Results
Solid Matrix
Our idea of a 3D-printer made it necessary to immobilize our cells inside a three dimensional matrix. We figured that the matrix needed to have the following properties:
- Clear substance with good transmission of light to enable us to actuate the immobilized cells precisely with light.
- Possibility to distribute the cells evenly within the matrix.
- Environment that ensures the survival of the bacteria.
The idea to immobilize our bacteria in something like a solid growth medium (like agar-plates) was a step in the right direction, but standard LB-agar was not the solution. In the end, we chose GELRITE as a gelling agent, “a highly-purified, natural anionic heteropolysaccharide that forms rigid, brittle, agar-like gels” (source: gelrite spec sheet, see labbook/methods).
Clear substance with good transmission of light:
The matrix should be prepared with minimal media such as M9 instead of LB, because LB shows a strong absorption in the lower range of visible light (hence its yellow color). Minimal media are clear, which is a great advantage.
The cell density in the matrix is also an important factor, because with increasing cell number the gel becomes blurry due to refraction of light (see diagrams).
Distribution of cells and cell survival:
To make sure that the cells are distributed evenly within the matrix, the bacteria need to be added to the medium before gelling occurs. The gelling temperature of GELRITE depends on both the amount of GELRITE powder and the salt concentration of the used liquid. A 0.5 % GELRITE gel prepared with M9 medium solidifies at around 46 °C. This means that the cells that shall be immobilized must survive such temperatures for a few minutes. This is why we made some experiments with the heat resistant E. coli strain BH28 (kindly provided by Jeanette Winter). Fluorescence microscopy showed that the cells can survive the gelling process and produce GFP or RFP upon induction. The temperature seems to be the most critical factor regarding cell survival, as minimal media, with which the gel is prepared, provide enough nutrients for the bacteria.
Cloning of constructs
Cloning of AND-Gate and reporter constructs were successful and plasmids have been verified via sequencing after every cloning step. Those sequences were entered into the registry. The cloning scheme for our AND-Gate and reporter constructs can be seen on our Design page.
High Fidelity PCR was performed on BBa_K322127 in order to amplify the ~3.9 kbp region of PcyA (Phycocyanobilin:ferredoxin oxidoreductase) gen and cph8 genes, as well as the OmpC promotor region. This PCR-product forms new part BBa_K568000.
A correct clone of our final optogenetical AND-Gate BBa_K568001 construct was successfully sequenced with VR primer into first 1000 bp of T7ptag region. Testing of this construct according to our Design notes in CP919 cells with GFP reporter part BBa_I746907 was not possible within timescale.
Size of our cloned reporter plasmid BBa_K568003, containing T7 promoter with RBS and lacZ is correct (T7promoter_RBS_lacZ approx. 3kbp pSB1AK8 approx. 3.4 kbp). One clone was verified via sequencing. This part was further characterized performing Miller Assays in BL21(DE3) cells. See "characterization of parts" or Registry entry for detailed information.
Characterisation of parts
Red Light Sensor
The red light sensor used is derived from BBa_K322127. We used this part in two ways: At first, we used PCR to amplify the parts needed for red light detection from this preexisting part, generating BBa_K568000. After that we compared the original part BBa_K322127 and our new part BBa_K568000.. To prove the proper function of these two red light sensor parts, we did several Miller Assays. Unfortunately, this part did not produce the results we hoped for.
Blue Light Sensor
The blue light promoter was fused to lacZ and expression of lacZ was measured wih the Miller Assay. The blue light promoter can be induced at 450 nm, which we accomplished with the appropriate LED. To fully characterize this part, cultures were grown at different conditions and their lacZ expression was measured.
Comparing samples grown at different lighting conditions showed that room light decreases the activity of the blue light promoter slightly, whereas blue light of 450 nm increases its activity.
As literature suggested a temperature dependency, we tested samples grown at room temperature (23 °C) and 37 °C, the usual incubation temperature for bacterial cultures. This proved that the blue light promoter yields higher expression rates at this lower temperature. Blue light is another input of a response pathway to cold stress and acts upon YcgF/YcgE. Under blue light the repressor YcgF binds to YcgE which in E. coli represses genes for biofilm formation, which then in turn detaches from its target. The underlying part for our construct is
BBa_K238013, we added lacZ with a preceding RBS.
Reporter Plasmids
lacZ Reporter
We tested the function of the reporter plasmid BBa_K568003 using a Miller Assay. The part was transformed into BL21(DE3) cells, which are able to express T7 polymerase upon stimulation with IPTG. We were able to show that the expression level of β-galactosidase increases about one hour after induction, if compared to the control incubated without IPTG. The data indicates a leaky expression of β-galactosidase, which might be due to a leaky production of T7 polymerase by the host strain. An increase in Miller Units could be shown for all tested concentrations of IPTG between 0.01 mM and 1.5 mM, which seem to be quantitative until 90 min after stimulation.
GFP Reporter
In order to test our AND-Gate construct in CP919 cells, we need another reporter than lacZ due to genomic ompC-lacZ fusion present in this strain. Therefore Part
BBa_I746907 has successfully been tested for proper function.
"
Results
Solid Matrix
Our idea of a 3D-printer made it necessary to immobilize our cells inside a three dimensional matrix. We figured that the matrix needed to have the following properties:
The idea to immobilize our bacteria in something like a solid growth medium (like agar-plates) was a step in the right direction, but standard LB-agar was not the solution. In the end, we chose GELRITE as a gelling agent, “a highly-purified, natural anionic heteropolysaccharide that forms rigid, brittle, agar-like gels” (source: gelrite spec sheet, see labbook/methods).
Clear substance with good transmission of light:
The matrix should be prepared with minimal media such as M9 instead of LB, because LB shows a strong absorption in the lower range of visible light (hence its yellow color). Minimal media are clear, which is a great advantage. The cell density in the matrix is also an important factor, because with increasing cell number the gel becomes blurry due to refraction of light (see diagrams).
Distribution of cells and cell survival:
To make sure that the cells are distributed evenly within the matrix, the bacteria need to be added to the medium before gelling occurs. The gelling temperature of GELRITE depends on both the amount of GELRITE powder and the salt concentration of the used liquid. A 0.5 % GELRITE gel prepared with M9 medium solidifies at around 46 °C. This means that the cells that shall be immobilized must survive such temperatures for a few minutes. This is why we made some experiments with the heat resistant E. coli strain BH28 (kindly provided by Jeanette Winter). Fluorescence microscopy showed that the cells can survive the gelling process and produce GFP or RFP upon induction. The temperature seems to be the most critical factor regarding cell survival, as minimal media, with which the gel is prepared, provide enough nutrients for the bacteria.
Cloning of constructs
Cloning of AND-Gate and reporter constructs were successful and plasmids have been verified via sequencing after every cloning step. Those sequences were entered into the registry. The cloning scheme for our AND-Gate and reporter constructs can be seen on our Design page.
High Fidelity PCR was performed on BBa_K322127 in order to amplify the ~3.9 kbp region of PcyA (Phycocyanobilin:ferredoxin oxidoreductase) gen and cph8 genes, as well as the OmpC promotor region. This PCR-product forms new part BBa_K568000.
A correct clone of our final optogenetical AND-Gate BBa_K568001 construct was successfully sequenced with VR primer into first 1000 bp of T7ptag region. Testing of this construct according to our Design notes in CP919 cells with GFP reporter part BBa_I746907 was not possible within timescale.
Size of our cloned reporter plasmid BBa_K568003, containing T7 promoter with RBS and lacZ is correct (T7promoter_RBS_lacZ approx. 3kbp pSB1AK8 approx. 3.4 kbp). One clone was verified via sequencing. This part was further characterized performing Miller Assays in BL21(DE3) cells. See "characterization of parts" or Registry entry for detailed information.
Characterisation of parts
Red Light Sensor
The red light sensor used is derived from BBa_K322127. We used this part in two ways: At first, we used PCR to amplify the parts needed for red light detection from this preexisting part, generating BBa_K568000. After that we compared the original part BBa_K322127 and our new part BBa_K568000.. To prove the proper function of these two red light sensor parts, we did several Miller Assays. Unfortunately, this part did not produce the results we hoped for.
Blue Light Sensor
The blue light promoter was fused to lacZ and expression of lacZ was measured wih the Miller Assay. The blue light promoter can be induced at 450 nm, which we accomplished with the appropriate LED. To fully characterize this part, cultures were grown at different conditions and their lacZ expression was measured. Comparing samples grown at different lighting conditions showed that room light decreases the activity of the blue light promoter slightly, whereas blue light of 450 nm increases its activity.
Reporter Plasmids
lacZ Reporter
We tested the function of the reporter plasmid BBa_K568003 using a Miller Assay. The part was transformed into BL21(DE3) cells, which are able to express T7 polymerase upon stimulation with IPTG. We were able to show that the expression level of β-galactosidase increases about one hour after induction, if compared to the control incubated without IPTG. The data indicates a leaky expression of β-galactosidase, which might be due to a leaky production of T7 polymerase by the host strain. An increase in Miller Units could be shown for all tested concentrations of IPTG between 0.01 mM and 1.5 mM, which seem to be quantitative until 90 min after stimulation.
GFP Reporter
In order to test our AND-Gate construct in CP919 cells, we need another reporter than lacZ due to genomic ompC-lacZ fusion present in this strain. Therefore Part BBa_I746907 has successfully been tested for proper function.