Part:BBa_K292006
Strong RBS + LacI repressor + double terminator
This part contains a strong ribosome binding site, the LacI repressor and a double terminator (BBa_B0030 + BBa_C0012 + BBa_B0014). This brick comes from the BBa_K292005.
History:
In E.Coli, pLac is a part of the lactose operon. LacI is constantly expressed and represses the pLac. In the presence of Lactose, LacI is inhibited and pLac is active and allows the transcription of beta-galactosidase. Lactose can be substituted by IPTG (Isopropyl β-D-1-thiogalactopyranoside).
Usage and Biology
The LacI repressor represses pLac promoter from the E.coli lactose operon. So LacI repressor and this bio-brick are really reliable to use when we want to control a gene expression by using pLac promoter. In fact when LacI is not expressed, pLac is activated, and when there is an expression of LacI, pLac is inhibited. We can easily design a system to induce the transcription of LacI by using another operon as the tetracycline operon and creates a failed feedback mechanism for pLac inhibition and so, for gene expression inhibition.
The LacI BBa_K292006 already contains a strong RBS and a double terminator, so this brick is ready to use!
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1168
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Functional Parameters
biology | T7TE-LuxIA |
direction | Bidirectional |
efficiency | 0.6 |
forward_efficiency | 0.604[CC]/0.96[JK] |
function | Rep |
ligands | allolactose, IPTG |
protein | LacI |
reversed_version | 2145 |
reverse_efficiency | 0.86[JK] |
swisspro | P03023 |
tag | LVA |
//function/regulation/transcriptional
biology | T7TE-LuxIA |
direction | Bidirectional |
efficiency | 0.6 |
forward_efficiency | 0.604[CC]/0.96[JK] |
function | Rep |
ligands | allolactose, IPTG |
protein | LacI |
reversed_version | 2145 |
reverse_efficiency | 0.86[JK] |
swisspro | P03023 |
tag | LVA |