Team:SDU-Denmark

From 2009.igem.org

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<div class="teaser">About our project</div>
 
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=The Problem=
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=Bacto-Bandage=
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[[Image:SDU-Denmark-Staphylococcus_aureus%2C_50%2C000x%2C_USDA%2C_ARS%2C_EMU.jpg|100px|thumb|right|Staphylococcus aureus]]
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(Picture of S. aureus)
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Our goal is to create an ''E. coli'' strain, which inhibits ''Staphylococcus aureus'' (''S. aureus'') biofilm formation in wounds by producing RNA III-inhibiting-peptide (RIP).
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S. aureus is one of the largest causes of hospital infections, each year infecting millions of people around the globe.  
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''S. aureus'' is one of the largest causes of hospital infections, each year infecting millions of people around the globe. ''S. aureus'' is normally commensal, but can create bacterial biofilms on implanted medical devices and in post-operational wounds. Biofilm is becoming increasingly hard to treat, as a result of growing resistance to many types of antibiotics.  
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S. aureus is normally commensal, but can create bacterial biofilm on implanted medical devices and in post-operational wounds.  
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By manipulating ''E. coli'' to express a synthetic RIP peptide tagged with an export signal, we hope to reach this goal. RIP has been shown to hinder the quorum-sensing processes essential for biofilm development in ''S. aureus'', thereby making it harder for the bacteria to spread and cause infections. We also propose making a bandage that contains our engineered bacteria behind a semipermeable membrane, allowing only small peptides such as RIP to pass through, into the wound.
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Biofilm formation, combined with resistancy to antibiotics in a growing number of S. aureus strains, is making S. aureus increasingly hard to treat. New ways for combating these bacteria could be immensely important.  
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We hope to show that biological machines could be used to fight different kinds of bacterial infections intelligently, to contribute with our RIP and export-signal parts and by better characterization of the older parts we've used.
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Here we have tried to create a biological machine, capable of stopping the bacterial signalling necessary for biofilm formation to proceed.
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[https://2009.igem.org/Team:SDU-Denmark/Project Our Project] | [https://2009.igem.org/Team:SDU-Denmark/Background Background for the project]
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Continue reading about our project.  
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Read more about S. aureus, biofilm formation, quorum-sensing and quorum-quenching.
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<div class="teaser">About our team</div>
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=The Machine=
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(Picture of bandage-e-coli)
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=University of Southern Denmark=
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[[Image:SDU2009-igemteam.jpg|300px|thumb|right|SDU Denmark. From left to right: Ann, Mike, John, Helle, Martin, Anna, Julius, Kir, Marc and Anne.]]
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We have created a simple biological machine that can inhibit biofilm formation, thereby making it easier to treat S. aureus.
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We are eight students from the [http://www.sdu.dk University of Southern Denmark], who shared a common wish to explore synthetic biology and decided to start the first iGEM team at our university.  
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This was done by genetically engineering E. coli using the BioBrick standard. BioBricks are standardized gene parts and by using this standard, we have been able to profit from older parts and contribute with new parts for others to use in the future.
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Our main achievement is the RNA III-inhibiting-peptide (RIP) part. In this project we show (for the first time), that it’s possible to express RIP in E. coli and that it can obstruct the quorum-sensing process necessary for biofilm formation in S. aureus.
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Continue reading about our project.
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Read more about our parts, and how we accomplished this project.
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=The Future=
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(Picture of Operation bandage)
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We propose making a bandage that contains our engineered bacteria behind a semipermeable membrane, allowing only small peptides such as RIP to pass through, into the wound.
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We have reason to hope, that this will weaken the biofilm, thereby making multiresistant bacteria easier to treat with conventional antibiotics.
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Also, our machine opens up for the possibility to combat infections more intelligently. A logical next step would be to couple other kinds of quorum-quenching molecules to our machine, together with different quorum-signaling receptors. This would allow for inhibition of only the bacteria that’s currently infecting the wound.
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Read more about the implications of our project.
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=About us=
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We are eight students from the University of Southern Denmark, who shared a common wish to explore synthetic biology and decided to start the first iGEM team at our university.
We are from diverse backgrounds such as nano-bio-science, molecular biology and medicine.
We are from diverse backgrounds such as nano-bio-science, molecular biology and medicine.
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Together with six advisors, we are spending the summer getting to grips with the up’s and down’s in synthetic biology, the lab, how to organize the project and everything in between.
Together with six advisors, we are spending the summer getting to grips with the up’s and down’s in synthetic biology, the lab, how to organize the project and everything in between.
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[https://2009.igem.org/Team:SDU-Denmark/Team Our Team] | [http://igem.sdu.dk See what we're up to on our blog]
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Our Team | See what we're up to on our blog
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Revision as of 09:15, 21 October 2009







The Problem

(Picture of S. aureus)

S. aureus is one of the largest causes of hospital infections, each year infecting millions of people around the globe.

S. aureus is normally commensal, but can create bacterial biofilm on implanted medical devices and in post-operational wounds.

Biofilm formation, combined with resistancy to antibiotics in a growing number of S. aureus strains, is making S. aureus increasingly hard to treat. New ways for combating these bacteria could be immensely important.

Here we have tried to create a biological machine, capable of stopping the bacterial signalling necessary for biofilm formation to proceed.

Continue reading about our project.

Read more about S. aureus, biofilm formation, quorum-sensing and quorum-quenching.

The Machine

(Picture of bandage-e-coli)

We have created a simple biological machine that can inhibit biofilm formation, thereby making it easier to treat S. aureus.

This was done by genetically engineering E. coli using the BioBrick standard. BioBricks are standardized gene parts and by using this standard, we have been able to profit from older parts and contribute with new parts for others to use in the future.

Our main achievement is the RNA III-inhibiting-peptide (RIP) part. In this project we show (for the first time), that it’s possible to express RIP in E. coli and that it can obstruct the quorum-sensing process necessary for biofilm formation in S. aureus.

Continue reading about our project.

Read more about our parts, and how we accomplished this project.

The Future

(Picture of Operation bandage)


We propose making a bandage that contains our engineered bacteria behind a semipermeable membrane, allowing only small peptides such as RIP to pass through, into the wound.

We have reason to hope, that this will weaken the biofilm, thereby making multiresistant bacteria easier to treat with conventional antibiotics.

Also, our machine opens up for the possibility to combat infections more intelligently. A logical next step would be to couple other kinds of quorum-quenching molecules to our machine, together with different quorum-signaling receptors. This would allow for inhibition of only the bacteria that’s currently infecting the wound.


Read more about the implications of our project.

About us

We are eight students from the University of Southern Denmark, who shared a common wish to explore synthetic biology and decided to start the first iGEM team at our university.

We are from diverse backgrounds such as nano-bio-science, molecular biology and medicine.

Together with six advisors, we are spending the summer getting to grips with the up’s and down’s in synthetic biology, the lab, how to organize the project and everything in between.

Our Team | See what we're up to on our blog



What do you think?

Feedback

We would love to get as much feedback as possible, both on our project and other work as well. Feel free to write, criticize or just say hallo.

Announcements

Oct. 21: Last minute panic updates are on the way :-)

Oct. 20: Brainstorm and team page updated.

Oct. 19: We made a [http://igem.sdu.dk/?p=354 sacrifice] to the Gods. Hopefully this will gives us the last bit of luck for the competition.

Oct. 18: We're been working hard on characterizing our parts and now we're getting ready for the final wiki upgrade

Oct. 16: We now have a couple on the team - Helle and Mike <3 congratulations! (Anne and Marc have actually been a couple for 4 years Anna)

Oct. 10: Colony-PCR protocol is uploaded.

SDU-Denmark-Valencia.gif

Oct. 3: Yes! We got a gold medal in [http://igemvalencia.questionpro.com Valencia's survery].

Oct. 1: Congratulation Anne! Happy Birthday.

Sep. 22: A lot of new info on the background page.

Sep. 16: We're featured in this months [http://intern.sdu.dk/enheder/natur/PerspektivMening/PerspektivMening3sept2009.pdf Perspektiv & Mening], a magazine at SDU.

Sep. 10: We got our 4-brick-part together. Wohu. Now we can start testing.

Aug. 26: [http://igem.sdu.dk/?p=314 Loading buffer on trail] at our blog. And we are getting ready to insert our different bricks into a backbone, yeah.

Aug. 25: More profiles on our team page.

Aug. 20: We updated the team page with most of our advisors.

Aug. 19: Wohu! Anna has returned after a five week trip to Africa where she helped deliver babies in Kenya. Good to have you back! Also we wrote about our [http://igem.sdu.dk/?p=307 ligation troubles on our blog].

Aug. 17: We updated the wiki with more protocols, our diary and changed the layout a bit.

Aug. 14: Julius left us to study at [http://www.northcarolina.edu/ University of North Carolina]. We miss you already, Mr. Misty Forrest Dragon!

Aug. 11: Kir's birthday! Happy birthday!

Check out the other teams

Be sure to check out all the other teams that are competing in this years iGEM.


Sponsors

[http://www.sdu.dk Check out University of Southern Denmark]

[http://www.dna-technology.dk/ Check out DNA Technology]