Literature DB >> 7012133

Transformation in Escherichia coli: stages in the process.

H E Bergmans, I M van Die, W P Hoekstra.   

Abstract

Transformation experiments with Escherichia coli recipient cells and linear chromosomal deoxyribonucleic acid (DNA) are reported. E. coli can be rendered competent for DNA uptake by a temperature shock (0 degrees C leads to 42 degrees C leads to 0 degrees C) of the recipient cells in the presence of a high concentration of either Ca2+ or Mg2+ ions. Uptake of DNA into a deoxyribonuclease-resistant form, for which the presence of Ca2+ is essential, was possible during the temperature shock but appeared to occur most readily after the heat shock during incubation at 0 degrees C. When DNA was added to cells that had been heat shocked in the presence of divalent cations only, DNA uptake also occurred. This suggests that competence induction and uptake may be regarded as separate stages. Under conditions used to induce competence, we observed an extensive release of periplasmic enzymes, probably reflecting membrane damage induced during development of competence. After the conversion of donor DNA into a deoxyribonuclease-resistant form, transformants could be selected. It appeared that incubation, before plating, of the transformation mixture in a medium containing high Ca2+ and Mg2+ concentrations and supplemented with all growth requirements increased the transformation frequency. This incubation probably causes recovery of physiologically labile cells.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7012133      PMCID: PMC216999          DOI: 10.1128/jb.146.2.564-570.1981

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


  23 in total

1.  The genetic and biochemical basis of the transformability of Escherichia coli K12.

Authors:  M Oishi; S D Cosloy
Journal:  Biochem Biophys Res Commun       Date:  1972-12-18       Impact factor: 3.575

2.  Genetic transformation in E. coli: the inhibitory role of the recBC DNase.

Authors:  W Wackernagel
Journal:  Biochem Biophys Res Commun       Date:  1973-03-17       Impact factor: 3.575

3.  The nature of the transformation process in Escherichia coli K12.

Authors:  S D Cosloy; M Oishi
Journal:  Mol Gen Genet       Date:  1973-07-31

4.  Purification of sex pili from Escherichia coli carrying a derepressed F-like R factor.

Authors:  J P Beard; T G Howe; M H Richmond
Journal:  J Bacteriol       Date:  1972-09       Impact factor: 3.490

5.  Mechanism of assembly of the outer membrane of Salmonella typhimurium. Isolation and characterization of cytoplasmic and outer membrane.

Authors:  M J Osborn; J E Gander; E Parisi; J Carson
Journal:  J Biol Chem       Date:  1972-06-25       Impact factor: 5.157

6.  Calcium-dependent bacteriophage DNA infection.

Authors:  M Mandel; A Higa
Journal:  J Mol Biol       Date:  1970-10-14       Impact factor: 5.469

7.  Enhanced uptake of donor DNA by Ca2+ treated Escherichia coli cells.

Authors:  A G Sabelnikov; A V Avdeeva
Journal:  Mol Gen Genet       Date:  1975-07-10

8.  Sensitivity of Escherichia coli to viral nucleic acid. 8. Idiosyncrasy of Ca2+-dependent competence for DNA.

Authors:  A Taketo
Journal:  J Biochem       Date:  1974-04       Impact factor: 3.387

9.  Sensitivity of Escherichia coli to viral nucleic acid, X. Ba2+-induced competence for transfecting DNA.

Authors:  A Taketo
Journal:  Z Naturforsch C Biosci       Date:  1975 Jul-Aug

10.  Nonchromosomal antibiotic resistance in bacteria: genetic transformation of Escherichia coli by R-factor DNA.

Authors:  S N Cohen; A C Chang; L Hsu
Journal:  Proc Natl Acad Sci U S A       Date:  1972-08       Impact factor: 11.205

View more
  23 in total

1.  Plasmid establishment in competent Haemophilus influenzae occurs by illegitimate transformation.

Authors:  M L Pifer
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

2.  Escherichia coli Free Radical-Based Killing Mechanism Driven by a Unique Combination of Iron Restriction and Certain Antibiotics.

Authors:  Li Ma; Yongjun Gao; Anthony W Maresso
Journal:  J Bacteriol       Date:  2015-09-21       Impact factor: 3.490

3.  The moxFG region encodes four polypeptides in the methanol-oxidizing bacterium Methylobacterium sp. strain AM1.

Authors:  D J Anderson; M E Lidstrom
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

4.  Can Ca2+-dependent competence be repeatedly induced in the same Escherichia coli cells?

Authors:  A G Sabelnikov; I V Gordienko; B N Ilyashenko
Journal:  Mol Gen Genet       Date:  1984

5.  Expression and loss of the pBR322 plasmid in Klebsiella aerogenes NCTC 418, grown in chemostat culture.

Authors:  A Sterkenburg; G A Prozée; P A Leegwater; J T Wouters
Journal:  Antonie Van Leeuwenhoek       Date:  1984       Impact factor: 2.271

6.  Ca2+-induced permeabilization of the Escherichia coli outer membrane: comparison of transformation and reconstitution of binding-protein-dependent transport.

Authors:  B Bukau; J M Brass; W Boos
Journal:  J Bacteriol       Date:  1985-07       Impact factor: 3.490

7.  Origin of the 2-amino-2-deoxy-gluconate unit in Rhizobium leguminosarum lipid A. Expression cloning of the outer membrane oxidase LpxQ.

Authors:  Nanette L S Que-Gewirth; Mark J Karbarz; Suzanne R Kalb; Robert J Cotter; Christian R H Raetz
Journal:  J Biol Chem       Date:  2003-01-15       Impact factor: 5.157

8.  Genetic transformation in freshwater: Escherichia coli is able to develop natural competence.

Authors:  B Baur; K Hanselmann; W Schlimme; B Jenni
Journal:  Appl Environ Microbiol       Date:  1996-10       Impact factor: 4.792

9.  Osmolability of Escherichia coli and modification of [125I]ampicillin-binding by competence induction for uptake of transforming DNA.

Authors:  E Fischer
Journal:  Arch Microbiol       Date:  1989       Impact factor: 2.552

10.  Sxy induces a CRP-S regulon in Escherichia coli.

Authors:  Sunita Sinha; Andrew D S Cameron; Rosemary J Redfield
Journal:  J Bacteriol       Date:  2009-06-05       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.