Literature DB >> 20298193

The type IIB restriction endonucleases.

Jacqueline J T Marshall1, Stephen E Halford.   

Abstract

The endonucleases from the Type IIB restriction-modification systems differ from all other restriction enzymes. The Type IIB enzymes cleave both DNA strands at specified locations distant from their recognition sequences, like Type IIS nucleases, but they are unique in that they do so on both sides of the site, to liberate the site from the remainder of the DNA on a short duplex. The fact that these enzymes cut DNA at specific locations mark them as Type II systems, as opposed to the Type I enzymes that cut DNA randomly, but in terms of gene organization and protein assembly, most Type IIB restriction-modification systems have more in common with Type I than with other Type II systems. Our current knowledge of the Type IIB systems is reviewed in the present paper.

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Year:  2010        PMID: 20298193     DOI: 10.1042/BST0380410

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  14 in total

Review 1.  Type II restriction endonucleases--a historical perspective and more.

Authors:  Alfred Pingoud; Geoffrey G Wilson; Wolfgang Wende
Journal:  Nucleic Acids Res       Date:  2014-05-30       Impact factor: 16.971

2.  A model for the evolution of prokaryotic DNA restriction-modification systems based upon the structural malleability of Type I restriction-modification enzymes.

Authors:  Edward K M Bower; Laurie P Cooper; Gareth A Roberts; John H White; Yvette Luyten; Richard D Morgan; David T F Dryden
Journal:  Nucleic Acids Res       Date:  2018-09-28       Impact factor: 16.971

3.  TstI, a Type II restriction-modification protein with DNA recognition, cleavage and methylation functions in a single polypeptide.

Authors:  Rachel M Smith; Christian Pernstich; Stephen E Halford
Journal:  Nucleic Acids Res       Date:  2014-03-14       Impact factor: 16.971

4.  Organization of the BcgI restriction-modification protein for the transfer of one methyl group to DNA.

Authors:  Rachel M Smith; Alistair J Jacklin; Jacqueline J T Marshall; Frank Sobott; Stephen E Halford
Journal:  Nucleic Acids Res       Date:  2012-11-11       Impact factor: 16.971

5.  Organization of the BcgI restriction-modification protein for the cleavage of eight phosphodiester bonds in DNA.

Authors:  Rachel M Smith; Jacqueline J T Marshall; Alistair J Jacklin; Susan E Retter; Stephen E Halford; Frank Sobott
Journal:  Nucleic Acids Res       Date:  2012-11-11       Impact factor: 16.971

6.  Concerted action at eight phosphodiester bonds by the BcgI restriction endonuclease.

Authors:  Jacqueline J T Marshall; Rachel M Smith; Sumita Ganguly; Stephen E Halford
Journal:  Nucleic Acids Res       Date:  2011-06-07       Impact factor: 16.971

7.  Illuminating the reaction pathway of the FokI restriction endonuclease by fluorescence resonance energy transfer.

Authors:  Christian Pernstich; Stephen E Halford
Journal:  Nucleic Acids Res       Date:  2011-10-12       Impact factor: 16.971

8.  ClpXP protease targets long-lived DNA translocation states of a helicase-like motor to cause restriction alleviation.

Authors:  Michelle Simons; Fiona M Diffin; Mark D Szczelkun
Journal:  Nucleic Acids Res       Date:  2014-09-26       Impact factor: 16.971

9.  Removal of a frameshift between the hsdM and hsdS genes of the EcoKI Type IA DNA restriction and modification system produces a new type of system and links the different families of Type I systems.

Authors:  Gareth A Roberts; Kai Chen; Laurie P Cooper; John H White; Garry W Blakely; David T F Dryden
Journal:  Nucleic Acids Res       Date:  2012-09-23       Impact factor: 16.971

Review 10.  Type I restriction enzymes and their relatives.

Authors:  Wil A M Loenen; David T F Dryden; Elisabeth A Raleigh; Geoffrey G Wilson
Journal:  Nucleic Acids Res       Date:  2013-09-24       Impact factor: 16.971

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