Difference between revisions of "Part:BBa K1680015"

Latest revision as of 03:16, 27 September 2015

pRS315 yeast shuttle vector with Biobrick MCS

This part is a biobricked shuttle vectors for Saccharomyces cerevisiae. It is part of a vector series with different auxotrophy markers (Part:BBa_K1680014, Part:BBa_K1680016). The vector was made compatible with the RFC10 standard and also contains a RFC10 cloning site. This part is derived from the wild type pRS315 vector Part:BBa_K950010.

• Request concerning submission for plasmid backbone was sent to HQ on 09/17

Further - not biobrick compatible - versions of this vector with different inserts can also be found in the registry: Part:BBa_K106006, Part:BBa_K106014, Part:BBa_K106670, Part:BBa_K106672, Part:BBa_K106693, Part:BBa_K106697, Part:BBa_K106698

This part encodes for an ampicillin resistance gene and replicates to high-copy numbers in E. coli. Furthermore, the CEN6/ARS4 (Chromosome VI centromere/Autonomously Replicating Sequence 4) cassette ensures that the plasmid stays at a low copy number in yeast, because they are treated as pseudo chromosomes. The vector also encodes for a LEU2 gene, which is used as an auxotrophy marker in yeast.

This part is mutagenized version of the wild type pRS315 vector (Sikorski 1989).

A EcoRI restriction site in the backbone was removed by mutagenesis PCR (see lane 1 & 2 in figure). Exchange of the wild type MCS for RFC10 compatible MCS could be shown by restriction with SalI restriction: The enzyme linearizes the vector with old MCS (lane 3) but does not cut the vector with the new MCS, as indicated by presence of supercoiled DNA (lane 4).

Agarose Gel of different Versions of the pRS313 vector. Lane 1: wild type vector, cut with EcoRI; lane 2: mutagenised vector cut with EcoRI; lane 3: mutagenised vector cut with SalI; lane 4: vector with RFC10 MCS cut with SalI.

Sequence and Features

This part is a RFC10 compatible shuttle vector for yeast.