Boston University

From 2007.igem.org

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(Project Progress)
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|- style="color:#990000;"
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| align="left" width="200pt" | '''Undergraduate Students'''  
| align="left" width="200pt" | '''Undergraduate Students'''  
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:[[Rahul Ahuja]] • [[Daniel Bellin]]
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:[[Boston_UniversityRA | Rahul Ahuja]] • [[Boston_UniversityDS | Daniel Bellin]]
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:[[Christian Ling]] • [[David Shi]]  
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:[[Boston_UniversityDS | Christian Ling]] • [[Boston_UniversityDS | David Shi]]  
'''Graduate Advisors'''
'''Graduate Advisors'''
:[[Frank Juhn]] • [[Kevin Litcofsky]]
:[[Frank Juhn]] • [[Kevin Litcofsky]]

Revision as of 17:13, 6 July 2007

Rhett2.JPG

About Us

Welcome to the wiki for Boston University's iGEM 2007 team!

Our team consists of David Shi, Rahul Ahuja, Christian Ling, and Danny Bellin, all soon-to-be juniors majoring in Biomedical Engineering at Boston University.

We are advised by Dr. Timothy Gardner, Assistant Professor of Biomedical Engineering, as well as Frank Juhn, Kevin Litcofsky, and Stephen Schneider, students in the Gardner Laboratory, where we work. We are grateful to our advisors for their time and support!

We are also grateful to Pfizer, the Boston University College of Engineering, and the Boston University Department of Biomedical Engineering, for their generous support of our team.

Our Project

The goal of our project is to use directed evolution to increase the current output of the electrogenic bacteria Shewanella oneidensis (affectionately referred to as Shewie in the Gardner Lab). As the name suggests, directed evolution consists of two main steps: intentionally mutating DNA and then selecting for the expression of desired traits.

In the case of S. oneidensis, certain global transcription regulators in its genome have been identified as being related to the metabolic processes of the bacteria. These global transcription regulators will be mutated via error-prone PCR and transformed into S. oneidensis in hopes of altering current output. Bacteria that express greater electrogenic capability will then be selected via flow cytometry or other viable selection methods. This process of directed evolution can be repeated with previously selected S. oneidensis in order to increase the level of electrogenesis even further.

Project Progress

Project Progress



Our Team Project Design Project Results Miscellany
Undergraduate Students
Rahul Ahuja Daniel Bellin
Christian Ling David Shi

Graduate Advisors

Frank JuhnKevin Litcofsky
Stephen Schneider

Principal Advisor

Prof. Timothy Gardner
Why S. oneidensis?

Directed Evolution

1. Plasmid Selection and Design
2. Mutation of GTFs
3. Transformation of GTFs into Shewie
TOPO Cloning • Conjugation • Zymo
4. Selection Methods
Fluorescence-Activated Cell Sorting
TOPO Cloning
TOPO Transformation
Bacterial Conjugation
Zymo Transformation
Electroporation
stv