Difference between revisions of "Part:BBa K1769003"
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This reporter is used to characterize the promoter J61051. GFP is produced when we add salicylic acid. | This reporter is used to characterize the promoter J61051. GFP is produced when we add salicylic acid. | ||
| − | ===Improvement=== | + | ===Improvement made by Nanjing_high_school,2020=== |
The composite part BBa_K3524005 of rephos project was improved based on the composite part BBa_K1769003 of the NYMU-Taipei igem team. The BBa_K1769003 part is a salicylic acid biosensor and there is an inducible promoter with GFP response as reporter. | The composite part BBa_K3524005 of rephos project was improved based on the composite part BBa_K1769003 of the NYMU-Taipei igem team. The BBa_K1769003 part is a salicylic acid biosensor and there is an inducible promoter with GFP response as reporter. | ||
The GFP is also used as a reporter in our part BBa_K3524005, when salicylic acid was added in the culture, we can detect the expression of EGFP. Besides, we did some modification: transcription factor NahR and Psal promoter are added in front of the EGFP gene. NahR can specifically bind to salicylic acid to activate the Psal promoter. | The GFP is also used as a reporter in our part BBa_K3524005, when salicylic acid was added in the culture, we can detect the expression of EGFP. Besides, we did some modification: transcription factor NahR and Psal promoter are added in front of the EGFP gene. NahR can specifically bind to salicylic acid to activate the Psal promoter. | ||
| − | [[File:T--Nanjing high school-BBa K3524005 improve.jpg|500px|thumb|center|Figure | + | [[File:T--Nanjing high school-BBa K3524005 improve.jpg|500px|thumb|center|Figure 1]] |
Besides, chassis engineering bacteria E. coli is replaced by Tatumella citrea, which can provide phosphorus for crops. The engineering Tatumella citrea can commensalism with crops when crops rhizospheres secrete salicylic acid. | Besides, chassis engineering bacteria E. coli is replaced by Tatumella citrea, which can provide phosphorus for crops. The engineering Tatumella citrea can commensalism with crops when crops rhizospheres secrete salicylic acid. | ||
| − | ===Contribution=== | + | |
| + | BBa_K3524005 is a bio-sensor (nahR and Psal) for the detection of salicylic acid. We adopted it originally on the chromosome of Pseudomonas Stutzeri. With the appearance of salicylic acid, the protein translated from nahR binds with the Psal promoter and initiates the expression of the enzyme that can utilize the acid as one of the energy sources for Pseudomonas Stutzeri. In our design, we replaced the essential gene with the GFP gene to test our framework. With GFP, the situation is that the edited bacteria can be fluorescent with the existence of salicylic acid. | ||
| + | |||
| + | ====Contribution==== | ||
To build up a regulable genetic circuit, we chose the bio-sensor (nahR gene and Psal promoter) for the detection of salicylic acid we adopted is originally on the chromosome of Pseudomonas Stutzeri. With the appearance of salicylic acid, the protein translated form nahR binds with PsaI promoter and initiates the expression of the enhancer green fluorescent protein (EGFP). | To build up a regulable genetic circuit, we chose the bio-sensor (nahR gene and Psal promoter) for the detection of salicylic acid we adopted is originally on the chromosome of Pseudomonas Stutzeri. With the appearance of salicylic acid, the protein translated form nahR binds with PsaI promoter and initiates the expression of the enhancer green fluorescent protein (EGFP). | ||
| − | [[File:T--Nanjing_high_school-BBa_K3524005 fig 0.jpg|500px|thumb|center|Figure | + | [[File:T--Nanjing_high_school-BBa_K3524005 fig 0.jpg|500px|thumb|center|Figure 2]] |
| + | |||
Our team has verified this bio-sensor worked well. The future iGEM teams can exchange the EGFP to other functional proteins to make some significant utiles. For example, our team choose an essential gene GAPDH, belongs to Tatumella citrea, which can provide phosphorus for crops[1][2] to replace the EGFP . As a result, in the presence of salicylic acid, GADPH can be expressed, and T. citrea can survive. Since salicylic acid is a root exudate, this genetic circuit that T. citrea can commensalism with crops. | Our team has verified this bio-sensor worked well. The future iGEM teams can exchange the EGFP to other functional proteins to make some significant utiles. For example, our team choose an essential gene GAPDH, belongs to Tatumella citrea, which can provide phosphorus for crops[1][2] to replace the EGFP . As a result, in the presence of salicylic acid, GADPH can be expressed, and T. citrea can survive. Since salicylic acid is a root exudate, this genetic circuit that T. citrea can commensalism with crops. | ||
| − | ===Engineering Success=== | + | |
| − | Build | + | ====Engineering Success==== |
| + | =====Build===== | ||
Results of plasmids construction: | Results of plasmids construction: | ||
| − | [[File:T--Nanjing_high_school-BBa_K3524005 table 1.jpg|500px|thumb|center|Table 1 | + | [[File:T--Nanjing_high_school-BBa_K3524005 table 1.jpg|500px|thumb|center|Table 1*n represents for pTrc99k-nahR plasmids.*G represents for pMW119-Psa1-EGFP plasmids.]] |
| − | + | ||
| − | + | ||
We then used the successfully constructed plasmids to examine the effectiveness of the bio-sensor system. | We then used the successfully constructed plasmids to examine the effectiveness of the bio-sensor system. | ||
| + | |||
Some possible factors that led to failure | Some possible factors that led to failure | ||
| − | 1.Mistakes in homologous recombination | + | 1. Mistakes in homologous recombination |
Unable to recombine the right fragments into the vector. | Unable to recombine the right fragments into the vector. | ||
| − | 2.Mistakes in PCR | + | 2. Mistakes in PCR |
During the amplification, the fragments may not be correctly amplified by PCR, so some of the recovered fragments are wrong fragments, which will cause problems when used for vector construction | During the amplification, the fragments may not be correctly amplified by PCR, so some of the recovered fragments are wrong fragments, which will cause problems when used for vector construction | ||
| − | Test: | + | |
| + | ====Test:===== | ||
| + | |||
The pTrc99k-NahR and pMW119-Psa1-EGFP plasmids were co-transformed into Tatumella Citrea and screened by Kanamycin resistance and Ampicillin resistance LB solid plates. The co-transformed strains were inoculated into fresh LB medium, cultured at 37°C until OD600 was approximately equal to 0.6. Different concentrations of salicylic acid (dissolved in absolute ethanol) were added. After 24 hours, observations with fluorescence microscope were used to show the regulatory effect of salicylic acid on the PsaI promoter and it was indicated by fluorescence intensity. | The pTrc99k-NahR and pMW119-Psa1-EGFP plasmids were co-transformed into Tatumella Citrea and screened by Kanamycin resistance and Ampicillin resistance LB solid plates. The co-transformed strains were inoculated into fresh LB medium, cultured at 37°C until OD600 was approximately equal to 0.6. Different concentrations of salicylic acid (dissolved in absolute ethanol) were added. After 24 hours, observations with fluorescence microscope were used to show the regulatory effect of salicylic acid on the PsaI promoter and it was indicated by fluorescence intensity. | ||
Data collected： | Data collected： | ||
| − | |||
| − | |||
| + | [[File:T--Nanjing_high_school-BBa_K3524002 fig 1.jpg|500px|thumb|center|Figure 3. Microscopic view of fluorescence shown by Tatumella Citrea]] | ||
| − | Learn | + | =====Learn===== |
| − | 1.With different salicylic acid concentration: | + | =====1.With different salicylic acid concentration:===== |
We measured the fluorescence intensity to obtain a quantitative result. The data is plotted as the following: the measured fluorescence intensity is divided by the number of cells (OD600) to obtain a homogenized fluorescence intensity. The fluorescence intensity of all samples added with salicylic acid is subtracted from the fluorescence intensity of the background without salicylic acid. It can be seen that from 1 μM to 100 μM salicylic acid, the fluorescence intensity rises sharply. Under the condition of 1000 μM salicylic acid, the fluorescence intensity decreased, which is presumably due to the influence of salicylic acid solvent (ethanol) on cell growth, or other unknown regulatory effects of salicylic acid and NahR. | We measured the fluorescence intensity to obtain a quantitative result. The data is plotted as the following: the measured fluorescence intensity is divided by the number of cells (OD600) to obtain a homogenized fluorescence intensity. The fluorescence intensity of all samples added with salicylic acid is subtracted from the fluorescence intensity of the background without salicylic acid. It can be seen that from 1 μM to 100 μM salicylic acid, the fluorescence intensity rises sharply. Under the condition of 1000 μM salicylic acid, the fluorescence intensity decreased, which is presumably due to the influence of salicylic acid solvent (ethanol) on cell growth, or other unknown regulatory effects of salicylic acid and NahR. | ||
| − | [[File:T--Nanjing_high_school-BBa_K3524002 fig 2.jpg|500px|thumb|center|Figure | + | |
| − | + | [[File:T--Nanjing_high_school-BBa_K3524002 fig 2.jpg|500px|thumb|center|Figure 4.Relative fluorescence unit under different Salicylic acid concentration]] | |
| − | 2.With different hours: | + | |
| + | ======2.With different hours:===== | ||
With the same concentration of salicylic acid, we also measured the change of fluorescence intensity over time. It can be seen from the figure 3. that within 3 to 22 hours after the addition of salicylic acid, the fluorescence intensity increases successively. But it mostly stops increasing at 24 hours. | With the same concentration of salicylic acid, we also measured the change of fluorescence intensity over time. It can be seen from the figure 3. that within 3 to 22 hours after the addition of salicylic acid, the fluorescence intensity increases successively. But it mostly stops increasing at 24 hours. | ||
| − | [[File:T--Nanjing_high_school-BBa_K3524002 fig 3.jpg|500px|thumb|center|Figure | + | [[File:T--Nanjing_high_school-BBa_K3524002 fig 3.jpg|500px|thumb|center|Figure 5 Relative fluorescence unit with different time after addition of salicylic acid]] |
| − | + | ||
The mechanism we created did work out well, and the expressions of EGFP protein was detected. This proves that the potential of the bio-sensor system we made is effective,. The two factors we examined are the most convenient, and available test we could conduct. For the concentration of salicylic acid, we found out that at 100 μM, it shows the highst fluorescence intensity. This means that the system works the best in that range of salicylic acid concentration. For the time after addition of salicylic acid, the highst fluorescence unit is shown at 22 hours, the trend is mainly increasing. But after 22 hours, it is decreasing. It is best to leave the mechanism for 15-22 hours after the addition of salicylic acid so it can show the most effective results. | The mechanism we created did work out well, and the expressions of EGFP protein was detected. This proves that the potential of the bio-sensor system we made is effective,. The two factors we examined are the most convenient, and available test we could conduct. For the concentration of salicylic acid, we found out that at 100 μM, it shows the highst fluorescence intensity. This means that the system works the best in that range of salicylic acid concentration. For the time after addition of salicylic acid, the highst fluorescence unit is shown at 22 hours, the trend is mainly increasing. But after 22 hours, it is decreasing. It is best to leave the mechanism for 15-22 hours after the addition of salicylic acid so it can show the most effective results. | ||
| − | + | ||
| − | + | ||
| − | + | ======Refernce====== | |
| − | Refernce | + | |
[1] Whitelaw, M.a. “Growth Promotion of Plants Inoculated with Phosphate-Solubilizing Fungi.” Advances in Agronomy, 1999, pp. 99–151., doi:10.1016/s0065-2113(08)60948-7. | [1] Whitelaw, M.a. “Growth Promotion of Plants Inoculated with Phosphate-Solubilizing Fungi.” Advances in Agronomy, 1999, pp. 99–151., doi:10.1016/s0065-2113(08)60948-7. | ||
| + | |||
[2] Bar-Yosef, B., et al. “Pseudomonas Cepacia-Mediated Rock Phosphate Solubilization in Kaolinite and Montmorillonite Suspensions.” Soil Science Society of America Journal, vol. 63, no. 6, 1999, pp. 1703–1708., doi:10.2136/sssaj1999.6361703x. | [2] Bar-Yosef, B., et al. “Pseudomonas Cepacia-Mediated Rock Phosphate Solubilization in Kaolinite and Montmorillonite Suspensions.” Soil Science Society of America Journal, vol. 63, no. 6, 1999, pp. 1703–1708., doi:10.2136/sssaj1999.6361703x. | ||
| + | |||
| + | Edited by Nanjing_high_school,2020. | ||
-------------------------------------------------------------------------------------------- | -------------------------------------------------------------------------------------------- | ||
Latest revision as of 20:50, 27 October 2020
Salicylic acid sensor
This reporter is used to characterize the promoter J61051. GFP is produced when we add salicylic acid.
Improvement made by Nanjing_high_school,2020
The composite part BBa_K3524005 of rephos project was improved based on the composite part BBa_K1769003 of the NYMU-Taipei igem team. The BBa_K1769003 part is a salicylic acid biosensor and there is an inducible promoter with GFP response as reporter. The GFP is also used as a reporter in our part BBa_K3524005, when salicylic acid was added in the culture, we can detect the expression of EGFP. Besides, we did some modification: transcription factor NahR and Psal promoter are added in front of the EGFP gene. NahR can specifically bind to salicylic acid to activate the Psal promoter.
Besides, chassis engineering bacteria E. coli is replaced by Tatumella citrea, which can provide phosphorus for crops. The engineering Tatumella citrea can commensalism with crops when crops rhizospheres secrete salicylic acid.
BBa_K3524005 is a bio-sensor (nahR and Psal) for the detection of salicylic acid. We adopted it originally on the chromosome of Pseudomonas Stutzeri. With the appearance of salicylic acid, the protein translated from nahR binds with the Psal promoter and initiates the expression of the enzyme that can utilize the acid as one of the energy sources for Pseudomonas Stutzeri. In our design, we replaced the essential gene with the GFP gene to test our framework. With GFP, the situation is that the edited bacteria can be fluorescent with the existence of salicylic acid.
Contribution
To build up a regulable genetic circuit, we chose the bio-sensor (nahR gene and Psal promoter) for the detection of salicylic acid we adopted is originally on the chromosome of Pseudomonas Stutzeri. With the appearance of salicylic acid, the protein translated form nahR binds with PsaI promoter and initiates the expression of the enhancer green fluorescent protein (EGFP).
Our team has verified this bio-sensor worked well. The future iGEM teams can exchange the EGFP to other functional proteins to make some significant utiles. For example, our team choose an essential gene GAPDH, belongs to Tatumella citrea, which can provide phosphorus for crops[1][2] to replace the EGFP . As a result, in the presence of salicylic acid, GADPH can be expressed, and T. citrea can survive. Since salicylic acid is a root exudate, this genetic circuit that T. citrea can commensalism with crops.
Engineering Success
Build
Results of plasmids construction:
We then used the successfully constructed plasmids to examine the effectiveness of the bio-sensor system.
Some possible factors that led to failure 1. Mistakes in homologous recombination Unable to recombine the right fragments into the vector. 2. Mistakes in PCR During the amplification, the fragments may not be correctly amplified by PCR, so some of the recovered fragments are wrong fragments, which will cause problems when used for vector construction
Test:=
The pTrc99k-NahR and pMW119-Psa1-EGFP plasmids were co-transformed into Tatumella Citrea and screened by Kanamycin resistance and Ampicillin resistance LB solid plates. The co-transformed strains were inoculated into fresh LB medium, cultured at 37°C until OD600 was approximately equal to 0.6. Different concentrations of salicylic acid (dissolved in absolute ethanol) were added. After 24 hours, observations with fluorescence microscope were used to show the regulatory effect of salicylic acid on the PsaI promoter and it was indicated by fluorescence intensity. Data collected：
Learn
1.With different salicylic acid concentration:
We measured the fluorescence intensity to obtain a quantitative result. The data is plotted as the following: the measured fluorescence intensity is divided by the number of cells (OD600) to obtain a homogenized fluorescence intensity. The fluorescence intensity of all samples added with salicylic acid is subtracted from the fluorescence intensity of the background without salicylic acid. It can be seen that from 1 μM to 100 μM salicylic acid, the fluorescence intensity rises sharply. Under the condition of 1000 μM salicylic acid, the fluorescence intensity decreased, which is presumably due to the influence of salicylic acid solvent (ethanol) on cell growth, or other unknown regulatory effects of salicylic acid and NahR.
=2.With different hours:
With the same concentration of salicylic acid, we also measured the change of fluorescence intensity over time. It can be seen from the figure 3. that within 3 to 22 hours after the addition of salicylic acid, the fluorescence intensity increases successively. But it mostly stops increasing at 24 hours.
The mechanism we created did work out well, and the expressions of EGFP protein was detected. This proves that the potential of the bio-sensor system we made is effective,. The two factors we examined are the most convenient, and available test we could conduct. For the concentration of salicylic acid, we found out that at 100 μM, it shows the highst fluorescence intensity. This means that the system works the best in that range of salicylic acid concentration. For the time after addition of salicylic acid, the highst fluorescence unit is shown at 22 hours, the trend is mainly increasing. But after 22 hours, it is decreasing. It is best to leave the mechanism for 15-22 hours after the addition of salicylic acid so it can show the most effective results.
Refernce
[1] Whitelaw, M.a. “Growth Promotion of Plants Inoculated with Phosphate-Solubilizing Fungi.” Advances in Agronomy, 1999, pp. 99–151., doi:10.1016/s0065-2113(08)60948-7.
[2] Bar-Yosef, B., et al. “Pseudomonas Cepacia-Mediated Rock Phosphate Solubilization in Kaolinite and Montmorillonite Suspensions.” Soil Science Society of America Journal, vol. 63, no. 6, 1999, pp. 1703–1708., doi:10.2136/sssaj1999.6361703x.
Edited by Nanjing_high_school,2020.
Usage and Biology
The NYMU-Taipei igem team characterize this inducible as an inducible promoter with GFP response as reporter. The following data was obtained by microplate reader:
The inducible promoter was induced with different concentration(0, 1.50E-07, 6.10E-07, 2.40E-06, 9.80E-06, 3.90E-05, 1.60E-04, 6.20E-04, 1.00E-03) every 30 minutes. We started the induction when the OD600 was 0.6-0.7. The fluorescence response was measured with plate reader.
The inducible promoter was induced with different concentration(0, 1.50E-07, 6.10E-07, 2.40E-06, 9.80E-06, 3.90E-05, 1.60E-04, 6.20E-04, 1.00E-03) every 30 minutes. We started the induction when the OD600 was 0.6-0.7. The fluorescence response was measured with plate reader. The red line indicate the Hill equation(P = Pmax*[SA]^n/([SA]^n+Km^n) ) fit of our dose-response data with error bar showing the standard deviation and the R square value of this fit is 0.99531. "n" indicates the hill coefficient(unitless), "Pmax" indicates the maximal promoter activity, and "K" is the salicylic acid concentration while P equals 1/2*Pmax
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 786
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 77
Illegal NgoMIV site found at 618 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1941