Team:TP CC-SanDiego/Mentors
From 2014hs.igem.org
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<h2>John DeFriel</h2> | <h2>John DeFriel</h2> | ||
- | <h3></h3> | + | <h3>Simply put, John is the Most Interesting Man in the World. Alternatively put, he used to be a helicopter snowboarding instructor. If that hasn't convinced you, John got his BA in Rhetoric when he was 20, then lived in a truck for 2 years at the bottom of Mt. Baker where he recorded snowfall for avalanche studies while flirting with the idea of becoming a professional snowboarder. Instead, he decided getting a BS in Chemical Engineering in 3 years was a more fitting challenge. John was on the 2011 Wisconsin-Madison iGem team and remembers seeing Spencer in his stupid checkered inspector hat and thinking "What a doofus!"</h3> |
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Revision as of 05:40, 12 June 2014
{
STATISTICS
Statistics that are quite relevant to the nature of this experiment
Statistics that are quite relevant to the nature of this experiment
Toxicity of aflatoxin is 10 times that of hydrocyanic acid and 68 times of arsenic.
This disease is the third-leading cause of cancer death globally according to WHO (2008), with about 550,000–600,000 new cases each year.
This disease is the third-leading cause of cancer death globally according to WHO (2008), with about 550,000–600,000 new cases each year
ENGINEERING
E. Coli Capable of Extracelluar Secretion of Mycotoxin Detoxifying Enzymes
E. Coli Capable of Extracelluar Secretion of Mycotoxin Detoxifying Enzymes
Microfungi that produce harmful mycotoxins flourish on improperly-stored nuts, grains, meat, and dairy. They especially thrive in developing countries, where the lack of advanced food storage and mycotoxin exposure causes 40% of the diseases. To lessen the problem, our team engineered E. coli strains using synthetic biology tools to produce chimeric mycotoxin-degrading fungal enzymes, Aflatoxin-Detoxifizyme (ADTZ) and Zearalenone Hydrolase (ZHD101), which are designed to be secreted to extra-cellular space by fusing with secretion signal peptides from alpha-amylase and beta-lactamase. In this study, we have successfully generated synthetic genetic materials to produce four chimeric mycotoxin-detoxifying enzymes. The levels of extracellular secretion is also characterized and analyzed. The project will allow a mass production of detoxification enzymes in cost effective way, preventing the squandering of harvested crops, and limiting mycotoxin-related diseases. Increased access to these proteins will have an immense commercial, industrial, agricultural, and health impact.