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| <tr> | | <tr> |
| <td height="58" colspan="2" td background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><p class="style3">RUTGERS iGEM TEAM WIKI</p> | | <td height="58" colspan="2" td background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><p class="style3">RUTGERS iGEM TEAM WIKI</p> |
- | <p class="style3"> </p>
| |
| <p class="style3">MYSIS<br /> | | <p class="style3">MYSIS<br /> |
| </p></td> | | </p></td> |
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| <h4 class="shadow"><img src="https://static.igem.org/mediawiki/2011/f/ff/Screen_Shot_2011-09-25_at_9.57.01_AM.jpg" width="901" height="643"></h4> | | <h4 class="shadow"><img src="https://static.igem.org/mediawiki/2011/f/ff/Screen_Shot_2011-09-25_at_9.57.01_AM.jpg" width="901" height="643"></h4> |
| <p class="stuff">It will open up a screen that will allow the user to manage which organisms and assembly standards the program handles.</p> | | <p class="stuff">It will open up a screen that will allow the user to manage which organisms and assembly standards the program handles.</p> |
| + | <p class="stuff"> </p> |
| <p class="stuff"> </p> | | <p class="stuff"> </p> |
| </td> | | </td> |
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| </tr> | | </tr> |
| <tr> | | <tr> |
- | <td width="69%" class="imgshadow2"><blockquote> | + | |
- | <table width="100%" border="0" cellspacing="0" cellpadding="0"><tr>
| + | |
- | <td colspan="7" td="td" background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><h1><span class="shadow"><img src="https://static.igem.org/mediawiki/2011/5/5c/58-bookmark.png" width="10" height="26" /> Memory Switch</span></h1></td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td colspan="6" class="stuff"><h4 class="shadow">Genetic Switch</h4>
| + | |
- | <p class="stuff">The memory switch, designed Pecking University 2007, will be used in order to allow the bacteria to remember if it has been exposed to laser light or not. This should allow the input signal to be amplified in some sense. The memory uses a modified pRM promoter from lambda phage. <img src="switch_button_off.png" width="209" height="303" align="left" /></p>
| + | |
- | <p class="stuff">When the bacterium is not yet exposed to light, we repress the pRM promoter with cI434. </p>
| + | |
- | <p class="stuff">CI434 is located on a transcript with a ptrpL promoter. </p>
| + | |
- | <p class="stuff">In the Select circuit, LovTap will repress the ptrpL promoter upon light exposure. This will stop repression of the pRM promoter, allowing transcription. Included in the transcript is cI, which is an activator of the pRM promoter, and trpR to repress ptrpL and thus the production of cI434. </p>
| + | |
- | <p class="stuff">Thus even though upon discontinuing light exposure, repression of pRM via cI4343 should occur, the switch represses cI434 and allows for the pRM promoter to continue being transcribed, in conjunction with the pRM activator cI. pRM transcription should stay on via this positive feedback loop. </p>
| + | |
- | <p class="stuff"> </p></td>
| + | |
- | <td width="25%" valign="top" background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png" class="stuff" td="td"><p> </p></td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </blockquote>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td width="69%" class="imgshadow2"><blockquote>
| + | |
- | <table width="100%" border="0" cellspacing="0" cellpadding="0"><tr>
| + | |
- | <td colspan="7" td="td" background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><h1><span class="shadow"><img src="https://static.igem.org/mediawiki/2011/5/5c/58-bookmark.png" width="10" height="26" /> mRFP</span></h1></td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td colspan="6" class="stuff"><h4 class="shadow">Red Fluorescent Proteins</h4>
| + | |
- | <p class="stuff">mRFP1, derived from the Discosoma sp. fluorescent protein "DsRed" by directed evolution first to increase the speed of maturation, then to break each subunit interface while restoring fluorescence, which cumulatively required 33 substitutions.
| + | |
- | he latest red version matures more completely, is more tolerant of N-terminal fusions and is over tenfold more photostable than mRFP1. </p>
| + | |
- | <p class="stuff"><img src="swpics/mrfp.png" width="210" height="184" /><-filler</p>
| + | |
- | <p class="stuff">Three monomers with distinguishable hues from yellow-orange to red-orange have higher quantum efficiencies.
| + | |
- | http://www.mendeley.com/research/improved-monomeric-red-orange-yellow-fluorescent-proteins-derived-discosoma-sp-red-fluorescent-protein/</p>
| + | |
- | <p class="stuff"> </p>
| + | |
- | <h4 class="shadow">Structural Properties</h4>
| + | |
- | <p class="stuff">In the functional conformation of the trp repressor, the protein is “loosely” bound to the alpha helix (of what?). </p>
| + | |
- | <p class="stuff">If LovTAP cannot bind the alpha helix, then the repressor will not function. AsLOV2 on the other hand, “tightly” binds a similar alpha helix in the dark. However, when exposed to 477 nm (blue) light, AsLOV2 undergoes a conformational change and cannot bind the alpha helix. </p>
| + | |
- | <p class="stuff">Thus, LovTap is a trp repressor in the light and is not active in the dark.</p>
| + | |
- | <p class="stuff"> </p>
| + | |
- | <h4 class="shadow">Induction</h4>
| + | |
- | <p class="stuff">In order to produce color a signal needs to be attached to pRM. This signal will be a T7 polymerase, which will activate a strong T7 promoter. Included on the transcript, along with the T7 promoter will be modified RFP (mRFP). Once the bacteria are exposed to light and the Select circuit is activated, the exposed bacteria should produce modified red fluorescent protein, which can be seen via the unaided eye. mRFP1 was derived from the Discosoma sp. fluorescent protein "DsRed"by direction evolution.</p>
| + | |
- | <p> </p>
| + | |
- | <h4 class="shadow">Issues</h4>
| + | |
- | <p class="stuff">Basal transcription can also be a problem at the T7 promoter. T7 is a very strong promoter, so if basal transcription occurs we predict we will get intense color randomly. </p>
| + | |
- | <p class="stuff">We can test other, weaker promoters in T7’s place to see if we still get significant color intensity. Putting a weaker promoter should not significantly affect the color intensity because we have placed this promoter on a high copy plasmid to amplify as much as possible.</p>
| + | |
- | <p class="stuff"> </p></td>
| + | |
- | <td width="25%" valign="top" background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png" class="stuff" td="td"> </td>
| + | |
- | </tr>
| + | |
- |
| + | |
- |
| + | |
- | </table>
| + | |
- | </blockquote>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td width="69%" class="imgshadow2"><blockquote>
| + | |
- | | + | |
- | <table width="100%" border="0" cellspacing="0" cellpadding="0"><tr>
| + | |
- | <td colspan="7" td background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><h1><span class="shadow"><img src="https://static.igem.org/mediawiki/2011/5/5c/58-bookmark.png" width="10" height="26" /> Issues</span></h1></td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- |
| + | |
- | <td colspan="6" class="stuff"><h4 class="shadow">I. Input</h4>
| + | |
- | <p class="stuff"><span id="internal-source-marker_0.4353755620644141">Writing </span>speed is probably the most important concern we will have in this project. We will need to test how long it takes for the bacteria to transcribe the genes and create the color. Seeing as how bacteria replicated very quickly (within half an hour), we predict that transcription occurs even faster since it is a process necessary for bacteria to replicate. Our guess is that this will not be too significant of a problem, envisioning the color to appear within a few minutes.</p>
| + | |
- | <p class="stuff"> </p>
| + | |
- | <h4 class="shadow">II. Processing</h4>
| + | |
- | <p class="stuff">?</p>
| + | |
- | <p> </p>
| + | |
- | <h4 class="shadow">III. Output</h4>
| + | |
- | <p class="stuff">The goal is to make the bacteria produce color in response to the light signal. The bacteria would be grown out into a lawn and then drawn on with the laser pointer and this drawing would appear in color, similar to drawing on a sketch pad. We are literally etching a sketch on the bacteria. </p>
| + | |
- | <p class="stuff">A concern is how long the bacteria will take to respond to the light and produce color. Moreover the bacteria should be sensitive enough so that only the bacteria that are exposed to the light should respond. Essentially there should be as little noise as possible in the coloring.
| + | |
- | A successful engineered Bacterial Etch-a-Sketch would allow a lawn of bacteria to be used as a sketch pad where we can draw on with a household laser pointer. </p>
| + | |
- | <p class="stuff">Depending on the application, this system has the ability to produce intracellular pigment when exposed to 477nm (blue) light. In the future, our bacteria could help solve problems that require a rapid response to light with a quick? visual output.</p>
| + | |
- | <p class="stuff"> </p></td>
| + | |
- | <td width="25%" valign="top" background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png" class="stuff" td></td>
| + | |
- | </tr>
| + | |
- | | + | |
- | </table> </blockquote> </td>
| + | |
| </tr> | | </tr> |
| <td colspan="2" td background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><table width="90%" border="0" cellspacing="5" cellpadding="0"> | | <td colspan="2" td background="https://static.igem.org/mediawiki/2011/9/96/Stripe.png"><table width="90%" border="0" cellspacing="5" cellpadding="0"> |