Literature DB >> 3005116

EcoK restriction during in vitro packaging of coliphage lambda DNA.

S M Rosenberg.   

Abstract

The K restriction system of Escherichia coli works in vitro [Meselson and Yuan, Nature 217 (1968) 1110-1114]. E. coli C lacks the K restriction system. I show that in vitro packaging in standard E. coli K-12-derived systems effects a loss of plaque-former output from K-unmodified lambda DNA relative to K-modified lambda DNA when compared with packaging in the E. coli C-derived system of Rosenberg et al. [Gene 38 (1985) 165-175]. I conclude that the EcoK restriction system is active in standard in vitro packaging systems. EcoK restriction during in vitro packaging could specifically depress recovery of some lambda and cosmid clones of eukaryotic DNA or any other DNA not modified for EcoK restriction.

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Year:  1985        PMID: 3005116     DOI: 10.1016/0378-1119(85)90330-0

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  5 in total

1.  Toward a physical map of the genome of the nematode Caenorhabditis elegans.

Authors:  A Coulson; J Sulston; S Brenner; J Karn
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

2.  Charomids: cosmid vectors for efficient cloning and mapping of large or small restriction fragments.

Authors:  I Saito; G R Stark
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

3.  Physical linkage of mouse lambda genes by pulsed-field gel electrophoresis suggests that the rearrangement process favors proximate target sequences.

Authors:  U Storb; D Haasch; B Arp; P Sanchez; P A Cazenave; J Miller
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

4.  Chain-bias of Escherichia coli Rec-mediated lambda patch recombinants is independent of the orientation of lambda cos.

Authors:  S M Rosenberg
Journal:  Genetics       Date:  1988-09       Impact factor: 4.562

5.  Bacillus subtilis phenylalanyl-tRNA synthetase genes: cloning and expression in Escherichia coli and B. subtilis.

Authors:  A A Brakhage; H Putzer; K Shazand; R J Röschenthaler; M Grunberg-Manago
Journal:  J Bacteriol       Date:  1989-02       Impact factor: 3.490

  5 in total

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