ULB/9 July 2009

From 2009.igem.org

(Difference between revisions)
(Begin of the page from Amandine's doc)
(Content update)
Line 335: Line 335:
</style>  
</style>  
</html>
</html>
 +
 +
== July 8-9, 2009 ==
Choice of bacteria strains :
Choice of bacteria strains :
Line 340: Line 342:
* ''Caulobacter crescentus'' (strain CB15N)
* ''Caulobacter crescentus'' (strain CB15N)
* ''E. Coli'' (strain K12 or DG1
* ''E. Coli'' (strain K12 or DG1
 +
 +
=== Constructions ===
 +
 +
==== Construction 1 ====
 +
 +
As Caulobacter crescentus genes of interest have E. coli homologs, we’ll first transfer HfsG et HfsH genes through the assembly standart 21 [figure 1] and we hope E. Coli will be able to produce the adhesive material.
 +
 +
Forward and reverse primers are designed.
 +
 +
hfsG and hfsH share a single nucleotide  HfsG : ---TG'''A'''  ;  HfsH : '''A'''TG---
 +
<br/>=> a blunt-end ligation(?) is possible
 +
 +
Terminator chosen : [http://partsregistry.org/wiki/index.php?title=Part:BBa_B0015 BBa_B0015]

Revision as of 08:37, 19 August 2009

iGEM Team:ULB-Brussels Wiki


July 8-9, 2009

Choice of bacteria strains :

  • Caulobacter crescentus (strain CB15N)
  • E. Coli (strain K12 or DG1

Constructions

Construction 1

As Caulobacter crescentus genes of interest have E. coli homologs, we’ll first transfer HfsG et HfsH genes through the assembly standart 21 [figure 1] and we hope E. Coli will be able to produce the adhesive material.

Forward and reverse primers are designed.

hfsG and hfsH share a single nucleotide HfsG : ---TGA  ; HfsH : ATG---
=> a blunt-end ligation(?) is possible

Terminator chosen : BBa_B0015