Team:Berkeley

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<p>Biosensors have widespread applications ranging from diagnostics to environmental monitoring. Vibrio cholerae's ToxR system can be used as a component in biological devices capable of detecting a wide variety of molecules. A periplasmic domain causes ToxR homodimerization, activating transcription of the ctx promoter. By replacing the periplasmic domain of ToxR with existing or engineered ligand-dependent homodimers, we hope to link ToxR dimerization (and gene expression) to the presence of specific ligands. Initially, ToxR constructs proved to be toxic to E. coli. To address ToxR toxicity, we constructed a stress-based negative feedback transcription system. This allowed us to express relatively high levels of toxic proteins so that we could continue to engineer ToxR chimeras. We then fused an estrogen dependent dimer with ToxR in hopes of creating an estrogen biosensor. We have observed a range of constitutive phenotypes and have more experiments planned to engineer a dose-dependent transcriptional response to estrogen. By fusing existing or engineered ligand dependent homodimers to ToxR, this modular system can be applied to develop new biosensors. </p>
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<p>Biosensors have widespread applications ranging from diagnostics to environmental monitoring. Vibrio cholerae's ToxR system can be used as a component in biological devices capable of detecting a wide variety of molecules. A periplasmic domain causes ToxR homodimerization, activating transcription of the ctx promoter. By replacing the periplasmic domain of ToxR with existing or engineered ligand-dependent homodimers, we hope to link ToxR dimerization (and gene expression) to the presence of specific ligands. Initially, ToxR constructs proved to be toxic to E. coli. To address ToxR toxicity, we constructed a stress-based negative feedback transcription system. This allowed us to express relatively high levels of toxic proteins so that we could begin to engineer ToxR chimeras. We fused an estrogen-dependent dimer with ToxR hoping to create an estrogen biosensor. We observed a range of constitutive phenotypes and have more experiments planned to engineer a dose-dependent transcriptional response to estrogen. By fusing existing or engineered ligand dependent homodimers to ToxR, this modular system can be applied to develop new biosensors. </p>
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Revision as of 18:31, 28 September 2011

Berkeley iGEM 2011

header
Mercury

Biosensors have widespread applications ranging from diagnostics to environmental monitoring. Vibrio cholerae's ToxR system can be used as a component in biological devices capable of detecting a wide variety of molecules. A periplasmic domain causes ToxR homodimerization, activating transcription of the ctx promoter. By replacing the periplasmic domain of ToxR with existing or engineered ligand-dependent homodimers, we hope to link ToxR dimerization (and gene expression) to the presence of specific ligands. Initially, ToxR constructs proved to be toxic to E. coli. To address ToxR toxicity, we constructed a stress-based negative feedback transcription system. This allowed us to express relatively high levels of toxic proteins so that we could begin to engineer ToxR chimeras. We fused an estrogen-dependent dimer with ToxR hoping to create an estrogen biosensor. We observed a range of constitutive phenotypes and have more experiments planned to engineer a dose-dependent transcriptional response to estrogen. By fusing existing or engineered ligand dependent homodimers to ToxR, this modular system can be applied to develop new biosensors.

A protein with great potential as a general biosensor system.

Chimeric proteins that drive translation off of the Pctx promoter.

Our method for expressing interesting (but toxic) proteins.

Bacteria engineered to detect the presence of estrogen.


We are Team Berkeley, a cohesive unit of 7 undergraduates and 3 advisers. Earlier this year we planned a complex project that was risky given the short amount of time iGEM made available. We quickly learned each others strengths and weaknesses in order to develop a system of organizational communication to synchronize our efforts for the task at hand. We created protocols and taught them to each other, and extensively used google docs to always keep up with what others were doing or what steps we have to take to complete the project. Through months of hard work, we have been able to fine tune our ability to work together. As a team, we have learned firsthand how the synthetic biology community relies on the goal-oriented cooperation of skilled individuals from very different backgrounds and skill sets. Some of us have a very strong engineering background and are very good at working with new technology while others of us have a strong biology background and work better with research problem solving. We are proud of the project that we have created which we will present at the Jamboree together in October.


The UC Berkeley iGEM team would like to thank Autodesk and Agilent for their financial support and Synberc, for their administrative support.