Difference between revisions of "Team:ECNUAS/Description"

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<div class="column full_size judges-will-not-evaluate">
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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2021.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2021.igem.org/Judging/Awards"> award listed below</a>. </p>
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<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2021.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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<h1>Project Description </h1>
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<h3>Bronze Medal Criterion #3</h3>
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<p>Describe how and why you chose your iGEM project.
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<br><br>
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Please see the <a href="https://2021.igem.org/Judging/Medals">2021 Medals Page</a> for more information.
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</p>
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<div class="column two_thirds_size">
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<h3>What should this page contain?</h3>
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<ul>
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<li> A clear and concise description of your project.</li>
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<li>A detailed explanation of why your team chose to work on this particular project.</li>
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<li>References and sources to document your research.</li>
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<li>Use illustrations and other visual resources to explain your project.</li>
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</ul>
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<div class="column third_size" >
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<div class="highlight decoration_A_full">
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<h3>Inspiration</h3>
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<p>See how other teams have described and presented their projects: </p>
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<ul>
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<li><a href="https://2019.igem.org/Team:Leiden/Description">2019 Leiden</a></li>
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<li><a href="https://2019.igem.org/Team:ITESO_Guadalajara/Description">2019 ITESO Guadalajara</a></li>
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<li><a href="https://2020.igem.org/Team:Technion-Israel/Description">2020 Technion Israel</a></li>
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<li><a href="https://2020.igem.org/Team:Botchan_Lab_Tokyo/Description">2020 Botchan Lab Tokyo</a></li>
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<li><a href="https://2020.igem.org/Team:St_Andrews/Description">2020 St Andrews</a></li>
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<li><a href="https://2020.igem.org/Team:MIT/Description">2020 MIT</a></li>
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</ul>
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</div>
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</div>
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<div class="column two_thirds_size" >
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<h3>Advice on writing your Project Description</h3>
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<p>
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We encourage you to put up a lot of information and content on your wiki, but we also encourage you to include summaries as much as possible. If you think of the sections in your project description as the sections in a publication, you should try to be concise, accurate, and unambiguous in your achievements. Your Project Description should include more information than your project abstract.
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</p>
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</div>
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<div class="column third_size">
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<h3>References</h3>
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<p>iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you thought about your project and what works inspired you.</p>
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    <title>ECNUAS</title>
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        <div class="sub-title">Project Description</div>
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        <div class="article-title">I. Background</div>
 +
        <div class="article-content" style="text-indent: 30px;">With the development of science and technology,
 +
            agriculture becomes the most crucial domain. It plays a vast role in the national construction and becomes
 +
            the basis impetus to develop the whole society. Agriculture is not only an indicator of the strength of a
 +
            country, but also shows the living conditions of the people.</div>
 +
        <div class="article-content" style="text-indent: 30px;">Agricultural chemicals are the indispensable part of the
 +
            development of agriculture. But there are still many problems about the agricultural chemicals. So this
 +
            year, our title is to test the content of cyanuric acid in atrazine.</div>
 +
        <div class="article-content" style="text-indent: 30px;">Atrazine is one of the most widely used herbicides in
 +
            the world. It is cheap and also effective on many crops. But it still has negative effects. Atrazine will
 +
            leave a residue in the soil called cyanuric acid, it has endocrine disruption, genotoxicity, reproductive
 +
            toxicity and other harm to mammals. Figure 1 shows the process of cyanuric acid accumulation. So we are
 +
            going to design portable instrument to detect the content of residue in herbicide. lt should be cheap and
 +
            convenient.</div>
 +
        <div class="img-wrap no-margin">
 +
            <img src="https://static.igem.org/mediawiki/2021/6/67/T--ECNUAS--Project_Description01.jpg" alt="">
 +
            <span>Figure 1. The process of Atrazine biodegradation.</span>
 +
        </div>
 +
        <div class="article-title">II. General concept </div>
 +
        <div class="article-content" style="text-indent: 30px;">On the principle of this sensor. By combining cyanuric
 +
            acid with a specific plasmid, it activates the promoter in the body, which activates the downstream gene
 +
            ,and induces gene expression to show the signs of fluorescence. The content of cyanuric acid is detected by
 +
            detecting the fluorescence concentration. Our general concept is shown in Figure 2.</div>
 +
        <div class="img-wrap no-margin">
 +
            <img src="https://static.igem.org/mediawiki/2021/a/a7/T--ECNUAS--Project_Description02.jpg" alt="">
 +
            <span>Figure 2. Genetic design of our biosensor</span>
 +
        </div>
 +
        <div class="article-content" style="text-indent: 30px;">So what we have to do is to combine the reporter gene
 +
            amil_GFP and pUC57_mini_Pprovoin5 to obtain plasmid B. After that, the two plasmids, plasmid B
 +
            (pUC57_mini_Pprovoin5_amilGFP), and plasmid A (pUC57_mini_Ptat_AtzR) are extracted and purified together to
 +
            be transformed into DH5a to obtain the target bacteria C. After screening by two antibiotics (kana&amp)
 +
            medium, positive transformant - bacteria C would be further cultured and used to detect cyanuric acid.</div>
 +
        <div class="article-content" style="text-indent: 30px;">Cell-free gene expression (CFE) has recently emerged as
 +
            a powerful strategy for rapid, field-deployable diagnostics for nucleic acids and chemical contaminants.One
 +
            reason for this success is that CFE reactions minimize many of the constraints of whole-cell sensors,
 +
            including mass transfer barriers, cytotoxicity, genetic instability, plasmid loss, and the need for
 +
            biocontainment. In addition, CFE reactions can be stabilized through freeze-drying and then are activated
 +
            upon rehydration, enabling the biosensors to be used outside the laboratory at the point of sampling in the
 +
            field.</div>
 +
        <div class="article-content" style="text-indent: 30px;">Therefore, we would introduce the concept of CFE into
 +
            our biosensor in order to produce a portable CFE Atrazine biosensor kit that could be easily used by normal
 +
            people in daily life outside the laboratory.</div>
 +
        <div class="article-title">III. Expected results</div>
 +
        <div class="article-content" style="text-indent: 30px;">1. Construct the gene system that can detect cyanuric
 +
            acid.</div>
 +
        <div class="article-content" style="text-indent: 30px;">2. Design cell-free Atrazine biosensor, and test its
 +
            function.</div>
 +
        <div class="article-title">Reference</div>
 +
        <div class="article-content">1. Zhang X, Huang Q, Zhao ZZ, Xu X, Li S, Yin H, Li L, Zhang J, Wang R. An Eco- and
 +
            User-Friendly Herbicide. J Agric Food Chem. 2019 Jul 17;67(28):7783-7792. doi: 10.1021/acs.jafc.9b00764.
 +
            Epub 2019 Jul 3. PMID: 31267752. </div>
 +
        <div class="article-content">2. Zhu M, Wang L, Wang Y, Zhou J, Ding J, Li W, Xin Y, Fan S, Wang Z, Wang Y.
 +
            Biointeractions of Herbicide Atrazine with Human Serum Albumin: UV-Vis, Fluorescence and Circular Dichroism
 +
            Approaches. Int J Environ Res Public Health. 2018 Jan 11;15(1):116. doi: 10.3390/ijerph15010116. PMID:
 +
            29324720; PMCID: PMC5800215.</div>
 +
        <div class="article-content">3. Silverman, Adam D., et al. "Deconstructing cell-free extract preparation for in
 +
            vitro activation of transcriptional genetic circuitry." ACS synthetic biology 8.2 (2018): 403-414.</div>
 +
        <div class="article-content">4. 1.Liu, Xiangyang, et al. "Design of a transcriptional biosensor for the
 +
            portable, on-demand detection of cyanuric acid." ACS synthetic biology 9.1 (2019): 84-94. </div>
 +
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Latest revision as of 16:15, 19 October 2021

ECNUAS

Project Description
I. Background
With the development of science and technology, agriculture becomes the most crucial domain. It plays a vast role in the national construction and becomes the basis impetus to develop the whole society. Agriculture is not only an indicator of the strength of a country, but also shows the living conditions of the people.
Agricultural chemicals are the indispensable part of the development of agriculture. But there are still many problems about the agricultural chemicals. So this year, our title is to test the content of cyanuric acid in atrazine.
Atrazine is one of the most widely used herbicides in the world. It is cheap and also effective on many crops. But it still has negative effects. Atrazine will leave a residue in the soil called cyanuric acid, it has endocrine disruption, genotoxicity, reproductive toxicity and other harm to mammals. Figure 1 shows the process of cyanuric acid accumulation. So we are going to design portable instrument to detect the content of residue in herbicide. lt should be cheap and convenient.
Figure 1. The process of Atrazine biodegradation.
II. General concept
On the principle of this sensor. By combining cyanuric acid with a specific plasmid, it activates the promoter in the body, which activates the downstream gene ,and induces gene expression to show the signs of fluorescence. The content of cyanuric acid is detected by detecting the fluorescence concentration. Our general concept is shown in Figure 2.
Figure 2. Genetic design of our biosensor
So what we have to do is to combine the reporter gene amil_GFP and pUC57_mini_Pprovoin5 to obtain plasmid B. After that, the two plasmids, plasmid B (pUC57_mini_Pprovoin5_amilGFP), and plasmid A (pUC57_mini_Ptat_AtzR) are extracted and purified together to be transformed into DH5a to obtain the target bacteria C. After screening by two antibiotics (kana&amp) medium, positive transformant - bacteria C would be further cultured and used to detect cyanuric acid.
Cell-free gene expression (CFE) has recently emerged as a powerful strategy for rapid, field-deployable diagnostics for nucleic acids and chemical contaminants.One reason for this success is that CFE reactions minimize many of the constraints of whole-cell sensors, including mass transfer barriers, cytotoxicity, genetic instability, plasmid loss, and the need for biocontainment. In addition, CFE reactions can be stabilized through freeze-drying and then are activated upon rehydration, enabling the biosensors to be used outside the laboratory at the point of sampling in the field.
Therefore, we would introduce the concept of CFE into our biosensor in order to produce a portable CFE Atrazine biosensor kit that could be easily used by normal people in daily life outside the laboratory.
III. Expected results
1. Construct the gene system that can detect cyanuric acid.
2. Design cell-free Atrazine biosensor, and test its function.
Reference
1. Zhang X, Huang Q, Zhao ZZ, Xu X, Li S, Yin H, Li L, Zhang J, Wang R. An Eco- and User-Friendly Herbicide. J Agric Food Chem. 2019 Jul 17;67(28):7783-7792. doi: 10.1021/acs.jafc.9b00764. Epub 2019 Jul 3. PMID: 31267752.
2. Zhu M, Wang L, Wang Y, Zhou J, Ding J, Li W, Xin Y, Fan S, Wang Z, Wang Y. Biointeractions of Herbicide Atrazine with Human Serum Albumin: UV-Vis, Fluorescence and Circular Dichroism Approaches. Int J Environ Res Public Health. 2018 Jan 11;15(1):116. doi: 10.3390/ijerph15010116. PMID: 29324720; PMCID: PMC5800215.
3. Silverman, Adam D., et al. "Deconstructing cell-free extract preparation for in vitro activation of transcriptional genetic circuitry." ACS synthetic biology 8.2 (2018): 403-414.
4. 1.Liu, Xiangyang, et al. "Design of a transcriptional biosensor for the portable, on-demand detection of cyanuric acid." ACS synthetic biology 9.1 (2019): 84-94.