Results

Building devices

During this summer we tried to build a lot of devices (17 exactly) but we finally realized that they were too many for our first time. We had many problems assembling parts and checking the constructions: PCR colony did not work (or it just worked sometimes), digestion enzymes did not cut always, we could hardly obtain pieces by PCR or site-directed mutagenesis products, etc. We think most problems were caused because of the lab conditions. We worked in a practices lab and the material we used was not the best. When we noticed that the Jamboree date was too close, we had to focus in some devices and forget assembling others. Prioritizing some devices helped us to finish proposed devices. Our work moved forward faster.

You can see below the devices we finally built and what they are for.

• Device 6. Quantify induction of PfecA promoter.
• Device 8. Production of chemoattractant aspartate mediated by signal transduction circuit 2 in response to ferric citrate.
• Device 9. Constitutive production of chemoattractant aspartate.
• Device 14. Production of chemoattractant salicylate (for P. putida) mediated by signal transduction circuit 2 in response to ferric citrate.

As you can see we could not assemble any device related to the Sensing part (link) of the project. Until the last day we tried to assemble the device that codes FecA/PrhA hybrid protein (an outer membrane protein) but we did not achieve it. It seemed that this protein could have some harmful effects in bacteria. We tried to express this protein under the control of a middle-strong constitutive promoter. First we did it using a high copy vector and last we changed it to a low copy plasmid, but we never obtained colonies that harvest the hybrid protein and could survive. Two days before Wiki freezing we looked up any inducible expression vector we could use instead of our constitutive promoter. We found TetR repressed POP/RIPS generator (meter link), which showed suitable features, but we had not enough time to test it before the Jamboree date. Anyhow, we thought that a good way to solve OM protein expression is to use inducible promoters.

Chemotaxis assays

The main way to test our project was to use chemotaxis assays. Over August we started to read as much articles about chemotaxis assays as we found. We soaked of these processes and tested some of them. In Assay site you can read more about all the different kinds of experiments we performed. Also we modified some of this assays.

When we started we used three bacterial strains: E. coli K-12, Pseudomonas sp. and Pseudomonas putida G7; and three chemoattractans, glutamate, aspartate and salycilate. Little by little we narrowed the possibilities to E. coli K-12 as strain and aspartate as attractant, because it is expected chemotactic response. However, we could not achieve good results with our chemotaxis assays using tip boxes as chemotaxis chambers and needles instead of capillaries. So we changed media conditions, needle thickness, we did different dilutions… but successful results did not arrive. Finally we realized the chance involved in our misfortune, our E. coli strain got a mutation which did not allow it to move or sense chemotaxis stimulus. We checked it by using a soft agarose plate assay.

Then we changed our strains for other known motile E. coli RP437 strain which came from Sandy Parkinson lab (chemotaxis researcher). Using the new strains we performed lower scale assays (1ul capillaries, no more that 1ml of bacterial suspensions), optimized some conditions and we achieved our goal. By microscopy and dilution and spread the chemotactic response of the bacteria towards aspartate was characterized.

Here some pictures of a capillary assay of E. coli chemotaxis toward aspartate are shown. As you can see while time passes more bacteria accumulate inside the capillary and in front of it. This is a fact that supports the chemotaxis response of E. coli.

In the last chemotaxis assay we performed before wiki freezing we used as chemotaxis chamber a flow-chamber with three channels and 1ul glass capillaries. In both edges of each channel there was a capillary, one with aspartate and other filled with buffer. We carried out experiments with two chambers, one was incubated at room temperature during 1h and the other at 30ºC. After incubation capillaries were cleaned with water and their contents were diluted and spread in agar plates. Then plates were incubated overnight at 37ºC and counted. Below results of this assay are shown. The response to aspartate is quite higher than to buffer and also the standard deviation is lower when the temperature is fixed at 30ºC.

Producing bacteria

Our goal was check if the sender bacteria could release chemoattractant enough to induce chemotactic behaviour in their partners. Although we had two different chemoattractants (salycilate and aspartate) we only did the experiments with aspartate, because it is the amino acid which causes the strongest chemotactic in response to E coli. Moreover, we started to do the chemotaxis assays quite late so we really wanted to focus in only the most important parts of the project, even if we had to dismiss the other possibilities.

We designed several growing media in which the expression of the plasmids could be analyzed. We set up inocula in these media and when they were saturated, we centrifugated and reject the pellets. The supernatants were used in chemotaxis assays