Plasmid_Backbone

Part:BBa_K1680016

Designed by: Katharina Sporbeck   Group: iGEM15_Tuebingen   (2015-09-17)

pRS316 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_K1680015). The vector was made compatible with the RFC10 standard and also contains a RFC10 cloning site. This part is derived from the wild type pRS316 vector Part:BBa_K950011.

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

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 URA3 gene, which is used as an auxotrophy marker in yeast.


This part is mutagenized version of the wild type pRS316 vector (Sikorski 1989).

A PstI and SacI restriction site in the backbone were removed by mutagenesis PCR (see lane 1-3 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 4) but does not cut the vector with the new MCS, as indicated by presence of supercoiled DNA (lane 5).


PRS315 mutated.png

Agarose Gel of different Versions of the pRS313 vector. Lane 1: wild type vector, cut with PstI; lane 2: mutagenised vector (PstI site) cut with PstI; lane 2: mutagenised vector (SacI site) cut with SacI; 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.


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 2040
    Illegal XbaI site found at 2025
    Illegal SpeI site found at 2017
    Illegal PstI site found at 2003
  • 12
    INCOMPATIBLE WITH RFC[12]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 2040
    Illegal SpeI site found at 2017
    Illegal PstI site found at 2003
    Illegal NotI site found at 2008
    Illegal NotI site found at 2032
  • 21
    INCOMPATIBLE WITH RFC[21]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 2040
  • 23
    INCOMPATIBLE WITH RFC[23]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 2040
    Illegal XbaI site found at 2025
    Illegal SpeI site found at 2017
    Illegal PstI site found at 2003
  • 25
    INCOMPATIBLE WITH RFC[25]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 2040
    Illegal XbaI site found at 2025
    Illegal SpeI site found at 2017
    Illegal PstI site found at 2003
    Illegal NgoMIV site found at 1668
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal BsaI site found at 1079
    Illegal BsaI.rc site found at 3414
    Illegal SapI site found at 2331
    Illegal SapI site found at 4435
    Illegal SapI.rc site found at 926



[edit]
Categories
//chassis/eukaryote/yeast
//dna
//plasmid
//plasmidbackbone
//plasmidbackbone/copynumber/low
Parameters
None