Difference between revisions of "Team:NEU China B"

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var y = event.clientY - c.getBoundingClientRect().top;
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window.location.href = 'https://2018.igem.org/Team:NEU_China_B/Human_Practices';
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window.location.href = 'https://2018.igem.org/Team:NEU_China_B/Human_Practices';
{
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window.location.href = 'https://2018.igem.org/Team:NEU_China_B/Human_Practices';
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tipsWarpper.y = y;
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tipsWarpper.msg = "Background";
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console.log("img 2");
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tipsWarpper.x = x;
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tipsWarpper.y = y;
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tipsWarpper.valid = true;
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tipsWarpper.msg = "Img 1";
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drawTips(x, y, 50, 50, "Basic Part");
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tipsWarpper.y = y;
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tipsWarpper.msg = "InterLab";
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tipsWarpper.valid = true;
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tipsWarpper.x = x;
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tipsWarpper.y = y;
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tipsWarpper.msg = "Human_Practices";
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tipsWarpper.y = y;
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tipsWarpper.msg = "??????";
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tipsWarpper.valid = true;
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<hr>
 
<hr>

Revision as of 05:33, 17 October 2018

Ruby - Responsive Corporate Tempalte

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Abstract


The role of L-lactate is not always beneficial for the yogurt fermentation due to excessive L-lactate can provide an optimized growth condition for yeast and mold. Therefore, it is important to detect the concentration of L-lactate. Acid-base titration is a common method for it, but this method is complicated and time-consuming. In order to monitor L-lactate quickly and conveniently, we designed a biosensor for detecting L-lactate concentration by using the lldPRD L-lactate operon and QS system in E. coli. One of these parts is able to induce the lldPRD genes expression, LuxS protein, in the presence of L-lactate. LuxS protein catalyzes the SAM cycle and produces a small signaling molecule AI-2 that motivates our second part promoter of LsrA&K to promote GFP expression. The optic fiber is able to detect the GFP signal and convert it into current. Simultaneously, the entire device container will be made by 3D printing.