Team:Uppsala/Project Killing
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- | document.getElementById("tab1").innerHTML = '<img class="assembly_plan" src="https://static.igem.org/mediawiki/2014/2/25/Uppsala-igem2014Killingsystem.png"><p>Figure 1. The assembly plan of the killing construct. The green arrow is the promotor, the red circle is the RBS and the yellow box is the gene which consist of an export tag, USP45 and the bacteriocin, colicin FyA fused together.</p><br><br><br><br><h2>Bacteriocin</h2><p>With the growing problems of antibiotics we decided to use bacteriocincs as our antimicrobial. A bacteriocin is a peptide that is produced naturally by certain bacteria. It target close relatives to the producing bacteria. Unlike antibiotics the targets of bacteriocins are very specifc. The bacteriocin, colicin Fy is produced from y. frederiksenii and it will only target other yersinia species. Bacteriocins will either attack the cellmembrane or within the cell such as gene expression or protein production. One of colicins Fy main target is the y.enterocolitica. It kills y. enterocolitica by creating pores in its cellmembrane. Y. enterocolitica is also one of the more common pathogens in the gut and it causes some serious symptoms. That is why we choose colicin as the bacteriocin we want to express.</p><br><br><h2>Spot42 RNA</h2><p>Our goal was to design a seek and kill system. This means that we only want to express the bacteriocins when our bacteria is close to the target. We choose to do this because it takes energy to express the bacteriocins and there’s no use in overproducing it when the bacteria is not in proximity to y.entercolitica. In order to make our bacteria too only express the colicin when we want, we have included a sRNA system. We have an antisense region of the spot42 to recognize the USP45. USP45 is the secretion tag that we have coupled to the colicin. The sRNA will stick to Hfq and bind to the mRNA of USP45-Colicin gene and that will block the translation.<br>But when our bacteria is in proximity to y.entercolitica we want it to start express the CFyA. Therefore the sensing group have been working on a yenbox system which will inactivate the promotor that regulate the spot42 when it is close to y.enterocolitica.<p>'; | + | document.getElementById("tab1").innerHTML = '<img class="assembly_plan" src="https://static.igem.org/mediawiki/2014/2/25/Uppsala-igem2014Killingsystem.png"><p>Figure 1. The assembly plan of the killing construct. The green arrow is the promotor, the red circle is the RBS and the yellow box is the gene which consist of an export tag, USP45 and the bacteriocin, colicin FyA fused together.</p><br><br><br><br><h2>Bacteriocin</h2><p>With the growing problems of antibiotics we decided to use bacteriocincs as our antimicrobial. A bacteriocin is a peptide that is produced naturally by certain bacteria. It target close relatives to the producing bacteria. Unlike antibiotics the targets of bacteriocins are very specifc. The bacteriocin, colicin Fy is produced from y. frederiksenii and it will only target other yersinia species. Bacteriocins will either attack the cellmembrane or within the cell such as gene expression or protein production. One of colicins Fy main target is the y.enterocolitica. It kills y. enterocolitica by creating pores in its cellmembrane. Y. enterocolitica is also one of the more common pathogens in the gut and it causes some serious symptoms. That is why we choose colicin as the bacteriocin we want to express.</p><br><br><h2>Spot42 RNA</h2><p>Our goal was to design a seek and kill system. This means that we only want to express the bacteriocins when our bacteria is close to the target. We choose to do this because it takes energy to express the bacteriocins and there’s no use in overproducing it when the bacteria is not in proximity to y.entercolitica. In order to make our bacteria too only express the colicin when we want, we have included a sRNA system. We have an antisense region of the spot42 to recognize the USP45. USP45 is the secretion tag that we have coupled to the colicin. The sRNA will stick to Hfq and bind to the mRNA of USP45-Colicin gene and that will block the translation.<br>But when our bacteria is in proximity to y.entercolitica we want it to start express the CFyA. Therefore the sensing group have been working on a yenbox system which will inactivate the promotor that regulate the spot42 when it is close to y.enterocolitica.<p><img src="https://static.igem.org/mediawiki/2014/4/41/Uppsala-igem2014Spot42_system.png"><p>Figure 2. The spot42 system'; |
Revision as of 16:42, 21 September 2014
Stephanie Herman
Teresa Reinli
Joakim Hellner
Alexander Virtanen
Jennifer Rosenius
Marcus Hong
Miranda Stiernborg
Tim Hagelby Edström
Viktor Blomkvist
Megha Biradar
Niklas Handin
Jonas Mattisson
Arina Gromov
Nils Anlind
Eric Sandström
Gunta Celma
Oliver Possnert
Martin Friberg
Kira Karlsson
Christoffer Andersson
Laura Pacoste
Andries Willem Boers
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