Team:Cambridge/Project/Amplification

From 2009.igem.org

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(Recreating Previous Work)
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'''Further work - Cambridge iGEM 2009'''
'''Further work - Cambridge iGEM 2009'''
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We hope more fully characterize the activator constructs.  First, we hope to characterize these activators as promoters compared to the Relative Promoter Unit (RPU).  Secondly, we will investigate the activators'  sensitivity to arabinose.
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We hope more fully characterize the activator constructs.  First, we hope to characterize these activators on low copy plasmids as promoters compared to the Relative Promoter Unit (RPU).  Secondly, we will investigate the activators'  sensitivity to arabinose.
== Recreating Previous Work ==
== Recreating Previous Work ==

Revision as of 07:49, 12 August 2009


A Reliable Amplification System

Introduction

Cambridge iGEM 2007

The Cambridge 2007 iGEM team developed a PoPS amplifier system using phage activators and promoters. The system works by using a PoPS input to make an activator protein, as shown in the diagram from their wiki below, which then binds to a promoter and generates a Pops output.

Amplifier07.jpg


In order to quantify the ratio between PoPS in and PoPS out, the team built the following construction on the high copy plasmid pSB1A2, with mRFP and GFP as PoPS reporters and 15 total combinations of different activators and reporters.

Construction07.jpg


They successfully quantified the PoPS amplification factors for each activator/promoter combination after arabinose induction.

Further work - Cambridge iGEM 2009

We hope more fully characterize the activator constructs. First, we hope to characterize these activators on low copy plasmids as promoters compared to the Relative Promoter Unit (RPU). Secondly, we will investigate the activators' sensitivity to arabinose.

Recreating Previous Work

We began by recreating the 2007 team's data with some select amplifier constructs. We have the advantage over the 2007 team in that we have a better plate reader that is able to take OD600 absorbance readings at the same time as taking RFP and GFP absorbance readings. For our transformations, we used the E. coli host strain BW27783. This host strain constitutively expresses arabinose transporters and is unable to metabolize arabinose, making it an ideal host for arabinose titration experiments.

Experiments

Results

where should we put this?