Team:HKUST-Hong Kong/Achievement

From 2012.igem.org

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           <p>From the day when our project was first  proposed in mid-March to the day when we stop wet lab work in mid-September,  we, our 2012 HKUST iGEM team have been working on our project for almost six  months. In our six-month iGEM life, we spent three month in wet lab. <br />
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  We are proud to say that within the three  months, we have achieved the following:</p>
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  <li>Successfully constructing the  parts for displaying recognition peptide, RPMrel, on the cell wall of Bacillus  subtilis. (BBa_733007)</li>
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  <li>Successfully constructing two  parts for BMP2 synthesis and excretion using signaling peptide ybdN and ydjM  respectively. (BBa_733016, BBa_K733017)</li>
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  <li>Successfully constructing cell  growth inhibitory device for regulating BMP2 production (BBa_K733012)</li>
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  <li>Successfully characterize the  low efficiency promoter pTms which used to drive the expression of antitoxin  ydcD. (BBa_K733009, BBa_K733018)</li>
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  <li>Successfully characterize  xylose inducible promoter which used to control the expression of BMP2 and  toxin ydcE.</li>
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  <li>Successfully characterize cell  growth inhibition device.</li>
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Revision as of 15:36, 24 September 2012

Team:HKUST-Hong Kong - 2012.igem.org

ACHIEVEMENT

From the day when our project was first proposed in mid-March to the day when we stop wet lab work in mid-September, we, our 2012 HKUST iGEM team have been working on our project for almost six months. In our six-month iGEM life, we spent three month in wet lab.
We are proud to say that within the three months, we have achieved the following:

  1. Successfully constructing the parts for displaying recognition peptide, RPMrel, on the cell wall of Bacillus subtilis. (BBa_733007)
  2. Successfully constructing two parts for BMP2 synthesis and excretion using signaling peptide ybdN and ydjM respectively. (BBa_733016, BBa_K733017)
  3. Successfully constructing cell growth inhibitory device for regulating BMP2 production (BBa_K733012)
  4. Successfully characterize the low efficiency promoter pTms which used to drive the expression of antitoxin ydcD. (BBa_K733009, BBa_K733018)
  5. Successfully characterize xylose inducible promoter which used to control the expression of BMP2 and toxin ydcE.
  6. Successfully characterize cell growth inhibition device.