From 2007.igem.org

See the Notebook

Contents 1 In progress : molecular biology part 2 To Do List 3 In Progress 3.1 FstZ strain caracterisation 3.2 Transduction of the deletion of DapA from the strain w121 into MG1655 and MG1655 FtsZ TS84 3.3 Caracterisation of w121 - MG1655 feeding supplementation 3.4 Caracterisation of Acinetobacter strain 4 Accomplishments 4.1 Transformation of 8 Biobricks

In progress : molecular biology part

Red : done Blue : fail Black : in progress... Big construct to be inserted in the chromosome
Construct : inducible CRE

Miscellaneous

DGAT and some other things are missing

To Do List

• Cloning of Lox71-FtsZ and Lox71-FtsA-FtsZ in J61002 with the constitutive promoter and with the pBad

This will allow us to see the effect of the overexpression of FtsZ and FtsA+FtsZ on the growth and phenotype. We expect the overexpression of FtsZ only to be lethal and the one of FtsA+FtsZ to form a viable mini-cell phenotype.

• Cloning of Lox66-DapA of Coli and Subtilis in the same 2 vectors

In Progress

FstZ strain caracterisation

We try to obtain a reliable TS clone, which would not grow at 42°C, but grow at 30°C

Transduction of the deletion of DapA from the strain w121 into MG1655 and MG1655 FtsZ TS84

The goal is, by transduction, to introduce DapA deletion into FtsZ TS strain

• We managed to build a stock of efficient phages (stock of 12.7.7)
• Transduction in progress

Caracterisation of w121 - MG1655 feeding supplementation

This part is just a preliminary work whose aim is to show that two strains can complement each other. A more detailed explanation of these experiments can be found in the team notebook.

• Several conditions were tested but the curves are difficult to interpret. See preliminary results.

Caracterisation of Acinetobacter strain

Goal : in the final construct, we will take the gene DGAT from this strain and put it in E. Coli.
Preliminary work has been done on acinetobacter :

• We confirmed the production of TG in acinetobacter when it is grown on minimal medium + a source of carbon (ask David from precise information). We were able to stain TG with Nile Red fluorescent dye (cf photos):
  • in a whole colony
  • on single cells
• We began cloning of DGAT gene on E. Coli (ask David for precise information)

Accomplishments

• PCR and Cloning of lox71-KmR-Lox66

• Cloning of lox71 and lox66

• Cloning of I0500 (inducible pBad) in [http://partsregistry.org/Part:BBa_J61002 J61002]

This will allow us to compare the strength of the pBad and the strengh of the constitutive promoter. Moreover, we'll be able to clone any gene we like after the promoter.

Transformation of 8 Biobricks

The goal is to extract DNA from the plates and make a stock of plasmid we need.

• BBa_I0500: Inducible pBad/araC in pSB2K3 (KanR)
• BBa_J23100: strong constitutive promoter in BBa_J61002 (AmpR)
• BBa_B0015: double terminator (B0010-B0012) in pSB1AK3 (AmpR)
• BBa_B0030: RBS (well 3G plate 1)
• BBa_E0422: ECFP (RBS+LVA+Term) (well 11G plate 1)
• BBa_E0241: PoPs to GFP converter (well 15c plate 2)
• BBa_E0840: gfp tri-part; strong rbs (well 16E plate 1)
• BBa_J61047: Cre ORF (well 8P plate 4)