Team:Newcastle

From 2010.igem.org

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__NOTOC__{{Team:Newcastle/mainbanner}}
__NOTOC__{{Team:Newcastle/mainbanner}}
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=BacillaFilla: Fixing cracks in Concrete=  
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=BacillaFilla: Fixing Cracks in Concrete=  
[[Image:Newcastle_iGEM_Teampic.jpeg|centre|468px]]
[[Image:Newcastle_iGEM_Teampic.jpeg|centre|468px]]
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<div style="text-align:justify;padding:5px">
<div style="text-align:justify;padding:5px">
===Project Description===
===Project Description===
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BacillaFilla, an engineered ''Bacillus subtilis'', aims to repair [[Team:Newcastle/problem|cracks in concrete]], which can cause catastrophic structural failure. BacillaFilla would be applied to structures by spraying onto their surface.
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BacillaFilla, an engineered ''Bacillus subtilis'', aims to repair [[Team:Newcastle/problem|cracks in concrete]] which can cause catastrophic structural failure. BacillaFilla would be applied to structures by spraying onto their surfaces.
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BacillaFilla swims deep into the cracks. Repair is effected by production of [[Team:Newcastle/Urease|CaCO<sub>3</sub>]], [[Team:Newcastle/Filamentous_Cells|filamentous ''Bacillus subtilis'' cells]] and [[Team:Newcastle/glue|levan]]. CaCO<sub>3</sub> expands at the same rate as concrete, making it the ideal filler. Filamentous ''Bacillus subtilis'' cells have similar tensile strength to the synthetic fibres used in fibre-reinforced concrete, and provide reinforcement. Levan glues CaCO<sub>3</sub> and filamentous cells in place.
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BacillaFilla would swim deep into the cracks. Repair would be effected by production of [[Team:Newcastle/Urease|CaCO<sub>3</sub>]], [[Team:Newcastle/Filamentous_Cells|filamentous ''B. subtilis'' cells]] and [[Team:Newcastle/glue|levansucrose glue]]. CaCO<sub>3</sub> expands at the same rate as concrete, making it an ideal filler. Filamentous ''B. subtilis'' cells have similar tensile strength to the synthetic fibres used in fibre-reinforced concrete, and provide reinforcement. Levansucrose glues CaCO<sub>3</sub> and filamentous cells in place.
''B. subtilis'' 168 sporulates, making it ideal for storage and transportation. The cells can be [[Team:Newcastle/solution#Alkalinity_resistance|made to be tolerant to concrete's high pH]].
''B. subtilis'' 168 sporulates, making it ideal for storage and transportation. The cells can be [[Team:Newcastle/solution#Alkalinity_resistance|made to be tolerant to concrete's high pH]].
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We designed a [[Team:Newcastle/Swarming|swarming]] BioBrick part for repairing ''B. subtilis'' 168's defective ''swrA'' and ''sfp'' genes and regaining motility. At the end of the crack the quorum sensing peptide [[Team:Newcastle/End_of_crack_%26_signalling_system|subtilin]] triggers a co-ordinated population response from a [[Team:Newcastle/End_of_crack_%26_signalling_system#2008Brick|subtilin-inducible promoter]]. Upregulating ''SR1'' and ''rocF'' promotes arginine and urea production, increasing exogenous  CaCO<sub>3</sub> deposition. Over-producing YneA induces the filamentous cell phenotype, while SacB converts extracellular sucrose to levan glue.
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We designed a [[Team:Newcastle/Swarming|swarming]] BioBrick part for repairing ''B. subtilis'' 168's defective ''swrA'' and ''sfp'' genes, regaining motility. At the end of the crack the quorum sensing peptide [[Team:Newcastle/End_of_crack_%26_signalling_system|subtilin]] triggers a co-ordinated population response from a [[Team:Newcastle/End_of_crack_%26_signalling_system#2008Brick|subtilin-inducible promoter]]. Upregulating ''SR1'' and ''rocF'' promotes arginine and urea production, increasing exogenous  CaCO<sub>3</sub> deposition. Over-producing YneA induces the filamentous cell phenotype, while SacB converts extracellular sucrose to levan glue.
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To protect the environment our project also includes a design for a [[Team:Newcastle/Non-target-environment_kill_switch| kill switch]].
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To protect the environment our project also includes a design for a [[Team:Newcastle/Non-target-environment_kill_switch| kill switch]].  
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Our project is summarised in the diagram below:
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[[Image:newcastle_summary.png|850px]]
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[[Image:newcastle_summary.png|600px|centre]]
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{|style cellpadding="20" cellspacing="0"
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! colspan="2" |<font size=4> <center>'''Summary of achievements:'''</center></font>
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===Summary of Our Achievements===
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{|style cellpadding="14" cellspacing="0"
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|<span style="color:Sienna">'''BRONZE:'''</span>
|<span style="color:Sienna">'''BRONZE:'''</span>
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|From the beginning of the project, we have successfully registered the team of two instructors, six advisors and eight members. We have completed and submitted a Project Summary form, developed ideas and shared them on our iGEM wikipedia page. We also entered information on one new BioBrick part, [http://partsregistry.org/Part:BBa_K302012 IPTG-induced filamentous cell formation], into the Registry of Parts. The BioBrick for the IPTG-induced filamentous cell formation has been submitted to the Parts Registry.
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|From the beginning of the project, we have successfully registered the team of two instructors, six advisors and eight members. We have completed and submitted a Project Summary form, developed ideas and shared them on our iGEM wikipedia page. We also entered 31 new BioBrick parts into the Registry of Parts. One part, [http://partsregistry.org/Part:BBa_K302012 IPTG-induced filamentous cell formation], the BioBrick for the IPTG-induced filamentous cell formation, was demonstrated to work as expected.
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|<span style="color:Silver">'''SILVER:'''</span>
|<span style="color:Silver">'''SILVER:'''</span>
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|<span style="color:Goldenrod">'''GOLD:'''</span>
|<span style="color:Goldenrod">'''GOLD:'''</span>
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|In order to obtain a gold, we investigated the benefits of an e-Science approach, focusing on workflows, to synthetic biology. Details can be found at [[Team:Newcastle/E-Science|here]]. This part of the project resulted in us proposing a new standard for a RESTful API which facilitates the discovery and publication of models of functional biological units. The standard has been submitted to the BioBricks Foundation as [[BBFRFC66|BBF RFC 66]]. We have also improved on existing BioBrick parts to produce hyperspankoid: [http://partsregistry.org/Part:BBa_K302003 BBa_K302003].
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|In order to obtain a gold, we investigated the benefits of an e-Science approach, focusing on workflows, to synthetic biology. Details can be found at [[Team:Newcastle/E-Science|here]]. This part of the project resulted in us proposing a new standard for a RESTful API which facilitates the discovery and publication of models of functional biological units. The standard has been submitted to the BioBricks Foundation as [[BBFRFC66|BBF RFC 66]].
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===Attribution and Contribution===
 
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The work on this project (including part design, computational modelling, lab work and graphic design) was completed entirely by a [[Team:Newcastle/the_team|multidisciplinary team of students]]. Details of this work can be found on the [[Team:Newcastle/solution|Solution]], [[Team:Newcastle/modelling|Modelling]] and [[Team:Newcastle/notebook|Lab book]] pages. This work is unrelated to the work done by the labs of our instructors and advisors.
 

Latest revision as of 19:13, 25 November 2010

iGEM Homepage Newcastle University BacillaFilla Homepage Image Map

BacillaFilla: Fixing Cracks in Concrete

Newcastle iGEM Teampic.jpeg

Project Description

BacillaFilla, an engineered Bacillus subtilis, aims to repair cracks in concrete which can cause catastrophic structural failure. BacillaFilla would be applied to structures by spraying onto their surfaces.

BacillaFilla would swim deep into the cracks. Repair would be effected by production of CaCO3, filamentous B. subtilis cells and levansucrose glue. CaCO3 expands at the same rate as concrete, making it an ideal filler. Filamentous B. subtilis cells have similar tensile strength to the synthetic fibres used in fibre-reinforced concrete, and provide reinforcement. Levansucrose glues CaCO3 and filamentous cells in place.

B. subtilis 168 sporulates, making it ideal for storage and transportation. The cells can be made to be tolerant to concrete's high pH.

We designed a swarming BioBrick part for repairing B. subtilis 168's defective swrA and sfp genes, regaining motility. At the end of the crack the quorum sensing peptide subtilin triggers a co-ordinated population response from a subtilin-inducible promoter. Upregulating SR1 and rocF promotes arginine and urea production, increasing exogenous CaCO3 deposition. Over-producing YneA induces the filamentous cell phenotype, while SacB converts extracellular sucrose to levan glue.

To protect the environment our project also includes a design for a kill switch.

Our project is summarised in the diagram below:

Newcastle summary.png


Summary of Our Achievements

BRONZE: From the beginning of the project, we have successfully registered the team of two instructors, six advisors and eight members. We have completed and submitted a Project Summary form, developed ideas and shared them on our iGEM wikipedia page. We also entered 31 new BioBrick parts into the Registry of Parts. One part, [http://partsregistry.org/Part:BBa_K302012 IPTG-induced filamentous cell formation], the BioBrick for the IPTG-induced filamentous cell formation, was demonstrated to work as expected.
SILVER: Our new BioBrick, the IPTG-inducible filamentous cell formation part works, so we characterised it and included the information, [http://partsregistry.org/Part:BBa_K302012:Experience BBa_K302012], on the Parts Registry.
GOLD: In order to obtain a gold, we investigated the benefits of an e-Science approach, focusing on workflows, to synthetic biology. Details can be found at here. This part of the project resulted in us proposing a new standard for a RESTful API which facilitates the discovery and publication of models of functional biological units. The standard has been submitted to the BioBricks Foundation as BBF RFC 66.


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