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EPF-Lausanne/9 September 2009
From 2009.igem.org
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==Wet Lab== | ==Wet Lab== | ||
| + | ===Culture=== | ||
| + | Made one new bottle of M9/min+AA+thiamine in 500 ml. | ||
| + | |||
| + | All clones (M9 & LB) have grown. M9 cultures have been redone in 25 ml M9 + antibiotics. 750 ul of overnight re-inoculated. Put in incubator at 37°C for 2 hours. We got different OD after this time, for RBS, LacI-RFP #1,2, RO2 #4,5,10, RO1 # 1,2,3. We normalized the OD to 0.06 for all of them by adding the appropriate amount of fresh medium to each erlen' (calculation was done linear). | ||
===Characterization=== | ===Characterization=== | ||
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| + | 50 ul of culture in each well. | ||
| + | |||
| + | Trp : 0.5 -> 1ul, 1 -> 2ul, 1.5 -> 3 ul. | ||
| + | |||
| + | ATC : 0.5 -> 0.5 ul (so about 50 ng/ml), 1 -> 1ul. | ||
| + | |||
| + | IPTG : 1x -> 5.5 ul -> 1 mM final. | ||
| + | |||
| + | Note : from the start of the induction to putting the plate in the machine, it took about 20 minutes (so some wells may already have been induced). | ||
'''Results of the characterization''' | '''Results of the characterization''' | ||
Revision as of 11:50, 2 October 2009
Wet Lab
Culture
Made one new bottle of M9/min+AA+thiamine in 500 ml.
All clones (M9 & LB) have grown. M9 cultures have been redone in 25 ml M9 + antibiotics. 750 ul of overnight re-inoculated. Put in incubator at 37°C for 2 hours. We got different OD after this time, for RBS, LacI-RFP #1,2, RO2 #4,5,10, RO1 # 1,2,3. We normalized the OD to 0.06 for all of them by adding the appropriate amount of fresh medium to each erlen' (calculation was done linear).
Characterization
| With Atc | Without Atc | |||
|---|---|---|---|---|
| With Trp |
| 1/2 Trp 1 Trp 3/2 Trp | ||
| Without Trp | 1/2 Atc 1 Atc 3/2 Atc | Without Atc nor Trp |
50 ul of culture in each well.
Trp : 0.5 -> 1ul, 1 -> 2ul, 1.5 -> 3 ul.
ATC : 0.5 -> 0.5 ul (so about 50 ng/ml), 1 -> 1ul.
IPTG : 1x -> 5.5 ul -> 1 mM final.
Note : from the start of the induction to putting the plate in the machine, it took about 20 minutes (so some wells may already have been induced).
Results of the characterization
For the RBS :
RBS was our negative control. We can see that there is no RFP fluorescence (because of course RBS has no RFP gene).
For LacI-RFP 1 + IPTG :
LacI-RFP 2 + IPTG show the same tendancy.
For Read Out 1
RO1#1 + 0.5 TRP :
RO1#2 + 0.5 TRP shows the same tendancy :
RO1#1 + 1 TRP :
Again, RO1#2 clone has the same behaviour :
RO1#1 without TRP:
Clone #2 has the same behaviour :
RO1#3 clones doesn't follow these tendancy. It actually seems that this clone isn't working at all. It is possible a spontaneous mutation occured in some place... On all different conditions, RO1#3 clones show a flat curve, like RBS. It doesn't express RFP which means either our construct wasn't inserted, either there has been a mutation in it. For example + 1 TRP :
For Read Out 2
RO2#1 without TRP :
RO2#3 has exactly the same curve shape :
RO2#1 + 0.5 TRP :
RO2#3 has a more "normal" shape :
RO2#1 + 1 TRP :
RO2#3 is the same :
RO2#1 + 1.5 TRP :
RO2#3 in the same conditions :
RO2#1 + 0.5 TRP + 0.5 ATC :
RO2#3 in the same conditions :
RO2#1 + 0.5 TRP + 1 ATC :
RO2#3 in the same conditions :
RO2#1 + 1 TRP + 0.5 ATC :
RO2#3 in the same conditions :
RO2#1 + 1 TRP + 1 ATC :
RO2#3 in the same conditions :
RO2#1 + 0.5 ATC :
RO2#3 in the same conditions :
RO2#1 + 1 ATC :
RO2#3 in the same conditions :
RO2#1 + 1.5 ATC :
RO2#3 in the same conditions :
Clone RO2#2 is not working, it has always a flat curve like this (for ex +0.5 ATC):
People in the lab
Mélanie, Caroline, Basile, Nicolas
