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From 2010.igem.org

Contents 1 Overview 2 Cloning strategy 3 Parts 4 working process 4.1 generation of parts 4.1.1 generation of storage vectors

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 decreasing 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 like this 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 anologue), tetR (binds tetO)

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 and this 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

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	plating of cells
CheY	C	plating of cells
CheR	N	plating of cells
CheR	C	plating of cells
CheB	N	plating of cells
CheB	C	plating of cells
TrigF	N (binds N-terminal to ribosome)	primers recieved
MreB	N	primers ordered
MreB	C	primers ordered
tetR	N	primers recieved
tetR	C	primers recieved
PhyB	N	primers ordered
PhyB	C	primers ordered
PhyB	N	primers ordered
PhyB	C	primers ordered
PIF3	N	primers ordered
PIF3	C	primers ordered
cyFP	N
cyFP	C
GFP	N
GFP	C