Difference between revisions of "Team:WPI Worcester/Attributions"

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<p>In the lab, Camille was involved in transforming E. coli strains with different proteins, including the various antifreeze proteins tested in this project. Camille also made competent EMG, DH5a, NCTC and BL21. She was heavily involved in running biofilm assay plates to test the antifreeze proteins’ abilities at disrupting and preventing biofilm growth. Camille ran agarose gel electrophoresis to visualize DNA fragments from the samples as well as his-tag gels to visualize the expressed proteins from the transformations. Camille also held the position of Content Master for the team’s wiki page. </p>
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<p>In the lab, Camille was involved in transforming E. coli strains with different proteins, including the various antifreeze proteins tested in this project. She performed Gibson assembly cloning and made competent EMG, DH5a, NCTC and BL21. She was heavily involved in running biofilm assay plates to test the antifreeze proteins’ abilities at disrupting and preventing biofilm growth. Camille ran agarose gel electrophoresis to visualize DNA fragments from the samples as well as his-tag gels to visualize the expressed proteins from the transformations. Camille also held the position of Content Master for the team’s wiki page. </p>
  
  

Revision as of 22:16, 12 October 2018

Attributions

The 2018 WPI iGEM Team would like to extend a sincere thanks to all those who contributed to the completion of our project! The team started working in D term, or late May, of 2018 and continued into October of 2018.

Team Members

What follows is a summary of the contributions of each team member.

Bailey Sweet:

Kylie Sumner:

In the lab, Kylie performed E. coli transformations, did Gibson assembly cloning, made competent E. coli of various strains, ran more DNA and protein gels than any person should ever have to, and tested the effect of different antifreeze proteins on the formation of biofilm growth. Kylie was also the Collaborations Chair for the team this year.

Alex Rebello:

Camille Pearce:

In the lab, Camille was involved in transforming E. coli strains with different proteins, including the various antifreeze proteins tested in this project. She performed Gibson assembly cloning and made competent EMG, DH5a, NCTC and BL21. She was heavily involved in running biofilm assay plates to test the antifreeze proteins’ abilities at disrupting and preventing biofilm growth. Camille ran agarose gel electrophoresis to visualize DNA fragments from the samples as well as his-tag gels to visualize the expressed proteins from the transformations. Camille also held the position of Content Master for the team’s wiki page.

Mei Hao:

Beck Arruda:

Arth Sharma:

In the lab, Arth tested the antimicrobial properties of curcumin (the active ingredient of turmeric) in biofilm assays. With subcloning and protein extraction experiments, he aided in preparing cultures, and measuring sample concentrations. Serving as Outreach and Engagement Chair, he aided the organization and documenting of public demonstrations and workshops in our lab.

Faculty:

A special thanks to the WPI faculty who have facilitated, assisted, and encouraged the ongoing research of iGEM and helped make the project possible.

Dr. Natalie Farny:

Advisor of WPI iGEM. Assisted in acquiring of plasmid vectors, reagents, ascertaining protocols, and in subcloning genes.

Mr. Mihail Bocka:

WPI Lab manager. Provided supplies and reagents for our experiments when needed.

Dr. Lou Roberts:

WPI teaching staff. Assisted in electroporation of NCTC.

Dr. Mike Buckholt:

WPI teaching staff. Aided in the usage of lab instruments.

Dr. Jill Rulfs:

WPI teaching staff. Provided assistance in troubleshooting broken equipment and gathering necessary lab supplies.

Project Inspiration:

With the recent outbreaks of pathogenic bacteria on leafy crops such as lettuce, we sought to address the problem with the research conducted by the 2015 WPI iGEM team. They had confirmed the antibacterial capacity of antifreeze proteins in disrupting biofilm development. Moreover, with the growing societal embracement of natural compounds to combat common pathologies, we assessed the utility of the flavonoid curcumin as an antibacterial.

Supporting Research

We borrowed the crystal violet assay protocol from the major qualifying project report, "Using Biofilms for the Detection and Bioremediation of Arsenic."

Outside Institutions

Alex, work your magic bro.

iGEM Teams

We would like to extend a deep thanks to the Pasteur Paris iGEM team for their biofilm assay protocol!