Literature DB >> 383579

Plasmids with temperature-dependent copy number for amplification of cloned genes and their products.

B E Uhlin, S Molin, P Gustafsson, K Nordström.   

Abstract

Miniplasmids (pKN402 and pKN410) were isolated from runaway-replication mutants of plasmid R1. At 30 degrees C these miniplasmids are present in 20--50 copies per cell of Escherichia coli, whereas at temperatures above 35 degrees C the plasmids replicate without copy number control during 2--3 h. At the end of this period plasmid DNA amounts to about 75% of the total DNA. During the gene amplification, growth and protein synthesis continue at normal rate leading to a drastic amplification of plasmid gene products. Plasmids pKN402 (4.6 Md) and pKN410 (10 Md) have single restriction sites for restriction endonucleases EcoRI and HindIII; in addition plamid pKN410 has a single BamHI site and carries ampicillin resistance. The plasmids can therefore be used as cloning vectors. Several genes were cloned into these vectors using the EcoRI sites; chromosomal as well as plasmid-coded beta-lactamase was found to be amplified up to 400-fold after thermal induction of the runaway replication. Vectors of this temperature-dependent class will be useful in the production of large quantities of genes and gene products. These plasmids have lost their mobilization capacity. Runaway replication is lethal to the host bacteria in rich media. These two properties contribute to the safe use of the plasmids as cloning vehicles.

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Year:  1979        PMID: 383579     DOI: 10.1016/0378-1119(79)90065-9

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


  41 in total

Review 1.  High-expression of a target gene and high-stability of the plasmid.

Authors:  M Kobayashi; Y Kurusu; H Yukawa
Journal:  Appl Biochem Biotechnol       Date:  1991-02       Impact factor: 2.926

2.  Construction of a Co1E1 plasmid bearing inducible high-copy-number phenotype.

Authors:  D Bachvarov; E Jay; I Ivanov
Journal:  Folia Microbiol (Praha)       Date:  1990       Impact factor: 2.099

3.  DnaG-dependent priming signals can substitute for the two essential DNA initiation signals in oriV of the broad host-range plasmid RSF1010.

Authors:  Y Honda; T Nakamura; K Tanaka; A Higashi; H Sakai; T Komano; M Bagdasarian
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

4.  Intron insertion facilitates amplification of cloned virus cDNA in Escherichia coli while biological activity is reestablished after transcription in vivo.

Authors:  I E Johansen
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-29       Impact factor: 11.205

5.  An efficient random mutagenesis technique using an E. coli mutator strain.

Authors:  A Greener; M Callahan; B Jerpseth
Journal:  Mol Biotechnol       Date:  1997-04       Impact factor: 2.695

6.  Properties of a mutant recA-encoded protein reveal a possible role for Escherichia coli recF-encoded protein in genetic recombination.

Authors:  M V Madiraju; A Templin; A J Clark
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

Review 7.  Biocatalysis made to order.

Authors:  G Tripathi
Journal:  Appl Biochem Biotechnol       Date:  1988-10       Impact factor: 2.926

Review 8.  Plasmid DNA vaccine vector design: impact on efficacy, safety and upstream production.

Authors:  James A Williams; Aaron E Carnes; Clague P Hodgson
Journal:  Biotechnol Adv       Date:  2009-02-20       Impact factor: 14.227

9.  Cloning and manipulation of the Escherichia coli cyclopropane fatty acid synthase gene: physiological aspects of enzyme overproduction.

Authors:  D W Grogan; J E Cronan
Journal:  J Bacteriol       Date:  1984-04       Impact factor: 3.490

10.  Role of mRNA translational efficiency in bovine growth hormone expression in Escherichia coli.

Authors:  B E Schoner; H M Hsiung; R M Belagaje; N G Mayne; R G Schoner
Journal:  Proc Natl Acad Sci U S A       Date:  1984-09       Impact factor: 11.205

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