Part:BBa_K3866022
pLac:RBS GB compatible with A1-B2
This lac promoter includes a CAP binding site and the lac operator sequence lacO.
Usage and Biology
The lac promoter is not as strong as the tac or the trc promoter, but in high copy-number vectors it allows expression of foreign proteins at respectable levels. In the absence of the lac repressor (LacI) expression from the lac promoter is turned on. Maximum induction of the lac promoter requires the action of the cAMP activator protein (CAP, crp gene product), which is most active when cells are grown in medium lacking glucose. Media that contain glucose as carbon source should not be used to express genes from this promoter. For inducible gene expression from the lac 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
Experimental Use and Experience
This part is used in BBa_
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]
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