BBa_K1355000

BBa_K1355000 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K1355000
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Luna Barroco de Lacerda
Date created: 2014-10-05 11:00:00
Date modified: 2016-01-13 10:34:49

Strong RBS + merA (mercuric ion reductase)+ terminator (BBa_ B0015)



Types
DnaRegion

Roles
Composite

engineered_region

Sequences BBa_K1355000_sequence (Version 1)

Description

The MerA gene is one of the most important gene into bacterial mercury-resistance operon. Transforms mercury Hg2+ in Hg0, which is volatile and moves passively out of the bacteria in gaseous form as shown in Figure above. The reduction of Hg2+ occurs by a NADPH-dependent system.

Notes

We analyzed all Mercury-resistance (Mer) operon genes, in these following strains available at NCBI: (1) Escherichia coli 042, (2) Escherichia coli O26 , (3) Escherichia coli ACN001, (4) Escherichia coli 838C-R1, (5) Escherichia coli APEC-O103, (6) Escherichia coli UMNK88, (7) Escherichia coli AR060302, (8) Escherichia coli PMV-1. It is showed that the mer genes from strains (1) - (2) - (3) - (4) - (5) is conserved among them. However strains (6) - (7) and (8) did not show any similarity. Therefore we used sequences from (1) to (5) due the consensus in E.coli.

Source

MerA gene sequence is found in the O26-CRL plasmid from Escherichia coli O26. We also added strong RBS from protein 10 found in phage 17 and the double terminator (BBa_B0015) to ensure efficient termination of transcription and messenger RNA recognition.

Sequence Annotation Location Component / Role(s)
rbs
BBa_ B0015
MerA
9,16
1652,1778
24,1639
feature/rbs ribosome_entry_site
feature/BioBrick engineered_region
CDS feature/cds
igem#experience
Works
 
igem#sampleStatus
In stock
igem#status
Available
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K1355000/1