Team:BCCS-Bristol/Notebook-Progress

Progress Reports

• 1st July - 8th July
  • Swimming agar assay testing different conditions
    • different agar concentrations, incubation temperatures, inoculation depths

• 9th July - 15th July

• 16th July - 22nd July

• 23rd July - 22nd July

• 24th July - 22th July

• 31st July - 6th August
  • BioBrick Transformation
    • Heat shock transformations with BioBrick DNA resulted in zero, one or two colonies per attempt
    • All colonies have been verified to possess the plasmids
    • Electroporation is much more successful
  • Agar plug assay
    • E. coli MG1655 moved apparently some beads!!!
    • but unfortunenately, no chemotaxis was observed

• 7th August - 13th August
  • BioBrick Transformation
    • The self-made electro competent E. coli DH5α cells are working
    • A longer incubation time of the punched paper disc in water seems to resolve more BioBrick DNA

• 14th August - 20th August
  • Agar plug assay
    • Repulsion achieved to some degree in the agar-plug assay.
  • BioBrick transformation
    • DH5α transformed with pRZ1(pRS415 containing cpxR responsive promotor - sent to us by T.Silhavy, Princeton)

• 2nd September - 9th September
  • BioBrick transformation

• 10th September - 16th September

Progress Report Details

1st July - 8th July

Swimming agar assay

We wanted to test different conditions for the swimming agar assay:

- different agar concentrations

- different incubation temperatures

- different inoculation depths

After an incubation overnight, we measured the diameter of the E. coli MG1655 swarms. Surprisingly, we observed two swarm layers: The lower one has a bigger diameter than the upper.

Agar (%)	Temperature ( o C)	Inoculation Depth	Number	JPG File	Inner Ring (cm)	Outer Ring (cm)
0.3	30	Deep	1	4828	4.6	5.3
0.3	30	Deep	2	4827	4.6	5.3
0.3	30	Deep	3	4829	4.7	5.2
0.3	30	Under Surface	1	4830	4.6	5.2
0.3	30	Under Surface	2	4831	4.6	5.2
0.3	30	Under Surface	3	4832	4.6	5.1
0.3	30	On Surface	1	4833	2.9	3
0.3	30	On Surface	2	4834	3.8	4.4
0.3	30	On Surface	3	4835	4.4	4.9
0.3	37.5	Under Surface	1	4836	7.2	7.6
0.3	37.5	Under Surface	2	4837	7.4	7.7
0.3	37.5	Under Surface	3	4838	7.1	7.4
0.3	25	Under Surface	1	4840	2.8	3.5
0.3	25	Under Surface	2	4839	3	3.6
0.3	25	Under Surface	3	4841	3.1	3.7
0.2	30	Under Surface	1	4842	8.6	8.6
0.2	30	Under Surface	2	4843	8.6	8.6
0.2	30	Under Surface	3	4844	8.6	8.6
0.5	30	Under Surface	1	4847	2.3	2.3
0.5	30	Under Surface	2	4845	1.9	1.9
0.5	30	Under Surface	3	4846	1.5	1.5

9th July - 15th July

Swimming agar assay with aspartic acid

We conducted a second swimming agar assay with E. coli MG1655. This time, we added paper discs that were soaked with a L-aspartic acid solution. We wanted to observe whether the bacteria are attracted by the amino acid. We tested again different parameters:

- agar concentrations of 0.15 %, 0.3 % and 0.5 %

- incubation temperatures of 25 ^oC, 30 ^oC and 37 ^oC

- inoculations depths of "on the surface", "under the surface" and "deep in the medium"

- aspartic acid concentrations of 0.2 %, 0.1 % and 0.01 %

Photos of swiming agar were taken and travelled distances measured. 0.3% agar was found to be the best for an overnight culture and a temperature of 37^oC was too high, since the swarms spread over the whole plate. All plates showed swarm spread at different levels giving inner and outer rings. Unfortunately, we observed no different movement/growth towards the L-aspartic acid compared with the control (water). It was assumed that this is due to the low concentration, but it wasn't possible to made a 0.4 % solution.

31st July - 6th August

BioBrick Transformation

Last Thursday, the primers VF2 and VR arrived. These primers allow a confirmation of a succesful transformation of most BioBrick parts by means of PCR. The resulting fragment length depends on the specific BioBrick DNA.

Using VF2 and VR, a colony PCR are was conducted with all colonies that were obtained with chemical competent cells so far. Two colonies with the yeast ADH1 promoter (No. 1 and 2, see left photo) and three colonies with a GFP generator (No. 3-5, see left photo) were identified as positive. Thus, all colonies are positive, but the transformation efficiency is too low, since the result was only one or zero colonies per transformation attempt.

Electroporation should give higher efficiencies. An attempt with a new BioBrick (ADH1 terminator) resulted in 69 colonies! Ten of them were analysed using PCR. The resulting fragment should have a length of 461 bp, but from the eigth positive colonies fragments between 650-750 bp were obtained (see right photo). This is probably due to a mutation which might result in a different binding location for one of the primers. Another explanation might be that the denoted length is wrong. Since this BioBrick is not important for our project, it will be disregarded.

L= HyperLadder I (BIOLINE) N= Negative control Numbers= See text

The transformation efficiency of the electroportation was significant higher than of the chemical competent cells. Therefore, an own stock of electric competent cells was made.

Agar plug assay

TR235 (E. coli with construct to detect adhesion to hydrophobic surfaces) arrived from Princeton (Thomas J. Silhavy). Cells are viable, growth curve done. 11µm PS beads shown to be moved by bacteria (MG1655); we observed ‘jiggling’ of beads when bacteria present (not seen in no-bacteria control). Also, we observed significant movement in different directions (distances of approx 1x to 5x length of the beads by eye) of beads that were close together, suggesting that movement was not due to currents in the medium. We saw no distance covered in almost all the control beads, a few moved small distances, so some currents are present. Bacteria and beads were left together for ~30mins to allow time for adhesion. No movement has yet been seen when the bacteria and beads are not left to adhere. We will look again at this, as we may have not previously looked closely enough (photographing over a time course of a few minutes).

		0 mins		1 min		2 mins

		Circles represent position at 0 mins, one colour for each bead. For example, the bead that starts in red circle moves down and right, while that in the yellow circle moves left.

Chemotaxis assay (Yu, H.S. et al. (1997) FEMS Microbiology Letters, 156, 265-269.) has not worked so far. Currents can be seen flowing from the aspartate plug, pushing bacteria away. The focus of this week will be on getting this fixed, with a view to combining chemotaxis and the ability to move beads, allowing us to move beads in a particular direction.

The GRN for switching on the chemotactic response by binding to a bead, and signaling to nearby bacteria that a particle is in the vicinity, is almost finalised.

7th August - 13th August

BioBrick Transformation

The self-made electro competent E. coli DH5α cells were tested twice. The transformation efficiency with pUC19 was 4.45 x 10⁸ cfu/µg and 5.67 x 10⁸ cfu/µg. The first attempt with BioBrick DNA failed, but this might be due to a too low cell amount compared to all the other decanted tubes. In the following transformations, the incubation of the punched paper disc with the DNA was varied in time (3 h and 5.5 h). It seems that a longer incubation increases the transformation efficiency. This has to be confirmed, since the transformations were conducted by different persons. Thereby, next to the yeast ADH1 promoter another BioBrick (enhanced version of EYFP, yeast-optimized YFP) was tested because the VF2-VR value of yeast ADH1 promoter we got didn't coincide with the value given on the iGEM page.

Agar Plug Assay

Evaporation and currents that were occurring in previous attempts at the agarose-in-plug assay were eliminated by ensuring water potentials of plug and chemotaxis buffer were as similar as possible. Both the beads and the bacteria were found to sink to the bottom of the chamber shortly after inoculation. This makes the model much simpler, as everything can be modelled in 2D. We showed that beads need to be left in bacteria for around 30mins in order for significant bead movement to occur. We currently have not determined if this is because the bacteria form a layer under the beads which stops them sticking to the slide, or if adherence itself is needed for bead movement. We determined the diffusion speed of bromophenol blue dye (which is three times larger than aspartate), and concluded that by 30mins aspartate would have diffused throughout the slide.

14th August - 20th August

Agar Plug Assay

We repeated the chemotaxis assays and found that the bacterial density surrounding the plug varied and therefore we obtained more valid results by using lower magnification and scanning around the whole plug (as opposed to focussing on one area for the whole time course). This gave a much better overview of changes in bacterial density.

We tried testing bacterial chemotaxis to 1% serine and 1% aspartate in the plug. Bacterial density around the plug was monitored for 1hr. Bacteria appeared to be repelled by both the serine (see below)and aspartate at this concentration compared with the control where no chemoattractant was present in the plug. Research group page (Professor Jong Yoon, Micro/nanofluidic Bio MEMS group) indicates that serine becomes chemorepellent 1M concentration (the same may be true of aspartate).

	Control		1%Serine in plug

We have been attempting a 'dead bacteria' control, but have been unable to successfully kill our bacteria without using a method that physically alters them. We have tried sodium azide (bacteriostatic)- but resuspension allows them to recover. Kanamycin and chloramphenicol were also used, but only for a few hours. We might try leaving a culture overnightin these two antibiotics - this should be sufficient to kill them!

BioBrick Transformation

The transformation efficiency should be increased. It was assumed that the quality of the BioBrick DNA is the most important factor to improve. Thus, two punched paper discs of the same BioBrick were incubated overnight at two different temperatures: 37^oC and room temperature. The room temparature DNA resulted in 63 colonies (compared to 14 colonies with the 37^oC-DNA), but it was not comparable since the 63 colonies were a result from a double electro shock. This may enhance the transformation efficiency. Thus, further tests should be conducted considering different incubation times and temperatures of the paper disc in water and as well single and double electroporation.

Electro competent cell of E. coli MG1655 were made and tested with pUC19. This resulted in zero colonies and may due to the high OD₆₀₀ of the cells when they were prepared. New cells should be made.

DH5α cells were transformed with pRZ1 (pRS415 containing cpxR responsive promotor). The efficiency was very high and 15 colonies were isolated.

21st August - 1st September

Change to a proof-of-concept

Unfortunately it was discovered that the Cpx response (activated by adhesion to hydrophobic surfaces) actually downregulates, via CpxR, chemotaxis through a number of genes. This means that our initial plan of using the Cpx system to detect adhesion to the beads will not work in its current form as the bacteria adhered to the bead will stop chemotaxing. Indeed, bacteria that adhere to the bead because of short or long-range co-ordination will also stop chemotaxing soon after they reach and adhere to the bead. There would be two ways around this problem: either we stop CpxR switching off chemotaxis by knocking-out the two binding regions that allow CpxR to downregulate the two operons downregulating the chemotactic genes, or we place these genes (eight of them) under the control of an activating CpxR region. In the time remaining, neither of these are achievable. Furthermore, it is likely that there are additional unknown genes required for chemotaxis, that are also downreguated by CpxR upon adhesion, therefore there is a good chance that neither strategy would work initially. As our experimental work has not yet confirmed whether bacteria adhered to beads, and able to chemotax, can actually direct bead movement towards a goal chemoattractant, at the least we would require the modelling work to suggest that this was indeed possible before any effort was made to maintain chemotaxis upon adhesion by either of the above strategies.

In light of this, the focus of the lab work will move towards producing proof-of-concept BioBricks that will allow us to demonstrate the communication of an adhesion event from an adhered to an unadhered bacteria. This can be achieved making extensive use of the available BioBricks. Specifically, sender cells (cells that have adhered to beads and are trying to communicate with unadhered cells), will contain the LuxI-GFP portion of BBa_J37015, fused downstream of a CpxR responsive promoter (modified from current version fused to LacZ provided courtesy of T.Silhavy, Princeton). Upon adhesion to beads, LuxI will produce AHL, which will diffuse into the medium, while GFP will give confirmation that the transcript is working. For receiver cells we will test both BBa_T9002 and BBa_I731014, which produce GFP and mCherry respectively upon activation by AHL. We will also BioBrick the CpxR responsive promoter itself, and aim to fuse BBa_E0840 (GFP) to the CxpR responsive promoter, creating a nice visual assay for adhesion (the CpxR-LuxI-GFP BioBrick will also do this, but producing AHL in addition may not be ideal for certain future applications). Therefore in total we aim to produce 3 BioBricks in total.

2nd September - 9th September

Biobrick transformations

A series of biobrick transformations (J37015, T9002, E0840 and I731014) were performed using electro-competent DH5α cells. After several attempts, only J37015 and T9002 appeared to work, but after carrying out colony PCR on the transformed bacteria we found that the J37015 part doesn’t appear to be in its plasmid (pSB1A3). The T9002 transformation, however, was successful, and this was verified by plasmid mini-prep and subsequent test digestion. Its activity as a luxR GFP receiver construct was also confirmed, by testing the fluorescence of the transformed bacteria when incubated with two different concentrations of AHL. (No GFP was produced in the control, un-transformed, bacteria). Since we have tried several times, unsuccessfully, to transform the other biobricks, strains already transformed with these biobricks were requested from iGEM HQ.

	DH5α T9002, 10E-6M AHL, Bright Field		DH5α T9002, 10E-6M AHL, GFP

10th September - 16th September

We received strains from iGEM HQ transformed with the following biobricks: J37015, pSB1A3, I731014, T9002, E0840.

The AHL test used to verify the activity of our T9002-transformed DH5α cells was repeated (see protocols page) to test the I731014 and T9002 strains provided by iGEM. We used pSB1A3-transformed strains as our control. Both test strains displayed fluorescence at both 10^-6M and 10^-8M AHL, whilst no fluorescence was detected in the negative control. The proportion of total I731014-transformed bacteria that actually fluoresced was quite low however. (T9002 fluorescence, in contrast, was near to 100% of total bacteria in the sample that was viewed).

Plasmid mini-preps and restriction digests were performed to test the identity of the plasmids. Single and double digests were carried out for each biobrick. The results for T9002 and E0840 were as expected and corresponded to the part sequence data. Both the single and double digests for J37015, however, produced only one band – all running just above the 2000bp marker. SpeI was used in both the single and double digest and according to the sequence data cuts once in the plasmid containing the J37015 part (pSB1A2). HindIII was the second restriction enzyme used in the double digests and should cut once in the J37015 part. We concluded from this information that the J37015 part is not in the plasmid – and the resulting single band corresponds to the linearised pSB1A2 plasmid! The digests for pSB1A3 and I731014 were rather confusing. We don’t know what went wrong here, especially as we had shown previously in the AHL test that the I731014 part appears to be functioning.

This week we also started on the road to making our first biobricks. The CpxR promoter was cloned out of the TR235 and MG1655 genomes, and was verified on a gel after restriction digest. The results of the digest of pSB1A3, however, did not make sense again, and doesn’t appear to correspond to what it is meant to be. We have now decided to obtain this plasmid by using the T9002 biobrick, cutting out the T9002 part, and inserting our CpxR promoter.

The second biobrick we want to make is luxI and GFP under the control of our CpxR promoter. Originally the LuxI and GFP portion were to be obtained from the J37015 biobrick, but since this doesn’t appear to be in the plasmid, we have started on building it ourselves using the separate LuxI (I15030) and GFP (E0840) parts. Transformations of electro-competent DH5α with the I15030 part were carried out.