Difference between revisions of "Part:BBa K1905004"

 
 
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<partinfo>BBa_K1905004 parameters</partinfo>
 
<partinfo>BBa_K1905004 parameters</partinfo>
 
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This part is based on part BBa_K1905001 (Riboswitch to detect L1 mRNA) with the blue fluorescent protein coding sequence.  For the practical purposes of our project, we needed a easily detectable result, so we decided to add the coding sequence for BFP, in order that the results could be reared according to color changing.  So when L1 mRNA interacts with the riboswitch, there will be expression of BFP.
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https://static.igem.org/mediawiki/2016/3/30/TecCEMHSRL1CP.png
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Figure 1. Biobrick design diagram
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This biobrick was chemically synthesised and cloned into both pSB1A3 and pSB1C3 vectors. These were transformed into E. coli TOP10 strain. It was grown at 37°C for 12 hours and then propagated on liquid LB medium. Miniprep plasmid extraction was carried out in order to document the plasmid, as observed on Figure 2.
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https://static.igem.org/mediawiki/2016/2/22/TecCEMHS_documentation2016.jpeg
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Figure 2. Agarose (0.8%) gel electrophoresis; Miniprep plasmid extraction. Lane 2:  BBa_K1905004 - L1 Riboswitch + BFP ligation
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Furthermore, this biobrick worked as initially expected for the techniques that were carried out. White colonies were seen upon plaquing transformed bacteria, as the riboswitch would only allow the expression of reporter protein (Red) only when in contact with the viral mRNA. As we cannot work with this kind of biological material, our characterisation consisted only in observing white colonies vs. coloured colonies (if the riboswitch turned out to be non-functional).

Latest revision as of 18:35, 24 October 2016


Riboswitch to detect L1 mRNA from HPV and express BFP

DNA coding for a riboswitch to detect L1 mRNA from Human Papillomavirus and express Blue Fluorescent Protein. This part includes a promoter (BB_R0010) and a RBS (BBa_B0034), the reverse complementary for a section of L1 DNA coding region, and the original sequence with one base changed, BFP coding region (BBa_K592009) and a terminator (BBa_B0015). When there is presence of L1 mRNA, the riboswitch turns on and it allows the expression of BFP as reporter protein.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


This part is based on part BBa_K1905001 (Riboswitch to detect L1 mRNA) with the blue fluorescent protein coding sequence. For the practical purposes of our project, we needed a easily detectable result, so we decided to add the coding sequence for BFP, in order that the results could be reared according to color changing. So when L1 mRNA interacts with the riboswitch, there will be expression of BFP.


TecCEMHSRL1CP.png


Figure 1. Biobrick design diagram


This biobrick was chemically synthesised and cloned into both pSB1A3 and pSB1C3 vectors. These were transformed into E. coli TOP10 strain. It was grown at 37°C for 12 hours and then propagated on liquid LB medium. Miniprep plasmid extraction was carried out in order to document the plasmid, as observed on Figure 2.


TecCEMHS_documentation2016.jpeg


Figure 2. Agarose (0.8%) gel electrophoresis; Miniprep plasmid extraction. Lane 2: BBa_K1905004 - L1 Riboswitch + BFP ligation


Furthermore, this biobrick worked as initially expected for the techniques that were carried out. White colonies were seen upon plaquing transformed bacteria, as the riboswitch would only allow the expression of reporter protein (Red) only when in contact with the viral mRNA. As we cannot work with this kind of biological material, our characterisation consisted only in observing white colonies vs. coloured colonies (if the riboswitch turned out to be non-functional).