"
Team:TU Munich/Project/Vector Design
From 2012.igem.org
IngmarPolte (Talk | contribs) (→Vector Design) |
|||
| Line 1: | Line 1: | ||
{{Team:TU_Munich/Header}} | {{Team:TU_Munich/Header}} | ||
| - | |||
| - | |||
= Vector Design = | = Vector Design = | ||
Revision as of 16:02, 26 September 2012
Contents |
Vector Design
What ist the use of DNA sequences coding for valuable enzymes without the possibility to express them and analyse the protein activity?
Therefore an important task at the beginning of our project was the design of an expression vector for yeast which is compatible to the iGEM cloning principles and standards. Based on the comercial available pYES 2 vector manufacted by Invirtogen we created an vector containing:
- a RFC 25 compatible multiple cloning site
- a strep-tag II
- a 2µ origin for high copy number replication in saccharomyces cerevisae
- the URA3 gene to use the uracil auxotrophy of XXX(Hefestamm) as a selection marker
- a pUC origin for high copy number replication in E.coli
- the ß-lactamase coding gene to use ampicillin as a selection marker for cloning applications in E.coli
- a galacotsoe inducible PGal promoter
- a CYC1 transcription terminator
Furthermore we designed several vectors containing our constitutive promoters and different additional terminators. The different versions of the vector have been successfully applied and tested in all other subprojects.
Design
vom Poster:
RFC25 COMPATIBILITY
To be able to test and quantify the expression of desired enzymes in yeast we designed an expression vector which is compatible to the iGEM RFC25 standard based on the commercially available pYES2 vector from Invitrogen.
DESIGN
This included an exchange of the original multiple cloning site by a multiple cloning site consisting of the restriction enzymes used in the iGEM RFC25 standard. Additionally the restriction sites of these enzymes in the vector backbone have been eliminated by quick-change mutagenisis. Furthermore we inserted a gene sequence coding for a strep-tag II straight behind the multiple cloning site in order to facilitate the extraction of expressed proteins. The successful introduction of these modifications has been confirmed via DNA sequencing. Additionally a second vector containing a His-tag instead of the strep-tag II and a vector giving the opportunity to test different promoters is currently planned.
Description of the original vector + 4 different modified versions.
