ULB/9 July 2009

From 2009.igem.org

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== July 8-9, 2009 ==
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Choice of bacteria strains :
Choice of bacteria strains :
* ''Caulobacter crescentus'' (strain CB15N)
* ''Caulobacter crescentus'' (strain CB15N)
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* ''E. Coli'' (strain K12 or DG1
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* ''E. Coli'' (strain K12 or DG1)
=== Constructions ===
=== Constructions ===
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==== Construction 1 ====
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*'''Construction 1'''
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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.
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As ''Caulobacter crescentus'' genes of interest have'' E. coli'' homologs, we’ll first transfer '''HfsG''' et '''HfsH''' genes through the assembly standard 21 [figure 1] and we hope E. Coli will be able to produce the adhesive material.
Forward and reverse primers are designed.
Forward and reverse primers are designed.

Revision as of 09:38, 1 October 2009

iGEM Team:ULB-Brussels Wiki



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 standard 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