Team:DTU-Denmark/Notebook/8 August 2013
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==Main purpose== | ==Main purpose== | ||
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- | Run experiment 2: "Measuring the production of N<sub>2</sub>O from Nitrite NO<sub>2</sub><sup>-<sup> | + | Run experiment 2: "Measuring the production of N<sub>2</sub>O from Nitrite NO<sub>2</sub><sup>-</sup> anaerobically" |
- | + | ''Control measurement'' | |
- | + | ||
==Who was in the lab== | ==Who was in the lab== |
Revision as of 11:56, 11 August 2013
8 August 2013
Contents |
lab 208
Main purpose
Who was in the lab
Kristian, Julia, Henrike
Procedure
PCR for AMO with USER endings
primers: 17a, 17b
template: gel purified AMO extraction fragment
Program: Standard with 54C annealing temperature and 3:00 extension time
Reaction Mix
component(per reaction) | without additives | using 5% DMSO | using 1M Betaine |
---|---|---|---|
dNTPs | 1uL | 1uL | 1uL |
HF buffer | 10uL | 10uL | 10uL |
X7 polymerase | 0.5uL | 0.5uL | 0.5uL |
MilliQ water | 31.5uL | 29uL | 21.5uL |
template | 1uL | 1uL | 1uL |
FW primer | 3uL | 3uL | 3uL |
RV primer | 3uL | 3uL | 3uL |
DMSO | - | 2.5uL | - |
Betaine | - | - | 10uL |
PCR for extraction of Nir1
primers: 41a, 41b
template: colony from plate. One colony was dissolved in 100 uL of MilliQ and 1 uL of this solution was taken as template
program: Touchdown PCR analog to program used on 01-08-2013 to amplify Nir.
Reaction Mix
component(per reaction) | without additives | using 5% DMSO | using 1M Betaine |
---|---|---|---|
dNTPs | 1uL | 1uL | 1uL |
HF buffer | 10uL | 10uL | 10uL |
X7 polymerase | 0.5uL | 0.5uL | 0.5uL |
MilliQ water | 31.5uL | 29uL | 21.5uL |
template | 1uL | 1uL | 1uL |
FW primer | 3uL | 3uL | 3uL |
RV primer | 3uL | 3uL | 3uL |
DMSO | - | 2.5uL | - |
Betaine | - | - | 10uL |
Comment
Both PCRs mentioned above were successful when DMSO was added.
Results
Gel on yesterdays PCR
- 1kb ladder
- Yesterdays sample 1
- Yesterdays sample 2
- Yesterdays sample 3
- Yesterdays sample 4
- Neg.
- Neg.
- Nir2
- cycAX Histag
- 1kb ladder
Gel on ON PCR samples
- 1kb ladder
- Nir1
- Nir1 5%DMSO
- Nir1 1M Betaine
- Nir1 3M Betaine
- Nir2 3M Betaine U
- Nir2 1M Betaine U
- Nir2 5%DMSO U
- Nir2 U
- Neg (Nir)
- Ref 0%DMSO
- Ref 2%DMSO
- Ref 5%DMSO
- AMO U
- AMO 2%DMSO U
- Neg (AMO)
- NirG 5%DMSO
- NirG
- 1kb ladder
Gel on todays PCR samples
- 1kb ladder
- Nir Q5 poly
- Nir 2%DMSO Q5 poly
- Nir 3M Betaine Q5 poly
- Nir 5%DMSO Q5 poly
- Nir1 Q5 poly
- Nir1 2%DMSO Q5 poly
- Nir1 5%DMSO Q5 poly
- Nir1 3M Betaine Q5 poly
- AMO USER primers
- AMO +DMSO USER primers
- AMO +Betaine USER primers
- Nir1 DMSO
- Nir1 Betaine
- 1kb ladder
Conclusion
lab 115
Main purpose
Run experiment 2: "Measuring the production of N2O from Nitrite NO2- anaerobically" Control measurement
Who was in the lab
Ariadni, Helen
Procedure
Following the protocol "Experiment 2: Measuring production of N2O from Nitrite NO2- anaerobically"
Changing the steps :
6. 2 ml of the overnight culture in 100 ml of medium.
7. Grow the cells for about 4 hours where the OD was measured ...... in 500 nm wavelength setup instead of 600 nm.
8. We didn't cool down the centrifuge because the experiment had to be done in 37 degrees.
11. The volume was 140 ml instead of 100 ml.
12. The OD was measured 0.1195 instead of 0.3.
15. 10 minutes of N2 saturation instead of 5 minutes.
19. Add 0.5 ml of nitrite solution and continue by adding 1 ml after 10 minutes then we took 1.8 ml of sample, we added then 0.5 ml and afterwards when there was any change in the curve we spiked with 0.9 ml of nitrite. We took 2.3 ml for sample in the end and another 2 ml for OD measurement where OD=0.1105.
The temperature in the end was 40.5 degrees C and not 37.
Results
Colorimetric results
Ammonium
Measuring range 2-75 mg/L NH4-N
start point- signal <2 mg/L
middle point- signal <2 mg/L
end point- signal <2 mg/L but 1.8 mg/L
Nitrate
Measuring range 1-25 mg/L NO3-N
start point- signal <1 mg/L
middle point- signal <1 mg/L
end point- signal 0.4 mg/L
Nitrite
Measuring range 0.02-1 mg/L NO2-N
start point- signal 0.07 mg/L
middle point- signal 0.57 mg/L after X10 dilution
end point- signal 0.47 mg/L after X10 dilution
Conclusion
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