The assembled construct PA2652 (BBa_K515102) and non-codon optimised mcpS in pRK415, have been inserted and tested for functionality in E. coli DH5α obtained from New England Biolabs. We carried out tests in an attempt to show the rewired chemotaxis towards L(-)malic acid. We separated testing of chemotaxis towards malate into behavioral, qualitative & quantitative analyses. One factor concerning the assays, which was severely underestimated at the start of the testing stage, but was quickly realised, was the difficulty of performing a functional assay to obtain results. Testing of the functionality of our construct therefore involved an enormous number of changes and troubleshooting modifications, just to find out that further changes were needed for a functioning assay.

To test bacterial uptake into the roots of the plants we worked with Arabidopsis thaliana to observe the uptake of bacteria into plant roots. A. thaliana is a common plant model organism. It belongs to the mustard family and fulfils many important requirements for a model organism. Its genome has been almost completely sequenced and replicates quickly, producing a large number of seeds. It is easily transformed and many different mutant strains have been constructed to study its different characteristics (National Institute of Health, no date). While Arabidopsis may not represent plant populations naturally occurring in arid areas threatened by desertification, it is a handy model organism we will be using to study the effect of the auxin plant hormone indole-3-acetic acid (IAA) on roots, observe chemotaxis towards them and look at uptake of bacteria into the roots.

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2.1 Behavioral analysis

Bacteria perform two types of movement, smooth swimming or tumbling. We have monitored probability of the bacteria performing tumbling compared to smooth swimming in the presence or absence of attractant. As bacteria recognise the attractant, we expect a difference in bacterial chemotaxis velocity.

This is in contrast to the bacteria, which do not recognise the attractant, but are capable of metabolising it. Due to the fact that chemoreceptors respond much faster to a newly introduced carbon source than the bacterial metabolism, we tried to measure transient change in velocity due to introduction of an attractant.

This observation has been performed with bacteria in mid-exponential phase (OD₆₀₀ 0.4-0.6) induced in motility buffer 2 hours prior to observation. The bacteria containing construct PA2652 (BBa_K515102) have been exposed to motility buffer (control), 10 mM serine (positive control) & 10 mM malate (test). Observation was performed using a Zeiss Axiovert 200 Inverted Fluorescent Microscope, with video collection Volocity software. ImageJ plug-in Manual Tracking was used to collect data and Chemotaxis Tool plug-in to analyze the data.

2.2 Qualitative analysis

Qualitative assays should inform us about the result of rewiring chemotaxis in E. coli with the engineered constructs mcpS or PA2652 (BBa_K515102). However it does not inform us about the cell count and the extent to which engineered bacteria can chemotax towards the attractant source.

A number of methods exist that show chemotaxis towards a source [1]. Most of them are based on the properties of semi - solid agar, which allows diffusion of molecules and bacterial movement. We have modified agar plug assay to observe chemotactic response. The bacteria used were in mid - exponential phase (OD₆₀₀ 0.4-0.6). Cells suspended in the semi solid agar were positioned 2 cm away from the attractant source and left overnight to grow and move. At the end of the assay the plates were imaged using Fujifilm LAS-3000 Imager.

DH5-α Escherichia coli cells were used as studied subject expressing our construct. Negative control used were cells without engineered construct, with selection marker for ampicillin and kanamycin. This was to show inability of the non-engineered cells to perform chemotaxis towards malate. Positive control used were cells with selectable markers for kanamycin and ampicillin but no engineered construct. The attractant used to test positive control was serine a chemical, which is recognised by native chemoreceptors of E. coli. This was to show that cells we are using to conduct our experiments have functional chemotaxis pathway and are capable of recognising an attractant gradient.The tested DH5-α Escherichia coli contained construct (BBa_K515102) PA2652 malate chemoreceptor. We have also tested cells containing non-codon optimised mcpS gene carried on pRK415 plasmid with selectable tetracycline. However due to the lack of information about the construct, and the fact that it is non-standard biobrick format, with several illegal restriction sites within the sequence, we did not test this construct further analyses.

Results expected from this assay should show clear differences in shape of the formed colony, since the bacteria attracted to source will move and therefore distort the shape of the colony into eliptical, directed shape towards the source, in comparison with the control, which are expected to look circular as bacteria are equally likely to swim into any direction.

Table 1: The concentrations of attractant tested

Positive control

Figure 1: Rising concentrations of serine were tested. a) 0 mM control - circular colony b) 0.01 mM - circular colony e) 0.1 mM - circular colony d) 1 mM - possible eliptical colony c) 10 mM - eliptical colony f) 100 mM - eliptical colony away from the attractant.

Figure 2: Rising concentrations of serine were tested. a) 0 mM control - circular colony, b)5 mM - eliptical colony c) 10 mM - eliptical colony d) 15 mM - eliptical colony e) 20 mM - eliptical colony f) 25mM - circular colony.

Negative control

Figure 3: Rising concentrations of malate were tested. a) 0 mM control - circular colony b) 0.01 mM - circular colony c) 0.1 mM - circular colony d) 1 mM - circular colony e) 10 mM - circular colony f) 100 mM - circular colony.

Figure 4: Rising concentrations of malate were tested. a) 0 M control - circular colony b)5 mM - circular colony c) 10 mM - circular colony d) 15 mM - circular colony e) 20 mM - circular colony, f) 25mM - circular colony.

McpS - pRK415

Figure 5: Rising concentrations of malate were tested. a) 0 mM control - circular colony b) 0.01 mM - circular colony c) 0.1 mM - circular colony d) 1 mM - circular colony e) 10 mM - circular colony f) 100 mM - circular colony.

Figure 6: Rising concentrations of serine were tested. a) 0 mM control - circular colony b)5 mM - circular colony c) 10 mM - eliptical colony formed not in the direction expected d) 15 mM - possible eliptical colony e) 20 mM - possible eliptical colony f) 25 mM - circular colony.

PA2652 - BBa_K515102

Figure 7: Rising concentrations of malate were tested. a) 0 M control - circular colony b) 0.01 mM - possible eliptical colony the shape is hard to analyze c) 0.1 mM - strange shape of colony observed, however this was not a result of mishandling with semi - solid agar d) 1 mM - colony shape is not perfectly circular however not eliptical either e) 10 mM - circular colony f) 100 mM - circular colony.

Figure 8: Rising consentrations of serine were tested. a) 0 mM control - circular colony b)5 mM - colony shape was rendered void due to mishandling with semi-solid agar c) 10 mM - possible eliptical shape colony d) 15 mM - circular colony e) 20 mM - colony shape was rendered void due to mishandling with semi - solid agar f) 25mM - circular colony.

The data obtained from this assay were not easily analysed. This assay is qualitative and therefore should provide us with positive or negative result. However upon analysis of the data a conclusion can not be drawn. This is because, set up of the assay gives space for ambiguity. This is due to a number of factors. Attractant is localised, and it diffuses to all directions, however the plate is not infinite and therefore loss of concentration gradient occurs over time. Another factor is the semi-solid agar itself. This medium is relatively difficult to manipulate with and a number of samples were ruined during the handling. Even considering that set up of this assay lead to vague results a number of points can be drawn. Positive control have shown that E. coli DH5α are capable of chemotaxis. It has also shown that when added attractant is of too high concentration (10^-1 M) bacteria do not swim directly towards the attractant source since the medium around the source is saturated. Instead they perform chemotaxis in a direction, where the attractant concentration gradient is set up, so that it is in the range for sensing by chemoreceptors. This occurs even if it means that the bacteria effectively move away from the attractant source. Negative control have shown that at any tested concentration of L(-)malic acid E. coli DH5α without PA2652 or mcpS construct do not perform chemotaxis towards attractant show. The assay have, however failed to conclude a result for mcpS or PA2652 construct as the colonies observed have a range of shapes at different attractant concentrations, that do not allow us to conclude positive or negative result.

2.3 Quantitative Analysis

In comparison to qualitative assays, quantitative assays are more informative as they provide cell count based on different attractant concentrations and therefore allow identification of the optimal attractant concentration for bacterial chemotaxis. Our analyses were based on the high throughput capillary assay ([2].

We have modified this assay to obtain cell count through flow cytometer BD FACScan in contrast to commonly used CFU count. The assay itself is based on a number of capillary tubes filled with different concentrations of attractant placed into bacterial suspension for a period of 30 minutes. Even though the assay itself sounds simple, the set up was proven to be very difficult to lead us to obtain any useful data.

Table 1: The concentrations of tested serine (control) & malate attractant.

The capillaries, however did not function in a way due to a number of issues, which we have not managed to fully address in our set up. First is the suspension of the liquid in the capillary, while capillary is not suspended in liquid. We have tried to parafilm the top of the glass capillary tubes but it did not seem to create full vaccuum. For this reason we have minimised our choice to capillaries that can suspend liquid,so we have continued testing with syringes and 10 µL BioRobotix™ tips with ART barrier. Second main problem we have found, was the generation of surface tension, when we tried to remove the capillaries at the end of the assay, this then influenced the result greatly.

Figure 9: Failed set up of high-throughput capillary assay, using syringes loaded with 100 µL of attractant. Possible reason for non-functionality of this assay is surface tension upon removal of the syringes from bacterial suspension.

Figure 10: Failed set up of high-throughput capillary assay, using 10 µL BioRobotix™ tips. Possible reason for non-functionality of this assay was the use of multichannel pippette.

To get around this we have tried to build a grid for the capillary tubes and perform the experiment on perfectly leveled surface, however removal of the rack was impossible without the result being influenced by surface tension. The surface tension influenced syringe capillaries to greater extent than 10 µL BioRobotix™ tips. The BioRobotix™ tips however seemed to have problem with releasing equal amounts of attractant with bacteria after the assay was finished and some of the tips did not release any of the liquid. One reason for this can be usage of multichannel pippette. These problems have been observed upon analysis of data. Data has been analyzed with Cyflogic^TM software, CyFlo Ltd, Finland.

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Figure 11. GFP-expressing E. coli cells inside Arabidopsis roots (data and imaging by Imperial College iGEM 2011).

One important part of our project is the uptake of our bacteria into plant roots. The observation that this occurs (albeit under controlled lab settings) is new and was only published last year ^[3]. As the amount of auxin needed for enhancing plant growth depends on whether our bacteria are producing the compound outside or inside the plants, we attempted to replicate these findings.

In preparation for confocal imaging, we met with Dr Martin Spitaler and Mark Scott who advised us on how to prepare samples and image them. Confocal microscopy is much more precise than conventional light field microscopy as it eliminates background light by focusing the laser through a pinhole (Mark Scott, oral communication). The confocal microscopy we conducted was focused on imaging GFP expressing bacteria inside Arabidopsis roots to show that uptake of the bacteria takes place.

In an imaging trial run we found that natural fluorescence can be measured in roots in a spectrum that does not interfere with measuring the superfolder GFP expressed by our E. coli cells (Video 2). We did therefore not need to dye the roots before imaging.

Video 2. Stack of wt Arabidopsis root. The root can be imaged at around 488nm. Imaging carried out by Dr Martin Spitaler for Imperial College iGEM 2011.

In order to prepare the GFP-expressing bacteria for plant uptake, they were spun down and media was exchanged prior to incubation at 37°C to reach exponential phase. Bacteria were then spun down and resuspended in wash buffer (5mM MES) to reach OD 30. 8 ml, 4 ml and 2 ml were added to separate flasks, containing 100ml of half-MS media each. 4ml and 6ml of wash buffer were added to the flasks containing 4ml and 2ml bacteria, respectively. 8 ml of wash buffer was added to the negative control. Ten Arabidopsis seedlings were distributed into each of the flasks. Incubation was carried out for 15 hours prior to imaging.

Prior to imaging, roots were washed in PBS to wash off bacteria and facilitate imaging. We imaged the plants incubated with 8ml of bacteria and were able to find bacteria inside one of the roots. A 3D picture was taken of uninfected roots and roots containing bacteria by taking a Z stack image using confocal microscopy (Video 3).

Video 3. Bacteria inside of Arabidopsis thaliana roots. These videos were put together using Z-stack images taken on a confocal microscope. These images can be converted into 3D pictures that allow us to verify that the bacteria can indeed be found inside the roots rather than on the surface (data and imaging by Imperial College iGEM 2011).

We repeated this experiment at a later date with plants that had been allowed to grow for a longer period of time. The bacteria were predominantly found in root hairs and inside of cells on the root surface (Fig. 11). These plants were older than the ones previously used for uptake experiments and bacterial uptake was much more predominant.

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Dendra is a photoconvertable protein that normally exhibits green fluorescence but can be switched, using single photon activation, to fluoresce red. This conversion cannot be reversed ^[4]. Dendra is therefore very useful for observing the metabolism of cells: if all protein in a cell is converted to red fluorescence and it subsequently expresses green fluorescence, the cell has to be metabolically active. As we wanted to know if our cells are metabolically active once they have been taken up into root cells, we performed another plant uptake experiment.

Dendra-expressing bacteria were also taken up into plant roots. Using a confocal microscope, we photoconverted the Dendra protein from green to red fluorescence. Conversion with the 405 nm laser was completed after about 15 rounds of bleaching at 50% laser intensity with the pinhole set to 3 airy units.

Figure 12. Dendra photoconversion in bacteria taken up inside plant roots. 1 is the area photoconverted using the 405nm laser. 2 is an individual bacterium whose Dendra protein has undergone photoconversion. 3 is a negative control consisting of a non-photoconverted bacterium. The bacteria found inside the roots can be seen on the right. The data on the left displays the conversion from green to red fluorescence for the highlighted areas. Ch2: emission in green spectrum. Ch3: emission in red spectrum. ChD: brightfield emission.

As is visible from Fig. 12, protein in bacteria that are inside the area targeted by the laser switches from green to red fluorescence after about fifteen rounds of bleaching. Protein in bacteria that were not targeted (DOI 3) remains green. The switch from green to red fluorescence can be visualised much more acutely when observing the change in fluorescence in a single bacterium (DOI 2).

This conversion can also be visualised via a time-lapse video (Video 4).

Video 4. Time-lapse of green-to-red photoconversion of Dendra in E. coli cells that have been taken up into wild type Arabidopsis roots

Due to time constraints, we were unfortunately not able to trace the metabolic activity of the cells inside the plant roots. However, we are planning to set up an experiment that consists of photoconverting Dendra in E. coli taken up by the roots and periodically image the same cells to assess whether they remain metabolically active once they are inside the plant. This is especially important as we would need to know whether the cells would be able to actively produce auxin inside the root cells.

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[1] Jain*, R.K., & Pandey, J. (2010) Chemotactic Responses. V K. N. Timmis, ed. Handbook of Hydrocarbon and Lipid Microbiology. Berlin, Heidelberg: Springer Berlin Heidelberg, pp. 3933-3955. Available at: http://www.springerlink.com/content/x458521h8420l478/ [Cited September 16, 2011].

[2] Bainer, R., Park, H. & Cluzel, P. (2003) A high-throughput capillary assay for bacterial chemotaxis.Journal of Microbiological Methods, 55, pp. 315 - 319.

[3] Paungfoo-Lonhienne, C. et al. (2010) Turning the table: plants consume microbes as a source of nutrients. PLoS One, 5(7), e11915.

[4] Gurskaya, N. et al. (2006) Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light. Nature Biotechnology 24, pp. 461-465.

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