BBa_J147002

BBa_J147002 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_J147002
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: MAX CARBONELL BALLESTERO
Date created: 2015-08-02 11:00:00
Date modified: 2015-08-31 04:08:32

RFP inducible device regulated by LuxR and C6-HSL through the Lux promoter



Types
DnaRegion

Roles
engineered_region

Composite

Sequences BBa_J147002_sequence (Version 1)

Description

Device composed of two modules, separated by a double terminator (BBa_B0014): First, a positively regulated Lux Promoter (BBa_R0062) drives the expression of a red fluorescent protein (BBa_E1010) with a medium ribosome binding site (BBa_B0032); second, a constitutive expression of Lux Receptor (BBa_C0062) and a green fluorescent protein (BBa_E0040) in tandem under a tet promoter (BBa_R0040) and both proteins with a weak RBS (BBa_B0033). This inducible device produces the expression of a red fluorescent protein upon the addition of lactone (C6-HSL) and the presence of the Lux Receptor in the cell.

This composite part has been used and extensively described in a paper published in Nucleic Acid Research in 2014 (open access). For further details and part experience, please freely download the paper or contact the authors. The reference and link are:

Carbonell-Ballestero, M. et al. A bottom-up characterization of transfer functions for synthetic biology designs: lessons from enzymology. Nucleic Acids Res (2014) doi: 10.1093/nar/gku964.

Notes

LuxR coding sequence and GFP coding sequence are in tandem, both placed after a Ribosome Binding Site sequence.

Source

This composite part has been created using the Biobrick assembly method with parts taken from the Spring 2010 iGEM distribution.

igem#sampleStatus
Not in stock
igem#status
Unavailable
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_J147002/1