Difference between revisions of "Team:Stuttgart/Rose and Limonene Fragrance"

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             <p>The plasmids from Guo et al. pET28a-KDC-YjgB-ARO8 and pET28a-ATF1, used in this study, were sucessfully confirmed by sequencing the plasmids at GATC (Figure 9 and 10).
 
             <p>The plasmids from Guo et al. pET28a-KDC-YjgB-ARO8 and pET28a-ATF1, used in this study, were sucessfully confirmed by sequencing the plasmids at GATC (Figure 9 and 10).
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              The rose genes KDC-YjgB-ARO8 and ATF1 were sucessfully amplified by PCR.
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              The agarosegel analysis (Fig.11) showed expected ties in the range between 4000-5000 kDa for KDC-YjgB-ARO8 and another tie at 1600 kDa for ATF1.
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              The arabiniose-inducable promotor pBAD (BBa_K206000 from the iGEM kit plate) could also be amplified by PCR. The purified PCR product showed a discrete tie at 130 kDa.
 +
              Additionally another PCR was perfomed, to couple the pBAD promotor to the gene complex with KDC-YjgB-ARO8.
 +
              The Verification by agarosegel electrophoresis showed that the coupling wasn't sucessfull.
 
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<h8>Figure 9: Sequenced rose plasmid (pET28a-ATF1) from Guo et al. </h8>
 
<h8>Figure 9: Sequenced rose plasmid (pET28a-ATF1) from Guo et al. </h8>
 
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<!--<https://static.igem.org/mediawiki/2017/d/d7/Rosescent.png">-->
 
<!--<https://static.igem.org/mediawiki/2017/d/d7/Rosescent.png">-->
 
<img src="https://static.igem.org/mediawiki/2017/7/77/PETKDCYjgBAro8.png" class="img-responsive"/>
 
<img src="https://static.igem.org/mediawiki/2017/7/77/PETKDCYjgBAro8.png" class="img-responsive"/>
 
<h8>Figure 10: Sequenced rose plasmid (pET28a-KDC-YjgB-ARO8) from Guo et al. </h8>
 
<h8>Figure 10: Sequenced rose plasmid (pET28a-KDC-YjgB-ARO8) from Guo et al. </h8>
 
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<!--<https://static.igem.org/mediawiki/2017/d/d1/Gelrose1.png">-->
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<img src="https://static.igem.org/mediawiki/2017/f/fa/Rosegel.png" class="img-responsive"/>
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<h8>Figure 11: Agaraose-gel electrophoresis of purified rose-PCR products</h8>
 
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            <p>
 
              The rose genes KDC-YjgB-ARO8 and ATF1 were sucessfully amplified by PCR.
 
              The agarosegel analysis (Fig.11) showed expected ties in the range between 4000-5000 kDa for KDC-YjgB-ARO8 and another tie at 1600 kDa for ATF1.
 
              The arabiniose-inducable promotor pBAD (BBa_K206000 from the iGEM kit plate) could also be amplified by PCR. The purified PCR product showed a discrete tie at 130 kDa.
 
              Additionally another PCR was perfomed, to couple the pBAD promotor to the gene complex with KDC-YjgB-ARO8.
 
              The Verification by agarosegel electrophoresis showed that the coupling wasn't sucessfull.
 
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  <!--<https://static.igem.org/mediawiki/2017/d/d1/Gelrose1.png">-->
 
  <img src="https://static.igem.org/mediawiki/2017/f/fa/Rosegel.png" class="img-responsive"/>
 
  <h8>Figure 11: Agaraose-gel electrophoresis of purified rose-PCR products</h8>
 
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   <p>HIER TEXT REINKOPIEREN</p>
 
   <p>HIER TEXT REINKOPIEREN</p>
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Revision as of 19:19, 30 October 2017

Results

Rose and Limonene Fragrance


Rose Fragrance

The plasmids from Guo et al. pET28a-KDC-YjgB-ARO8 and pET28a-ATF1, used in this study, were sucessfully confirmed by sequencing the plasmids at GATC (Figure 9 and 10). The rose genes KDC-YjgB-ARO8 and ATF1 were sucessfully amplified by PCR. The agarosegel analysis (Fig.11) showed expected ties in the range between 4000-5000 kDa for KDC-YjgB-ARO8 and another tie at 1600 kDa for ATF1. The arabiniose-inducable promotor pBAD (BBa_K206000 from the iGEM kit plate) could also be amplified by PCR. The purified PCR product showed a discrete tie at 130 kDa. Additionally another PCR was perfomed, to couple the pBAD promotor to the gene complex with KDC-YjgB-ARO8. The Verification by agarosegel electrophoresis showed that the coupling wasn't sucessfull.

Figure 9: Sequenced rose plasmid (pET28a-ATF1) from Guo et al.
Figure 10: Sequenced rose plasmid (pET28a-KDC-YjgB-ARO8) from Guo et al.
Figure 11: Agaraose-gel electrophoresis of purified rose-PCR products

HIER TEXT REINKOPIEREN

Figure 10: HIER TEXT REINKOPIEREN

HIER TEXT REINKOPIEREN

Figure 11:HIER TEXT REINKOPIEREN

HIER TEXT REINKOPIEREN