Difference between revisions of "Part:BBa K2984042"

 
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<partinfo>BBa_K2984042 short</partinfo>
 
<partinfo>BBa_K2984042 short</partinfo>
  
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This part is composed of the PsaD promoter (BBa_K2984008), a B2-B2 linker (BBa_K2984034), the MHETase enzyme (BBa_K3002037), kindly provided by the iGEM TU Kaiserslautern 2019 team, a YFP tag (BBa_K2984020), and the Rbcs2 terminator (BBa_K2984018). The part can be used to express the MHETase enzyme in C. reinhardtii. The YFP-mVenus tag can be used to detect expression of the MHETase.  
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This vector is a part of the <a href="https://2019.igem.org/Team:Humboldt_Berlin/Part_Collection">Chlamy-HUB-Collection</a>. This part is composed of the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984008">PsaD promoter</a>, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984034">B2-B2 linker</a>, the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K3002037">MHETase enzyme</a>, kindly provided by the iGEM TU Kaiserslautern 2019 team, a YFP <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984020">mVenus</a> tag, and the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984018">Rbcs2 terminator</a>. The part can be used to express the MHETase enzyme in C. reinhardtii. The YFP-mVenus tag can be used to detect expression of the MHETase.  
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<partinfo>BBa_K2984042 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2984042 SequenceAndFeatures</partinfo>
  
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==Characterization==
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<figure>
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<img src="https://2019.igem.org/wiki/images/a/aa/T--Humboldt_Berlin--Konstruk_11.jpg" alt="colonies_total" width="500">
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<figcaption>Fig.1 - Image of a successful transformation in E.coli after ligation of the construct. The construct can then be isolated from E. coli to be transformed in C. reinhardtii</figcaption>
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</figure>
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<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Revision as of 10:36, 17 October 2019


L1c-PsaD-MHETase-YFP-RbcS2

This vector is a part of the Chlamy-HUB-Collection. This part is composed of the PsaD promoter, a B2-B2 linker, the MHETase enzyme, kindly provided by the iGEM TU Kaiserslautern 2019 team, a YFP mVenus tag, and the Rbcs2 terminator. The part can be used to express the MHETase enzyme in C. reinhardtii. The YFP-mVenus tag can be used to detect expression of the MHETase.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1609
    Illegal PstI site found at 1933
    Illegal PstI site found at 2276
    Illegal PstI site found at 3086
    Illegal PstI site found at 3519
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1609
    Illegal PstI site found at 1933
    Illegal PstI site found at 2276
    Illegal PstI site found at 3086
    Illegal PstI site found at 3519
    Illegal NotI site found at 1944
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2854
    Illegal BamHI site found at 4
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1609
    Illegal PstI site found at 1933
    Illegal PstI site found at 2276
    Illegal PstI site found at 3086
    Illegal PstI site found at 3519
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1609
    Illegal PstI site found at 1933
    Illegal PstI site found at 2276
    Illegal PstI site found at 3086
    Illegal PstI site found at 3519
    Illegal NgoMIV site found at 1542
    Illegal NgoMIV site found at 2003
    Illegal NgoMIV site found at 2033
    Illegal NgoMIV site found at 2348
    Illegal NgoMIV site found at 2366
    Illegal NgoMIV site found at 2402
    Illegal NgoMIV site found at 3045
  • 1000
    COMPATIBLE WITH RFC[1000]


Characterization

colonies_total
Fig.1 - Image of a successful transformation in E.coli after ligation of the construct. The construct can then be isolated from E. coli to be transformed in C. reinhardtii