BBa_K1361006

BBa_K1361006 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K1361006
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Shoujie Sun
Date created: 2014-10-06 11:00:00
Date modified: 2015-05-08 01:10:04

Curli Fiber generator where CsgBtrunc, a dissociative nucleator, under the control of Pbad promoter



Types
DnaRegion

Roles
Generator

engineered_region

Sequences BBa_K1361006_sequence (Version 1)

Description

This part contains the major subunit of curli fiber CsgA and its nucleator CsgBtrunc, in which CsgA is constitutive expression whereas CsgBtrunc is under the control of Pbad promotor. CsgBtrunc is different from native CsgB from the deletion of C-terminal amino acid from 133 to 155 that it cannot attach cell outer membrane. And CsgBtrunc itself is highly aggregative in the culture.
This part is designed to be used for immediate generate of large amount of curli fiber after adding of the inducer and a stronger promoter for CsgA was chosen to parallel with BBa_K1361002.
This part cannot functioning alone without expression of CsgEFG genes in the same cell, for they coding the outer membrane channel secrete system for CsgA and CsgB.

Notes

The PstI loci within CsgA sequence has been replaced from CTGCAG to CTGCCG.

Source

CsgAC and CsgBtrunc were collected by PCR from genome of E coli DH5alpha respectively.

igem#sampleStatus
It's complicated
igem#status
Planning
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K1361006/1