Part:BBa_K3052030
Light-fluoresce circuit (GFP&RFP)
This circuit uses a light control system wherein the central protein Cph8 is a photosensitive protein that can response to red light and block the expression of downstream genes. The shift of the two alternations can be testified by measuring the fluoresce intensity of sfGFP and mRFP in our project.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 5032
Illegal NheI site found at 5055 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2298
Illegal BglII site found at 6592
Illegal XhoI site found at 405 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 6145
Illegal AgeI site found at 4801
Illegal AgeI site found at 4913 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 2504
2019 Team XJTU-CHINA's improvement of BBa_K2598038
Overview
This year team XJTU-CHINA aim to improve a well-characterized red-light-activated sensor which is part of the GRB system of 2018 team UCAS-China(Part:BBa_K2598038). This part contains red-light sensor cph8(BBa_I15010) and repressor CI (BBa_C0051) under its regulation. Base on this red-light-activated sensor, we add a CI regulated promoter -Pλ to this part and enable it to realize the function of two-phases switch (BBa_K3052030). Besides, we also added two fluorescent proteins -superfolder GFP (BBa_K3052041) and mRFP (BBa_K3052042) under the control of pomp (BBa_R0082) and Pλ(BBa_K1145005) respectively to report the expression level of each phase. Theoretically, RFP will expresses under red light and GFP expresses in the absence of red light.
UCAS-2018 tested the change of fluorescence intensity with the change of illumination intensity. When there is no light, fluorescence is not expressed, but when there is light, fluorescence starts to be expressed, and with the increase of time and the increase of light intensity, fluorescence intensity increases, which is shown as a one-way switch. Cite:http://2018.igem.org/Team:UCAS-China/Demonstrate
Reference [1]Schmidl, S. R., Sheth, R. U., Wu, A., & Tabor, J. J. (2014). Refactoring and optimization of light-switchable Escherichia coli two-component systems. ACS synthetic biology, 3(11), 820-831.
[2]http://2018.igem.org/Team:UCAS-China/Design
Characterization
The light-fluorescent circuits (see circuits) were constructed by two-step Golden Gate Assembly and were confirmed by colony PCR. The length of this fragment is 1467 bp and the following results showed the successful constructions.
In order to validate the effectiveness of this switch, we qualitatively measure the fluorescent of this circuit at different time. Sample of DH5α E. coli transformed with BBa_K3052030 is incubated for 24 hours without red light and then continue incubating 24 hours with red light. We photographed both the sample of control group (DH5α E.coli wildtype) and experimental group(E.coli with light-fluorescent circuit ) by a fluorescence microscope at 24 hours (24 hours without light treatment) and 48 hours (24 h without light treatment and 24 h with red light treatment). The figure indicated that the bidirectional switch was functional to switch from GFP to RFP.
Furthermore, we used COFOCAL to sensitively detect GFP and RFP while switch is shifting. After the sample above had been incubated for 24 hours without light treatment, it was treated with intense red light (wavelength=640nm). After incubating for another 3 hours with red light treatment, we took out some of the sample and perform CONFOCAL imaging. The result shows that the RFP was appearing with red light treatment, which indicates this switch can be effectively triggered by red light.
To quantitatively test the efficiency of this light switch, we decided to cultivate the cells in dark environment first and then trigger the switch with intense red light. When they had been incubated for 30 hours without red light, we start to put intense red light around the medium. During the experiment, we measured the GFP and RFP intensity of the sample every 2 hours.
From the above figure we can see that the GFP intensity increased gradually while RFP intensity maintained to be at a low basic level without red light. But after red light treatment, GFP intensity dropped sharply to a low and stable value in 4 hours, and slow increase of RFP intensity was obviously observed. The results clearly indicates the effectiveness of this bidirection switch and the fast response time to the red-light stimulation.
All in all, the results quantitively and quantitatively demonstrated the light controlled switch is functional. Compared to the previous part which achieved the monodirectional regulations (BBa_K2598038 of UCAS_China 2018), our improved version can efficiently achieve bidirectional regulation of two genes, leading to more flexible and selective regulations. BBa_K3052030 in our project is the proof of concept of this bidirectional switch, and the fluorescent proteins will be alternated with our selected linalool synthase and limonene synthase which have also been proved to be functional, to achieve the selective production of linalool and limonene.
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