Davidson Missouri W/Results2

From 2007.igem.org

Gene Splitting

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. Figure 2 shows a plate of cells containing split RFP.

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.

Figure 2: Cells containing split RFP (pLac-RBS-RFP1-hixC-RFP2) after overnight incubation at room temperature.

Graphs

Once we managed to split two genes, we proceeded to implement two different 3-node graphs into plasmids. These graphs were named Graphs A and B and are shown below. For each graph, we wanted to find a Hamiltonian Path from the node represented by RFP (colored in green) to the node represented by the transcriptional terminator (colored in red). The plasmid representation of Graph A is not be capable of flipping into a false positive orientation, while the plasmid representation of Graph B does provide that possibility.

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.

Starting Orientations

We constructed the following Hamiltonian Path Problem (HPP) constructs to test our bacterial computer system for Graphs A and B. Constructs that are built to solve Graph A are labeled HPP-A. Constructs that are built to solve Graph B are labeled HPP-B. A subscript equal to 0 denotes a plasmid in a solved orientation. A subscript that is greater than 0 denotes a plasmid that is in an unordered starting orientation.

• HPP₀ (Positive Control for HPP-A and HPP-B constructs)
  
  
  
• HPP-A₀ (Solved Orientation)
  
  
• HPP-A₁
  
  
• HPP-A₂
  
  
• HPP-B₁
  
  

Controls

Because are graphs require that solved colonies be selected for by double fluorescence (both red and green), we first performed control experiments to ensure that we could distinguish solved and unsolved colonies. To test fluorescence phenotypes when both split GFP and split RFP are the same cell, we used our positive control constructs ([http://partsregistry.org/Part:BBa_I715045 HPP₀] and [http://partsregistry.org/Part:BBa_I715042 HPP-A₀]) with split RFP and split GFP both downstream of the T7 polymerase promoter. In the presence of T7 polymerase, cells with the split RFP/GFP plasmid should demonstrate both green and red fluorescence.

We first tried cotransforming our HPP₀ construct with a T7 RNA polymerase plasmid construct ([http://partsregistry.org/Part:BBa_I715038 BBa_I715038]). As can be seen in Figure 3 below, this cotransformation resulted in bright green colonies that demonstrated minimal red fluorescence. When we measured the fluorescence of the cotransformed control, RFP was not present at detectable levels (See fluorescence data below).

We then tried transforming our HPP-A₀ control plasmid into cells that already contained T7 polymerase in their chromosome (T7 RNAP cells). As can be seen in Figure 4 below, these colonies displayed the yellowish color we expected. Based on our fluorescence data, (shown below), we were able to show that GFP and RFP were present at detectable levels in this control. We hypothesize that the difference in the two controls is due to higher concentrations of T7 RNA polymerase in the T7 RNAP cells than in the cotransformants. We therefore used the T7 RNAP cells for future experiments.

Figure 3: Colonies containing both the T7 RNA polymerase plasmid and the HPP₀ control plasmid demonstrated strong green fluorescence, but minimal red fluorescence.

Figure 4: T7 RNAP colonies that contain the HPP-A₀ control plasmid demonstrated the expected yellow fluorescence.

In addition to the regular split RFP/GFP controls, we also tested 2 "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 ([http://partsregistry.org/Part:BBa_I715036 BBa_I715036]) and Plac-RBS-GFP1-hixC-RFP2 ([http://partsregistry.org/Part:BBa_I715035 BBa_I715035]). 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 (See fluorescence data below).

Flipping Detection by Phenotype

To test for flipping by phenotype, we used our 3 - Graph A constructs from above, HPP-A₀, HPP-A₁, HPP-A₂. As expected, unflipped HPP-A₀ fluoresced yellow, unflipped HPP-A₁ fluoresced red, and unflipped HPP-A₂ demonstrated no fluorescence when transformed into the T7 RNAP cells (See Figures 5-7 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 8 and 11). The Hin HPP-A₁ + Hin plate contained red, green and yellow colonies (See Figures 9 and 12). The HPP-A₂ + Hin plate contained mostly nonfluorescent colonies with a few green and red colonies (See Figures 10 and 13).

Click twice on the images below for higher resolution.

Figure 5: HPP-A₀ - These colonies fluoresced yellow

Figure 6: HPP-A₁ - These colonies fluoresced red

Figure 7: HPP-A₂ - These colonies do not fluoresce

Figure 8: HPP-A₀ + Hin - The addition of Hin has produced green, red, and yellow colonies

Figure 9: HPP-A₁ + Hin - The addition of Hin has produced green, red, and yellow colonies

Figure 10: HPP-A₂ + Hin - The addition of Hin has produced green and red colonies

Figure 11: HPP-A₀ + Hin - closeup of Figure 8

Figure 12: HPP-A₁ + Hin - closeup of Figure 9

Figure 13: HPP-A₂ + Hin - closeup of Figure 10

Flipping Detection by PCR

In order to provide physical evidence of Hin-mediated DNA rearrangement of our HPP-A + Hin constructs, we designed PCR primers that would allow us to determine the position of the GFP2 gene half. The experiment below shows the results of PCR using the universal reverse primer [http://partsregistry.org/Part:BBa_G00101 G00101], which binds to the 3' biobrick suffix, and a GFP2-forward primer.

Here is how the primers bind to the 3 HPP-A constructs:

PCR Primer Binding: (from top to bottom) HPP-A₀, HPP-A₁, HPP-A₂

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 fluorometer to measure the fluorescence of various HPP constructs. First, we had to determine the excitation and emission wavelengths that would allow us to detect the green and red fluorescence of split genes. Scans were conducted in order to find these wavelengths. The graphs below show 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. We used these scans to pick a peak emission wavelength for further testing.

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.

Normalized Fluorimetry Results

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 HPP-B₁ construct, which contains RBS-RFP1-hixC-GFP2, appears dark green on the UV box, but does not fluoresce green or red by spectroscopy.