From 2007.igem.org

Results

Gene Splitting

Figure 1: The negative control (hixC-GFP2) on the left does not fluoresce, but the experimental split GFP (Plac-RBS-GFP1-hixC-GFP2) on the right does.

We were able to split two genes: GFP and RFP. Split GFP has strong green fluorescence. Split RFP's red color is much reduced compared to wild-type RFP. It takes overnight incubation at room temperature for the red color to be visible in white light. Both colors are fluorescent under UV light, although the green color predominates. In Figure 1 below, a negative-control (on the left) does not fluoresce, but split GFP (on the right) does. Click here to view a picture of cells containing split RFP.

We also wanted to test fluorescence phenotypes with both proteins in the same cells. Figure 2 shows cells containing both split GFP and split RFP, downstream of the T7 RNA polymerase promoter and co-transformed with T7 RNA polymerase plasmid ([http://partsregistry.org/Part:BBa_I715038 BBa_I715038]). These cells look bright green, but the red color is hard to see under UV light. Under white light, the green color is not apparent, but the cells are a little pink. The cells only containing split RFP, on the right, are clearly pink under UV light. However, not all cells are equally colored and some even contain a dark green fuorescene, which is a curious result as the cells do not contain GFP of any form.

Figure 2: On the left, cells with the T7 RNA polymerase plasmid and a plasmid containing both split RFP and split GFP. These cells fluoresce a bright green under UV light and look pink under white light. On the right, cells with the T7 RNA polymerase and only split RFP demonstrate red fluorescence of varying intensities.

In addition to the regular split GFP and split RFP constructs, we also wanted to test some "hybrid" constructs to ensure that they would not fluoresce. GFP and RFP have similar structures and functions. Previous studies have shown that it is possible to modify GFP to display a wide range of color phenotypes. We created the following parts: Plac-RBS-RFP1-hixC-GFP2 and Plac-RBS-GFP1-hixC-RFP2. A plasmid may, at some point during its flipping process, contain such sequences. We tested to make sure that the similarity of these two proteins did not make them compatible enough to fluoresce. It was found that neither of these parts show any fluorescence or color change.

Constructs

Once we managed to split two genes, we proceeded to implement two different graphs in plasmids.

Graph A: This graph contains 3-nodes and 3-edges. We wanted to find a Hamiltonian path from the node representing RFP (colored in green) to the node representing the transcriptional terminator (colored in red).

Graph B: This graph also contains 3-nodes and 3-edges, however it provides the possibility of a false positive solution.

We built the following constructs:

• Positive Control for HPP-A and HPP-B constructs
  
• HPP-A₀
  
• HPP-A₁
  
• HPP-A₂
  
• HPP-B₁
  

Part Flipping and Computation

Co-transformation of the unsolved HPP plasmids with the Hin vector begins flipping and computation. Subsequent co-transformation with the T7 RNA polymerase vector then initiates transcription.

We have found that all colonies with the HPP plasmids showed unexpected green color. The green is distinguishable by eye or fluorometer from GFP's color. As a control, we showed that the T7 RNA polymerase vector does not create the green color, so we are confident that the HPP vectors are responsible.

One possibility we had tested was that hybrid parts, such as RFP1-hixC-GFP2 and GFP1-hixC-RFP2 produced functional fluorescent proteins. However, we created these parts and tested them, and found that there was no fluorescence when the pLac promoter was upstream (parts [http://partsregistry.org/Part:BBa_I715035 BBa_I715035] and [http://partsregistry.org/Part:BBa_I715036 BBa_I715036]).

Another possibility is that these hybrid proteins cannot fluoresce independently, but will emit color when in tetramers. Wild-type GFP and RFP are tetrameric, but the registry versions of the parts, [http://partsregistry.org/Part:BBa_E0040 BBa_E0040] and [http://partsregistry.org/Part:BBa_E1010 BBa_E1010] are monomeric mutants. It would be possible to test this hypothesis by running purified protein on a non-denaturing gel.

Figure 3: Cells with only the T7 RNA polymerase plasmid, shown under UV light. There is no fluorescence.

Figure 4: Cells with both the T7 RNA polymerase plasmid and the flipped Hamiltonian Path Problem plasmid, shown under UV light. There is visible green fluorescence.

Flipping Detection by Phenotype

To test for flipping by phenotype, we built 3 constructs, each representing a different starting orientation for Graph A. They were labeled HPP-A₀, HPP-A₁, HPP-A₂, with HPP-A₀ already in the solved orientation, HPP-A₁ demonstrating only red fluorescence initially, and HPP-A₂ demonstrating no initial fluorescence (See Figure 5 below).

Figure 5: From top to bottom: HPP-A₀, ([http://partsregistry.org/Part:BBa_I715042 I715042]), HPP-A₁, ([http://partsregistry.org/Part:BBa_I715043 I715043]) and HPP-A₂, ([http://partsregistry.org/Part:BBa_I715044 I715044])

Each of the 3 constructs, HPP-A₀, HPP-A₁, and HPP-A₂, were transformed into E. coli cells expressing T7 RNAP. As expected, the colonies containing HPP-A₀ fluoresced yellow (red + green), the HPP-A₁ colonies fluoresced red, and the HPP-A₂ colonies did not fluoresce. (See Figures 7-9 below).

A fragment containing the Hin expression cassette (pLac-RBS-Hin-LVA, [http://partsregistry.org/Part:BBa_S03536 BBa_S03536]) was ligated in front of each of the 3 HPP-A constructs. These HPP-A + Hin plasmids were then transformed into T7 RNAP cells. A colony from each transformation was picked and grown overnight for plasmid mini-prep. Each of the 3 constructs was restriction digested and the insert sizes were verified to be correct. The 3 constructs were then retransformed into T7 RNAP cells, and the resulting transformation mixture was streaked for colony isolation. The HPP-A₀ + Hin plate contained mostly yellow colonies but also red and green (See Figures 10 and 13). The Hin HPP-A₁ + Hin plate contained red, green and yellow colonies (See Figures 11 and 14). The HPP-A₂ + Hin plate contained mostly nonfluorescent colonies with a few green and red colonies (See Figures 12 and 15).

Click twice on the images below for higher resolution.

Figure 7: HPP-A₀ - These colonies glow yellow

Figure 8: HPP-A₁ - These colonies glow red

Figure 9: HPP-A₂ - These colonies do not glow

Figure 10: HPP-A₀ + Hin - The addition of Hin has produced green, red, and yellow colonies

Figure 11: HPP-A₁ + Hin - The addition of Hin has produced green, red, and yellow colonies

Figure 12: HPP-A₂ + Hin - The addition of Hin has produced green and red colonies

Figure 13: HPP-A₀ + Hin - closeup of Figure 10

Figure 14: HPP-A₁ + Hin - closeup of Figure 11

Figure 15: HPP-A₂ + Hin - closeup of Figure 12

Flipping Detection by PCR

In order to provide physical evidence of Hin-mediated DNA rearrangement, we designed PCR primers that would allow us to determine the position of one of the GFP2 gene half. The experiment below shows the results of PCR using the universal primer G00101, which binds to vector sequence 3' to the biobrick suffix, and primer GFP2-forward.
Here is how the primers bind to the 3 HPP-A constructs:

Lane 1 : MW marker (50, 100, 200, 300, 400, 500, 750, 1000, 1400/1550, 2000, 3000, 4000 bp), Lanes 2 : HPP-A₀, Lanes 3 : HPP-A₁, Lanes 4 : HPP-A₂, Lanes 5 : Hin+HPP-A₀, Lanes 6 : Hin+HPP-A₁, Lanes 7 : Hin+HPP-A₂

Left Gel - Lane 1 : MW marker (50, 100, 200, 300, 400, 500, 750, 1000, 1400/1550, 2000, 3000, 4000 bp), Lanes 2,3 : ClaI digest of Hin+HPP-A₀, Lanes 4,5 : ClaI digest of Hin+HPP-A₁, Lanes 6,7 : ClaI digest of Hin+HPP-A₂, Right Gel - Lane 1 : MW marker (50, 100, 200, 300, 400, 500, 750, 1000, 1400/1550, 2000, 3000, 4000 bp), Lane 3 : EcoRI+PstI digest of Hin+HPP-A₀, Lanes 5 : EcoRI+PstI digest of Hin+HPP-A₁, Lanes 7 : EcoRI+PstI digest of Hin+HPP-A₂

Dectection of Fluoresence by Spectroscopy

We used a fluorescent spectrometer to measure the fluorescence of wild type GFP, wild type GFP, the versions of these two split by hix sites, and new combinations of the GFP and RFP gene halves. We were able to detect fluorescence in bacterial cells by simply mixing the cells with 200 ul of water and measuring in a microtiter plate.

We first had to determine the excitation and emission wavelengths that would allow us to detect the green and red fluorescence. Scans were conducted in order to find these wavelengths. For example, the graphs below shows scans of excitation wavelengths that produce fluorescence at an emission wavelength of 515 nm, the wavelength we found to be best for green, and 608 nm, the best wavelength for red.

Sample 1 = pLac GFP1-hix-GFP2, glows green on UV box
Sample 2 = pT7-RFP1-hix-RFP2-GFP1-hix-GFP2-TT-hix-RFP2-TT-hix , glows yellow on UV box
Sample 3 = pT7-RFP1-hix-RFP2-GFP1-hix-RFP2-TT-hix-GFP2-TT-hix , glows red on UV box
Sample 4 = pT7-RFP1-hix-GFP2-TT-hix-RFP2-GFP1-hix-RFP2-TT-hix , does not glow on UV box

On the basis of these scans, we used excitation/emission wavelengths of 450 nm / 515 nm for green and 560 nm / 608 nm for red.

Probability of at least k solutions on m plasmids for Adelman's 14-edge graph

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Conclusions: We have been able to detect both green and red fluorescence in bacteria. When both of these are present, a yellow color can be observed. A surprise was that the construct that produces RFP1-GFP2 and GFP1-RFP2 is yellow on the UV box, but does not fluoresce green or red by spectroscopy.