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Team:Glasgow
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| - | < | + | <h1>DISColi: Bio-photolithography in Device Engineering Using Different Wavelengths of Light</h1> |
| - | <p> | + | <p>Light is ubiquitous. Systems that respond to light exist throughout nature, from unicellular photosynthetic organisms to the phototropism response in plants. Light is an abundantly available resource, offering precise control over a system even in remote locations. <br/><br/> |
| - | + | ||
| + | This is why we chose to work with light. DISColi is a novel bio-photolithographic system for engineering biofilms and the use of light allows the precision control needed to create functional 2D and 3D structures and devices. Such technology already has applications in fields as microfluidics, nanotechnology and tissue engineering. <br/><Br/> | ||
| + | |||
| + | Our work with light responsive constructs has allowed us to fully take advantage of the modular nature of synthetic biology. The main aims of our project can be separated into three light-controlled components: the designed sculpting of biofilms; 3D printing for encapsulation of cells; and the controlled modular synthesis of a variety of products. We expect our technology to have applications for material synthesis and compound manufacture in remote locations, for example outer space. | ||
| + | <br/><br/><b> | ||
| + | 1.) The sculpting of Biofilms</b><br/><Br/> | ||
| + | |||
| + | The complex 3D structures formed by microorganisms provide an ideal model for sculpting. However, biofilms are also medically significant and can cause problems for human health. Our first priority therefore was researcher safety. We also had to deal with the problem of a lack of shuttle vector between E.coli and common biofilm forming lab strains, such as Pseudomonas sp. For this reason, we have worked with a novel biofilm forming synthetic biology chassis, E.coli Nissle 1917. We intend to make this available to the Registry to allow future teams who wish to have a safer alternative that is still compatible with existing parts on the registry, to work with biofilms..<br/><Br/> | ||
| + | |||
| + | In order to sculpt shapes into the biofilm, it is necessary to disperse some of the microorganisms. We have developed three novel biobricks designed to cause dispersal of the biofilm. Under control of the light responsive promoters, we can use light to cause targeted dispersal of the biofilm. <br/><br/> | ||
| + | |||
| + | Phosphodiesterase, an enzyme isolated from Pseudomonas aeruginosa PA01, breaks down the signalling molecule cyclic diguanylate (c-di-GMP). This molecule is extremely important in biofilm formation and motility, and so the targeted overexpression of phosphodiesterase is designed to interfere with biofilm formation. <br/><br/> | ||
| + | |||
| + | We have also created two biobricks of novel surfactant proteins. These are Latherin and Ranaspumin, which are surfactant proteins with antimicrobial properties. Both these proteins are studied for their antibiofilm activity. <br/><br/> | ||
| + | |||
| + | To further enhance biofilm dispersal, we have also used two biobricks from the registry – Colicin E2 (Part BBa_ K131000) and T4 endolysin (Part BBa_K112806). All five of these proteins have been modelled to predict their diffusion through a biofilm. This allowed us to understand how large an area would be affected by triggering dispersal using our light responsive constructs. This meant we could predict how fine a resolution we could get when sculpting with light. <br/><br/> | ||
| + | |||
| + | DIScoli centres on the use of three light responsive promoters – the BLUF domain (Part BBa_K238013) which is activated by blue light, OmpC (Part BBa_R0082) which is activated by green light and OmpF (Part BBa_R0084) which is inhibited by red light. We have collaborated with the University of Edinburgh team, who shared with us the improved versions of OmpC and OmpF. <br/><br/> | ||
| + | |||
| + | To characterise the light promoters, we developed two novel reporters, LOV2 and iLOV. These reporters have numerous advantages over GFP derived fluorescent proteins, such as their small size and, in the case of iLOV, the ability to quickly recover from photobleaching. Another key advantage of the reporters LOV2 and iLOV is their ability to function under anoxic conditions. This unique ability was particularly desirable to our team due to our work with biofilms. We are using biofilms to engineer functional 2D and 3D structures using our light responsive constructs. Bio-photolithography has many applications, including the creation of structures for tissue engineering and manufacturing nanodevices. <br/><br/> | ||
| + | |||
| + | <b> | ||
| + | 2.) 3D printing for encapsulation</b><br/><br/> | ||
| + | |||
| + | The third component of our final product is encapsulation. For this we have chosen colanic acid, which is an exopolysaccharide that is naturally produced by E.coli in order to protect from acidic environments. Colanic acid was previously worked on by the 2009 Imperial College London team, and its production can be overexpressed using biobricks of the transcription factors RcsA and RcsB. <br/><br/><b> | ||
| + | |||
| + | 3.) The controlled modular synthesis of a variety of products</b><br/><br/> | ||
| + | |||
| + | A key component of DISColi is flexibility in manufacturing. Taking advantage of the modular nature of synthetic biology, our engineered bacteria will be able to produce a variety of useful compounds simply by inserting the genes for the desired compound into the system. <br/><br/> | ||
| + | |||
| + | This would mean the ability to use different wavelengths of light to select your desired product from a single precursor molecule. As a proof of principle of manufacturing in response to light, we have been working with the carotenoid pathway. In 2009, Cambridge submitted a number of biobricks involved in this pathway. We have improved this by synthesizing the fourth gene, crtY, in the pathway and testing it under a pBAD promoter. <br/><br/> | ||
| + | |||
| + | |||
| + | We believe it is vital to include a constant interaction with the public throughout our project. We aim to accomplish this through the use of regular Vlogs and personal Blogs. Uniquely, we have also created a daily time-lapse, with the hope that others can gain an insight into life in the lab. Check out the rest of our wiki to find out what else we’ve been up to!><br/><br/> | ||
| + | |||
<h2>News</h2> | <h2>News</h2> | ||
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features: { | features: { | ||
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loop: false, | loop: false, | ||
live: false, | live: false, | ||
Revision as of 07:41, 20 September 2011
DISColi: Bio-photolithography in Device Engineering Using Different Wavelengths of Light
Light is ubiquitous. Systems that respond to light exist throughout nature, from unicellular photosynthetic organisms to the phototropism response in plants. Light is an abundantly available resource, offering precise control over a system even in remote locations.
This is why we chose to work with light. DISColi is a novel bio-photolithographic system for engineering biofilms and the use of light allows the precision control needed to create functional 2D and 3D structures and devices. Such technology already has applications in fields as microfluidics, nanotechnology and tissue engineering.
Our work with light responsive constructs has allowed us to fully take advantage of the modular nature of synthetic biology. The main aims of our project can be separated into three light-controlled components: the designed sculpting of biofilms; 3D printing for encapsulation of cells; and the controlled modular synthesis of a variety of products. We expect our technology to have applications for material synthesis and compound manufacture in remote locations, for example outer space.
1.) The sculpting of Biofilms
The complex 3D structures formed by microorganisms provide an ideal model for sculpting. However, biofilms are also medically significant and can cause problems for human health. Our first priority therefore was researcher safety. We also had to deal with the problem of a lack of shuttle vector between E.coli and common biofilm forming lab strains, such as Pseudomonas sp. For this reason, we have worked with a novel biofilm forming synthetic biology chassis, E.coli Nissle 1917. We intend to make this available to the Registry to allow future teams who wish to have a safer alternative that is still compatible with existing parts on the registry, to work with biofilms..
In order to sculpt shapes into the biofilm, it is necessary to disperse some of the microorganisms. We have developed three novel biobricks designed to cause dispersal of the biofilm. Under control of the light responsive promoters, we can use light to cause targeted dispersal of the biofilm.
Phosphodiesterase, an enzyme isolated from Pseudomonas aeruginosa PA01, breaks down the signalling molecule cyclic diguanylate (c-di-GMP). This molecule is extremely important in biofilm formation and motility, and so the targeted overexpression of phosphodiesterase is designed to interfere with biofilm formation.
We have also created two biobricks of novel surfactant proteins. These are Latherin and Ranaspumin, which are surfactant proteins with antimicrobial properties. Both these proteins are studied for their antibiofilm activity.
To further enhance biofilm dispersal, we have also used two biobricks from the registry – Colicin E2 (Part BBa_ K131000) and T4 endolysin (Part BBa_K112806). All five of these proteins have been modelled to predict their diffusion through a biofilm. This allowed us to understand how large an area would be affected by triggering dispersal using our light responsive constructs. This meant we could predict how fine a resolution we could get when sculpting with light.
DIScoli centres on the use of three light responsive promoters – the BLUF domain (Part BBa_K238013) which is activated by blue light, OmpC (Part BBa_R0082) which is activated by green light and OmpF (Part BBa_R0084) which is inhibited by red light. We have collaborated with the University of Edinburgh team, who shared with us the improved versions of OmpC and OmpF.
To characterise the light promoters, we developed two novel reporters, LOV2 and iLOV. These reporters have numerous advantages over GFP derived fluorescent proteins, such as their small size and, in the case of iLOV, the ability to quickly recover from photobleaching. Another key advantage of the reporters LOV2 and iLOV is their ability to function under anoxic conditions. This unique ability was particularly desirable to our team due to our work with biofilms. We are using biofilms to engineer functional 2D and 3D structures using our light responsive constructs. Bio-photolithography has many applications, including the creation of structures for tissue engineering and manufacturing nanodevices.
2.) 3D printing for encapsulation
The third component of our final product is encapsulation. For this we have chosen colanic acid, which is an exopolysaccharide that is naturally produced by E.coli in order to protect from acidic environments. Colanic acid was previously worked on by the 2009 Imperial College London team, and its production can be overexpressed using biobricks of the transcription factors RcsA and RcsB.
3.) The controlled modular synthesis of a variety of products
A key component of DISColi is flexibility in manufacturing. Taking advantage of the modular nature of synthetic biology, our engineered bacteria will be able to produce a variety of useful compounds simply by inserting the genes for the desired compound into the system.
This would mean the ability to use different wavelengths of light to select your desired product from a single precursor molecule. As a proof of principle of manufacturing in response to light, we have been working with the carotenoid pathway. In 2009, Cambridge submitted a number of biobricks involved in this pathway. We have improved this by synthesizing the fourth gene, crtY, in the pathway and testing it under a pBAD promoter.
We believe it is vital to include a constant interaction with the public throughout our project. We aim to accomplish this through the use of regular Vlogs and personal Blogs. Uniquely, we have also created a daily time-lapse, with the hope that others can gain an insight into life in the lab. Check out the rest of our wiki to find out what else we’ve been up to!>
News
Sponsors
With many thanks to our generous sponsors, without whom this project would not have been possible.
