Team:DTU-Denmark/Notebook/22 August 2013

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Adjusting the temperature at 37 degrees and calibrating the probes as described in Appendix 5.
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Adjusting the temperature at 37 degrees and calibrating the probes as described in [[Team:DTU-Denmark/Methods/Calibrating_Electrodes|Calibration]].

Revision as of 17:45, 25 August 2013

22 August 2013

Contents

lab 208


Main purpose


Who was in the lab


Kristian, Henrike

Procedure


USER ligation and transformation

Redid for HAO and cyc in arabinose inducible pZA21::araBAD and for Nir fragments

PCR for Biobrick parts

Set up a new PCR reaction for Biobrick parts using HF buffer and 5% DMSO but no MgCl2. PCR was run on a touchdown program

primers: 53a, 53b

template: Sec2 miniprep

program:

temperature time cycles
98C 2:00 -
98C 0:10 10
63C 1:00 10
-0.5C per cycle
72C 1:00 10
98C 0:10 25
53C 1:00 25
72C 1:00 25
72C 5:00 -
10C hold -

Gel purification

Gel purified the linearized plasmid pZA21::ara with USER endings

colony pPCR to verify AMO insert

Picked 10 colonies from yesterday's cloning for colony PCR. Diluted cells in 50 uL of MilliQ and took 1 uL as template

primers: 53a, 53b

program:

temperature time cycles
98C 10:00 -
98C 0:10 36
56C 0:30 36
72C 2:00 36
72C 5:00 -
10C hold -

Results


nanodrop measurement of ara spl plasmids

Nd ara spl.jpg

Conclusion



lab 115


Main purpose


Run Experiment 2 in two different samples anaerobically in order to characterize the behavior of E.coli.

Who was in the lab


Ariadni, Helen

Procedure


Adjusting the temperature at 37 degrees and calibrating the probes as described in Calibration.


Following the protocol Experiment 2

Changing the steps :

6. 3 ml of the overnight culture (from glycerol stock) in 200 ml of medium with OD=0.0317.

7. Then added 3 ml more after 2 hours and the OD was 0.1046. The OD after 1 hour was 0.1340. Afterwards we added glycerol 1g in 10 ml of water and then added in our growing culture. Then after 40 min the OD was 0.2737. (Setup wavelength 600 nm).

12. The OD was measured 0.1324 instead of 0.3.

19. Add 0.5 ml of nitrite solution and continue by adding 0.5 ml after 10 minutes then we took 2.2 ml of sample, we added then 1 ml and we saw a slow response after 6 minutes. Afterwards when there was any change in the curve we spiked with 1 ml of nitrite. We continued as there was no response by adding 1 ml more and then by adding 2 ml more. We took 2 ml for sample in the end and another 2 ml for OD measurement where OD=0.1350. One hour after we took 2 ml of sample and then we spiked with 1 ml of NO2. There was no response after 12 minutes. Then we spiked with 0.5 ml of N2O and we show a big response.

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


Nitrate

Measuring range 1-25 mg/L NO3-N

start point- signal <1 mg/L

middle point- signal <1 mg/L but visible pinker

end point- signal <1 mg/L but much visible pinker


Nitrite

Measuring range 0.02-1 mg/L NO2-N

start point- signal <0.02 mg/L

middle point- signal 0.29 mg/L

end point- signal 0.70 mg/L after X2 dilution


Point before spiking with NO2 at the end measurement 1.03 mg/L (x2 dilution)- 0.5 mg/L (x4 dilution)

Conclusion


The E.coli didn't grow as usual and the problem might be the minimal medium.


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