Difference between revisions of "Team:NCKU Tainan/Improve"
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| − | + | After analyzing the experiment result for our pH-sensing system, we have concluded that we should try to improve one of our pH-sensitive promoters, P<sub>gadA</sub>. We found out that although P<sub>gadA</sub> can be induced under neutral and weak acidic condition. But the fluorescent intensity is too slow to be observed. We planned to increase the fluorescent intensity and shorten the time interval of induction. We thus add a RiboJ sequence at the downstream of the P<sub>gadA</sub>. | |
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Revision as of 15:09, 16 October 2018
Improve
Part Improvement
After analyzing the experiment result for our pH-sensing system, we have concluded that we should try to improve one of our pH-sensitive promoters, PgadA. We found out that although PgadA can be induced under neutral and weak acidic condition. But the fluorescent intensity is too slow to be observed. We planned to increase the fluorescent intensity and shorten the time interval of induction. We thus add a RiboJ sequence at the downstream of the PgadA.
Based on our research, RiboJ first described as it is an insulator in genetic construct but there has no any data shown this insulation effected the downstream genetic parts. In 2018, there was a team has proved that RiboJ could increase the expression of the downstream gene and they are from collage of William and Mary. Hence, our team, NCKU_Tainan has decided to enhance the expression of promoter gadA by adding a gene, riboJ at the downstream of promoter gadA.
For the function determination, we have measured the fluorescent density of the plasmid with and without RiboJ in different pH environment. We incubated the bacteria in pH adjacent M9 medium and measure the fluorescent intensity (absorbance: 480nm, excitation: 510 nm) in a short period of time.
Experiment Result
Figure 1: The fluorescent intensity expressed by PgadA of 24 hours in four different pH value of M9 medium.
Figure 2: The fluorescent intensity expressed by PgadA-RiboJ of 24 hours in four different pH value of M9 medium.
Figure 3: The fluorescent intensity between PgadA and PgadA-RiboJ in pH 6 and pH 7.
Conclusion
Based on our functional determination test results, the improvement that we did has succeeded. As you could see, E. coli that carrying promoter gadA with RiboJ (Figure 2) has the higher fluorescent level than the E. coli that carrying promoter gadA but without RiboJ (Figure 1). From our experiment result, we also could conclude that RiboJ not only can enhance expression but it could also strengthen the signal and increase the specificity of the downstream gene of it. So, our team has successfully improve the part of promoter gadA with the addition of RiboJ gene.