Literature DB >> 2993851

Processive cleavage of concatemer DNA duplexes by Eco RII restriction endonuclease.

A A Yolov, E S Gromova, Z A Shabarova.   

Abstract

Eco RII restriction endonuclease cleaves synthetic DNA-duplexes in which the recognition sites of this enzyme (5'...CCATGG...) are repeated every 9 base pairs with the alternating orientation of the central AT pair. It operates in a processive mode, i.e. the bound enzyme molecule slides along the substrate toward neighboring recognition sites. Nona-nucleotides are the main products of the cleavage. The data obtained neighboring recognition sites. Nona-nucleotides are the main products of the cleavage. The data obtained point to the capability of Eco RII endonuclease to recognize and cleave the substrate under both possible orientations of the central AT-pair of the recognition site with respect to the bound enzyme molecule. These data also show the close similarity of DNA structures in a complex with the enzyme and without.

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Year:  1985        PMID: 2993851     DOI: 10.1007/bf00778525

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  6 in total

1.  Four-stranded DNA structure and DNA base methylation in the mechanism of action of restriction endonucleases.

Authors:  A Stasiak; T Kłopotowski
Journal:  J Theor Biol       Date:  1979-09-07       Impact factor: 2.691

2.  Nucleotide sequence specificity of restriction endonucleases.

Authors:  H O Smith
Journal:  Science       Date:  1979-08-03       Impact factor: 47.728

3.  Does the specific recognition of DNA by the restriction endonuclease EcoRI involve a linear diffusion step? Investigation of the processivity of the EcoRI endonuclease.

Authors:  J Langowski; J Alves; A Pingoud; G Maass
Journal:  Nucleic Acids Res       Date:  1983-01-25       Impact factor: 16.971

Review 4.  Studies on sequence recognition by type II restriction and modification enzymes.

Authors:  P Modrich
Journal:  CRC Crit Rev Biochem       Date:  1982

5.  [Isolation, purification and properties of restriction endonuclease EcoRII].

Authors:  V G Kosykh; S A Puntezhis; Ia I Bur'ianov; A A Baev
Journal:  Biokhimiia       Date:  1982-04

6.  Interaction of EcoRII restriction and modification enzymes with synthetic DNA fragments. EcoRII endonuclease cleavage of substrates with repeated natural and modified recognition sites.

Authors:  A A Yolov; E S Gromova; E A Romanova; T S Oretskaya; A A Oganov; Z A Shabarova
Journal:  FEBS Lett       Date:  1984-02-13       Impact factor: 4.124

  6 in total
  3 in total

1.  Interaction of EcoRII restriction and modification enzymes with synthetic DNA fragments. V. Study of single-strand cleavages.

Authors:  A A Yolov; E S Gromova; E A Kubareva; V K Potapov; Z A Shabarova
Journal:  Nucleic Acids Res       Date:  1985-12-20       Impact factor: 16.971

2.  Interaction of EcoRII restriction and modification enzymes with synthetic DNA fragments. VI. The binding and cleavage of substrates containing nucleotide analogs.

Authors:  A A Yolov; M N Vinogradova; E S Gromova; A Rosenthal; D Cech; V P Veiko; V G Metelev; V G Kosykh; Y I Buryanov; A A Bayev
Journal:  Nucleic Acids Res       Date:  1985-12-20       Impact factor: 16.971

3.  Pairing nanoarchitectonics of oligodeoxyribonucleotides with complex diversity: concatemers and self-limited complexes.

Authors:  Anastasia A Zamoskovtseva; Victor M Golyshev; Valeria A Kizilova; Georgiy Yu Shevelev; Dmitrii V Pyshnyi; Alexander A Lomzov
Journal:  RSC Adv       Date:  2022-02-23       Impact factor: 3.361

  3 in total

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