Team:NCTU Formosa

From 2013.igem.org

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<div id="description" class="page" data-stellar-background-ratio="0.5"><div class="boxwrap" data-stellar-ratio="1.25"><div class="box"><div class="title">E.colightuner</div><span  
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<div id="title">E.colightuner by NCTU_Formosa</div>
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<div id="contenttext"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. </p>
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<p>Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro.</p><p>By using the sRNA-regulated system, red light induced ooperator, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable system that is capable of expressing four different genes under different conditions. In other words, it is a multitask machine. </p><p id="freeze">wiki freeze time remaining: <span id="day"></span> days <span id="ho"></span> hours <span id="min"></span> minutes <span id="sec"></span> seconds.</div>
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class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. </p>
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{
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<p>Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro.</p>
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var time = new Date()
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<p>By using the sRNA-regulated system, red light induced ooperator, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable system that is capable of expressing four different genes under different conditions. In other words, it is a multitask machine.</p></div></div></div></div>
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<div id="copyright">&copy; 2013  <a title="NCTU_Formosa" href="https://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa">NCTU_Formosa</a></div>
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Revision as of 04:38, 14 September 2013

E.colightuner
by NCTU_Formosa

We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions.

Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro.

By using the sRNA-regulated system, red light induced ooperator, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable system that is capable of expressing four different genes under different conditions. In other words, it is a multitask machine.

Retrieved from "http://2013.igem.org/Team:NCTU_Formosa"