Difference between revisions of "Team:Jilin China/Collaborations"

2.NPU-China

We cooperated with NPU-China this year, a team from Northwestern Polytechnical University in China.

Our team helped NPU-China characterized two parts because their team was short of staff to characterize all parts. The two parts are coding sequences of Saccharomyces cerevisiae mitochondrial genome. The cob codes cytochrome oxidase b which is the composition of the electron transport chain. And the introns of cob were all deleted. The var1 codes ribosomal protein. We helped them measure the growth curve to verify if the two parts are toxic to cells.

Figure 3. The figure’s horizontal axis represents the time, and the vertical axis represents OD value. The blue line is the growth curve of Blank, the orange line is the growth curve of cob and the gray line is the growth curve of var1.

As the results shows, the two genes almost don’t have influence on bacterial growth. The result indicated that the two genes are not toxic to cells.

NPU-China also helped us a lot. We designed hundreds of RNA-based thermosensors this year. We need to get their melting temperature, intensity and sensitivity. We have measured some heat-inducible RNA-based thermosensors by ourselves. Nevertheless, we know that at different laboratories and under different experimental conditions, the experimental results could differ. To ensure the accuracy of our experimental results, we sent 5 samples to NPU-China. They helped us measure sfGFP expression at different temperatures. (The 5 samples: RT1-4, RT1-33, K2541003, K2541004, K2541010 ).

Figure 4. The bar colors blue, orange and gray represent the temperatures 31, 35 and 39°C, respectively. The height of the bars corresponds to the normalized fluorescence.

As shown in figure 4, the fluorescence intensity of K2541003, K2541004 and K2541010 increase with elevated temperatures. While the fluorescence intensity of RT1-4 and RT1-33 don’t increase with elevated temperatures. This is consistent with our own measurement results (figure 5).

Figure 5. Comparison of measurement results between Jilin_Chian and NPU-China. K2541003_J, K2541004_J, K2541010_J are the measurement results of Jilin_China, and K2541003_N, K2541004_N, K2541010_N are the measurement results of NPU-China. The height of the bars corresponds to the normalized fluorescence.

We are very grateful to NPU-China for helping us with this experiment.

3.NEU_China_A

This year our team and NEU_China_A sent experimental materials in the Distribution Kit each other. These materials greatly helped both sides. We sent Nitrate reporter: PyeaR-GFP composite (BBa_K381001) and Test Device 4 for interlab (BBa_J364007) to them. PyeaR is a nitrate and nitrite sensitive promoter and NEU_China_A replaced GFP with a blue protein. The promoter PyeaR expressed the blue protein under the induction of nitric oxide. So they can use this part (BBa_K381001) to detect nitric oxide. NEU_China_A sent superfolder GFP (BBa_I746916) to us for part improvement. This year, We used sfGFP_optimism (BBa_K2541400) as an improvement part. Compared with iGEM superfolder GFP (BBa_I746916), it has no BbsI restriction site and can be used for Golden Gate assembly. So we used the part (BBa_I746916) from NEU_China_A to verify that it contains BbsI restriction site.

4.TUST_China

This year, we built a friendly relationship with TUST_China. During the meet-up in NKU and CCiC, we exchangd ideas about projects.

TUST_China focused on tetracycline detecting and degradation this year, so they would like to collect polluted water in most places in China. There is a river called Yongchun River which is closed to several bio-product factories near Jilin university. We provided a water sample from Yongchun River to TUST_China so they can detect antibiotic pollution to enrich their projects.

Back again to our SynRT, we used sfGFP_optimism as our reporter protein in the measurement device. Due to the high quality of sfGFP_optimism, we would standardize it and compete for best basic part. However, after several trials, we failed in ligation, then we decided to request TUST_China to help us. We sent them our plasmid for fluorescence measurement and primers for the construction of sfGFP_optimism. Luckily, they finished the construction for us and provided useful suggestions in ligation: you can increase the ratio of insert to vector, from 3:1 to 10:1. After the construction, they sequenced and sent it to us, which was correct.

Figure 6. Each gel pore reprenents 1kb marker, original plasmid, plasmid + EcoRI, plasmid + PstI and plasmid + EcoRI + PstI.

We really appreciated it that they helped us in such an important experiment. Hoping that we can build long-time friendship and work for synthetic biology.

5.XJTU-CHINA

This year we collaborated with XJTU-CHINA from Xi'an Jiaotong University and we helped them measure fluorescence, so they could get the relation between the concentration of psicose and fluorescence intensity. Furthermore, the relation between different concentration of psicose and pPsi promoter activation efficiency was obtained. We helped them verify that their Device A (figure 7) works.

Figure 7. The plasmid backbone of device A.

PsiR is a repressor protein that binds to the pPsi promotor, rendering it inactive. Psicose and PsiR repressor proteins are combined to form a negative regulation induction system (similar to the IPTG and LacI), and psicose is added to the system to induce EGFP expression.

When they measured the Device A, the results were not quite as expected. They suspected that both LB culture medium and psicose in the system may probably make the bacteria grow. What’s more, the amount of psicose solution added to the system is not consistent, so different osmotic pressure may lead different growth conditions of bacteria. When our team did the measurement, we cultured the bacteria to OD=0.6 and then re-suspended the bacterial precipitation with MM culture medium. We cultured the bacteria with different concentration of psicose and measured the Abs₆₀₀ and fluorescence intensity once per hour.

The results are as follows:

Figure 8. Abs₆₀₀ and fluorescence intensity once per hour in different psicose solution.

From the above results, we can see that with the increasing of psicose concentration, the fluorescence intensity increases, which basically accord with their assumption.

XJTU-CHINA has also helped us a lot. For our experimental design this year, we have lots of RNA-based thermosensors to submit to the part registry, which is a huge and challenging task. If we use the traditional construction method, the time and cost of constructing these parts will be a huge problem for us. Fortunately, we met XJTU-CHINA at the CCiC conference, and they would like to help us design an intermediate device for constructing standardized parts.

In combination with their own experience in using Golden Gate assembly, they inserted an only 60bp DNA fragment into pSB1C3 plasmid. The DNA fragment contains BsaI restriction site. Golden Gate assembly will enable fast and efficient parts construction. They sent the device to us as quickly as possible so we could complete the construction of about 50 parts before deadline, which greatly reduced our workload, improved our experimental efficiency, and solved our problem.

Figure 9. The intermediate device for constructing standardized parts.

The plasmid was confirmed to be constructed as expected by enzyme digestion (original plasmid, BsaI single digestion, and EcoRI and PstI double digestion). The agarose gel electrophoresis (figure 10) showed that these enzyme-digested products were all normal, and the brightness was also normal (5bp and 60bp fragment cannot be fully displayed on the electropherogram due to its length is very short). Furthermore, they sequenced it. The sequencing results showed that the ligation of plasmid and insert was correct, and the sequencing results were of good quality.

Figure 10. Each gel pore reprenents 1kb marker, original plasmid, plasmid + BsaI and plasmid + EcoRI + PstI.

In our follow-up experiments, the constructing device was fully applicable, and the success rate exceeded our expectation, which greatly reduced our workload. We constructed all basic parts before deadline.

After this cooperation, we have established a deep friendship with XJTU-CHINA. We often discuss some problems encountered in Golden Gate assembly. We also discuss some questions about modeling.

6.ShanghaiTech

This year, we cooperated with Shanghai Tech. They helped us measure heat-inducible RNA-based thermosensors in cell-free protein synthesis (CFPS). CFPS is the production of protein using biological machinery in a cell-free system, that is, without the use of living cells. According to recent article reported, cell-free system is more sensitive to detect RNA behavior than traditional measurement method. With the help of CFPS, we can get more precise experimental results in vitro.

For cell-free measurement, we construct a new measurement device with T7 promotor. Then we sent ten Glycerin bacteria and plasmid to them. They express ten plasmids in cell-free system under three temperature conditions: 29°, 37°and 42°. Then they read the relative fluorescence intensity by microplate reader. Finally, we received their data and computed the fold-change of the response in the given temperature range.

Figure 11. Fold change of the heat-inducible RNA-based theromsensors. Each plot represents an individual theromsensor. The purple horizontal represents the fold change of positive control. The purple vertical represents the normalized fluorescence of negative control.

As these results show, the heat-inducible RNA thermosensor we designed can work in CFPS. The fluorescence value increases with temperature elevated. Besides, the difference in fluorescence intensity and the rate of increase points to the diversity in thermosensor response.

We appreciate Shanghai Tech to help us measure the heat-inducible RNA-based theromsensos. Hoping that we can maintain the long-time friendship and collaborate with each other in the future.