Team:Paris Liliane Bettencourt/Notebook/2011/09/15/

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Microscopy experiments of today.
Microscopy experiments of today.
-
As we begin to master totally the Nikon microscope we chose to run three settings for the 3610 gfp-/3610 gfp+ experiments. The aim is to see which way is the best to plate them on our slides and more important at which growth state. We start for the same overnight culture and then create three microscopic slides from our two 3610 strains:
+
As we begin to master totally the Nikon microscope we chose to run three settings for the 3610 gfp-/3610 gfp+ experiments. The aim is to see which is the best way to plate the cells on our slides and more importantly at which growth state. We started from the same overnight culture and then created three microscopic slides from our two 3610 strains (gfp+ and gfp-):
#One directly from the overnight culture in stationnary phase.
#One directly from the overnight culture in stationnary phase.
-
#One diluting until the OD reached 0.1. We then wait for the OD to grow to 0.8 (roughly 2 hours) and we concentrate it as usual (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).
+
#One with dilution until the OD reached 0.1. We then waited for the OD to grow to 0.8 (roughly 2 hours) and then concentrated the cells (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).
-
#One by diluting 1/500 the overnight culture. We then wait for the OD to grow to 0.8 (roughly 4 hours) and we concentrate it as usual (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).
+
#One by diluting the overnight culture in the ratio  1/500. We then waited for the OD to grow to 0.8 (roughly 4 hours) and then concentrated the cells (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).
-
===First conclusions on our methods===
+
===First conclusions of our methods===
-
Despite what we thought, the autofocus programme on the Nikon is not perfect. We need to adjust it a little bit to our needs. It gave us slightly blurry image for the second serie of slide (dilution to an OD of 0.1) and catastrophic results for the stationnary phase slide. Fortunately, the stationnary phase means that bacteria do not grow and we were able to interpret the results even missing over an hour of images.
+
The autofocus programme on the Nikon was not perfect so it was adjusted to our needs. It gave us slightly blurry image for the second serie of slide (dilution to an OD of 0.1) and bad results for the stationnary phase slide. Fortunately, the stationnary phase means that bacteria do not grow so we were able to interpret the results even after missing more than an hour of images.
-
Our slide for the 1/500 dilution was very faulty. We could not see anything clearly and we will have to retry it tomorrow. Letting the drop dry or not is the primary issue here. We will try both ways tomorrow to see which seems better.
+
The slide for the 1/500 dilution was very faulty. We could not see anything clearly and we will have to retry it tomorrow. To let the drop of cells dry or not, is the primary issue here. Both ways will be tried tomorrow to see which one is suitable.
===Stationnary phase===
===Stationnary phase===
Line 25: Line 25:
===Dilution to an OD of 0.1===
===Dilution to an OD of 0.1===
-
The slide was one of the best we've done so far. We were able to see clearly zones with a monolayer of roughly 50/50 GFP and non-GFP cells. And we finally found some evidence of deiffusion in one of the followed sites!
+
The slide was one of the best we've done so far. We were able to see clearly zones with a monolayer of roughly 50/50 GFP/non-GFP cells. We finally found some evidence of GFP diffusion in one of the followed regions of the slide! The cells gaining fluorescence are circled in red. Note that, gfp+ cells lost their fluorescence with time whilst gfp- (the ones circled in red) gained fluorescence. We also run positive controls but took pictures of this slide only at the end of the experiment.
 +
{| border="1" class="wikitable" style="text-align: center;"
 +
|+3610 gfp-/3610 gfp+ in exponantial phase at 37°C
 +
|-
 +
|[[File:0914_3610_classic_w1TRANS_s5_t1.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=0min position 5 (trans image)]]
 +
|[[File:0914_3610_classic_w2GFP_s5_t1.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=0min position 5 (gfp image)]]
 +
|-
 +
|[[File:0914_3610_classic_w1TRANS_s5_t9.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=45min position 5 (trans image)]]
 +
|[[File:0914_3610_classic_w2GFP_s5_t9.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=45min position 5 (gfp image)]]
 +
|-
 +
|[[File:0914_3610_classic_w1TRANS_s5_t12.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=60min position 5 (trans image)]]
 +
|[[File:0914_3610_classic_w2GFP_s5_t12.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ at 37°C t=60min position 5 (gfp image)]]
 +
|-
 +
|[[File:0914_3610_classic_w1TRANS_s5_t23.png|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=180min position 5 (trans image)]]
 +
|[[File:0914_3610_classic_w2GFP_s5_t23.jpg|450px|thumb|center|3610 gfp- and 3610 gfp+ strains at 37°C t=180min position 5 (gfp image)]]
 +
|}
== Kevin ==
== Kevin ==
Line 34: Line 49:
== cyrille ==
== cyrille ==
-
Treatment of the ligations done yesterday. PVeg T7a TT + pT7 gfp TT worked. 16 col putted in culture.
+
Treatment of the ligations done yesterday. PVeg T7a TT + pT7 gfp TT worked. 16 colonies put in culture.
-
For the other ligations, the results of the positive control indicates that the transformation failed. 1 clone was found for p/eg tRNA rfp, and 3 pVeg tRNA tt rfp they were insulated. PCR colonie failed. The cultures will be minkprepped tomorow.
+
For the other ligations, the results of the positive control indicates that the transformation failed. 1 clone was found for pVeg tRNA rfp, and 3 pVeg tRNA tt rfp they were insulated. PCR colonie failed. The cultures will be miniprepped tomorow.
-
The ligation that are supposed to have failed were done again. As we were short on pHM3, the S99 was not done again.
+
The ligation that are supposed to have failed were done again. As we were short of pHM3, the S99 was not done again.
Miniprep of pHM3 overday.
Miniprep of pHM3 overday.
-
Suspicion on pHM3 on the lost of replication origin for subtilis due to the analysis of the sequencing. 7 miniprep of the original pHM3 were launched.
+
Suspicion of pHM3 on the lost of replication origin for subtilis due to the analysis of the sequencing. 7 minipreps of the original pHM3 were launched.
-
Double digestion in HincIII and PstI was help to see if the region was indeed lost. HindIII cut several times in the replication origin region.
+
Double digestion in HincIII and PstI will help to see if the region was indeed lost. HindIII cut several times in the replication origin region.
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   </div>
   </div>
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<div id="scroll_left"><a href="https://2011.igem.org/Team:Paris_Bettencourt/ComS_diffusion"><img src="https://static.igem.org/mediawiki/2011/0/0a/Arrow-left-big.png" style="width:100%;"></a><a href="https://2011.igem.org/Team:Paris_Bettencourt/ComS_diffusion">To the design for ComS diffusion!</a></div>
 
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<div id="scroll_right"><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/ComS_diffusion"><img src="https://static.igem.org/mediawiki/2011/e/e0/Arrow-right-big.png" style="width:100%;"></a><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/ComS_diffusion">To the experiments for ComS diffusion!</a></div>
 
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</html>

Latest revision as of 14:58, 20 September 2011

Team IGEM Paris 2011

Contents

Baptiste, Hovannes & Ouriel

Microscopy experiments of today.

As we begin to master totally the Nikon microscope we chose to run three settings for the 3610 gfp-/3610 gfp+ experiments. The aim is to see which is the best way to plate the cells on our slides and more importantly at which growth state. We started from the same overnight culture and then created three microscopic slides from our two 3610 strains (gfp+ and gfp-):

  1. One directly from the overnight culture in stationnary phase.
  2. One with dilution until the OD reached 0.1. We then waited for the OD to grow to 0.8 (roughly 2 hours) and then concentrated the cells (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).
  3. One by diluting the overnight culture in the ratio 1/500. We then waited for the OD to grow to 0.8 (roughly 4 hours) and then concentrated the cells (4000 rpm during 10 min and then put 200 microliters of LB on the pellet).

First conclusions of our methods

The autofocus programme on the Nikon was not perfect so it was adjusted to our needs. It gave us slightly blurry image for the second serie of slide (dilution to an OD of 0.1) and bad results for the stationnary phase slide. Fortunately, the stationnary phase means that bacteria do not grow so we were able to interpret the results even after missing more than an hour of images. The slide for the 1/500 dilution was very faulty. We could not see anything clearly and we will have to retry it tomorrow. To let the drop of cells dry or not, is the primary issue here. Both ways will be tried tomorrow to see which one is suitable.

Stationnary phase

As expected, no growth and no diffusion was observed.

3610 gfp-/3610 gfp+ in stationnary phase at 37°C
3610 gfp- and 3610 gfp+ strains stationary phase at 37°C t=0min position 1 (trans image)
3610 gfp- and 3610 gfp+ strains stationary phase at 37°C t=0min position 1 (gfp image)
3610 gfp- and 3610 gfp+ strains stationary phase at 37°C t=120min position 1 (trans image)
3610 gfp- and 3610 gfp+ strains stationary phase at 37°C t=120min position 1 (gfp image)

Dilution to an OD of 0.1

The slide was one of the best we've done so far. We were able to see clearly zones with a monolayer of roughly 50/50 GFP/non-GFP cells. We finally found some evidence of GFP diffusion in one of the followed regions of the slide! The cells gaining fluorescence are circled in red. Note that, gfp+ cells lost their fluorescence with time whilst gfp- (the ones circled in red) gained fluorescence. We also run positive controls but took pictures of this slide only at the end of the experiment.

3610 gfp-/3610 gfp+ in exponantial phase at 37°C
3610 gfp- and 3610 gfp+ strains at 37°C t=0min position 5 (trans image)
3610 gfp- and 3610 gfp+ strains at 37°C t=0min position 5 (gfp image)
3610 gfp- and 3610 gfp+ strains at 37°C t=45min position 5 (trans image)
3610 gfp- and 3610 gfp+ strains at 37°C t=45min position 5 (gfp image)
3610 gfp- and 3610 gfp+ strains at 37°C t=60min position 5 (trans image)
3610 gfp- and 3610 gfp+ at 37°C t=60min position 5 (gfp image)
3610 gfp- and 3610 gfp+ strains at 37°C t=180min position 5 (trans image)
3610 gfp- and 3610 gfp+ strains at 37°C t=180min position 5 (gfp image)

Kevin

Following step for characterisation of tetO array

Double transformation works ! Tomorrow microscopy.

cyrille

Treatment of the ligations done yesterday. PVeg T7a TT + pT7 gfp TT worked. 16 colonies put in culture.

For the other ligations, the results of the positive control indicates that the transformation failed. 1 clone was found for pVeg tRNA rfp, and 3 pVeg tRNA tt rfp they were insulated. PCR colonie failed. The cultures will be miniprepped tomorow.

The ligation that are supposed to have failed were done again. As we were short of pHM3, the S99 was not done again.

Miniprep of pHM3 overday.

Suspicion of pHM3 on the lost of replication origin for subtilis due to the analysis of the sequencing. 7 minipreps of the original pHM3 were launched. Double digestion in HincIII and PstI will help to see if the region was indeed lost. HindIII cut several times in the replication origin region.

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