EpsE

BBa_K143032 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K143032
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Chris Hirst
Date created: 2008-09-17 11:00:00
Date modified: 2015-05-08 01:10:24

EpsE Molecular Clutch Gene of B. subtilis



Types
DnaRegion

Roles
Coding

CDS

Sequences BBa_K143032_sequence (Version 1)

Description

The epsE gene of the exopolysaccharide synthesis operon of B. subtilis has been suggested to function in a manor similar to a molecular clutch#1. If expressed inside a cell it will prevent flagellar movement causing the cell to no longer be able to swim effectively and instead only tumble. As such EpsE could potentially be used as a controller of B. subtilis movement.

Though the EPS operon is normally repressed in B. subtilis, if EpsE is synthetically expressed it would be beneficial for the original copy of epsE to be knocked out. This can be achieved by integrating over the EesE gene with the epsE integration Biobricks (BBa_K143005 and BBa_K143006) which contain 2 in-frame stop codons.

Although many bacterial flaggelar assemblies contain proteins that are similar in shape, there is no guarantee that the epsE gene will function correctly in any host cell other than B. subtilis

Notes

The epsE(aka yveO) sequence was located in the B. subtilis chromosome#1 and the PstI restriction site removed before synthesis by GeneArt

Source

The epsE gene sequence was taken from the B. subtilis chromosome and was synthesised by GeneArt.

Sequence Annotation Location Component / Role(s)
EpsE Molecular Clutch Gene
start
stop
stop
1,834
1,3
838,840
835,837
CDS feature/cds
feature/start start_codon
stop_codon feature/stop
feature/stop stop_codon
igem#experience
Works
 
igem#partStatus
Released HQ 2013
igem#sampleStatus
In stock
igem#status
Available
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K143032/1