Difference between revisions of "Part:BBa K3183002:Design"
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<partinfo>BBa_K3183002 short</partinfo>
 
<partinfo>BBa_K3183002 short</partinfo>
  
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The part was identified in the article by Lizier et al; the gene was codon optimised for L. reuteri and synthesized by IDT. The part was leter assembled by Gibson Assembly into composite parts such as: BBa_K3183103, BBa_K3183100 etc., which were finally assembled into the pTRKH3 vector BBa_K3183050, again by Gibson Assembly  
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The part was identified in the article by Lizier et al; the gene was codon optimised for L. reuteri and synthesized by IDT. The part was leter assembled by Gibson Assembly into the composite part BBa_K3183101, which was finally assembled into the pTRKH3 vector (BBa_K3183050), again by Gibson Assembly  
  
 
<partinfo>BBa_K3183002 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K3183002 SequenceAndFeatures</partinfo>

Revision as of 00:32, 21 October 2019


Lactate Dehydrogenase Constitutive Promoter for Lactobacillus sp.

The part was identified in the article by Lizier et al; the gene was codon optimised for L. reuteri and synthesized by IDT. The part was leter assembled by Gibson Assembly into the composite part BBa_K3183101, which was finally assembled into the pTRKH3 vector (BBa_K3183050), again by Gibson Assembly


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 219


Design Notes

n/a


Source

The promoter is derived from the lactate dehydrogenase (ldlL) promoter from Lactobacillus acidophilus.

References

Lizier, Michela, et al. “Comparison of Expression Vectors in Lactobacillus Reuteri  Strains.” FEMS Microbiology Letters, vol. 308, no. 1, Aug. 2010, pp. 8–15., doi:10.1111/j.1574-6968.2010.01978.x.