Team:Lyon-INSA-ENS/Realisation/Week8
From 2011.igem.org
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- | < | + | <FONT COLOR="red"> <b>Strain construction : Prcn-GFP(LVA)</b> </FONT> <br><br> |
+ | |||
<b>Digestion</b> of the plasmid with Prcn (S+P) = linearization -> error: the part goes out from the plasmid <br> | <b>Digestion</b> of the plasmid with Prcn (S+P) = linearization -> error: the part goes out from the plasmid <br> | ||
-> use of other enzyme tubes, with the same results, same with a simple digestion -> our enzyme tubes are contaminated<br> | -> use of other enzyme tubes, with the same results, same with a simple digestion -> our enzyme tubes are contaminated<br> | ||
digestion of the plasmid with strong RRB-GFP (X+P) -> OK<br> | digestion of the plasmid with strong RRB-GFP (X+P) -> OK<br> | ||
<br> | <br> | ||
+ | |||
+ | </p> | ||
+ | <p style=" line-height : 1.5em"><FONT COLOR="blue"><b>Strain Collection</b></FONT> <br><br> | ||
<b>Storage</b> of MC4100 (Str) = S7, NM522 = S11, NMYO = S13 and NM522/NicoT (Amp) = S14 | <b>Storage</b> of MC4100 (Str) = S7, NM522 = S11, NMYO = S13 and NM522/NicoT (Amp) = S14 | ||
</p> | </p> |
Revision as of 15:52, 13 September 2011
Week 8
From Monday the 1st of August to Friday the 5th of August 2011
Monday
Adherence Tests
24 well plate with LB/2 or M63 medium to test bacterial adherence in response to cobalt :
positive control with an adherent strain PHL818 ( MG1655 malT::Tn10 adr101=OmpR234 ), negative control with a non adherent strain NM522, and our synthesized part Rcn-CsgBAEFG (Amp) with increasing concentrations of cobalt ( in CoCl2 form).
Flocculation test for the same strains with LB/2 or M63G medium.
Strain construction
Miniprep of the transformed colonies with the following plasmids : Prcn / Pcurli-GFP / Pcurli - Operon curli.
-> none of the isolated clones had the Prcn or Pcurli-GFP plasmid, start of liquid culture of new clones.
-> two clones had the Pcurli-curli operon part : storage in the collection
Tuesday
Adherence Tests
In LB/2, the flocculation tests show flocculation for the adherent strain (PHL818), none for the negative control. Our strain shows a small flocculation that increases with the concentration in cobalt.
No flocculation in M63 medium for our strain : LB/2 will be used only for the next tests.
New flocculation tests with a wider range of cobalt concentration in LB or LB/2 and using the Rcn-CsgBAEFG (Cm) synthesized part
Revealing of the 24 well plate from the previous day, using 2 different methods : methyl violet (to visualise the formation of the biofilm at the surface of the well ) or direct OD600 measure.
Strain construction
Miniprep of the clones started the previous day
-> two clones have the Prcn part and one Pcurli-GFP.
Storage of PHL818, PHL1273, Rcn-CsgBAEFG (Cm) = S3 = S17, Rcn-CsgBAEFG (Amp) = S4 = S18
Wednesday
Adherence Tests
Measurement of the OD600 of the LB/2 plate, which gives an adherence percentage for each strain.
Revealing of the M63 medium 24 well plate using the methyl violet ( 1 well) or OD600 method ( 3 wells ).
The flocculation tests from the previous day give better results in LB/2 compared to LB , but they're not significative. We'll use LB/2 for future tests.
The flocculation tests from the previous day give better results in LB/2 compared to LB , but they're not significative. We'll use LB/2 for future tests.
Plasmid Collection
Nanodrop quantification of some plasmids in the collection.
Thursday
Adherence Tests
Start of new 24 well plates, to study:
- the effect of cobalt (in increasing concentration),
- the difference between Amp or Cm strains, -> it works better in Amp
- the effect of the presence of antibiotic, -> it works better with Antibiotic
- the effect of prior treatment of the plate with EDTA, -> it is better when plate is rinse
- the effect of EDTA (in increasing concentration) on the strain. -> no useful
Characterization of OmpR234 with a 24 well plate and a flocculation test.
Test in CFA medium to show the formation of biofilms by colouring them red using the following strains( 10µL each ) :
PHL818 (positive control),NM522 (negative control), and test bacteria containing 18A promoter ( alone without the coding part ),our synthesized parts (Amp or Cm)
-> not very conclusive, a little circle of light around the bacteria.
Strain construction : Prcn-GFP(LVA)
Digestion of the plasmid with Prcn (S+P) = linearization -> error: the part goes out from the plasmid
-> use of other enzyme tubes, with the same results, same with a simple digestion -> our enzyme tubes are contaminated
digestion of the plasmid with strong RRB-GFP (X+P) -> OK
Strain Collection
Storage of MC4100 (Str) = S7, NM522 = S11, NMYO = S13 and NM522/NicoT (Amp) = S14
Friday
Adherence Tests
Repeat of the flocculation test for the characterization of OmpR234.
Repeat of the CFA medium test.
Revealing of the four 24 well plates from thursday.