Difference between revisions of "Part:BBa K2984018"

 
 
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[[Image:Terminator.png]]
 
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<partinfo>BBa_K2984018 parameters</partinfo>
 
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<partinfo>BBa_K2984018 short</partinfo>
 
<partinfo>BBa_K2984018 short</partinfo>
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* To terminate the transcription of a gene a signal on the DNA is required. The nucleotide sequence mediating this signal to the RNA-polymerase is called terminator. In 1986 a <i>Chlamydomonas reinhardtii</i> native gene for the small subunits of the ribulose bisphosphate carboxylase/oxygenase (Rubisco) was characterized (Goldschmidt-Clermont and Rahire, 1968; Stevens et al., 1996).
 
  
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This part is a part of the <a href="https://2019.igem.org/Team:Humboldt_Berlin/Part_Collection">Chlamy-HUB-Collection</a>. To terminate the transcription of a gene a signal on the DNA is required. The nucleotide sequence mediating this signal to the RNA-polymerase is called terminator. In 1986 a <i>Chlamydomonas reinhardtii</i> native gene for the small subunits of the ribulose bisphosphate carboxylase/oxygenase (Rubisco) was characterized (Goldschmidt-Clermont and Rahire, 1968; Stevens et al., 1996).
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'''Secondary Structure'''
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This part was designed to be used with the MoClo standard and has B5-C1 overhangs.
  
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[[Image:Mfold-K2984018-1.png]]
 
  
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<hr>
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<span class='h3bb'>Sequence and Features</span>
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'''Measurement'''
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<partinfo>BBa_K2984018 SequenceAndFeatures</partinfo>
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* [http://openwetware.org/wiki/Cconboy:Terminator_Characterization/Results How these parts were measured]
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==Characterization==
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<html>
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<figure>
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<img src="https://static.igem.org/mediawiki/parts/1/11/T--Humboldt_Berlin--RbcS2_B5-C1.png" alt="Cloning scheme L0-RbcS2 B5-C1" width="500">
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<figcaption>Fig.1 - Cloning scheme of L0-RbcS2_B5-C1 into <i>E. coli</i>. <B>A</B>  RbcS2 B5-C1 PCR product on agarose gel. <B>B + C</B> Successful transformation into <i>E. coli</i>. <B>D + E</B> Sequencing results of L0-RbcS2_B5-C1.</figcaption>
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</figure>
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<!-- Uncomment this to enable Functional Parameter display
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===Functional Parameters===
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<partinfo>BBa_K2984009 parameters</partinfo>
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<!-- -->
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==References==
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<ol>
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<li>
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Goldschmidt-Clermont, M., & Rahire, M. (1986). Sequence, evolution and differential expression of the two genes encoding variant small subunits of ribulose bisphosphate carboxylase/oxygenase in Chlamydomonas reinhardtii. Journal of molecular biology, 191(3), 421-432.
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</li>
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<li>Stevens, D. R., Purton, S., & Rochaix, J.-D. (1996). The bacterial phleomycin resistance geneble as a dominant selectable marker inChlamydomonas. Molecular and General Genetics MGG, 251(1), 23–30. https://doi.org/10.1007/BF02174340
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</li>
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</ol>

Latest revision as of 21:03, 21 October 2019


RbcS2 - Terminator B5-C1

This part is a part of the Chlamy-HUB-Collection. To terminate the transcription of a gene a signal on the DNA is required. The nucleotide sequence mediating this signal to the RNA-polymerase is called terminator. In 1986 a Chlamydomonas reinhardtii native gene for the small subunits of the ribulose bisphosphate carboxylase/oxygenase (Rubisco) was characterized (Goldschmidt-Clermont and Rahire, 1968; Stevens et al., 1996).

This part was designed to be used with the MoClo standard and has B5-C1 overhangs.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 258
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Characterization

Cloning scheme L0-RbcS2 B5-C1
Fig.1 - Cloning scheme of L0-RbcS2_B5-C1 into E. coli. A RbcS2 B5-C1 PCR product on agarose gel. B + C Successful transformation into E. coli. D + E Sequencing results of L0-RbcS2_B5-C1.


References

  1. Goldschmidt-Clermont, M., & Rahire, M. (1986). Sequence, evolution and differential expression of the two genes encoding variant small subunits of ribulose bisphosphate carboxylase/oxygenase in Chlamydomonas reinhardtii. Journal of molecular biology, 191(3), 421-432.
  2. Stevens, D. R., Purton, S., & Rochaix, J.-D. (1996). The bacterial phleomycin resistance geneble as a dominant selectable marker inChlamydomonas. Molecular and General Genetics MGG, 251(1), 23–30. https://doi.org/10.1007/BF02174340