"
Team:Edinburgh/Project
From 2013.igem.org
(Difference between revisions)
Hristianita (Talk | contribs) |
|||
| (7 intermediate revisions not shown) | |||
| Line 3: | Line 3: | ||
<div class='content'> | <div class='content'> | ||
| - | |||
| - | |||
<h3> Results summary </h3> | <h3> Results summary </h3> | ||
| - | |||
* '''We tested [[Team:Edinburgh/Project/Results/Chassis |the growth]] of our experimental strain, <i>Bacillus subtilis 168</i>, under various conditions relevant to the work we are going to perform.''' | * '''We tested [[Team:Edinburgh/Project/Results/Chassis |the growth]] of our experimental strain, <i>Bacillus subtilis 168</i>, under various conditions relevant to the work we are going to perform.''' | ||
| Line 21: | Line 18: | ||
| - | * '''We cloned a Neisserial Ferric binding protein A ([[Team:Edinburgh/Project/Results/ | + | * '''We cloned a Neisserial Ferric binding protein A ([[Team:Edinburgh/Project/Results/Metal_binding_Results|FbpA]]) as a BioBrick.''' |
| - | * '''We generated a [[ | + | * '''We generated a [[Team:Edinburgh/Project/Results/Bioethanol_Results| fusion]] of Pyruvate decarboxylase (Pdc) and Alcohol dehydrogense B (AdhB). We characterised it thoroughly and demonstrated that such co-localisation can increase ethanol production at least twofold.''' |
Latest revision as of 23:57, 4 October 2013
  
| 
| class="nomargin" 
| |||
  
|   
|   
|   
|   
| |
| Home | Team | Lab work | Modeling | Human practices | GenBrick |
Results summary
- We tested the growth of our experimental strain, Bacillus subtilis 168, under various conditions relevant to the work we are going to perform.
- We tested the Kanamycin resistance conferred by pTG262 in B.subtilis and E.coli.
- We created an assembly to demonstrate that Fur box is able to repress gene expression upon exposure to high iron concentrations.
- We cloned out and characterised a Fur transcription factor.
- We cloned a Neisserial Ferric binding protein A (FbpA) as a BioBrick.
- We generated a fusion of Pyruvate decarboxylase (Pdc) and Alcohol dehydrogense B (AdhB). We characterised it thoroughly and demonstrated that such co-localisation can increase ethanol production at least twofold.
- We cloned SinR and analysed biofilm formation in WT B.subtilis.
- We had a great summer, and plan to have fun at the Regional Jamboree.
| 
| 
| 
| 
| 
|
| This iGEM team has been funded by the MSD Scottish Life Sciences Fund. The opinions expressed by this iGEM team are those of the team members and do not necessarily represent those of MSD | |||||
