Types | DnaRegion
|
Roles | Plasmid
plasmid
|
Sequences | BBa_K823054_sequence (Version 1)
|
Description
For N-terminal fusion proteins with cgeA (display on B. subtilis spores).==
Sporovector==
Our
Sporovector is specially designed to give you the opportunity to easily create Sporobeads with any proteins you can think of. It is available as BioBrick in pSB1C3 and can be cloned in any of our empty
B. subtilis vectors. We also offer it ???precloned??? in pSB
Bs4S which in this version lacks
NgoMIV restriction sites.
The
Sporovector was created by ligation of three cut PCR-products. It is designed to allow N-terminal fusion of genes in Freiburg standard (
RCF25). Therefore, the gene to be inserted must be cut with
XbaI and
AgeI and the vector must be digested with
XbaI and
NgoMIV. By this digest, the RFP cassette will be removed from this vector to allow easy selection for the integration of the new insert. After ligation, there is a scar of six nucleotides between both genes but no restriction site left.
The gene fusion is controlled by the P
cotYZ-promoter which was the strongest one in our promoter evaluations. The C-terminal gene part is
cgeA, one of the two known spore crust proteins.
The vector is cloned but has not been tested with an insert, yet.
We are working on further
Sporovectors to offer also fusion with
cotZ as well as C-terminal fusions.
Notes
For N-terminal fusion proteins with cgeA (display on B. subtilis spores)
Source
Assembly of several PCRs.