Literature DB >> 9068647

Reduction of conjugal transfer efficiency by three restriction activities of Anabaena sp. strain PCC 7120.

J Elhai1, A Vepritskiy, A M Muro-Pastor, E Flores, C P Wolk.   

Abstract

The efficiency of conjugal transfer of plasmids from Escherichia coli to the cyanobacterium Anabaena sp. strain PCC 7120 was quantitated as a function of the number of restriction sites for the restriction enzymes carried by the recipient. In addition to the previously recognized isoschizomers of AvaI and AvaII, PCC 7120 was found to possess an isoschizomer of AvaIII. Plasmids modified in E. coli with methylases that protect in vitro against restriction by the three enzymes were transferred with high efficiency, nearly independent of the number of restriction sites on the plasmid. Plasmids left unprotected against one of the three restriction enzymes were transferred with lower efficiencies. For low numbers of sites, the efficiency of conjugal transfer decreased as an exponential function of the number of unprotected sites. The methods presented may be used to increase the efficiency of conjugal transfer into restriction-competent bacteria.

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Year:  1997        PMID: 9068647      PMCID: PMC178925          DOI: 10.1128/jb.179.6.1998-2005.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  69 in total

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Review 2.  DNA modification and restriction.

Authors:  W Arber; S Linn
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3.  Restriction of infectious bacteriophage fd DNA's and an assay for in vitro host-controlled restriction and modification.

Authors:  R Benzinger
Journal:  Proc Natl Acad Sci U S A       Date:  1968-04       Impact factor: 11.205

4.  Conjugal transfer of DNA to cyanobacteria.

Authors:  J Elhai; C P Wolk
Journal:  Methods Enzymol       Date:  1988       Impact factor: 1.600

5.  The pIC plasmid and phage vectors with versatile cloning sites for recombinant selection by insertional inactivation.

Authors:  J L Marsh; M Erfle; E J Wykes
Journal:  Gene       Date:  1984-12       Impact factor: 3.688

6.  Use of a transposon with luciferase as a reporter to identify environmentally responsive genes in a cyanobacterium.

Authors:  C P Wolk; Y Cai; J M Panoff
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

7.  Specific-purpose plasmid cloning vectors. II. Broad host range, high copy number, RSF1010-derived vectors, and a host-vector system for gene cloning in Pseudomonas.

Authors:  M Bagdasarian; R Lurz; B Rückert; F C Franklin; M M Bagdasarian; J Frey; K N Timmis
Journal:  Gene       Date:  1981-12       Impact factor: 3.688

8.  Electroporation and conjugal plasmid transfer to members of the genus Aquaspirillum.

Authors:  P A Eden; R P Blakemore
Journal:  Arch Microbiol       Date:  1991       Impact factor: 2.552

9.  A versatile class of positive-selection vectors based on the nonviability of palindrome-containing plasmids that allows cloning into long polylinkers.

Authors:  J Elhai; C P Wolk
Journal:  Gene       Date:  1988-08-15       Impact factor: 3.688

10.  Studies on transformation of Escherichia coli with plasmids.

Authors:  D Hanahan
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

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  130 in total

1.  Signal transduction protein P(II) is required for NtcA-regulated gene expression during nitrogen deprivation in the cyanobacterium Synechococcus elongatus strain PCC 7942.

Authors:  M Fadi Aldehni; Jörg Sauer; Christian Spielhaupter; Roland Schmid; Karl Forchhammer
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

2.  Novel DNA-binding proteins in the cyanobacterium Anabaena sp. strain PCC 7120.

Authors:  Olga A Koksharova; C Peter Wolk
Journal:  J Bacteriol       Date:  2002-07       Impact factor: 3.490

3.  Natural transformation of the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1: a simple and efficient method for gene transfer.

Authors:  K Onai; M Morishita; T Kaneko; S Tabata; M Ishiura
Journal:  Mol Genet Genomics       Date:  2003-11-25       Impact factor: 3.291

4.  Open reading frame all0601 from Anabaena sp. strain PCC 7120 represents a novel gene, cnaT, required for expression of the nitrate assimilation nir operon.

Authors:  José E Frías; Antonia Herrero; Enrique Flores
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

5.  The insertion sequences of Anabaena sp. strain PCC 7120 and their effects on its open reading frames.

Authors:  C Peter Wolk; Sigal Lechno-Yossef; Karin M Jäger
Journal:  J Bacteriol       Date:  2010-07-23       Impact factor: 3.490

6.  Negative regulation of expression of the nitrate assimilation nirA operon in the heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120.

Authors:  José Enrique Frías; Enrique Flores
Journal:  J Bacteriol       Date:  2010-03-26       Impact factor: 3.490

7.  Inactivation of a heterocyst-specific invertase indicates a principal role of sucrose catabolism in heterocysts of Anabaena sp.

Authors:  Rocío López-Igual; Enrique Flores; Antonia Herrero
Journal:  J Bacteriol       Date:  2010-08-20       Impact factor: 3.490

8.  A Salt-Inducible Mn-Catalase (KatB) Protects Cyanobacterium from Oxidative Stress.

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Journal:  Plant Physiol       Date:  2015-12-08       Impact factor: 8.340

9.  HetR-dependent and -independent expression of heterocyst-related genes in an Anabaena strain overproducing the NtcA transcription factor.

Authors:  Elvira Olmedo-Verd; Enrique Flores; Antonia Herrero; Alicia M Muro-Pastor
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

10.  Heterocyst-specific excision of the Anabaena sp. strain PCC 7120 hupL element requires xisC.

Authors:  Claudio D Carrasco; Scott D Holliday; Alfred Hansel; Peter Lindblad; James W Golden
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

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