Team:TU-Delft/Project

From 2011.igem.org

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Latest revision as of 10:10, 20 September 2011

StickE. Coli : Single Protein Attachment of Escherichia coli

Natural attachment of micro-organisms relies on a complex network of varying compounds known as biofilms. This complexity hinders an easy control and regulation of attachment and detachment. We will give Escherichia coli a simple, effective and controllable mechanism for biofilm formation, based on the strong glue from mussel feet. E. coli, expressing the strongest-binding mussel foot protein Mfp5 on the outer cell surface, can robustly attach to a wide variety of surfaces, including glass, plastic and itself.
Using highly sensitive TIRF microscopy and atomic force measurements we visualize and characterize the localization and attachment of cells. Combining these results with our mathematical models allows us to predict the attachment speed and stability as well as cell clustering and settling. The controllable, strong attachment opens up new possibilities for the use of bacterial machines in environmental applications, medicine and industry.

Workflow

Our workflow has been designed in such a way that each project is individual and independent. All the projects however can enhance each-other and contribute to one greater project.

In March we started by gathering project ideas with the team members, advisors, and supervisors. In April we did a lot of research on bio-adhesion and mussel foot proteins. In May we started with sponsoring and working on our wiki. In June we designed our first BioBrick. We did some modelling and worked on our lab plan. Also, we made a plan to make the Dutch society aware of synthetic biology. Now, in July, we continue with all the subprojects we started. By the end of September, we hope to have succeeded in all our separate projects and reached our goal on a scientific level. We hope to have a good modeling plan, well characterized Biobricks, a fruitful collaboration with other iGEM teams and the Rathenau Institute and a wonderful exposition in the Science Centre.

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-=='''Project Overview''' ==
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+=='''StickE. Coli : Single Protein Attachment of Escherichia coli''' ==
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-Our aim of competing in the 2011 iGEM competition is to engineer a bacterial strain to give it new properties in order to achieve controllable adhesion of microbial reactors. The main theme to achieve this aim is to control cell-cell attachment and cell-surface attachment in such a way that it is applicable for industry and fundamental research.
-In our project we strive for full control of the attachment and detachment of cells. In nature attachment consists of a complex network involving an extracellular matrix containing a wide variety of compounds. This complexity has hindered easy regulation. We will give ''Escherichia coli'' a much simpler but equally effective way of binding: mussel glue. Expressing the strongest protein responsible for the attachment of mussels to rocks, we can allow ''E. coli'' to strongly attach to even glass and plastic, whenever we want it, and subsequently releasing it again. This system should be viewed in the same category as “ the wheel”, by itself it is just a neat trick, but combination is key. Combining it for example with an ''E. coli'' capable biocatalytic conversion , one can create microbial production lines, use attachment for temporary rapid settling of biomass before product removal, or achieve fundamental premiers like bacterial cells forming a micro circle on command.
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+Natural attachment of micro-organisms relies on a complex network of varying compounds known as biofilms. This complexity hinders an easy control and regulation of attachment and detachment. We will give Escherichia coli a simple, effective and controllable mechanism for biofilm formation, based on the strong glue from mussel feet. E. coli, expressing the strongest-binding mussel foot protein Mfp5 on the outer cell surface, can robustly attach to a wide variety of surfaces, including glass, plastic and itself.<br/>
+Using highly sensitive TIRF  microscopy and atomic force measurements  we visualize and characterize the localization and attachment of cells. Combining these results with our mathematical models allows us to predict the attachment speed and stability as well as cell clustering and settling. The controllable, strong attachment opens up new possibilities for the use of bacterial machines in environmental applications, medicine and industry.
 ===Workflow===
-Our workflow has been designed in such a way that each project is individual and independent. All the projects however contribute to one greater project.
+Our workflow has been designed in such a way that each project is individual and independent. All the projects however can enhance each-other and contribute to one greater project.
 [[File:TUDelft-Horizontal_Workflow.jpg]]
-In March we started by gathering project ideas with the team members, advisors, and supervisors. In April we did a lot of research on bioadhesion and mussel foot proteins. In May we started with sponsoring and working on our wiki. In June we designed our first BioBrick. We did some modeling and worked out our lab plan. Also, we made a plan to make the Dutch society aware of synthetic biology. Now, in July, we go on with al the subprojects we started. By the end of September, we hope to have succeeded in all our separate projects and reached our goal on scientific level. We hope to have a good modeling plan, well characterized Biobricks, a fruitful collaboration with other iGEM teams and the Rathenau Institute and  wonderful exposition in the Science Centre.
+In March we started by gathering project ideas with the team members, advisors, and supervisors. In April we did a lot of research on bio-adhesion and mussel foot proteins. In May we started with sponsoring and working on our wiki. In June we designed our first BioBrick. We did some modelling and worked on our lab plan. Also, we made a plan to make the Dutch society aware of synthetic biology. Now, in July, we continue with all the subprojects we started. By the end of September, we hope to have succeeded in all our separate projects and reached our goal on a scientific level. We hope to have a good modeling plan, well characterized Biobricks, a fruitful collaboration with other iGEM teams and the Rathenau Institute and a wonderful exposition in the Science Centre.
-=='''Safety proposal''' ==
-====1. Would any of your project ideas raise safety issues in terms of: researcher safety, public safety or environmental safety?====
-====2. Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?====
-====3. Is there a local biosafety group, committee, or review board at your institution?====
-Since 1997 Dr. L.A. (Lesley) Robertson is the Biological Safety Officer (BSO) of the Faculty of Applies Sciences of Delft University of Technology, she manages biological safety issues. She has knowledge of the laboratory practices and procedures within the faculty and oversees the biological safety program of the faculty.
-Our faculty has ML-1 laboratories and one ML-2 laboratory, but we are only allowed to work in ML-1 labs for which the basic microbiology laboratory rules apply. Internationally, there are strict rules on genetically modified organisms (GMO). A license is required to be allowed to work with GMO’s. Only if the risks to humans and the environment are minimal to negligible, the government grants a license. The rules for working with GMO’s have to be followed by the laboratory researchers. For each laboratory one person is responsible for the compliance to the rules on that specific lab. Dr. L.A. Robertson has the final responsibility for all the labs. This means that she always knows what biological material is used, where and by whom.
-Before you are allowed to work in a laboratory you have to pass a biosafety test, which includes identifying of possible hazards in a lab, and doing a so called washing test. This include all the basic rules for researches to be allowed to work on the lab. All team members passed this test. Afterwards she explained us under which permits our project is conducted and which permits we should verify to be sure it is allowed.
-Therefore, a research proposal was provided to Dr. L.A. Robertson. The research proposal included a table containing the micro-organisms, plasmids and existing BioBricks we intend to use. To ensure that we’ll work within the permit, there are two lists which state all the allowed vectors and hosts. These lists are provided, just like the permit, by the Dutch Minsitry of Housing, Spatial planning and the environment. During the writing of our research proposal, we constantly verified in these lists if our plans were allowed. After Dr. L.A. Robertson read or research proposal and verified all the vectors and hosts, she gave us the permission for our project.  Now we could start are project, during the future we will inform our BSO Dr. L.A. Robertson regularly on our progression in the lab and what we are planning to do in the near future.
-====4. Do you have other ideas to deal with safety issues that could be useful for future iGEM competitions? How could parts, devices and systems be made even safer through biosafety engineering?====
-The iGEM competition should keep working with well-known organisms. Off course a project can be about toxicity, but then it should be well contained and guided by experienced supervisors. Students should be well informed on lab regulations, especially when working as interdisciplinary teams.
-A categorized and government controlled system of lab experience certificates should be implemented. This is already in place for nuclear laboratories, but not jet for the biohazard laboratories. This will give more clarity on who is capable to work in such environments and this creates the awareness that these hazards deserve.
-The most obvious answer is to make Event Tree Analysis (ETA) and Fault Tree Analysis (FTA) a compulsory part of the iGEM-designing phase. This will significantly limit the risks on all iGEM projects and student will learn to take biosafety into account even before they are going to work in the laboratory.
-Also for biosafety engineering it is recommended to use a well-known microorganism, because there is more knowledge on how internal systems work and intertwine. This will make an ETA and FTA more effective and therefore the risks are lower.
-It is well known that genetic engineering has a negative public perception. Genetic engineering is exotic, controlled by others, build up of natural parts, but manmade, it has unknown benefits, imposed, most do not trust the companies. The public thinks they are after the money. The overall media coverage is limited, but iGEM strives to communicate with the media. All with all, this makes that media communication should be approached carefully. This is also a biosafety precaution that should be taken into account. Prevent negative media attention, but never cover up the truth.
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