Team:Groningen

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Revision as of 19:23, 25 October 2010

iGEM Groningen 2010

Hydrophobofilm
pushing coatings into a greener future

  • A self assembling bio-based coating is form, a rigid biofilm.
    Expression of hydrophobic proteins called chaplins is induced by the biofilm causing strong surface hydrophobicity.
    The strongly hydrophobic biofilm will die off by a killswitch, leaving a nice hydrophobic biological coating.

    Self assembling hydrophobic biofilm

    We aim to design a biological coating as an alternative to for example chemical coatings. For this we, unconventionally, utilized a Bacillus subtilis biofilm. We wanted to enable our biofilm to be equipped with an interesting property which is automatically initiated. So we introduced an expression trigger which relies on quorum sensing. Our project was directed at finding an alternate solution to biofouling, since regular, chemical coatings which are widely in use pose a threat to the environment. In nature the lotus leaves show self-cleansing properties ascribed to their extreme surface hydrophobicity. In the prokaryotic domain we stumbled upon chaplins, strongly hydrophobic proteins originating from Streptomyces coelicolor. Surface hydrophobicity is a very useful property and is used in many applications ranging from not only antifouling coatings but also other applications which require water repellence to applications in the field of medical sciences. During our project we have contributed to the parts registry whit numerous BioBricks.


    We believe that there is a great future for biological coatings as demonstrated within the project. Hydrophobic biological coatings can provide a greener antifouling solution. However using the underlying mechanisms of biofilm triggered expression for other systems like dynamic painting, sensing of environmental changes or even the integration with silicon chips might be within the realm of possibilities. So we challenge coming iGEM teams to further explore and brainstorm about the possibilities of using biofilms as a host for a wide range of applications.

    Team
    This year a team of young inspired undergraduates from the [http://www.rug.nl University of Groningen] participated in the amazing challenge of iGEM. A multi-disciplinary team of Molecular Biologists, Chemists, Computer Scientists, Journalists and others spend the summer creating a wonderful project in the emerging field of synthetic biology
    Modeling
    Using computer models we worked on the frontiers of knowledge. Gene expression was simulated and a simple explanation for cell differentiation was proposed. Also aiding in ethics and practical feasibility a kill switch system was studied. Finally a new standard was proposed for characterizing Biobrick parts so future can be streamlined.
    Human Practices
    Because we believe that synthetic biology can better the lives of people and ensure long term prosperity for all humans we spend time educating high school students. But not all is perfect so risks were assessed and we philosophized on the ethical aspects of synthetic biology.


    Our sponsors

    Sigma Aldrich DSM NGI GBB Kluyver Center Bioké Stichting biotechnology Nederland (SBN) 101 promotions Center for Synthetic Biology

  • Self assembling hydrophobic biofilm

    Chaplin cell.jpg

    Surface hydrophobicity is a very useful property and is used in many applications ranging from raincoats, antifouling coatings, anti-bacterial and anti-fungal coatings and applications in the field of biomedical sciences to protection of highly sensitive sensor equipment. Hydrophobicity keeps a surface water free and thereby clean and dry, this prevents micro-organisms from fouling surfaces and corrosion from forming. Most hydrophobic coatings used today are either costly or contain harmful chemicals. So why not create an organism that does the work for you.

    The idea is to engineer a bacterium that once applied on a surface, starts forming a rigid biofilm. Completion of the biofilm will trigger the expression of hydrophobic proteins by the biofilm forming bacterium. These hydrophobic proteins will be incorporated in the rigid biofilm, causing strong hydrophobic surface activity. After the hydrophobic biofilm production, a kill switch would be activated to kill of all bacteria. The result of these processes will be a surface that is coated by a rigid biofilm with embedded hydrophobic proteins, leaving the coated surface extremely hydrophobic.

    Producing a hydrophobic biocoating that is self assembling, would have a lot of advantages. Firstly it is relatively cheap to apply bacteria to surfaces. And since the coating process will be done by the bacteria themselves, there is no high-tech treatment involved and there are no expensive chemicals necessary to attain the hydrophobicity. Secondly, because these hydrophobins are proteins, they are in contrast to many chemical hydrophobins non-toxic to the environment. Applications of this hydrophobic biofilm could range from antifouling coatings on ships, antifungal coatings and corrosion and water protecting coatings.

  • Human Practices

    We of the iGEM Groningen 2010 team thought it to be very important to not only direct our attention to the scientific part of our project, but we also focused on increasing general knowledge about synthetic biology and science overall amongst the general public since it can sometimes appear an increasingly large fissure is forming between scientists and the man in the street. Especially in these times when biotechnology is advancing so greatly, new discoveries can come off as wacky inventions from for example Star Trek.

    We reached out to the public by visiting high schools to present our project and synthetic biology in general. Moreover we offered high schools the opportunity to send their students over to our lab for a master class in which we tried to get teenagers interested in the life sciences and to show them all life on earth is build up from basic parts which are shared by humans and organisms as different to us as tomatoes. And in addition to this we were involved in a monthly returning event in which scientist reach out to the public in an informal setting. We also conducted a survey amongst the participants in these events.

    Of course we think ethics and safety are very important within our project to since we are dealing with genetically engineered organisms which we – in theory – would apply outside the lab, so we need to consider this. However, since a lot was already written on ethics by last years’ iGEM Groningen team we decided to focus on education.

    MasterclassScholieren2.jpg
  • Modeling

    Modeling in iGEM

    Laura model.jpg

    Together with the rise of synthetic biology, more and more computational tools and methods to improve and model biological systems were developed. Biological systems are often very complicated networks and it can be hard to study their behaviour without the help of computers. This is why mathematical descriptions of biochemical processes have become an important way of studying biological systems aside from wetwork. Computer simulations can for example predict system behaviour or screen for possible drug targets. Models can also show were the gaps in our understanding of a biological system are, because they might show that the assumed mechanism is not right.

    In synthetic biology, modelling is important because it can save time and money and improve the final product. Mathematical models do have to be validated by comparing experimental and simulation results, this is why models have become a tool for use in parallel with experimental approaches. However, modeling in synthetic biology is an interdisciplinary task, because one needs to understand both the biology of the systems which will be modeled and posess the mathematical knowledge needed to build the model. Therefore, modelling is a collaborative effort of different fields of science.


    Our modeling goals

    Djoke model.jpg

    When it became clear that our project involved biofilms, we looked into models that describe biofilm formation. We found that such models existed and visited an expert on biofilm models in Delft. After this visit, it became clear that although these models are pretty mathematical, we could make a simple model with biofilm formation and diffusion.

    We modeled gene expression of our hydrofobic proteins. The modelers were actually the ones who discovered the qurom sensing pathway used in our project when looking in the partsregistry. The Com XPA system has since then been studied and we found that the biological pathways involved are far more complex than our model could describe. We therefore chose to model how the ComXPA system could activate the expression of our proteins.

    We also looked into killswitch mechanisms because the applications of our biofilm in for example anti-fouling coatings are outside the lab. Since most GMO's are not allowed to leave the lab alive, it would be nice to kill our bacteria after they formed a biofilm with our hydrofobic proteins. Therefore we modeled a simple toxin anti-toxin killswitch mechanism.

    Finally we wrote an information standard which hopefully provides more and easier searchable information for the partsregistry.


    References

    Lukas Endler, Nicolas Rodriguez, Nick Juty, Vijayalakshmi Chelliah, Camille Laibe, Chen Li and Nicolas Le Novère, Designing and encoding models for synthetic biology, Journal of the Royal Society Interface, 2009, online April 1, http://rsif.royalsocietypublishing.org/content/early/2009/03/27/rsif.2009.0035.focus.full. Yiannis N Kaznessis, Models for synthetic biology, BMC Systems Biology 2007, 1:47, http://www.biomedcentral.com/1752-0509/1/47.

  • == Team ==

    Our team

    (f.l.t.r: Ramon, Arend Jan, Peter, Jorrit, Geeske, Maarten, David, Arend, Djoke, Joël)

    Go check out the members of our team, with whom we collaborated or our publicly available pictures! If you still have questions you can always contact us!

    Our advisors

    • prof. dr. Oscar Kuipers: [http://molgen.biol.rug.nl/molgen/index.php Molecular Genetics] (Head)
    • dr. Dennis Claessen: [http://www.rug.nl/staff/d.claessen/index Microbial Physiology]
    • prof. dr. Jan Kok: [http://molgen.biol.rug.nl/molgen/index.php Molecular Genetics]
    • prof. dr. Bert Poolman: Biochemistry; [http://www.centreforsyntheticbiology.eu/ Centre for Synthetic Biology] (Director)
    • prof. dr. Roel Bovenberg: Synthetic biology and Cell engineering; Corporate Scientist Biotechnology, [http://www.dsm.com/ DSM]

Judging Form

Below you find the judging form as we filled it in via the iGEM site, but with some more links so it will be easy to see where the actual proof of this achievements can be found on our wiki
Team:Groningen
Track:New Application
Project Name:Hydrophobofilm --- a self assembling hydrophobic biofilm
Project Abstract: Surface hydrophobicity is a useful property and has many applications. Hydrophobicity keeps a surface clean and dry preventing micro-organisms from attaching to a surface. Most chemical coatings used presently are costly or harmful to the environment. Our idea is to engineer Bacillus subtilis which when applied to a surface, automatically forms a hydrophobic biofilm coating. Succesful biofilm formation will serve as a trigger for the expression of hydrophobic proteins called Chaplins. The result of this process will be a rigid biofilm with embedded hydrophobic proteins, leaving a coated surface which is extremely hydrophobic. Producing a self-assembling hydrophobic biofilm is cheap, there is no high-tech treatment involved and there are no hazardous chemicals necessary to attain a hydrophobic coating. Applications of this hydrophobic biofilm range from anti-fouling coatings on ships to anti-corrosion coatings used to protect sensory equipment.
iGEM Medals
We believe our team deserves the following medal:BronzeSilverGold
Because we met the following criteria (check all that apply and provide details where needed)

Requirements for a Bronze Medal:
Register the team, have a great summer, and plan to have fun at the Jamboree.
Successfully complete and submit this iGEM 2010 Judging form.
Create and share a Description of the team's project using the iGEM wiki and the team's parts using the Registry of Standard Biological Parts.
Plan to present a Poster and Talk at the iGEM Jamboree.
Enter information detailing at least one new standard BioBrick Part or Device in the Registry of Standard Biological Parts. Including:
Primary nucleaic acid sequence
Description of function
Authorship
Safety notes, if relevant.
Acknowedgment of sources and references
Submit DNA for at least one new BioBrick Part or Device to the Registry.

Additional Requirements for a Silver Medal:
Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected; characterize the operation of your new part/device.
Enter this information and other documentation on both the iGEM 2010 wiki and the Registry.
Part Number(s): BBa_K305011
iGEM Wiki Page Name: Expression

Additional Requirements for a Gold Medal: (one OR more)
Characterize or improve an existing BioBrick Part or Device and enter this information back on the Registry.
Part Number(s): BBa_J04450, BBa_E0240
Help another iGEM team by, for example, characterizing a part, debugging a construct, or modeling or simulating their system.
Link to this information on your wiki. Page name: Collaboration
Develop and document a new technical standard that supports the: (check all that apply)
design of BioBrick Parts or Devices, or
construction of BioBrick Parts or Devices, or
characterization of BioBrick Parts or Devices, or
analysis, modeling, and simulation of BioBrick Parts or Devices, or
sharing BioBrick Parts or Devices, either via physical DNA, or via the Internet
Please provide the BBF RFC number for your standard:
Outline and detail a new approach to an issue of Human Practice in synthetic biology as it relates to your project, such as safety, security, ethics, or ownership, sharing, and innovation.
Link to this information on your wiki.
Page name: Human Practices
iGEM Prizes
All teams are eligible for prizes in their track, the grand prize, and for special prizes. The special prizes include Best Wiki, Best Poster, Best Presentation, Best New BioBrick Part (Natural or Engineered). To help the judges, please indicate if you feel you should be evaluated for any of the following special prizes:
Best Human Practice Advance
Best Experimental Measurement
Best Model
Please explain briefly why you should receive any of these three special prizes:
Best Human Practices advance - We believe that it is very important to look further than the scientific part of our project. Therefore we focused on increasing general knowledge about synthetic biology and science overall amongst the general public. We presented our project at high schools and participated in events which were ment to reach out to the public.
Team_Parts
To help the judges evaluate your parts , please identify 3 of your parts that you feel are best documented and are of the highest quality.
Part Number(s): BBa_K305003, BBa_K305007, BBa_K305011
Your team has listed these parts as your team favorites.
iGEM Safety
For iGEM 2010 teams are asked to detail how they approached any issues of biological safety associated with their projects.
The iGEM judges expect that you have answered the four safety questions (Safety page) on your iGEM 2010 wiki.
Please provide the link to that page:
Page name: Safety
Attribution and Contributions
For iGEM 2010 the description of each project must clearly attribute work done by the team and distinguish it from work done by others, including the host labs, advisors, and instructors.
Please provide the link to that page:
Page name: Attribution and Contributions
Comments
If there is any other information about your project you would like to highlight for the judges,
please provide a link to your wiki page here: Education

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