Team:DTU-Denmark/Experiments
From 2013.igem.org
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{{:Team:DTU-Denmark/Templates/StartPage|Experiments}} | {{:Team:DTU-Denmark/Templates/StartPage|Experiments}} | ||
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== Initial Characterization of ''E. coli'' == | == Initial Characterization of ''E. coli'' == | ||
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=== Toxicity of Nitrite, Nitrate and Ammonium to ''E. coli'' === | === Toxicity of Nitrite, Nitrate and Ammonium to ''E. coli'' === | ||
- | + | The purpose of this experiment was to determine whether the ions nitrite, nitrate and ammonium are toxic to ''E. coli'', and at what concentration. We used the BioLector to grow an ''E. coli'' strain that constitutively expresses RFP in the presence of these ions (at a range of concentrations), and measure the OD and fluorescence of the cells as a proxy for growth. We found that at high concentrations ammonium (>=500mM) and nitrate (>=25mM) were toxic to ''E. coli''. However, these concentrations are much higher than we would expect to find in wastewater, so we do not expect these ions to be toxic to our cells under normal operating conditions. | |
[[Team:DTU-Denmark/ToxicityExperiment|Experiment details -- Toxicity of Nitrite, Nitrate and Ammonium to ''E. coli'']] | [[Team:DTU-Denmark/ToxicityExperiment|Experiment details -- Toxicity of Nitrite, Nitrate and Ammonium to ''E. coli'']] | ||
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=== Nitrite stability in anaerobic ''E. coli'' === | === Nitrite stability in anaerobic ''E. coli'' === | ||
- | To | + | To measure how much nitrite would be consumed by competing pathways in Mutant 2, we grew untransformed ''E. coli'' anaerobically in the presence of varying concentrations of nitrite and measured the amount of ammonia and nitrite present. We found that a pathway to convert nitrite to ammonium is active, and therefore our Nir pathway will need to outcompete this pathway. |
[[Team:DTU-Denmark/Experiment1a|Experiment details -- Nitrite stability in anaerobic ''E. coli']] | [[Team:DTU-Denmark/Experiment1a|Experiment details -- Nitrite stability in anaerobic ''E. coli']] | ||
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== Verification of Transformants == | == Verification of Transformants == | ||
- | In order to verify and characterize our transformants, we performed the following experiments | + | In order to verify and characterize our Mutant 1 (aerobic, Ammonia -> Nitrite) and Mutant 2 (anaerobic, Nitrite -> Nitrous Oxide) transformants, we performed the following experiments. |
=== Anaerobic production of nitrous oxide from nitrite === | === Anaerobic production of nitrous oxide from nitrite === | ||
- | Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide produced. Controls are untransformed ''E. coli'' and ''P.aeroginosa''. | + | Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide produced. Controls are untransformed ''E. coli'' and ''P.aeroginosa''. The results from this experiment are complicated by the fact that measurements of nitrous oxide are extremely sensitive and the sensors did not always give reliable data. |
[[Team:DTU-Denmark/Experiment2|Experiment details -- Anaerobic production of nitrous oxide from nitrite]] | [[Team:DTU-Denmark/Experiment2|Experiment details -- Anaerobic production of nitrous oxide from nitrite]] |
Revision as of 12:07, 29 September 2013
Experiments
Contents |
Initial Characterization of E. coli
Initially, we did two experiments to characterize untransformed E. coli under conditions that would be present during wastewater treatment.
Toxicity of Nitrite, Nitrate and Ammonium to E. coli
The purpose of this experiment was to determine whether the ions nitrite, nitrate and ammonium are toxic to E. coli, and at what concentration. We used the BioLector to grow an E. coli strain that constitutively expresses RFP in the presence of these ions (at a range of concentrations), and measure the OD and fluorescence of the cells as a proxy for growth. We found that at high concentrations ammonium (>=500mM) and nitrate (>=25mM) were toxic to E. coli. However, these concentrations are much higher than we would expect to find in wastewater, so we do not expect these ions to be toxic to our cells under normal operating conditions.
Experiment details -- Toxicity of Nitrite, Nitrate and Ammonium to E. coli
Nitrite stability in anaerobic E. coli
To measure how much nitrite would be consumed by competing pathways in Mutant 2, we grew untransformed E. coli anaerobically in the presence of varying concentrations of nitrite and measured the amount of ammonia and nitrite present. We found that a pathway to convert nitrite to ammonium is active, and therefore our Nir pathway will need to outcompete this pathway.
Experiment details -- Nitrite stability in anaerobic E. coli'
Verification of Transformants
In order to verify and characterize our Mutant 1 (aerobic, Ammonia -> Nitrite) and Mutant 2 (anaerobic, Nitrite -> Nitrous Oxide) transformants, we performed the following experiments.
Anaerobic production of nitrous oxide from nitrite
Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide produced. Controls are untransformed E. coli and P.aeroginosa. The results from this experiment are complicated by the fact that measurements of nitrous oxide are extremely sensitive and the sensors did not always give reliable data.
Experiment details -- Anaerobic production of nitrous oxide from nitrite
Aerobic consumption of ammonium and hydroxylamine
Grow AMO and HAO transformants aerobically in the presence of ammonia; measure concentration of ammonia.
Experiment details -- Aerobic consumption of ammonium and hydroxylamine
Bioreactor
Finally, in order to see if the long term behaviour of our Nir transformant, we grew it in a bioreactor.
Experiment details -- Growth of Nir transformant in Bioreactor