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From 2010.igem.org

Revision as of 12:34, 29 July 2010 (view source) Luzi (Talk | contribs) ← Older edit		Revision as of 12:40, 29 July 2010 (view source) Luzi (Talk | contribs) (→generation of storage vectors) Newer edit →
Line 36:		Line 36:
	|-		|-
	! CheY		! CheY
-	| N || plating of cells	+	| N || clone selection
	|-		|-
	! CheY		! CheY
-	| C || plating of cells	+	| C || clone selection
	|-		|-
	! CheR		! CheR
-	| N || plating of cells	+	| N || clone selection
	|-		|-
	! CheR		! CheR
-	| C || plating of cells	+	| C || clone selection
	|-		|-
	! CheB		! CheB
-	| N || plating of cells	+	| N || clone selection
	|-		|-
	! CheB		! CheB
-	| C || plating of cells	+	| C || clone selection
	|-		|-
	! TrigF		! TrigF
-	| N (binds N-terminal to ribosome) || primers recieved	+	| N (binds N-terminal to ribosome) || primers ordered
	|-		|-
	! MreB		! MreB
Line 63:		Line 63:
	|-		|-
	! tetR		! tetR
-	| N || primers recieved	+	| N || PCR
	|-		|-
	! tetR		! tetR
-	| C || primers recieved	+	| C || PCR
	|-		|-
	! PhyB		! PhyB
Line 86:		Line 86:
	| C || primers ordered		| C || primers ordered
	|-		|-
-	! cyFP	+	! YFP
-	| N ||	+	| N || PCR
	|-		|-
-	! cyFP	+	! YFP
-	| C ||	+	| C || PCR
	|-		|-
	! GFP		! GFP

---

Revision as of 12:40, 29 July 2010

Overview

The goal of our iGEM project E.lemming is to take over the control of the tumbling frequency of E. coli. This is achieved by reversibly localizing certain elements of the chemotactic pathway (che-proteins) and thus affecting their activity. For localization we use the PhyB-PIF3 system found in plants. PhyB or PIF3 is fused to a che-protein while the other one is fused to a localized protein (localizer) within the cell. Upon a light stimulus of a certain wavelength PhyB is activated, binds PIF3 and thereby localizes the che-protein. A light stimulus of a different wavelength reverses this process.
In order to increase the probability that the system will work we will try out a lot of combinations of several proteins:

• che-proteins: cheY, cheB and cheR
• localizer: trigger factor (binds the ribosome), MreB (actin analogue), tetR (binds tetO)

The goal of the wet lab team is to implement this localization system into E. coli.

Cloning strategy

As we plan to generate several fusion proteins with different linkers, we decided to use the cloning strategy BBF RFC 28: A method for combinatorial multi-part assembly based on the Type IIs restriction enzyme AarI (http://dspace.mit.edu/handle/1721.1/46721). The advantage of this strategy is that we can clone up to 3 different inserts into one vector simultaneously in a 96 well format.

Parts

Currently we are working on putting all the BioBricks into a storage vector. The image shows all the constructs we plan to clone.

working process

generation of parts

generation of storage vectors

We use the vector pSEVA of Victor de Lorenzo's lab. It has a kanamycin resistance and a BBR1 origin. The working process for the generation of the storage vectors is as follows:
Ordering of primers (if template is available) -> PCR -> clean-up of PCR product -> ligation into storage vector -> transformation of competent cells -> plating of cells -> selection of clones (blue-white-screening) -> sequencing
For proteins for which no template is available we let the let the genes synthesize directly.

subparts

Protein	terminus on fusion	status
CheY	N	clone selection
CheY	C	clone selection
CheR	N	clone selection
CheR	C	clone selection
CheB	N	clone selection
CheB	C	clone selection
TrigF	N (binds N-terminal to ribosome)	primers ordered
MreB	N	primers ordered
MreB	C	primers ordered
tetR	N	PCR
tetR	C	PCR
PhyB	N	primers ordered
PhyB	C	primers ordered
PhyB	N	primers ordered
PhyB	C	primers ordered
PIF3	N	primers ordered
PIF3	C	primers ordered
YFP	N	PCR
YFP	C	PCR
GFP	N
GFP	C

generation of acceptor vectors

testing of parts

generation of E. coli mutants

experimental plan