Difference between revisions of "Part:BBa K3866001"
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===Verification of cloning=== | ===Verification of cloning=== | ||
− | [[File:T--Thessaly-- | + | [[File:T--Thessaly--pTrc pLac--digestion.png|500px|thumb|none|<i><b>Figure 3.</b> (C= Cut, U=Uncut) Restriction digestion of pTrc:RBS (C1 + C2) with: EcoRI + EcoRV, Expected bands: 1280bp, 896bp, Positive result: C1 + C2</i>]] |
===Source=== | ===Source=== |
Latest revision as of 19:31, 25 September 2021
pTrc:RBS GB compatible with A1-B2
The trc promoter is a hybrid of the lac and trp promoters which is a stronger promoter in comparison to the lac promoter.
Usage and Biology
The trc promoter was created by insertion of 1 bp into the 16 bp sequence between the consensus -35 and -10 sequences of the tac promoter, to obtain the optimal consensus distance of 17 bp between the -35 and -10 signal. This promoter includes the Lac Operator sequence lacO, which can be bound by the Lac repressor lacI, as well as an RBS BBa_B0034. For inducible gene expression from the trc promoter the lac repressor (LacI) is necessary. The repressor binds to the operator DNA with high specificity and inhibits gene expression until an inducer like allolactose or the analog IPTG (Isopropyl-?-D-thio-galactoside) is added to the medium. The inducer binds to the repressor, causing a change in its shape. Thus altered, the repressor is unable to bind to the operator, allowing RNA polymerase (RNAP) to transcribe the following genes and thereby leading to high levels of the encoded proteins.
Design Notes
The sequence was domesticated. We removed BsmBI, BsaI, BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in pUPD2 BBa_K3505007 and has overhangs compatible for Golden Braid cloning. This has position A1-B2.
Verification of cloning
Source
Synthesized by IDT.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]