Difference between revisions of "Part:BBa K2918005"

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<partinfo>BBa_K2918005 short</partinfo>
 
<partinfo>BBa_K2918005 short</partinfo>
  
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A T7 promoter with a strength that should give 10% of normal expression
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A T7 promoter with a strength that should give about 10% expression compared to wild type T7 promoter.
  
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K2918005 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2918005 SequenceAndFeatures</partinfo>
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The part has been confirmed by sequencing and there are no mutations.
  
 
===Usage and Biology===
 
===Usage and Biology===
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The T7 promoter variant was obtained by performing biased randomization of the wild type T7 promoter. The promoter variant contains a single base substitution compared to the wild type promoter.
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The T7 promoter variant was obtained by performing biased randomization of the wild type T7 promoter. The promoter variant contains a single base substitution compared to the wild type promoter <html><body><a href="#ryo"> (Ryo Komura et al., 2018)</a></body></html>.
  
 
===Strain Construction===
 
===Strain Construction===
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The DNA sequence of the part was synthesized by IDT with flanking BpiI sites and respective MoClo compatible promoter overhangs. The promoter was then cloned in a level 0 MoClo backbone <html>(<a target=”_blank” href=”https://www.addgene.org/47984/”>pICH41233</a>)</html> and the sequence was confirmed by sequencing. The cloning protocol can be found in the MoClo section below.
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The DNA sequence of the part was synthesized by IDT with flanking BpiI sites and respective Modular Cloning (MoClo) compatible promoter overhangs. The promoter was then cloned in a level 0 MoClo backbone <html><a href="http://www.addgene.org/47984">pICH41233</a></html> and the sequence was confirmed by sequencing. The cloning protocol can be found in the modular cloning section below.
  
 
===Modular Cloning===
 
===Modular Cloning===
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Modular Cloning (MoClo) is a system which allows for efficient one pot assembly of multiple DNA fragments. The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening).
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Modular Cloning (MoClo) is a system that allows for efficient one-pot assembly of multiple DNA fragments. The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening).
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For the protocol, you can find it <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a>.</html>
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Click <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a> </html> for the protocol.
  
  
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<b>Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2. The complete sequence of our parts including backbone can be found <html><a href="http://2019.igem.org/Team:TUDelft/Experiments" target="_blank">here</a>.</html></b>
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<b>Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2. </b>
  
  
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         </table>
 
         </table>
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     </body>
 
     </body>
 
</html>
 
</html>
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===Characterization===
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We have used this promoter to characterize the functioning of our <html><body><a href="https://parts.igem.org/Part:BBa_K2918040" target="_blank">optimized incoherent feed-forward loop</a></body></html>.
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===References===
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<html><body><ol><li><a href="https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0196905" target="_blank"> Ryo Komura, W. A., Keisuke Motone, Atsushi Satomura, Mitsuyoshi Ueda (2018). "High-throughput evaluation of T7 promoter variants using biased randomization and DNA barcoding." <i>PLOS ONE.</i></a></li></ol></body></html>
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Latest revision as of 17:02, 6 December 2019

Weak T7 promoter

A T7 promoter with a strength that should give about 10% expression compared to wild type T7 promoter.

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]

The part has been confirmed by sequencing and there are no mutations.

Usage and Biology

The T7 promoter variant was obtained by performing biased randomization of the wild type T7 promoter. The promoter variant contains a single base substitution compared to the wild type promoter (Ryo Komura et al., 2018).

Strain Construction

The DNA sequence of the part was synthesized by IDT with flanking BpiI sites and respective Modular Cloning (MoClo) compatible promoter overhangs. The promoter was then cloned in a level 0 MoClo backbone pICH41233 and the sequence was confirmed by sequencing. The cloning protocol can be found in the modular cloning section below.

Modular Cloning

Modular Cloning (MoClo) is a system that allows for efficient one-pot assembly of multiple DNA fragments. The MoClo system consists of Type IIS restriction enzymes that cleave DNA 4 to 8 base pairs away from the recognition sites. Cleavage outside of the recognition site allows for customization of the overhangs generated. The MoClo system is hierarchical. First, basic parts (promoters, UTRs, CDS and terminators) are assembled in level 0 plasmids in the kit. In a single reaction, the individual parts can be assembled into vectors containing transcriptional units (level 1). Furthermore, MoClo allows for directional assembly of multiple transcriptional units. Successful assembly of constructs using MoClo can be confirmed by visual readouts (blue/white or red/white screening). Click here for the protocol.


Note: The basic parts sequences of the Sci-Phi 29 collection in the registry contain only the part sequence and therefore contain no overhangs or restriction sites. For synthesizing MoClo compatible parts, refer to table 2.


Table 1: Overview of different level in MoClo

Level Basic/Composite Type Enzyme
Level 0 Basic Promoters, 5’ UTR, CDS and terminators BpiI
Level 1 Composite Transcriptional units BsaI
Level 2/M/P Composite Multiple transcriptional units BpiI

For synthesizing basic parts, the part of interest should be flanked by a BpiI site and its specific type overhang. These parts can then be cloned into the respective level 0 MoClo parts. For level 1, where individual transcriptional units are cloned, the overhangs come from the backbone you choose. The restriction sites for level 1 are BsaI. However, any type IIS restriction enzyme could be used.


Table 2: Type specific overhangs and backbones for MoClo. Green indicates the restriction enzyme recognition site. Blue indicates the specific overhangs for the basic parts

Basic Part Sequence 5' End Sequence 3' End Level 0 backbone
Promoter NNNN GAAGAC NN GGAG TACT NN GTCTTC NNNN pICH41233
5’ UTR NNNN GAAGAC NN TACT AATG NN GTCTTC NNNN pICH41246
CDS NNNN GAAGAC NN AATG GCTT NN GTCTTC NNNN pICH41308
Terminator NNNN GAAGAC NN GCTT CGCT NN GTCTTC NNNN pICH41276

Characterization

We have used this promoter to characterize the functioning of our optimized incoherent feed-forward loop.

References

  1. Ryo Komura, W. A., Keisuke Motone, Atsushi Satomura, Mitsuyoshi Ueda (2018). "High-throughput evaluation of T7 promoter variants using biased randomization and DNA barcoding." PLOS ONE.