pKSS (ATCC® 87446)

Applications: expression vectorvector for constructing cDNA librariesvector permitting RNA synthesis in vitrovector permitting allelic exchange of cloned insertsvector permitting positive selection for inserts beta-galactosidase beta-D-galactosidasevector permitting production of single-stranded DNA  /  Depositors: P Kast

Permits and Restrictions

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Designations pKSS
Depositors P Kast
Biosafety Level 1
Vector Information
Size (kb): 4.1329998970031740
Vector: pKSS (phagemid)
Promoters: Promoter for expression lacZ
Construction: pBLS, pheS
Marker(s):ampR,pheS
Construct size (kb): 4.132999897003174
Features: marker(s): ampR
promoter for expression: lacZ
promoter for in vitro transcription: T3
promoter for in vitro transcription: T7
replicon: f1
replicon: pMB1
MCS: KpnI...SmaI
MCS: SacI...BamHI
coding sequence: pheS
Applications
expression vector
vector for constructing cDNA libraries
vector permitting RNA synthesis in vitro
vector permitting allelic exchange of cloned inserts
vector permitting positive selection for inserts beta-galactosidase beta-D-galactosidase
vector permitting production of single-stranded DNA
Comments
Restriction digests of the clone give the following sizes (kb): BamHI/EcoRI--3.0, 1.2; PstI--4.1; PvuII--2.5, 1.0, 0.6.
Culture distributed in quantities of 0.4 ml in liquid nitrogen vials. Plasmid is not stable when freeze dried.
The vector can be used for integration of E. coli alleles at the corresponding locus in the host chromosome by cloning an allele of interest, containing a selectable marker, into MCSII.
The plasmid can then be transformed into a recA+ host, selecting for the cloned marker in the presence of p-Cl-Phe (in media lacking tryptone and ampicillin).
The host strain DH5alpha is not recommended for preparation of the vector due to the slow growth of transformed cells.
High efficiency positive selection cloning vector encoding a gene for dominant sensitivity to p-chloro-phenylalanine (No. 13,071-0, Aldrich, Milwaukee, WI).
The Gly294 mutant pheS gene is protected by a patent from Hoechst (Frankfurt, Germany).
Recombinant plasmids (containing cloned inserts that interrupt or replace the pheS gene) can be selected for by growth on rich media lacking tryptone and supplemented with 10 mM D,L-p-chloro-phenylalanine and 200 ug/ml ampicillin.
(The recommended media is YEG-Cl described in the reference below.)
The Ala294-->Gly mutant pheS gene encoded in the plasmid produces an enzyme with relaxed substrate specificity, and is dominantly lethal over the chromosomal pheS gene in the presence of p-Cl-Phe.
Media ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Growth Conditions
Temperature: 37.0°C
References

Kast P, Hennecke H. Amino acid substrate specificity of Escherichia coli phenylalanyl-tRNA synthetase altered by distinct mutations. J. Mol. Biol. 222: 99-124, 1991. PubMed: 1942071

Kast P. pKSS--a second-generation general purpose cloning vector for efficient positive selection of recombinant clones. Gene 138: 109-114, 1994. PubMed: 8125286

Peter Kast, personal communication

Shipped frozen
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