Team:Brasil-SP/Project/ResponseModule

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<h3 align="center">Response Module</h3>
<h3 align="center">Response Module</h3>
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<p><div align="justify">Blood sample from a person with low levels of circulating Cystatin C triggers the expression of the reporter gene GFP in the biodetector, resulting in fluorescent signals. On the other hand, blood sample with high levels of Cystatin C does not induce the production of GFP, resulting in absent of fluorescence. Our test is carried out with patients plasma (without blood cells) filtered through a microfluidics device. In this device, our modified Bacillus subtilis will stored as spores, which are activated by rich medium (Luria-Bertani [LB]) before being used in the device. In order to induce the spore formation, the bacteria are incubated in a minimal nutrient medium (Difco Sporulation Medium [DSM]).</div></p>
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<p><div align="justify">A blood sample from a healthly person, which has low levels of circulating Cystatin C, when in contact with B. subtilis cells triggers the expression of the reporter gene GFP in the biodetector, resulting in fluorescent signals. However, when a blood sample from a sickness person, wich has high levels of circulating Cystatin C, contacts B. subtilis cells it doesn’t induce the production of GFP, generating a negative signal.</p>
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<p>The GFP was chosen because the facility to found in our laboratory, we could use another reporter gene, like YFP (yellow fluorescence protein) or RFP (red florescence protein) for exemple.</p>
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<p>All the blood samples will be filtered through a microfluidics device, extracting just the plasma, that will be analyzed after it contacts with our modified B. subtilis.</p>
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<p>In this device, we will store B. subtilis as spores, which are activated by rich medium (Luria-Bertani [LB]) before being used in the device. In order to induce the spore formation, the bacteria are incubated in a minimal nutrient medium (Difco Sporulation Medium [DSM]).
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Revision as of 22:18, 11 October 2014

Response Module

A blood sample from a healthly person, which has low levels of circulating Cystatin C, when in contact with B. subtilis cells triggers the expression of the reporter gene GFP in the biodetector, resulting in fluorescent signals. However, when a blood sample from a sickness person, wich has high levels of circulating Cystatin C, contacts B. subtilis cells it doesn’t induce the production of GFP, generating a negative signal.

The GFP was chosen because the facility to found in our laboratory, we could use another reporter gene, like YFP (yellow fluorescence protein) or RFP (red florescence protein) for exemple.

All the blood samples will be filtered through a microfluidics device, extracting just the plasma, that will be analyzed after it contacts with our modified B. subtilis.

In this device, we will store B. subtilis as spores, which are activated by rich medium (Luria-Bertani [LB]) before being used in the device. In order to induce the spore formation, the bacteria are incubated in a minimal nutrient medium (Difco Sporulation Medium [DSM]). .