Difference between revisions of "Part:BBa K606035:Experience"
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As a positive control we have saturated a strain with a lot of IPTG. After 1h50 of growth, we compare the fluorescence of the gradient of IPTG with the saturated cells. We see a clear increase of the fluorescence wereas the saturated strains is quite stable. | As a positive control we have saturated a strain with a lot of IPTG. After 1h50 of growth, we compare the fluorescence of the gradient of IPTG with the saturated cells. We see a clear increase of the fluorescence wereas the saturated strains is quite stable. | ||
| − | [[Image:pT7GFPSaturated.png|center|thumb| | + | [[Image:pT7GFPSaturated.png|center|thumb|600px|Fig2: Comparison of the Fluo/OD ratio for transcription saturated and non saturated cells]] |
The offset of the curves is here renormalize at the inflexion point of the growth, when the cells start have passed the IPTG stress and are growing again. | The offset of the curves is here renormalize at the inflexion point of the growth, when the cells start have passed the IPTG stress and are growing again. | ||
Revision as of 10:22, 21 September 2011
We hae characterized this part transforming it into a BL21 strain. This strain carries insite the chromosome a T7 polymerase under the control of an IPTG inducible promoter. This strain is mostly used for protein expression for protein purification application.
Growth measurements
The measurements had been carried on in a TECAN i-control machine, at 37°C under transcient shaking, for 4h, for several colonies and several range of IPTG concentration. The OD 600nm and the fluorescence of the GFP (exc: 470nm / meas:515 nm) was measured every 5 min, and the ratio of the two was calculated.
The offset values for these curves was adjusted for better visualisation. The values given are in arbitrary units.
First we see an inflexion in the curve, that is due to the stong influence of the IPTG on the metabolism of the cells. Then, this loss it taken up and the bacteria start growing again. We see a clear increase of the fluorescence with the IPTG concentration, that is to say with the quantity of T7 polymerase in the cell
Comparison of the growth with the traduction saturated cells
As a positive control we have saturated a strain with a lot of IPTG. After 1h50 of growth, we compare the fluorescence of the gradient of IPTG with the saturated cells. We see a clear increase of the fluorescence wereas the saturated strains is quite stable.
The offset of the curves is here renormalize at the inflexion point of the growth, when the cells start have passed the IPTG stress and are growing again.
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