Difference between revisions of "Team:JiangnanU China/Collaborations"
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| − | <div class=" | + | <div class="fm_22"><b>We iGEMers dedicate to utilizing synbio methodology for amazing applications, though we indeed have a long way to go and thankfully we won’t walk alone. Here, we’d like to review all the collaboration with other teams. The team Fudan inspired us with a paper about ANN prediction, which greatly helped us in our model. Meanwhile, the team OUC-China has identified phage infection in their lab with our phage-free booklet and we together improved it with their feedback. What’s more, together with team Jilin_China, we organized a Meetup with other four teams, and then we helped them with their strength measurement of Anderson promoter family. |
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Revision as of 16:54, 21 October 2019
Collaboration
We iGEMers dedicate to utilizing synbio methodology for amazing applications, though we indeed have a long way to go and thankfully we won’t walk alone. Here, we’d like to review all the collaboration with other teams. The team Fudan inspired us with a paper about ANN prediction, which greatly helped us in our model. Meanwhile, the team OUC-China has identified phage infection in their lab with our phage-free booklet and we together improved it with their feedback. What’s more, together with team Jilin_China, we organized a Meetup with other four teams, and then we helped them with their strength measurement of Anderson promoter family.
OUC-China
Phage infection occurs accidentally not only in the fermentation factories but also in the lab, and it
might get worse and worse without appropriate treatment. Therefore, we’d like to dedicate a booklet
about prevention, identification, and control of bacteriophage infection. By coincidence, we met team
OUC-China in the CCiC whose strain died abnormally in the shaking flask. Having heard our anti-phage
project, they wanted to figure out whether they encountered a phage infection. We sent the script of our
booklet to them, and they easily checked that the death strain was not caused by phage. Meanwhile, with
the feedback of their identification, we together improved the PICP (Prevention, Identification, Control
of Phage) booklet（链接）, allowing more teams to maintain a phage-free lab environment.
Fudan
Our team achieved an anti-phage strategy against infection in different infection periods. Therefore,
it’s essential to control the promoter strength for the potential leakage or inclusion body problems.
Fortunately, team Fudan inspired us that it might be interesting to use ANN for promoter strength
prediction, which will save us a lot of time for test hundreds of promoters one by one in experiment.
Then, they gave us a paper1 about the similar prediction method, allowing us to establish an ANN
promoter strength prediction model of our own. With their help we can select more suitable promoters
designed by computer simulation.
Jilin
1. Measurement
Team Jilin_China has measured the relative promoter strength of the P59 to Anderson promoter family, however the measurement results based on fluorescence different due to various experiment conditions. Therefore, they’d like to know whether they could repeat the experiment and get the same result in different labs. So they invited us to measure the 6 parts in our lab. Jilin_China have sent BBa_J23119、BBa_J23104、BBa_J23108、BBa_J23105、BBa_J23114 and P59 promoters to us for measurement, and the results are similar at 485 nm (excitation) / 530 nm (emission). Click here for more Jinlin_China measurement data.
Team Jilin_China has measured the relative promoter strength of the P59 to Anderson promoter family, however the measurement results based on fluorescence different due to various experiment conditions. Therefore, they’d like to know whether they could repeat the experiment and get the same result in different labs. So they invited us to measure the 6 parts in our lab. Jilin_China have sent BBa_J23119、BBa_J23104、BBa_J23108、BBa_J23105、BBa_J23114 and P59 promoters to us for measurement, and the results are similar at 485 nm (excitation) / 530 nm (emission). Click here for more Jinlin_China measurement data.
Figure 1. Relative fluorescence (fluorescence/OD(sub)600(subed)) intensity at emission wavelength 528 nm under excitation wavelength 485 nm of each promoter measured by (A) Jilin_China and (B) JiangnanU_China over time.
We aimed to construct a phage-resistant E. coli strain which can be applied to industrial
fermentation production in the future, so we need to verify experiment under same protocol condition
in different laboratories, thus we invited Jilin_China to help to test whether E. coli will use a
large amount of energy to express anti-phage parts, which greatly affects their own growth. The grey
relation analysis they made will be applied to our model to select the anti-phage part that has the
least impact on bacterial growth.
