Difference between revisions of "Team:NAWI Graz/Description"

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         <h2 class="section-sub">Detailed Project Description</h2>
 
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         We designed two different plasmids, which are transformed in an <i>E. coli</i>  strain. Each of the plasmids contains a pH-sensitive promoter. The promoters are induced by different pH-levels. An acidic pH leads to the expression of a red fluorescent protein, mCardinal, and an alkaline pH to a green fluorescent protein, mNeonGreen.  
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         We designed <a href="https://2017.igem.org/Team:NAWI_Graz/pHPlasmid">two different plasmids</a>, which are transformed in an <i>E. coli</i>  strain. Each of the plasmids contains a pH-sensitive promoter. The promoters are induced by different pH-levels. An acidic pH leads to the expression of a red fluorescent protein, mCardinal, and an alkaline pH to a green fluorescent protein, mNeonGreen.  
 
Both fluorescent proteins contain a N-terminal TEV-site followed by a F-degron. The TEV-site allows the degradation by the TEV-protease. Once the TEV-site is cleaved off, the F-degron can be recognized by the endogenous ClpAP-machinery. This ClpAP-machinery induces the degradation of the fluorescent proteins and enables a faster change in fluorescence, when a pH-shift occurs. This addition could be beneficial in the future to avoid accumulation of fluorescence protein, if you plan to use the same bacterial culture for an extended amount of time. Therefore, the TEV-protease has to be integrated into the genome by CRISPR/Cas9, a novel method for gene-editing.  
 
Both fluorescent proteins contain a N-terminal TEV-site followed by a F-degron. The TEV-site allows the degradation by the TEV-protease. Once the TEV-site is cleaved off, the F-degron can be recognized by the endogenous ClpAP-machinery. This ClpAP-machinery induces the degradation of the fluorescent proteins and enables a faster change in fluorescence, when a pH-shift occurs. This addition could be beneficial in the future to avoid accumulation of fluorescence protein, if you plan to use the same bacterial culture for an extended amount of time. Therefore, the TEV-protease has to be integrated into the genome by CRISPR/Cas9, a novel method for gene-editing.  
 
The fluorescence signals are detected by a camera, leading to maneuvering the robot through an arena. Depending on the fluorescent color of the media, the robot turns either left or right.
 
The fluorescence signals are detected by a camera, leading to maneuvering the robot through an arena. Depending on the fluorescent color of the media, the robot turns either left or right.

Revision as of 18:06, 1 November 2017

PROJECT DESCRIPTION


Vid. 1: Video about our project. This video gives a short overview of project

The aim of our project was to create a robot-bacteria interface, where information processing is done by a bacterial culture that exhibits a feedback loop with a mobile robot. To enable communication between bacteria and robot, we decided to engineer Escherichia coli cells to respond to changes in pH with a change in fluorescence. To achieve pH-dependent expression of fluorescence protein, we used two different promoters: the acid inducible asr promoter and the alkaline inducible alx promoter.

Introduction

An important area at the cutting edge of technology is the integration of biological systems in mechanical and automated systems. For our iGEM project we therefore chose to take a new approach on the integration of biology into technology. Our goal was the creation of a robot-bacteria interface that acts in a constant feedback loop. The first step was to make communication between bacteria and a technical system possible. Therefore, we created a pH-sensitive E. coli strain that expresses detectable proteins according to pH-level. The pH-level is determined by the position of a mobile robot in an arena with a virtual pH-gradient. The pH-level indicated by the robot's position is passed on to a bacterial culture in a bioreactor. As a response to the pH-shift, a shift in fluorescence protein expression is achieved due to the pH-sensitive promoters alx and asr. This altered expression correlates with a change in color, that is detectable with an optical system. The data from the optical signal is then sent back to the robot resulting in a response in the form of a directional change. Thus, we can control the motion of the robot through the arena with a constant feedback loop to the bioreactor.

Detailed Project Description

We designed two different plasmids, which are transformed in an E. coli strain. Each of the plasmids contains a pH-sensitive promoter. The promoters are induced by different pH-levels. An acidic pH leads to the expression of a red fluorescent protein, mCardinal, and an alkaline pH to a green fluorescent protein, mNeonGreen. Both fluorescent proteins contain a N-terminal TEV-site followed by a F-degron. The TEV-site allows the degradation by the TEV-protease. Once the TEV-site is cleaved off, the F-degron can be recognized by the endogenous ClpAP-machinery. This ClpAP-machinery induces the degradation of the fluorescent proteins and enables a faster change in fluorescence, when a pH-shift occurs. This addition could be beneficial in the future to avoid accumulation of fluorescence protein, if you plan to use the same bacterial culture for an extended amount of time. Therefore, the TEV-protease has to be integrated into the genome by CRISPR/Cas9, a novel method for gene-editing. The fluorescence signals are detected by a camera, leading to maneuvering the robot through an arena. Depending on the fluorescent color of the media, the robot turns either left or right.

Applications and Implications

One of the possible applications could be a bioreactor with bacteria that control their environment via active feedback. This enables the bacteria to give a signal, if they are in need of a different media composition. For example, if more nutrients or a correction of the pH-level become necessary, bacteria will indicate it and a robot automatically adapts the medium to the circumstances. The technology also holds potential in the creation of reusable biosensors or a controlled bioremediation effort, where bacteria are mobile due to the connection to a robot host.