๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Replication and maintenance of theKluyveromyceslinear pGKL plasmids

โœ Scribed by N. Gunge; K. Kitada


Publisher
Springer
Year
1988
Tongue
English
Weight
552 KB
Volume
4
Category
Article
ISSN
0393-2990

No coin nor oath required. For personal study only.

โœฆ Synopsis


Lactis -Killer character

Two new linear plasmids, pK192L (4.9 kb) and pK192S (2.4 kb), were isolated from a Kluyveromyces lactis killer strain carrying pGKL1 and pGKL2, pK192L was a deletion plasmid of pGKL1, derived from a part of the ORF1, and had a palindrome structure of a 215 bp unique sequence flanked by 2.35 bp inverted repeats, pK192S was a hairpin plasmid produced by selfannealing of a single-stranded pK192L DNA. In genetic analysis, pK192L and pK192S always coexisted and replicated in cells harboring pGKL2 and pGKL1, in contrast to other pGKLl-derived deletion plasmids, such as F1, F2 and pGKLIS, which could replicate in cells carrying pGKL2 only. Based on these and other lines of evidence, it was concluded that the reason for the pGKL1 dependent replication of the pK192L/S plasmids was the absence of the intact pGKL1-ORF1 gene and that the ORF1 function was necessary for the replication of the pGKL1 genome. This finding is in good agreement with a recent view reporting that ORF1 may encode a DNA polymerase of pGKL1. In a separate experiment, four new linear plasmids were isolated from a Saccharomyces cerevisiae strain carrying pGKL1 and pGKL2. Structural analysis showed that they consisted of two pairs of hairpin-palindrome type plasmids, each derived from different parts ofpGKL2, respectively. pGKL1 stabily replicated in cells carrying both these pGKL2 derived deletion plasmids.


๐Ÿ“œ SIMILAR VOLUMES


Kluyveromyces lactiskiller system:ORF1of
โœ R. Schaffrath; M. J. R. Stark; N. Gunge; F. Meinhardt ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer-Verlag ๐ŸŒ English โš– 929 KB

To functionally characterize the genes encoded by the larger killer plasmid pGKL2 from Kluyveromyces lactis a previously developed in-vivo recombination system was exploited. An in-vitro modified version of the cytoplasmically expressible LEU2 gene cartridge (LEU2\*) flanked by appropriate pGKL2 seg

Replication of Fpoh + plasmid in mafA mu
โœ Wada, Chieko ;Yura, Takashi ;Hiraga, Sota ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Springer ๐ŸŒ English โš– 652 KB

A class of F' plasmids, designated Fpoh+, was previously shown to be able to replicate extra-chromosomally on Hfr strains by virtue of carrying the specific site or region poh+ (permissive on Hfr) of the E. coli chromosome (Hiraga, 1975, 1976a). These plasmids were now found to replicate on E. coli

Replication of ColE2 and ColE3 plasmids:
โœ Tajima, Yoshitaka ;Horii, Toshihiro ;Itoh, Tateo ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Springer ๐ŸŒ English โš– 572 KB

We have identified and localized two incompatibility determinants (IncA and IncB) within a 1.3 kb segment of ColE2 sufficient for autonomous replication. The IncA determinant is localized in a region shorter than 250 bp and expresses incompatibility against both ColE2 and ColE3. The region which det