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

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                    <b>Collaboration</b>
 
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                <b>OUC-China</b>
 
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                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.
 
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                <b>Fudan</b>
 
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                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.
 
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                    <b>Jilin</b>
 
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                    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) / 528 nm (emission).
 
                    Click <a href="https://2019.igem.org/Team:Jilin_China/Collaborations">here</a>for more Jilin_China measurement
 
                    data.
 
   
 
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                    Figure 1. Relative fluorescence (fluorescence/OD(sub)600(subed)) intensity at emission wavelength 528 nm
 
                    under xcitation wavelength 485 nm of each promoter measured by (A) Jilin_China and (B) JiangnanU_China over time.</div><br/>
 
 
 
 
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                    We aimed to construct a phage-resistant <i>E. coli</i> strain which can be applied to industrial
 
                    fermentation production in the future, so we needed to verify experiment under the same protocol condition
 
                    in different laboratories, thus we invited Jilin_China to help to test whether <i>E. coli</i> would use a
 
                    large amount of energy to express anti-phage parts, which greatly affected their own growth. The curve of <i>E. coli</i> growth they made was applied to our model to select the anti-phage part that had the
 
                    least impact on bacterial growth.
 
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Revision as of 15:52, 21 October 2019