Difference between revisions of "Part:BBa K1223008"

 
 
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<partinfo>BBa_K1223008 short</partinfo>
 
<partinfo>BBa_K1223008 short</partinfo>
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the cassette is cloned between BamHI and XbaI restriction sites.  
 
the cassette is cloned between BamHI and XbaI restriction sites.  
  
<!-- Add more about the biology of this part here
+
===Design Notes===
 +
used for amplification and extraction of P.A.S.E2 cassette. P.A.S.E. 2 cassette is intended to be incorporated into E.coli BL21 genome by recombineering, and therefore has a homolgy region in each side that direct the recombination into the right place in the genome.
 +
this cassette is used to replace the native promoter and regulatory sequences upstream of the CDS of the TyrS gene that encodes for the enzyme Tyrosine synthetase. the native promoter is replaced with an IPTG/Arabinose induced promoter (BBa_k354000) and BBa_b0034 RBS.
 +
the cassettes has a kanamycin resistance gene (KanR) to aid in selection of the desired transformants.
 +
 
 +
the sixth amino acid in the TyrS sequence was replaced with an amber stop codon (TAG) in order to further reduce unwanted 'leakage' of the promoter. the TAG stop codon is used for the incorporation of unnatural amino acids (UAAs) into the protein sequence. this system gives us better control of the translation process and prevents expression of TyrS when the unnatural amino acid is not present in the medium.
 +
incorporation of unnatural amino acids into the protein sequence require three things:
 +
- insertion of the amber stop codon (TAG) in the DNA sequence, where we want the UAA to be incorporated. we also need to replace the stop codon at the end of the CDS to the TGA or TAA stop codons (preferably TAA).
 +
- an orthogonal tRNA that will be loaded with the UAA to be incorporated into the protein.
 +
- an orthogonal tRNA synthetase that recognizes both the orthogonal tRNA and the UAA. 
 +
 
 +
both the tRNA and the tRNA synthetase are encoded in the UAA incoporation machinery plasmid.
 +
 
 +
The part was characterized through sequencing and restriction digest with BamHI and XbaI.
 +
 
 +
[[File:tb2.png]]
 +
 
 +
lane1: undigested pUC57-P.A.S.E.2 cassette
 +
 
 +
lane2: pUC57-P.A.S.E.2 digested XbaI and BamHI
 +
 
 +
lane3: DS5000 ladder
 +
 
 +
 
 +
== Creating the world’s first UAA logic AND gate ==
 +
 
 +
The sixth amino acid in the TyrS sequence was replaced with an amber stop codon (TAG). The TAG stop codon is used for the incorporation of unnatural amino acids (UAAs) into the protein sequence. This system gives us better control of the translation process and prevents expression of TyrS when the unnatural amino acid is not present in the medium.
 +
The fail proof aspect of this system is achieved by creating a logic AND gate which is depended on IPTG/Arabinose AND UAA in order to synthesize an active TyrS protein.
 +
 
 +
[[File:tb1.png]]
 +
 
 +
===Source===
 +
 
 +
this construct was synthesized in one piece.
 +
the sources of the sequences used in this part are genbank (TyrS CDS, KanR) and the iGEM catalog (BBa_k354000,BBa_b0034).
 +
 
 +
===References===
 +
Wang, L.; Brock, A.; Herberich, B.; Schultz, P. G. Science 2001, 292, 498.
 +
 
 +
Milles, S.; Tyagi, S.; Banterle, N.; Koehler, C.; VanDelinder, V.; Plass, T.; Neal, A. P.; Lemke, E. A. Journal of the American Chemical Society 2012, 134, 5187.
 
===Usage and Biology===
 
===Usage and Biology===
  

Latest revision as of 13:35, 12 October 2013

pUC-57-P.A.S.E.2

P.A.S.E2 cassette cloned into pUC-57 (ampicillin resistance).

the cassette is cloned between BamHI and XbaI restriction sites.

Design Notes

used for amplification and extraction of P.A.S.E2 cassette. P.A.S.E. 2 cassette is intended to be incorporated into E.coli BL21 genome by recombineering, and therefore has a homolgy region in each side that direct the recombination into the right place in the genome. this cassette is used to replace the native promoter and regulatory sequences upstream of the CDS of the TyrS gene that encodes for the enzyme Tyrosine synthetase. the native promoter is replaced with an IPTG/Arabinose induced promoter (BBa_k354000) and BBa_b0034 RBS. the cassettes has a kanamycin resistance gene (KanR) to aid in selection of the desired transformants.

the sixth amino acid in the TyrS sequence was replaced with an amber stop codon (TAG) in order to further reduce unwanted 'leakage' of the promoter. the TAG stop codon is used for the incorporation of unnatural amino acids (UAAs) into the protein sequence. this system gives us better control of the translation process and prevents expression of TyrS when the unnatural amino acid is not present in the medium. incorporation of unnatural amino acids into the protein sequence require three things: - insertion of the amber stop codon (TAG) in the DNA sequence, where we want the UAA to be incorporated. we also need to replace the stop codon at the end of the CDS to the TGA or TAA stop codons (preferably TAA). - an orthogonal tRNA that will be loaded with the UAA to be incorporated into the protein. - an orthogonal tRNA synthetase that recognizes both the orthogonal tRNA and the UAA.

both the tRNA and the tRNA synthetase are encoded in the UAA incoporation machinery plasmid.

The part was characterized through sequencing and restriction digest with BamHI and XbaI.

Tb2.png

lane1: undigested pUC57-P.A.S.E.2 cassette

lane2: pUC57-P.A.S.E.2 digested XbaI and BamHI

lane3: DS5000 ladder


Creating the world’s first UAA logic AND gate

The sixth amino acid in the TyrS sequence was replaced with an amber stop codon (TAG). The TAG stop codon is used for the incorporation of unnatural amino acids (UAAs) into the protein sequence. This system gives us better control of the translation process and prevents expression of TyrS when the unnatural amino acid is not present in the medium. The fail proof aspect of this system is achieved by creating a logic AND gate which is depended on IPTG/Arabinose AND UAA in order to synthesize an active TyrS protein.

Tb1.png

Source

this construct was synthesized in one piece. the sources of the sequences used in this part are genbank (TyrS CDS, KanR) and the iGEM catalog (BBa_k354000,BBa_b0034).

References

Wang, L.; Brock, A.; Herberich, B.; Schultz, P. G. Science 2001, 292, 498.

Milles, S.; Tyagi, S.; Banterle, N.; Koehler, C.; VanDelinder, V.; Plass, T.; Neal, A. P.; Lemke, E. A. Journal of the American Chemical Society 2012, 134, 5187.

Usage and Biology

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 396
    Illegal XbaI site found at 425
    Illegal PstI site found at 1238
    Illegal PstI site found at 1637
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 396
    Illegal PstI site found at 1238
    Illegal PstI site found at 1637
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 396
    Illegal BglII site found at 1451
    Illegal BamHI site found at 1619
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 396
    Illegal XbaI site found at 425
    Illegal PstI site found at 1238
    Illegal PstI site found at 1637
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 396
    Illegal XbaI site found at 425
    Illegal PstI site found at 1238
    Illegal PstI site found at 1637
    Illegal NgoMIV site found at 787
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2974
    Illegal SapI site found at 727
    Illegal SapI site found at 937
    Illegal SapI site found at 1891