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 | ||
<partinfo>BBa_K3183002 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3183002 SequenceAndFeatures</partinfo> | ||
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===References=== | ===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. |
Revision as of 00:31, 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 composite parts such as: BBa_K3183103, BBa_K3183100 etc., which were finally assembled into the pTRKH3 vector BBa_K3183050, again by Gibson Assembly
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE 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.