=Frankfurt Official Team Profile]
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Welcome to our page and greetings from the Goethe University Frankfurt am Main. In the near future we will add some basic information about our project, the people involved and the place we study at.
 
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= Current Project Description =
 
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Many widespread diseases such as obesity, type 2 diabetes, caries et cetera, especially common in western countries, are directly or indirectly linked to high sugar consumption. In order to reduce calorie intake and minimize health impact, many artificial sweeteners have been developed over the past decades, though virtually all with specific downsides.
 
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A recent example of a family of prospective sweeteners of plant origin are Rebaudiosides, diterpene glycosides from paraguyan herb ''Stevia rebaudiana'', which has been used regionally for probably centuries. Its extremely sweet tasting leaves and stems can be used dried, but are more recently commercially extracted for their Rebaudioside contents.
 
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The Rebaudiosides are a family of differently glycosylated Steviol diterpenes, of which Rebaudioside A has the best properties in taste and sweetness, though other members of this family have varying taste deficiencies such as bitterness.
 
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Therefore, we aim to develop biobricked pathway expressing all necessary genes for Rebaudioside A production in common baker's yeast ''Saccharomyces cerevisae'', a well known, safe organism used in food production for millenia.
 
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As a precursor for the diterpene Steviol is geranylgeranyl pyrophosphate (GGPP), an intermediate of the mevalonate pathway and the steroid metabolism, we plan to overexpress certain key enzymes of this pathway in order to create a favorable amount of educts for Steviol biosynthesis, as literature research hinted at this particular bottleneck.
 
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Furthermore, we aim to clone, biobrick and express the enzymes for a bifunctional cyclase from ''Gibberella fujikuroi'' catalyzing a two step cyclisation from GGPP to ''ent''-Kaurene, the ''ent''-Kaurene oxidase, as well from ''Gibberella fujikuroi'', catalyzing the reaction from ''ent''-Kaurene to ''ent''-Kaurenoic acid, and a ''ent''-Kaurenoic acid hydroxylase from ''Stevia rebaudiana'', catalyzing the final step producing Steviol.
 
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Finally, we will try introduce certain uracil-glycosil transferases (UGTs) from ''Stevia rebaudiana'', catalyzing various glycosilation reactions necessary to produce Rebaudiosides. As one UGT believed to be necessary for Rebaudioside A production is not yet known, we might conduct experiments to find this particular UGT or a viable substitute.
 
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Basing upon a microorganism producing stevia sweetener, other problems such as purification and product recovery might be improved biotechnologically, and stevia sweetener producing biobricks might prove useful in other organisms and use scenarios.
 

Latest revision as of 22:42, 26 September 2012

Team: iGEM Frankfurt - 2012.igem.org


Welcome to our page and greetings from the Goethe University Frankfurt am Main. We are pleased about your visit of our website. You will find more details about our project using the menu above. We appreciate your critic and comments.

Steviomyces - it's gonna be sweet

Project Description

iGEM at the Night of Science - it's gonna be sweet. You can see the stevia plant, a self-made stevia cake and german stevia götterspeise. There is also some commercial stevia chocolate available

Therefore, we aim to develop biobricked pathway expressing all necessary genes for rebaudioside A production in common baker's yeast Saccharomyces cerevisae, a well known, safe organism used in food production for millenia. As a precursor for the diterpene steviol is geranylgeranyl pyrophosphate (GGPP), an intermediate of the mevalonate pathway and the steroid metabolism, we plan to overexpress certain key enzymes of this pathway in order to create a favorable amount of educts for steviol biosynthesis, as literature research hinted at this particular bottleneck. Furthermore, we aim to clone, biobrick and express the enzymes for a bifunctional cyclase from Gibberella fujikuroi catalyzing a two step cyclisation from GGPP to ent-kaurene, the ent-kaurene oxidase, as well from Gibberella fujikuroi, catalyzing the reaction from ent-kaurene to ent-kaurenoic acid, and a ent-kaurenoic acid hydroxylase from Stevia rebaudiana, catalyzing the final step producing steviol. Finally, we will try to introduce certain uracil-glycosil transferases (UGTs) from Stevia rebaudiana, catalyzing various glycosilation reactions necessary to produce rebaudiosides. As one UGT believed to be necessary for rebaudioside A production is not yet known, we might conduct experiments to find this particular UGT or a viable substitute.

Basing upon a microorganism producing stevia sweetener, other problems such as purification and product recovery might be improved biotechnologically. Furthermore, the biobricks for stevia production can be used in other organisms and for other applications.

Aims and Achievements of our Project

In our participation in the 2012 iGEM Competition we were able to successfully test the gen assembly method via gap repair cloning and construct a plasmid for increased Geranylgeranyl Pyrophosphate production and transformed it into yeast. We presented our idears to the general, professional and university public and discussed them both with regard to technical, social and ethical implications. Last but not least we were able to gain financial, technical and administrative support and overcame the obstacles to create an iGEM Team for the first time at our institution. We are planning to establish the iGEM competition as an fixed part of the educational proposals at the Goethe University.


Regrettably we were not able to conduct many biochemical trials to investigate the function of our gen cassette. We are going to concetrate on those biochemical methods in the next years competition. For that purpose we will try to analyze the metabolome of our modified pathways and do protein assays. Additionally we want to create the final steps to Steviol in yeast and also give some attention in the production of different Diterpene compounts.


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