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Team:Yale/Project Validate
From 2013.igem.org
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| + | <div id="header">{{Template:Team:Yale2013/Templates/Header}}</div> | ||
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| + | {| class = "bar" style="color:#3399CC;background-color:#737CA1;" cellpadding="2" cellspacing="1" border="1" bordercolor="#fff" width="75%" align="center" | ||
| + | !align="center"|[[Team:Yale/Project_Overview|Project Overview]] | ||
| + | !align="center"|[[Team:Yale/Project_Validate|Validate PLA synthesis]] | ||
| + | !align="center"|[[Team:Yale/Project_Bioassay|Develop bioassay]] | ||
| + | !align="center"|[[Team:Yale/Project_MAGE|Apply MAGE]] | ||
| + | !align="center"|[[Team:Yale/Project_Export|Introduce export system]] | ||
| + | !align="center"|[[Team:Yale/Project_Bioplastic|Make a bioplastic]] | ||
| + | |} | ||
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== Aims for the Project == | == Aims for the Project == | ||
#'''Engineer strains of ''E. coli'' to validate PLA synthesis'''<br> | #'''Engineer strains of ''E. coli'' to validate PLA synthesis'''<br> | ||
Revision as of 01:08, 22 August 2013
| Project Overview | Validate PLA synthesis | Develop bioassay | Apply MAGE | Introduce export system | Make a bioplastic |
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Aims for the Project
- Engineer strains of E. coli to validate PLA synthesis
- Develop bioassay to screen PLA production
- Apply MAGE to optimize PLA production, guided by FBA
- Introduce type 1 secretion system to export and extract PLA
- Make a bioplastic
Engineer strains of E. coli to validate PLA synthesis
| This was our plan in order to validate PLA synthesis. In order to save money we ordered each of the two heterologous genes in four pieces from IDT giving us 8 GBlocks. |
