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Team:NCTU Formosa/index
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<div id="description" class="page" data-stellar-background-ratio="0.5"><div class="box"><div class="title">E.colightuner</div><span | <div id="description" class="page" data-stellar-background-ratio="0.5"><div class="box"><div class="title">E.colightuner</div><span | ||
Revision as of 16:34, 26 August 2013
We have developed and 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, light induced promoter, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable circuit to adjust the concentration of IAA, an important factor for plant growth. This circuit is proven to be practical in a closed system of plant tissue.
