Team:Evry/Project/Compounds/Sensing
From 2014.igem.org
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<li><b><u><h5>Advantages of bio-sensing</h5></u></b> <br> | <li><b><u><h5>Advantages of bio-sensing</h5></u></b> <br> | ||
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In response of those recent awareness, different systems of detection have been developed. <br> | In response of those recent awareness, different systems of detection have been developed. <br> | ||
But with the approach of bio-sensing, we develop tool which are able to detect a pollutant with a very high efficiency, and with a great specificity. <br> | But with the approach of bio-sensing, we develop tool which are able to detect a pollutant with a very high efficiency, and with a great specificity. <br> | ||
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So besides having effective and cheap systems, biosensors are totally biological and non-polluting tools.<br> | So besides having effective and cheap systems, biosensors are totally biological and non-polluting tools.<br> | ||
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<li><b><u><h5>Systems</h5></u></b> <br> | <li><b><u><h5>Systems</h5></u></b> <br> | ||
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+ | <p> | ||
To devellop our tools, we search in the scientific litterature, some natural systems based on promoters inducibles by our compounds of interest. It's often promoters wich allow the expression of a set of genes which correspond to the cell's response to the compound.<br> | To devellop our tools, we search in the scientific litterature, some natural systems based on promoters inducibles by our compounds of interest. It's often promoters wich allow the expression of a set of genes which correspond to the cell's response to the compound.<br> | ||
- | For phenols, an a set of genes called Dmp operon in <i>Pseudomonas CF600 </i> is able to degrade phenol with the aim to produce acetyl CoA, and use these compounds as an energy source. <br> | + | For phenols, an a set of genes called Dmp operon in <i>Pseudomonas CF600 </i> is able to degrade phenol with the aim to produce acetyl CoA, and use these compounds as an energy source. <br></p> |
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<FONT color=#003333><b><u>Figure6: </u></b>The catabolic pathway for degradation of phenol and the organization of Dmp operon. (Powlowski J, Shingler V., 1994)</font><br> | <FONT color=#003333><b><u>Figure6: </u></b>The catabolic pathway for degradation of phenol and the organization of Dmp operon. (Powlowski J, Shingler V., 1994)</font><br> | ||
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The transcription of this operon is regulated by the DmpR regulator element which bind phenol and activate the transcription of the phenol hydroxylase promoter by allowing the fixation of the RNA polymerase (more information, see the section <a href="https://2014.igem.org/Team:Evry/Biology/Sensors">Sensors</a>). <br> | The transcription of this operon is regulated by the DmpR regulator element which bind phenol and activate the transcription of the phenol hydroxylase promoter by allowing the fixation of the RNA polymerase (more information, see the section <a href="https://2014.igem.org/Team:Evry/Biology/Sensors">Sensors</a>). <br> | ||
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Aerobic bacteria which live in oxygenated environments and anaerobic bacteria which live in oxygen free environments such as aquatic sediments. They use different mechanisms, aerobes attack PCBs oxidatively, breaking open the carbon ring and destroying the compounds. Anaerobes, on the other hand, leave the biphenyl rings intact while removing the chlorines. <br> | Aerobic bacteria which live in oxygenated environments and anaerobic bacteria which live in oxygen free environments such as aquatic sediments. They use different mechanisms, aerobes attack PCBs oxidatively, breaking open the carbon ring and destroying the compounds. Anaerobes, on the other hand, leave the biphenyl rings intact while removing the chlorines. <br> | ||
The evidence in the literature suggests that PCDD/F compounds are subject to biodegradation in the environment as part of the natural chlorine cycle.<br> | The evidence in the literature suggests that PCDD/F compounds are subject to biodegradation in the environment as part of the natural chlorine cycle.<br> | ||
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- | <br><div align="center"> | + | <br><div align="center"><p> |
<img src="https://static.igem.org/mediawiki/2014/8/81/PathwayPCB.jpg" alt="text to print if image not found" /><br> | <img src="https://static.igem.org/mediawiki/2014/8/81/PathwayPCB.jpg" alt="text to print if image not found" /><br> | ||
- | <FONT color=#003333><b><u>Figure7: </u></b>The catabolic pathway for degradation of biphenyl by aerobic bacteria and the organization of bph gene cluster (Kensuke F., Hidehiko F., 2008) .</font><br> | + | <FONT color=#003333><b><u>Figure7: </u></b>The catabolic pathway for degradation of biphenyl by aerobic bacteria and the organization of bph gene cluster (Kensuke F., Hidehiko F., 2008) .</font><br></p> |
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The transcription of this set of genes is regulated by bphR2 wich bind PCBs and activate the transcription of pbhR1 gene (more information, see the section <a href="https://2014.igem.org/Team:Evry/Biology/Sensors">Sensors</a>). <br> | The transcription of this set of genes is regulated by bphR2 wich bind PCBs and activate the transcription of pbhR1 gene (more information, see the section <a href="https://2014.igem.org/Team:Evry/Biology/Sensors">Sensors</a>). <br> | ||
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For nitrites, degradation pathway are very well known because they belong to the nitrite cycle. And for heavy metals, a lot of operon which allows the cell's tolerance to these compounds exist and have promoter answering specifically to the metal concentration. <br> | For nitrites, degradation pathway are very well known because they belong to the nitrite cycle. And for heavy metals, a lot of operon which allows the cell's tolerance to these compounds exist and have promoter answering specifically to the metal concentration. <br> | ||
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<li><b><u><h5>Futur : degradation?</h5></u></b> <br> | <li><b><u><h5>Futur : degradation?</h5></u></b> <br> | ||
<br><div align="justify"> | <br><div align="justify"> | ||
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Sensing's constructions are very simple and easy to realize. But in a larger framework we can imagine one day be able to clone all the enzymes of the degradation pathway of phenol and PCBs in our bacteria. In fact we can create, more than a sensor system based on sponge, a complete filtrating system which can not only sense pollutants, but totally remove them. <br> | Sensing's constructions are very simple and easy to realize. But in a larger framework we can imagine one day be able to clone all the enzymes of the degradation pathway of phenol and PCBs in our bacteria. In fact we can create, more than a sensor system based on sponge, a complete filtrating system which can not only sense pollutants, but totally remove them. <br> | ||
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<FONT color=#003333><b><u>Figure8: </u></b>Nitrogen cycle.</font><br> | <FONT color=#003333><b><u>Figure8: </u></b>Nitrogen cycle.</font><br> | ||
</div> | </div> | ||
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Unfortunately, when we talk about heavy metals we talk about atoms which cannot just be degraded by a biological pathway. But we can imagine some ways of accumulation of these elements in bacteria that we can remove and treated after like chemical waste.<br> | Unfortunately, when we talk about heavy metals we talk about atoms which cannot just be degraded by a biological pathway. But we can imagine some ways of accumulation of these elements in bacteria that we can remove and treated after like chemical waste.<br> | ||
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Revision as of 18:37, 13 October 2014
The sensing approach
Advantages of bio-sensing
In response of those recent awareness, different systems of detection have been developed.
But with the approach of bio-sensing, we develop tool which are able to detect a pollutant with a very high efficiency, and with a great specificity.
Biological elements necessary to built those tools have a very low cost, are very easy to obtain and the assembling is quite easy and don’t emit any pollutant.
So besides having effective and cheap systems, biosensors are totally biological and non-polluting tools.
Systems
To devellop our tools, we search in the scientific litterature, some natural systems based on promoters inducibles by our compounds of interest. It's often promoters wich allow the expression of a set of genes which correspond to the cell's response to the compound.
For phenols, an a set of genes called Dmp operon in Pseudomonas CF600 is able to degrade phenol with the aim to produce acetyl CoA, and use these compounds as an energy source.
Figure6: The catabolic pathway for degradation of phenol and the organization of Dmp operon. (Powlowski J, Shingler V., 1994)
The transcription of this operon is regulated by the DmpR regulator element which bind phenol and activate the transcription of the phenol hydroxylase promoter by allowing the fixation of the RNA polymerase (more information, see the section Sensors).
For PCBs, two distinct classes of bacteria have now been identified as being able to degrade PCBs.
Aerobic bacteria which live in oxygenated environments and anaerobic bacteria which live in oxygen free environments such as aquatic sediments. They use different mechanisms, aerobes attack PCBs oxidatively, breaking open the carbon ring and destroying the compounds. Anaerobes, on the other hand, leave the biphenyl rings intact while removing the chlorines.
The evidence in the literature suggests that PCDD/F compounds are subject to biodegradation in the environment as part of the natural chlorine cycle.
Figure7: The catabolic pathway for degradation of biphenyl by aerobic bacteria and the organization of bph gene cluster (Kensuke F., Hidehiko F., 2008) .The transcription of this set of genes is regulated by bphR2 wich bind PCBs and activate the transcription of pbhR1 gene (more information, see the section Sensors).
For nitrites, degradation pathway are very well known because they belong to the nitrite cycle. And for heavy metals, a lot of operon which allows the cell's tolerance to these compounds exist and have promoter answering specifically to the metal concentration.
But for this project, we chose to develop systems based on promoters presents in our bacteria strain Pseudovibrio denitrificans.
In that way, we made an RNA sequencing approach to detect promoter able to answer to the pollutant presence (more information, see the section RNAseq).
Our bacteria strain is known to live in sponge and may provide them a better tolerance to pollutants like heavy metals. This fact is actually study by the 'Molecules of defence and communication in the microbial ecosystems' team of the National museum of natural history of Paris (their web page here)
Futur : degradation?
Sensing's constructions are very simple and easy to realize. But in a larger framework we can imagine one day be able to clone all the enzymes of the degradation pathway of phenol and PCBs in our bacteria. In fact we can create, more than a sensor system based on sponge, a complete filtrating system which can not only sense pollutants, but totally remove them.
for nitrites it exist different biologic denitrification systems to reduce nitrates concentration in water that use bacteria as Pseudomonas with a denitrification yield of 80%. Bacteria are fixated on a mineral support and feed with acetic acid or ethanol (SNIDE). The major drawback is the production of nitrous and nitric oxide that are greenhouse gas.
To make a bacterium able to transforme nitrite into nitrogen we just have to add two enzymes:
-> Hydroxylamine oxydase from Parococcus denitrificans: nitrite + H2O = hydroxylamine
-> Hydrazine oxydoreductase from Candidatus Brocadia anammoxidans: hydroxylamine + NH3 + acceptor = N2 + H2O + reduced acceptor
Figure8: Nitrogen cycle.
Unfortunately, when we talk about heavy metals we talk about atoms which cannot just be degraded by a biological pathway. But we can imagine some ways of accumulation of these elements in bacteria that we can remove and treated after like chemical waste.