BBa_K523002

BBa_K523002 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K523002
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Sylvia Ispasanie, Mun Ching Lee
Date created: 2011-07-18 11:00:00
Date modified: 2015-05-08 01:12:33

RBS + bglX (E. coli perisplasmic β
-glucosidase)



Types
DnaRegion

Roles
Translational_Unit

engineered_region

Sequences BBa_K523002_sequence (Version 1)

Description

This is the E. coli beta-glucosidase gene bglX. The part contains the native Ribosome Binding Site.

The part was made using the strategy outlined in BBa_K523000, and therefore contains 4 extra bases at the 5' end which generate a BglII restriction site.

Notes

The part was made using the strategy outlined in BBa_K523000, and therefore contains 4 extra bases at the 5' end which generate a BglII restriction site.

The part was created from a lab E. coli strain using primers:

*Forward: ACT AGATCT gcc acg tcg ggc aac
**adds BglII site; starts upstream of gene to catch RBS; RFC10 compliant after replacement of BBa_K523000 in a normal BioBrick vector.

*Reverse: ACT ACTAGT A TTA tta cag caa ctc aaa ctc gcc
**adds SpeI site; RFC10 compliant after insertion into vector; has double stop codon.

Source

The source E. coli genome sequence can be seen using GenBank U00096.2

Sequence Annotation Location Component / Role(s)
BglII
Native RBS
bglX
ATG
TAATAA
PstI site removed
G to T silent mutation
Predicted (cleaved) signal peptide
1,4
22,25
38,2338
38,38
2333,2333
85,85
2122,2122
38,97
feature/misc sequence_feature
sequence_feature feature/misc
feature/cds CDS
feature/start start_codon
feature/stop stop_codon
feature/s_mutation point_mutation
feature/s_mutation point_mutation
feature/misc sequence_feature
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_K523002/1