Team:Hong Kong-CUHK

From 2012.igem.org

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Latest revision as of 03:40, 27 September 2012

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WELCOME!

“Let there be light”, it’s the start of our universe. We see the first light from sunrise and wake up. Have you imagined the bacteria can acquire the function of eyes, to “see” the color and respond to it? Our iGEM team applied the knowledge of synthetic biology to engineer the bacteria in order to make them sense different light color and decide to move toward or away from it. To play safe, we proposed a new biosafety approach to control the engineered bacteria from gene level. Below is the abstract of our project and you will find more information in our wiki website!

LIGHT OF NO RETURN

Although the sensory technology has been deeply explored and implemented in various means, most of the developed sensors are chemically-dependent promoters which regulate downstream gene expression. We exploited the use of halobacterial sensors, the sensory rhodopsins which are sensitive to a wide spectrum of readily available light source and build a series of sensing systems to control cellular movement and gene regulation. This system can be executed as a fundamental part for further applications, such as cell targeting and refining. Furthermore, to counter the safety issues caused by the leakage of bioengineered cells, this sensing method altogether with the CRISPR/Cas sytem can target and achieve the cleavage of the transformed plasmid under the stimulation of natural light sources.

Address: Rm. 184, Science Centre, CUHK
Email: kingchan@cuhk.edu.hk Tel: (852)-39434420 Fax: (852)-26037246

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-       <p class="aloveofthunder" style="line-height:normal">WELCOME!</p>
-       <p>When Alexander Fleming won the Nobel Prize in Physiology or Medicine in 1945 for his discovery of the first antibiotic penicillin, he acknowledged and warned the world that the misusage of antibiotics would bring a threat of antibiotic resistant microbes. Indeed, in the past decades, the occurrence of antibiotics resistance in microbes has appeared more frequently and it has become more difficult to treat these infections. Therefore, we aim to manipulate a bacterial immune system, CRISPR/Cas to combat antibiotic resistance.</p>
-      <p>The CRISPR/Cas system is the adaptive immune system presented in many bacteria, and it protects them from the invading genetic materials such as the viral DNA. When a foreign double stranded DNA (dsDNA) invade these specific bacteria, a portion of the DNA is captured by their system and incorporated into spacer sequence. Further invasion of the same dsDNA is recognized by the spacers incorporated earlier and destroyed by the CRISPR-associated protein, Cas3. Through engineering the spacer sequence, we can make the system target any dsDNA that is complementary to the spacer(s). </p>
+ <td colspan="2" style="background-color:#FFF; padding:25px"><!-- InstanceBeginEditable name="EditRegion1" -->
-      <p>How are we going to make use of such intrinsic system to fight against the antibiotic resistant microbes? Bacillus subtilis could have their materials exchanged with both gram positive and negative bacteria through forming nanotubes. As B. subtilis lack of the CRISPR/Cas system, we need to engineer this immune system into B. subtilis. Upon the success of such implantation, the immune components could pass to the others’ cytoplasm through the nanotubes in between, and by manipulating the spacer sequence, the antibiotic resistance gene and any other DNA sequence of interest can be destroyed. </p>
+      <p>&nbsp;</p>
-<p>&nbsp;</p>
+       <p class="aloveofthunder" style="line-height:normal; margin-bottom:35px">WELCOME!</p>
-      <p style="line-height:normal; font-size:36px">ABSTRACT</p>
+       <p><strong><span style="color:#00C;font-size:16px"><em>&ldquo;Let there be light&rdquo;</em></span></strong>, it&rsquo;s the start of our universe. We see the first light from sunrise and wake up. Have you imagined the bacteria can acquire the function of eyes, to &ldquo;see&rdquo; the color and respond to it? Our iGEM team applied the knowledge of synthetic biology to engineer the bacteria in order to make them sense different light color and decide to move toward or away from it. To play safe, we proposed a new biosafety approach to control the engineered bacteria from gene level. Below is the abstract of our project and you will find more information in our wiki website!</p> <p>&nbsp;</p>
-       <p>Although the sensory technology has been deeply explored and implemented in various means, most of the developed sensors are chemically-dependent promoters which regulate downstream gene expression. We exploited the use of halobacterial sensors, the sensory rhodopsins which are sensitive to a wide spectrum of readily available light source and build a series of sensing systems to control cellular movement and gene regulation. This system can be executed as a fundamental part for further applications, such as cell targeting and refining. Furthermore, to counter the safety issues caused by the leakage of bioengineered cells, this sensing method altogether with the CRISPR/Cas sytem can targart and achieve the cleavage of the transformed plasmid under the stimulation of natural light sources.    </p>
+<p style="line-height:normal; font-size:36px; margin-bottom:30px">LIGHT OF NO RETURN      </p>
-     <!-- TemplateEndEditable --></td>
+       <p>Although the sensory technology has been deeply explored and implemented in various means, most of the developed sensors are chemically-dependent promoters which regulate downstream gene expression. We exploited the use of halobacterial sensors, the sensory rhodopsins which are sensitive to a wide spectrum of readily available light source and build a series of sensing systems to control cellular movement and gene regulation. This system can be executed as a fundamental part for further applications, such as cell targeting and refining. Furthermore, to counter the safety issues caused by the leakage of bioengineered cells, this sensing method altogether with the CRISPR/Cas sytem can target and achieve the cleavage of the transformed plasmid under the stimulation of natural light sources.    </p>
+     <!-- InstanceEndEditable --></td>
    </tr>
 </table>