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Team:INSA-Lyon/Project/Stage3/Theory
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| - | <p>In an other way, we | + | <p>In an other way, we wanted to use the combination of the promoter pBad/araC and the promoter LuxR/cI.</p> <br> |
<p>Without arabinose, LuxR and LuxI proteins are synthesized constitutively. LuxI is involved in the synthesis of HomoSerine Lactone (HSL). The fixation of HSL in LuxR protein causes a conformational change of the protein. In this conformation, LuxR protein can interact with the promoter and positively regulate it. This leads to PHB synthesis and when PHB molecules are accumulated enough, they organize themselves in granules. | <p>Without arabinose, LuxR and LuxI proteins are synthesized constitutively. LuxI is involved in the synthesis of HomoSerine Lactone (HSL). The fixation of HSL in LuxR protein causes a conformational change of the protein. In this conformation, LuxR protein can interact with the promoter and positively regulate it. This leads to PHB synthesis and when PHB molecules are accumulated enough, they organize themselves in granules. | ||
Revision as of 17:51, 26 October 2010
Regulation
The system of protein purification needs to be regulated to be fit. In fact, the cell machinery has limited energy sources to cope with the DNA replication, the proliferation, and simultaneously, the granule and the protein synthesis. We need to space out the synthesis of the different other elements.
As described in the article (Banki et al., Protein Science, 2005), we planned to induce first the granule synthesis during 30 hours and then to start the protein synthesis, which can bind directly to the granules already shaped. The rate of synthesis will be better if we stop the granules synthesis at this time. So we need promoters which turn each other ON and OFF.
We thought of two distinct systems in order to have an alternative if one of the promoters would not have been as good as expected.
First, we wanted to use the curli promoter in one of the system. We want to take advantage of the ability of this promoter to be ON at 28°C and OFF at higher temperatures. We looked for an iGEM promoter regulated by temperature, we chose a thermometer RNA. It is switched on above 32°C, allowing the transcription (BBa_K115017).
When the two constructs, functional, are in the same cell, the culture is moved at 28°C so that the PHB granules are formed under the control of Curli promoter. Then, the culture is moved at 37°C allowing the synthesis of the target proteins, activated by the thermometer RNA. At 37°C, the Curli promoter is off and the PHB granules are not synthesized anymore.
In an other way, we wanted to use the combination of the promoter pBad/araC and the promoter LuxR/cI.
Without arabinose, LuxR and LuxI proteins are synthesized constitutively. LuxI is involved in the synthesis of HomoSerine Lactone (HSL). The fixation of HSL in LuxR protein causes a conformational change of the protein. In this conformation, LuxR protein can interact with the promoter and positively regulate it. This leads to PHB synthesis and when PHB molecules are accumulated enough, they organize themselves in granules. The promoter Pbad/araC, without arabinose, is off.
When arabinose is added in the medium, it interacts with Pbad/araC and induces the synthesis of cI protein and phasin-intein construction. cI protein negatively regulates the promoter LuxR/HSL and stops PHB synthesis. Its effect is more efficient than the effect of the LuxR/HSL complex. Therefore, the LuxR/HSL regulated promoter is totally off. During this step, phasin and intein proteins are synthesized and get into PHB granules.
