Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2012 | 59 | 4 | 669-672

Article title

A rapid and simple method for detection of type II restriction endonucleases in cells of bacteria with high activity of nonspecific nucleases

Content

Title variants

Languages of publication

EN

Abstracts

EN
In this work we describe a novel, rapid and simple microscale procedure for identification of restriction endonuclease activity in bacteria lysates, which contain high levels of non-specific DNA nucleases.

Year

Volume

59

Issue

4

Pages

669-672

Physical description

Dates

published
2012
received
2012-07-23
revised
2012-10-16
accepted
2012-10-29
(unknown)
2012-11-06

Contributors

  • Department of Molecular Evolution, University of Gdańsk, Gdańsk, Poland
  • Department of Microbiology, University of Gdańsk, Gdańsk, Poland
  • Department of Microbiology, University of Gdańsk, Gdańsk, Poland
author
  • Department of Microbiology, University of Gdańsk, Gdańsk, Poland

References

  • Arber W (1979) Promotion and limitation of genetic exchange. Science 205: 361-365.
  • Belavin PA, Dedkov VS, Degtiarev SKh (1988) A simple technique for detection of restriction endonucleases in bacterial colonies. Appl Biochem Microbiol (Russia) 24: 121-124.
  • Bickle TA, Krüger DH (1993) Biology of DNA restriction. Microbiol Rev 57: 434-450.
  • Edberg SC, Clare D, Moore MH, Singer JM (1979) Rapid identification of Enterobacteriaceae from blood cultures with the Micro-ID system. J Clin Microbiol 10: 693-697.
  • Edwards PR and Ewing W H (1972) Identification of Enterobacteriaceae. Burgess, Minneapolis 3rd edN.
  • Greene PJ, Heyneker HL, Bolivar F, Rodriguez RL, Betlach MC, Covarrubias AA, Backman K, Russel DJ, Tait R, Boyer HW (1978) A general method for purification of restriction enzymes. Nucleic Acids Res 5: 2373-2380.
  • Isenberg HD (2007) Clinical microbiology procedures handbook. Washington DC: Am Soci for Microbiol 2nd edn.
  • Kaida T, Ginting L, Kanda K, Murata A, Kato F (1999) Screening of type II restriction endonuclease from soil bacteria. Bull Fac Agr 84: 1-9.
  • Krüger DH, Bickle A (1983) Bacteriophage survival: multiple mechanisms for avoiding the deoxyribonucleic acid restriction systems of their hosts. Microbiol Rev 47: 345-360.
  • Mruk I, Kaczorowski T (2003) Genetic organization and molecular analysis of the EcoVIII restriction-modification system of Escherichia coli E1585-68 and its comparison with isospecific homologs. Appl Environ Microbiol 69: 2638-2650.
  • Pingoud A, Jeltsch A (2001) Structure and function of type II restriction endonucleases. Nucl Acids Res 29: 3705-3727.
  • Poch MT, Somkuti GA (1993) Rapid screening of lactic acid bacteria for endonuclease activity. Biotechnol Tech 7: 781-784.
  • Poch MT, Somkuti GA (1995) Isolation of SagI, a new HaeIII isoschizomer from Streptococcus agalactiae. Appl Microbiol Biotechnol 43: 282-284.
  • Puchkova LI, Ushakova TA, Mikhailova VK, Serov GD, Krivopalova GN, Repin VE (2002) Testing and isolation of high-purity restriction endonucleases. Appl Biochem Microbiol 38: 20-24.
  • REBASE http://rebase.neb.com
  • Roberts RJ (2005) How restriction enzymes became the workhorses of molecular biology. Proc Natl Acad Sci 102: 5905-5908.
  • Sambrook J, Fritsch E.T, Maniatis T (1989) Molecular Cloning: A laboratory manual. Cold Spring Harbor Laboratory Pr; 2nd edn.
  • Smith DI, Blattner FR, Davies J (1976) The isolation and partial characterization of a new restriction endonuclease from Providencia stuartii. Nucleic Acids Res 3: 343-353.
  • Whitehead PR, Brown NL (1985) A simple and rapid method for screening bacteria for type II restriction endonucleases: enzymes in Aphanothece halophytica. Arch Microbiol 141: 70-74.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv59p669kz
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.