Literature DB >> 2539102

'Star' activity and complete loss of specificity of CeqI endonuclease.

Z Izsvák1, E Duda.   

Abstract

Restriction endonuclease CeqI, an isoschizomer of EcoRV, exhibits 'star' activity, a relaxation of specificity in the presence of Mn2+, dimethyl sulphoxide or glycerol. The enzyme cleaves a set of sequences that differ from the canonical GATATC by only one nucleotide in positions 2, 3, 4 or 5. Two of these sequences are not cleaved if modified by dam methylase. A further loss of specificity can be observed in circumstances less favourable for the enzyme, namely low-ionic-strength buffers of pH values below 6.0 or above 9.4. This activity seems to cleave DNA at any sequence, producing a smear instead of well-defined bands. Partial renaturation of the denatured enzyme gives rise to a similar non-specific nuclease activity.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2539102      PMCID: PMC1138355          DOI: 10.1042/bj2580301

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  14 in total

1.  Studies on the cleavage of bacteriophage lambda DNA with EcoRI Restriction endonuclease.

Authors:  M Thomas; R W Davis
Journal:  J Mol Biol       Date:  1975-01-25       Impact factor: 5.469

2.  Altering the specificity of restriction endonuclease: effect of replacing Mg2+ with Mn2+.

Authors:  M Hsu; P Berg
Journal:  Biochemistry       Date:  1978-01-10       Impact factor: 3.162

3.  Specificity of substrate recognition by the EcoRI restriction endonuclease.

Authors:  B Polisky; P Greene; D E Garfin; B J McCarthy; H M Goodman; H W Boyer
Journal:  Proc Natl Acad Sci U S A       Date:  1975-09       Impact factor: 11.205

4.  Purification and crystallization of the EcoRV restriction endonuclease.

Authors:  A D'Arcy; R S Brown; M Zabeau; R W van Resandt; F K Winkler
Journal:  J Biol Chem       Date:  1985-02-25       Impact factor: 5.157

5.  The effect of several nucleic acid binding drugs on the cleavage of d(GGAATTCC) and pBR 322 by the Eco RI restriction endonuclease.

Authors:  M Goppelt; J Langowski; A Pingoud; W Haupt; C Urbanke; H Mayer; G Maass
Journal:  Nucleic Acids Res       Date:  1981-11-25       Impact factor: 16.971

6.  The cleavage site for the restriction endonuclease EcoRV is 5'-GAT/ATC-3'.

Authors:  I Schildkraut; C D Banner; C S Rhodes; S Parekh
Journal:  Gene       Date:  1984-03       Impact factor: 3.688

7.  The effects of base analogue substitutions on the cleavage by the EcoRI restriction endonuclease of octadeoxyribonucleotides containing modified EcoRI recognition sequences.

Authors:  C A Brennan; M D Van Cleve; R I Gumport
Journal:  J Biol Chem       Date:  1986-06-05       Impact factor: 5.157

8.  Relaxed specificity of the EcoRV restriction endonuclease.

Authors:  S E Halford; B M Lovelady; S A McCallum
Journal:  Gene       Date:  1986       Impact factor: 3.688

9.  Alteration of the specificity of restriction endonucleases in the presence of organic solvents.

Authors:  E Malyguine; P Vannier; P Yot
Journal:  Gene       Date:  1980-01       Impact factor: 3.688

10.  [EcoRV restrictase: physical and catalytic properties of homogenous enzyme].

Authors:  N P Kuz'min; S P Loseva; R Kh Beliaeva; A N Kravets; A S Solonin
Journal:  Mol Biol (Mosk)       Date:  1984 Jan-Feb
View more
  3 in total

1.  Positive co-operative interaction between the subunits of CeqI restriction endonuclease.

Authors:  Z Jobbágy; Z Izsvák; E Duda
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

2.  Cofactor requirement of HpyAV restriction endonuclease.

Authors:  Siu-Hong Chan; Lars Opitz; Lauren Higgins; Diana O'loane; Shuang-Yong Xu
Journal:  PLoS One       Date:  2010-02-05       Impact factor: 3.240

3.  The Fidelity Index provides a systematic quantitation of star activity of DNA restriction endonucleases.

Authors:  Hua Wei; Caitlin Therrien; Aine Blanchard; Shengxi Guan; Zhenyu Zhu
Journal:  Nucleic Acids Res       Date:  2008-04-15       Impact factor: 16.971

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.