Boston University

From 2007.igem.org

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[[Image:BU_banner.JPG|center]]
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== About Us ==
== About Us ==
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Welcome to the wiki for Boston University's iGEM 2007 team!
Welcome to the wiki for Boston University's iGEM 2007 team!
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[[Image:BU_bubio.jpg|right]]
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Our team consists of [[Boston_University/DS | David Shi]], [[Boston_University/RA | Rahul Ahuja]], [[Boston_University/CL | Christian Ling]], and [[Boston_University/DB | Danny Bellin]],
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all soon-to-be juniors majoring in Biomedical Engineering at Boston University.
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Our team consists of the following members:
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We are advised by [http://www.bu.edu/dbin/bme/faculty/?prof=tgardner Dr. Timothy Gardner], Assistant Professor of Biomedical Engineering, as well as [[Boston_University/FJ | Frank Juhn]], [[Boston_University/KL | Kevin Litcofsky]], and [[Boston_University/SS | Stephen Schneider]], students in the [http://gardnerlab.bu.edu/ Gardner Laboratory], where we work.  We are grateful to our advisors for their time and support!
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Undergraduates: David Shi, Rahul Ahuja, Christian Ling, Danny Bellin
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We are also grateful to [http://www.pfizer.com Pfizer], the [http://www.bu.edu/eng Boston University College of Engineering], and the [http://www.bu.edu/eng/bme Boston University Department of Biomedical Engineering], for their generous support of our team.
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Faculty Advisor:  [http://www.bu.edu/dbin/bme/faculty/?prof=tgardner Dr. Timothy Gardner]
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== Our Project==
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Graduate Student Advisors: Frank Juhn, Stephen Schneider
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The goal of our project is to use [[Directed_Evolution | directed evolution]] to increase the current output of the electrogenic bacteria [[Shewanella_oneidensis | 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.
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In the case of S. oneidensis, certain [[GTRs_in_S_oneidensis | 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 | error-prone PCR]] and transformed into S. oneidensis in hopes of altering current output.
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We work at the the [http://www.gardnerlab.bu.edu Gardner Laboratory].
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Bacteria that express greater electrogenic capability will then be selected via [[Boston_University/Fluorescence-Activated_Cell_Sorting | flow cytometry]] or other viable selection methods.  
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== Our Project Plan ==
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This process of directed evolution can be repeated with previously selected S. oneidensis in order to increase the level of
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Our project is aimed at increasing current production from Shewanella Oneidensis by directed evolution of global transcription factors
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electrogenesis even further.
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Our plan so far:
 
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# Mutate global transcription factors
 
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## [[Design primers for amplification]]
 
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## [[Perform error-prone PCR]]
 
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# Transform mutated genes into E. coli
 
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## Choose plasmids
 
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## Restriction enzyme digestion
 
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## Ligation
 
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## Transformation into E. coli
 
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# Conjugate E. coli with Shewanella
 
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# Screen/select for increased current production due to mutations
 
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== Week's Goals ==
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{| align="center" style="color:white;" border="1"
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|-
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| bgcolor="#990000" color="white" height="30pt" align="center" | '''Our Team'''
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| bgcolor="#990000" color="white" align="center" | '''Project Design'''
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| bgcolor="#990000" color="white" align="center" | '''Project Results'''
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| bgcolor="#990000" color="white" align="center" | '''Miscellany'''
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|- style="color:#990000;"
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| align="left" width="375pt" |
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:'''Undergraduate Students'''
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::[[Boston_University/RA | Rahul Ahuja]] • [[Boston_University/DB | Daniel Bellin]]
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::[[Boston_University/CL | Christian Ling]] • [[Boston_University/DS | David Shi]]
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:'''Graduate Advisors'''
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::[[Boston_University/Frank Juhn | Frank Juhn]] • [[Boston_University/Kevin Litcofsky | Kevin Litcofsky]]
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::[[Boston_University/Stephen Schneider | Stephen Schneider]]
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:'''Principal Advisor'''
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::[http://www.bu.edu/dbin/bme/faculty/?prof=tgardner Dr. Timothy Gardner]
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| align="left" width="350pt"|
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:'''[[Boston_University/Why_Shewie | Why ''S. oneidensis''?]] '''
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:'''Directed Evolution'''
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::1. [[Boston_University/Plasmid Selection and Design | Plasmid Selection and Design]]
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::2. [[Boston_University/Mutation of GTFs | Mutation of GTFs]]
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::3. Transformation of GTFs into Shewie
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::::[[Boston_University/TOPO Cloning | TOPO Cloning]] • [[Boston_University/Conjugation | Conjugation]] [[Boston_University/Zymo | Zymo]]
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::4. Selection Methods
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::::[[Boston_University/Microencapsulation | Microencapsulation ]]
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::::[[Boston_University/Redox-sensitive fluorescent dye | Redox-sensitive fluorescent dye]]
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::::[[Boston_University/Fluorescence-Activated Cell Sorting | Fluorescence-Activated Cell Sorting]]
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| align="left" width="250pt" |
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:'''[[Boston_University/Zymo Transformation Results | Zymo Transformation]]'''
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:'''[[Boston_University/Electroporation Results | Electroporation]]'''
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:'''[[Boston_University/Bacterial Conjugation Results | Bacterial Conjugation]]'''
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:'''[[Boston_University/Plasmid Customization | Plasmid Customization]]'''
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:'''[[Boston_University/TOPO Cloning Results | TOPO Cloning]]'''
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:'''[[Boston_University/TOPO Transformation Results | TOPO Transformation]]'''
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:'''[[Hi-Scores and Other Greatness]]'''
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| align="left" width="250" |
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:'''[[Boston_University/Project Progress | Project Progress]]'''
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:'''[[Boston_University/Protocols | Protocols]]
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:'''[[Boston_University/Lab Photos | Lab Photos]]
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<!--:'''[[Boston_University/Team Photos | Team Photos]]-->
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:'''[[Boston_University/BU Photos | BU Photos]]
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:'''[[Boston_University/Image Dump | Image Dump (56k stay away!)]]
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|-
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|}
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Wednesday 5/30
 
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# Get all protocols
 
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#  Identify materials/prepare order
 
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#  Design Primers
 
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#  Learn about budget/POs
 
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Thursday 5/31
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<!--
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# Do primer order
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[[Image:shewie.jpg]]
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# Start conjugation practice
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[[Image:shewie2.jpg]]
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# Confirm restriction enzymes, ligases
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[[Image:pjq200.jpg]]
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# Order confirmed/needed materials
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[[Image:conjugation.jpg]]
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# Team Revew Meeting
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[[Image:fluorescent1.jpg]]
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[[Image:fluorescent2.jpg]]
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[[Image:fluorescent3.jpg]]
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[[Image:fluorescent4.jpg]]
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[[Image:facs.jpg]]
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[[Image:topo.jpg]]
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[[Image:topo2.jpg]]
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[[Image:bulogo.jpg]]
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[[Image:gardnerlogo.jpg]]
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[[Image:bu_collegeofengineering.jpg]]
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[[Image:gardner_logo.jpg]]
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[[Image:bubio.jpg]]
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!-->
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Friday 6/1
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==Supported By==
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# Evaluate/continue conjugation, practice electroporation for E. coli
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{| align="center" style="color:white;"
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# Meeting with Tim: Budgets/protocols, Pfizer/fundraising, iGEM registration, beads
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|-
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| width="150pt" | [[Image:BU_pfizer.gif]]
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| width="325pt" | [[Image:bu_collegeofengineering.gif]]
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|[[Image:Bu_Gardner_logo_small.jpg]]
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|-
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|}

Latest revision as of 22:29, 20 October 2007

BU banner.JPG


About Us

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

BU bubio.jpg

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 [http://www.bu.edu/dbin/bme/faculty/?prof=tgardner Dr. Timothy Gardner], Assistant Professor of Biomedical Engineering, as well as Frank Juhn, Kevin Litcofsky, and Stephen Schneider, students in the [http://gardnerlab.bu.edu/ Gardner Laboratory], where we work. We are grateful to our advisors for their time and support!

We are also grateful to [http://www.pfizer.com Pfizer], the [http://www.bu.edu/eng Boston University College of Engineering], and the [http://www.bu.edu/eng/bme 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.


Our Team Project Design Project Results Miscellany
Undergraduate Students
Rahul Ahuja • Daniel Bellin
Christian Ling • David Shi
Graduate Advisors
Frank Juhn • Kevin Litcofsky
Stephen Schneider
Principal Advisor
[http://www.bu.edu/dbin/bme/faculty/?prof=tgardner Dr. 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
Microencapsulation
Redox-sensitive fluorescent dye
Fluorescence-Activated Cell Sorting
Zymo Transformation
Electroporation
Bacterial Conjugation
Plasmid Customization
TOPO Cloning
TOPO Transformation
Hi-Scores and Other Greatness
Project Progress
Protocols
Lab Photos
BU Photos
Image Dump (56k stay away!)


Supported By

BU pfizer.gif Bu collegeofengineering.gif Bu Gardner logo small.jpg
Retrieved from "http://2007.igem.org/wiki/index.php/Boston_University"