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<h2 style="margin:0; background:#003366; font-size:140%; font-weight:bold; border:1px solid #002447; text-align:left; padding:0.3em 0.4em; color: white;">Introduction</h2>
<h2 style="margin:0; background:#003366; font-size:140%; font-weight:bold; border:1px solid #002447; text-align:left; padding:0.3em 0.4em; color: white;">Introduction</h2>
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????Blurb about BOL????These are the projects we are undertaking this year:
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In order to engineer interesting and useful functions in biology, a robust and extensive range of inter- and intra-cellular signalling pathways must be available. By analogy with the Internet, such a system must allow communication between cells of different heritage and structure (different “operating systems”). In the course of this project we attempted to implement candidates for both types of signalling mechanism, and additionally made progress towards adding a new Gram-positive platform for synthetic biology to the Registry.
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<span style="font-weight:bold; font-size:120%;">Standardising the Agr signalling system</span>
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<span style="font-weight:bold; font-size:120%;">Peptide signalling</span>
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The Accessory Gene Regulator (Agr) system in ''S. aureus'' is an oligopeptide-based quorum sensing mechanism. We aim to convert it into a reusable interbacterial signalling system for communication amongst and between both Gram-positive species (''B. subtilis'') and Gram-negative bacteria (''E. coli''), based on controllable secretion and detection of the signalling peptide AIP.
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The Accessory Gene Regulator (Agr) system in ''S. aureus'' is an oligopeptide-based quorum sensing mechanism. We worked on converting it into a reusable interbacterial signalling system for communication amongst and between both Gram-positive species (''B. subtilis'') and Gram-negative bacteria (''E. coli''), based on controllable secretion and detection of the signalling peptide AIP.
For more information, see [[Signalling project description]].
For more information, see [[Signalling project description]].
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<span style="font-weight:bold; font-size:120%;">''Bacillus subtilis'' SynBio Chassis</span>
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<span style="font-weight:bold; font-size:120%;">Gram-positive chassis</span>
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Most synthetic biology so far has involved Gram-negative bacteria, which are more widely used in molecular biology research; however, the biotechnology industry relies on Gram-positive bacteria. We are trying to make a "chassis" out of ''Bacillus subtilis'', a common Gram-positive bacterium, into which genetic engineers can add BioBrick parts and control circuits.
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Most synthetic biology so far has involved Gram-negative bacteria, which are more widely used in molecular biology research; however, the biotechnology industry relies on Gram-positive bacteria. We worked on constructing a "chassis" out of ''Bacillus subtilis'', a common Gram-positive bacterium, into which genetic engineers can add BioBrick parts and control circuits.
For more information, see [[Bacillus subtilis SynBio chassis]]
For more information, see [[Bacillus subtilis SynBio chassis]]
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<span style="font-weight:bold; font-size:120%;">PoPS amplifier</span>
<span style="font-weight:bold; font-size:120%;">PoPS amplifier</span>
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We aim to build a standard amplifier which can be used in any synthetic (BioBricked) system, which would take in a standard PoPS input and give a PoPS output of a known amplification factor.
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We built a standard amplifier which can be used in any synthetic transcriptional system, taking in a standard PoPS input and giving a PoPS output of a known amplification factor. In addition, the activator-promoter pairs tested have characterised crosstalk giving the potential for a controlled multifaceted response.
For more details, have a look at the [[amplifier project]].
For more details, have a look at the [[amplifier project]].

Revision as of 21:26, 25 October 2007

Cambridge 2007 logo.png

BOL: Bacteria OnLine

University of Cambridge iGEM 2007

Introduction

In order to engineer interesting and useful functions in biology, a robust and extensive range of inter- and intra-cellular signalling pathways must be available. By analogy with the Internet, such a system must allow communication between cells of different heritage and structure (different “operating systems”). In the course of this project we attempted to implement candidates for both types of signalling mechanism, and additionally made progress towards adding a new Gram-positive platform for synthetic biology to the Registry.

Peptide signalling

The Accessory Gene Regulator (Agr) system in S. aureus is an oligopeptide-based quorum sensing mechanism. We worked on converting it into a reusable interbacterial signalling system for communication amongst and between both Gram-positive species (B. subtilis) and Gram-negative bacteria (E. coli), based on controllable secretion and detection of the signalling peptide AIP.

For more information, see Signalling project description.

Gram-positive chassis

Most synthetic biology so far has involved Gram-negative bacteria, which are more widely used in molecular biology research; however, the biotechnology industry relies on Gram-positive bacteria. We worked on constructing a "chassis" out of Bacillus subtilis, a common Gram-positive bacterium, into which genetic engineers can add BioBrick parts and control circuits.

For more information, see Bacillus subtilis SynBio chassis

PoPS amplifier

We built a standard amplifier which can be used in any synthetic transcriptional system, taking in a standard PoPS input and giving a PoPS output of a known amplification factor. In addition, the activator-promoter pairs tested have characterised crosstalk giving the potential for a controlled multifaceted response.

For more details, have a look at the amplifier project.

[http://www.ccbi.cam.ac.uk/iGEM2007/index.php/Main_Page Go to the Cambridge iGEM 2007 team's official wiki!] (with more details about the team and how we came up with this idea)

[http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2007&group=Cambridge BioBricks we have contributed to the Registry]

Meet the team!


The Cambridge iGEM 2007 team!

Front row, from left: Narin Hengrung, Yi Han, David Wyatt

Second row, from left: Zhizhen Zhao (Jane), Stefan Milde, Dmitry Malyshev, Xinxuan Soh (Sheila)

Third row, from left: Yi Jin Liew, John Crowe (faculty), Lovelace Soirez, Stephanie May, Yue Miao

Back row, from left: James Brown (PhD student mentor), Jim Haseloff (faculty supervisor), Gos Micklem (faculty supervisor)

Not in photo: Jim Ajioka (faculty supervisor), Lorenz Wernisch (faculty), Tony Southall (PhD student)

The mailing list for the whole Cambridge iGEM2007 team is igem2007 [at] ccbi.cam.ac.uk

Sponsors

We are extremely grateful to the following organisations for their support of our project:

Major sponsors

[http://www.cam.ac.uk https://static.igem.org/mediawiki/2007/9/95/Cambridge_UofC_coat_of_arms.png]     [http://www.dna20.com https://static.igem.org/mediawiki/2007/1/16/Cambridge_DNA2_0_logo.png]

Other sponsors

  • The Isaac Newton Trust-funded UROP scheme
  • EU SynBioComm programme