Team:Minnesota/Project/UV Absorption

From 2012.igem.org

(Difference between revisions)
Line 141: Line 141:
<!---END-->
<!---END-->
-
<a href="https://2012.igem.org/Team:Minnesota/Project">Click here to return to Projects page.</a>
+
<br><a href="https://2012.igem.org/Team:Minnesota/Project">Click here to return to Projects page.</a>
</div>
</div>

Revision as of 01:43, 4 October 2012

Team:Minnesota - Main Style Template Team:Minnesota - Template

Like us on FB and follow us on Twitter!

Synthesizing UV-Protective Compounds in Bacteria


      Our first idea was to engineer the production of the Micosprine-like Amino Acids (MAAs) in E. coli. These compounds confer UV protection in Anabaena variabilis and are currently used in sunscreen that protects against the entire UVA and UVB spectrum. To obtain these compounds for use in industry, the current method is direct extraction from A. variabilis. To develop an alternate way of producing these compounds, genes coding for enzymes in their production pathways were taken from A. variabilis and cloned into E. coli using BioBrickTM techniques. The result: E. coli that can produce UV protectant compounds, which has several implications. E. coli are cheap, easy to produce, grow quickly, are preferred for use in industry, and can be grown up in giant bioreactors. Therefore the speed and ease at which MAA-producing bacteria can be grown, as well as the amount that can be grown would drastically increase. Additionally, promoters and mechanisms of down-regulation in E. coli are well characterized, making modification and control of the pathway much simpler. These parts could easily be employed in future experiments where increased UV tolerance is desired (for example, in the characterization of a UV-sensitive promoter). Alternatively, a skin-based, UV-protectant probiotic could eventually be developed if these parts are incorporated into a native, non-pathogenic skim bacterium chassis, such as Staphylococcus epidermidis. Imagine a “sunscreen” that grows naturally on your skin!
Click here to return to Projects page.