Introduction

In this anaerobic experiment we add nitrite (NO₂^- ) in a series of spikes to:

• an untransformed strain of E. coli
• an untransformed strain of P. aeruginosa
• Mutant 2: a strain of E. coli transformed with the Nir gene from P. aeruginosa

in order to characterize how readily nitrite is converted to nitric oxide (NO), and subsequently to nitrous oxide (N₂O). We also monitor nitrite, ammonia and nitrate concentrations before each spike. The concentrations of nitrous oxide is measured continually and the ammonia, nitrite and nitrate concentrations are measured at a series of time points around the spike. For some experiments, we have data for the concentration of nitric oxide as well, however, the sensor frequently gave unreliable results and was replaced during the summer. While we were waiting for the new one to arrive, we were not able to take NO measurements.

Methods

The experimental procedure follows Protocol for Experiment 2.

For the calibration of the N₂O and NO electrodes we follow the calibration protocol.

Results and Discussion

In the following diagrams, the y-axis shows mg of Nitrogen (as nitrite, nitrous oxide or other N-source) per litre vs time. Vertical lines indicate the time at which we spiked with nitrite. All experiments were performed anaerobically.

Control: Untransformed E. coli -- Round 1

It appears that we observed a response from the cells after the third spike. However, this could also be due to fluctuations in the sensor.

Control: Untransformed E. coli -- Round 2

We repeated the experiment to try to reproduce the response that we saw in round 1. We were not able to see a response in either replicate that we did this round.

Untransformed P. aeruginosa

We also did not see a response for the P. aeruginosa, which we would expect.

Nir Transformed E. coli

Finally, we measured both N₂O and NO, but did not see an increase in N₂O. The NO sensor did not stabilize over the course of the experiment, and these results are not realistic.