Team:UGent

From 2013.igem.org

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This is a template page. READ THESE INSTRUCTIONS.
 
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
 
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You <strong>MUST</strong> have all of the pages listed in the menu below with the names specified. PLEASE keep all of your pages within your teams namespace. 
 
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{|align="justify"
 
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
 
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|[[Image:UGent_logo.png|200px|right|frame]]
 
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''Tell us more about your project.  Give us background.  Use this as the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
 
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|[[Image:UGent_team.png|right|frame|Your team picture]]
 
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|align="center"|[[Team:UGent | Team UGent]]
 
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<!--- The Mission, Experiments --->
 
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
!align="center"|[[Team:UGent|Home]]
!align="center"|[[Team:UGent|Home]]
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!align="center"|[[Team:UGent/Attributions|Attributions]]
!align="center"|[[Team:UGent/Attributions|Attributions]]
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Image:UGent_2013_logo.jpg
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The main goal of the industrial biotechnology is to increase the yield of the synthesis of biochemical products using microorganisms as production hosts. In general, this includes engineering large synthetic pathways and improving their expression. Overexpression of endogenous and/or heterologous genes has hitherto mainly been achieved by using high or medium copy plasmids. However, studies have demonstrated that cells containing plasmids for the overexpression of the desired product lose their productivity fairly quickly as a result of genetic instability. To avoid these problems a new method was developed for the overexpression of a gene of interest in the bacterial chromosome: Chemically Inducible Chromosomal evolution or CIChE. In this technique the chromosome is evolved to contain a higher number of gene copies by adding a chemical inducer. The original model for CIChE, however, results in bacterial strains containing a large number of antibiotic resistance genes. To make this valuable technique more widely applicable in the industry, we developed a new model for chromosomal evolution, based on a toxin-antitoxin system instead of antibiotic resistance.
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<!--- The Mission, Experiments --->

Revision as of 10:06, 21 July 2013

Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions
You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.


The main goal of the industrial biotechnology is to increase the yield of the synthesis of biochemical products using microorganisms as production hosts. In general, this includes engineering large synthetic pathways and improving their expression. Overexpression of endogenous and/or heterologous genes has hitherto mainly been achieved by using high or medium copy plasmids. However, studies have demonstrated that cells containing plasmids for the overexpression of the desired product lose their productivity fairly quickly as a result of genetic instability. To avoid these problems a new method was developed for the overexpression of a gene of interest in the bacterial chromosome: Chemically Inducible Chromosomal evolution or CIChE. In this technique the chromosome is evolved to contain a higher number of gene copies by adding a chemical inducer. The original model for CIChE, however, results in bacterial strains containing a large number of antibiotic resistance genes. To make this valuable technique more widely applicable in the industry, we developed a new model for chromosomal evolution, based on a toxin-antitoxin system instead of antibiotic resistance.