Difference between revisions of "Part:BBa K2918031"

 
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A level 1 with 0.1 T7 promoter, a universal RBS, GFP and a T7 terminator
 
A level 1 with 0.1 T7 promoter, a universal RBS, GFP and a T7 terminator
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===Usage and Biology===
 
  
 
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<partinfo>BBa_K2918031 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2918031 SequenceAndFeatures</partinfo>
  
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===Toxicity===
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Our Sci-Phi 29 tool is based on four components of the Φ29 bacteriophage: DNAP, TP, p5 and p6. However, overexpression of these proteins are toxic for the cell. In order to determine the optimal expression levels of the proteins in live cells, we carried out viability assays in <i>E. coli</i> BL21(DE3) pLysS. The results are shown in the graphs below.
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<div><ul>
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  <li style="display: inline-block;"> [[File:T--TUDelft--0.1GFP-nomM.png|thumb|none|444px|<b>Figure 3A:</b> The growth curve of GFP under a WT T7 promoter in hours with 1 mM IPTG induction]] </li>
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  <li style="display: inline-block;"> [[File:T--TUDelft--0.1GFP-1mM.png|thumb|none|444px|<b>Figure 3B:</b> The growth curve of GFP under a WT T7 promoter in hours with 1 mM IPTG induction]] </li>
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    <li> [[File:T--TUDelft--0.1GFP-10mM.png|thumb|center|444px|<b>Figure 3C:</b> The growth curve of GFP under a WT T7 promoter in hours with 10 mM IPTG inductionn]] </li>
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    </ul></div>
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===Usage and Biology===
  
 
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Revision as of 09:54, 4 October 2019


Weak T7 promoter - Universal RBS - GFP - T7 terminator

A level 1 with 0.1 T7 promoter, a universal RBS, GFP and a T7 terminator

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 465
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 465
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 465
    Illegal BamHI site found at 674
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 465
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 465
  • 1000
    COMPATIBLE WITH RFC[1000]

Toxicity

Our Sci-Phi 29 tool is based on four components of the Φ29 bacteriophage: DNAP, TP, p5 and p6. However, overexpression of these proteins are toxic for the cell. In order to determine the optimal expression levels of the proteins in live cells, we carried out viability assays in E. coli BL21(DE3) pLysS. The results are shown in the graphs below.

  • Figure 3A: The growth curve of GFP under a WT T7 promoter in hours with 1 mM IPTG induction
  • Figure 3B: The growth curve of GFP under a WT T7 promoter in hours with 1 mM IPTG induction
  • Figure 3C: The growth curve of GFP under a WT T7 promoter in hours with 10 mM IPTG inductionn