Difference between revisions of "Part:BBa K2984051"

 
 
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<partinfo>BBa_K2984051 short</partinfo>
 
<partinfo>BBa_K2984051 short</partinfo>
  
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This part is composed of the PsaD promoter (BBa_K2984008), a bleomycin resistance with self cleaving peptide scp (BBa_K2984045), a B2-B2 linker (BBa_K2984034), a YFP mVenus marker (BBa_K2984017), and the Rbcs2 terminator (BBa_K2984018).  
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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_K2984045">bleomycin resistance</a> with self cleaving peptide scp, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984034">B2-B2 linker</a>, a YFP <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984017">mVenus</a> marker, and the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984018">Rbcs2 terminator</a>.  
  
 
This Level 1 construct is designed for comparison of locus dependent expression through fluorescence intensity measuerments.
 
This Level 1 construct is designed for comparison of locus dependent expression through fluorescence intensity measuerments.
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</html>
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The bleomycin resistance leads to a higher expression of the enzyme, due to its working mechanism. For every two bleomycin molecules, the bleomycin resistance gene must be expressed once. The resistance works in a ratio of 1:2 to the antibiotic (Hayes et al., 1990). By having the resistance in the same open reading frame, the enzyme is also expressed, leading to a higher expression of the enzyme (Lumbreras et al. 1998).
  
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K2984051 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2984051 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/a2/T--Humboldt_Berlin--Konstruk_17.jpg" alt="colonies_total" width="500">
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<figcaption>Fig.1 - Image of a successful transformation in <i>E. coli</i> after ligation of the construct. The construct can then be isolated from <i>E. coli</i> to be transformed in <i>C. reinhardtii</i>.</figcaption>
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<partinfo>BBa_K2984051 parameters</partinfo>
 
<partinfo>BBa_K2984051 parameters</partinfo>
 
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==References==
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<ol>
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<li>
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Lumbreras, V., Stevens, D. R., & Purton, S. (1998). Efficient foreign gene expression in <i>Chlamydomonas reinhardtii</i> mediated by an endogenous intron. The Plant Journal, 14(4), 441-447.
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</li>
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<li>
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Hayes, J. D., & Wolf, C. R. (1990). Molecular mechanisms of drug resistance. Biochemical Journal, 272(2), 281.
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</li>
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</ol>

Latest revision as of 23:03, 19 October 2019


L1c-PsaD-bleRscp-YFP-RbcS2

This vector is a part of the Chlamy-HUB-Collection. This part is composed of the PsaD promoter, a bleomycin resistance with self cleaving peptide scp, a B2-B2 linker, a YFP mVenus marker, and the Rbcs2 terminator. This Level 1 construct is designed for comparison of locus dependent expression through fluorescence intensity measuerments.

The bleomycin resistance leads to a higher expression of the enzyme, due to its working mechanism. For every two bleomycin molecules, the bleomycin resistance gene must be expressed once. The resistance works in a ratio of 1:2 to the antibiotic (Hayes et al., 1990). By having the resistance in the same open reading frame, the enzyme is also expressed, leading to a higher expression of the enzyme (Lumbreras et al. 1998).

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1833
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1833
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 4
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1833
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1833
    Illegal NgoMIV site found at 1453
    Illegal NgoMIV site found at 2310
  • 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.


References

  1. Lumbreras, V., Stevens, D. R., & Purton, S. (1998). Efficient foreign gene expression in Chlamydomonas reinhardtii mediated by an endogenous intron. The Plant Journal, 14(4), 441-447.
  2. Hayes, J. D., & Wolf, C. R. (1990). Molecular mechanisms of drug resistance. Biochemical Journal, 272(2), 281.