IGEM:IMPERIAL/2008/New/Cloning Strategy

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A summary of the aims of each phase and constructs to be produced within each phase, is given below:
A summary of the aims of each phase and constructs to be produced within each phase, is given below:
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====== Phase 1 ======
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====== Phase 1; Constitutive Promoter Testing ======
Testing and characterisation of constitutive promoters. We will test 4 combinations of 2 promoters and 2 RBSs to characterise them. An antibiotic resistance cassette is placed at the 5' end of the construct, to prevent any readthrough by the native trancriptases from reaching the regulated biobricks.
Testing and characterisation of constitutive promoters. We will test 4 combinations of 2 promoters and 2 RBSs to characterise them. An antibiotic resistance cassette is placed at the 5' end of the construct, to prevent any readthrough by the native trancriptases from reaching the regulated biobricks.
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<html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase1.png"></html>
<html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase1.png"></html>
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====== Phase 2 ======
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====== Phase 2; Inducible Promoter Testing ======
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Testing and characterisation of inducible promoters; those marked with a 'c' are chemically-inducible and those marked with an 'l' are light-inducible. RFP is used instead of GFP as a quantifiable output as ytvA responds to blue light - GFP may cause positive feedback. 'Rep' genes encode a repressor for the chemically-inducible promoters to stop leaky expression.
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Testing and characterisation of inducible promoters; those marked with a 'C' are chemically-inducible and those marked with an 'L' are light-inducible. RFP is used instead of GFP as a quantifiable output as ytvA responds to blue light - GFP may cause positive feedback. 'Rep' genes encode a repressor for the chemically-inducible promoters to stop leaky expression.
<html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase2A.png">
<html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase2A.png">
<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase2B.png"></html>
<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase2B.png"></html>
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====== Phase 3 ======
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====== Phase 3; Clutch and Biomaterial Characterisation ======
Testing and characterisation of the clutch (''epsE'') and biomaterial synthesis (SB - signal sequence & biomaterial).
Testing and characterisation of the clutch (''epsE'') and biomaterial synthesis (SB - signal sequence & biomaterial).
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<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase3B.png"></html>
<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase3B.png"></html>
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====== Phase 4 ======
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====== Phase 4; Device Characterisation ======
Combining of light induction and epsE/biomaterial expression, and testing of feasibility.
Combining of light induction and epsE/biomaterial expression, and testing of feasibility.
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<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase4B.png"></html>
<img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/Phase4B.png"></html>
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====== Final Construct ======
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====== Final Construct; System Characterisation ======
Combination of light sensing and light-induced expression of epsE and biomaterial. Each gene has its own RBS because in ''B. subtilis'', it has been shown that levels of expression decreases as one moves along an operon.
Combination of light sensing and light-induced expression of epsE and biomaterial. Each gene has its own RBS because in ''B. subtilis'', it has been shown that levels of expression decreases as one moves along an operon.
<p><html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/S1L.png"></html></p>
<p><html><img width="100%" src="http://i59.photobucket.com/albums/g305/Timpski/S1L.png"></html></p>

Revision as of 10:33, 16 September 2008




Cloning Strategy

The Imperial iGEM 2008 team faces the task of working with a chassis that has been rarely used - and never characterised - in the competition to date. While the B. subtilis chassis offers us many advantages, working from the ground up presents many challenges.

Our cloning strategy is complex. In order to build the required constructs for our final product, we need to build, test and characterise intermediary parts and devices that will lead to the final system. The diagram below shows the critical pathway for our cloning strategy with a large number of closely-linked steps.



A summary of the aims of each phase and constructs to be produced within each phase, is given below:

Phase 1; Constitutive Promoter Testing

Testing and characterisation of constitutive promoters. We will test 4 combinations of 2 promoters and 2 RBSs to characterise them. An antibiotic resistance cassette is placed at the 5' end of the construct, to prevent any readthrough by the native trancriptases from reaching the regulated biobricks.

Phase 2; Inducible Promoter Testing

Testing and characterisation of inducible promoters; those marked with a 'C' are chemically-inducible and those marked with an 'L' are light-inducible. RFP is used instead of GFP as a quantifiable output as ytvA responds to blue light - GFP may cause positive feedback. 'Rep' genes encode a repressor for the chemically-inducible promoters to stop leaky expression.

Phase 3; Clutch and Biomaterial Characterisation

Testing and characterisation of the clutch (epsE) and biomaterial synthesis (SB - signal sequence & biomaterial).

Phase 4; Device Characterisation

Combining of light induction and epsE/biomaterial expression, and testing of feasibility.

Final Construct; System Characterisation

Combination of light sensing and light-induced expression of epsE and biomaterial. Each gene has its own RBS because in B. subtilis, it has been shown that levels of expression decreases as one moves along an operon.

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