Team:HKUST-Hong Kong/Achievement
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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 | + | <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 months in wet lab. <br /> |
We are proud to say that within the three months, we have achieved the following:</p> | We are proud to say that within the three months, we have achieved the following:</p> | ||
<ol> | <ol> | ||
- | <li>Successfully | + | <li>Successfully constructed the parts for displaying recognition peptide, RPMrel, on the cell wall of <i>Bacillus subtilis</i>. (BBa_K733007)</li> |
- | <li>Successfully | + | <li>Successfully constructed two parts for BMP-2 synthesis and excretion using signaling peptides YbdN and YdjM respectively. (BBa_K733016, BBa_K733017)</li> |
- | <li>Successfully | + | <li>Successfully constructed cell growth inhibitory device for regulating BMP-2 production (BBa_K733012)</li> |
- | <li>Successfully | + | <li>Successfully characterized the low efficiency promoter pTms which was used to drive the expression of antitoxin YdcD. (BBa_K733009, BBa_K733018)</li> |
- | <li>Successfully | + | <li>Successfully characterized xylose inducible promoter which was used to control the expression of BMP-2 and toxin YdcE.</li> |
- | <li>Successfully | + | <li>Successfully characterized cell growth inhibition device.</li> |
</ol> | </ol> | ||
</div> | </div> |
Revision as of 18:24, 24 September 2012
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 months in wet lab.
We are proud to say that within the three months, we have achieved the following:
- Successfully constructed the parts for displaying recognition peptide, RPMrel, on the cell wall of Bacillus subtilis. (BBa_K733007)
- Successfully constructed two parts for BMP-2 synthesis and excretion using signaling peptides YbdN and YdjM respectively. (BBa_K733016, BBa_K733017)
- Successfully constructed cell growth inhibitory device for regulating BMP-2 production (BBa_K733012)
- Successfully characterized the low efficiency promoter pTms which was used to drive the expression of antitoxin YdcD. (BBa_K733009, BBa_K733018)
- Successfully characterized xylose inducible promoter which was used to control the expression of BMP-2 and toxin YdcE.
- Successfully characterized cell growth inhibition device.