Literature DB >> 1908806

SOS induction as an in vivo assay of enzyme-DNA interactions.

J Heitman1, P Model.   

Abstract

We have constructed strains which are convenient and sensitive indicators of DNA damage and describe their use. These strains utilize an SOS::lac Z fusion constructed by Kenyon and Walker [Proc. Natl. Acad. Sci. USA 77 (1980) 2819-2823] and respond to DNA damage by producing beta-galactosidase. They can be used to characterize restriction systems and screen for restriction endonuclease mutants. Applications include the study of other enzymes involved in DNA metabolism, such as DNA methyltransferases, topoisomerases, recombinases, and DNA replication and repair enzymes.

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Year:  1991        PMID: 1908806     DOI: 10.1016/0378-1119(91)90383-m

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  24 in total

1.  Conditional growth of Escherichia coli caused by expression of vaccinia virus DNA topoisomerase I.

Authors:  M E Fernandez-Beros; Y C Tse-Dinh
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

2.  Stress-based identification and classification of antibacterial agents: second-generation Escherichia coli reporter strains and optimization of detection.

Authors:  Elyse Shapiro; François Baneyx
Journal:  Antimicrob Agents Chemother       Date:  2002-08       Impact factor: 5.191

3.  The isolation of strand-specific nicking endonucleases from a randomized SapI expression library.

Authors:  James C Samuelson; Zhenyu Zhu; Shuang-yong Xu
Journal:  Nucleic Acids Res       Date:  2004-07-09       Impact factor: 16.971

4.  Bacterial cell killing mediated by topoisomerase I DNA cleavage activity.

Authors:  Bokun Cheng; Shikha Shukla; Sarinnapha Vasunilashorn; Somshuvra Mukhopadhyay; Yuk-Ching Tse-Dinh
Journal:  J Biol Chem       Date:  2005-09-13       Impact factor: 5.157

5.  Isolation of SOS constitutive mutants of Escherichia coli.

Authors:  Erin K O'Reilly; Kenneth N Kreuzer
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

6.  Stability of EcoRI restriction-modification enzymes in vivo differentiates the EcoRI restriction-modification system from other postsegregational cell killing systems.

Authors:  Asao Ichige; Ichizo Kobayashi
Journal:  J Bacteriol       Date:  2005-10       Impact factor: 3.490

7.  Cloning and sequence comparison of AvaI and BsoBI restriction-modification systems.

Authors:  H Ruan; K D Lunnen; M E Scott; L S Moran; B E Slatko; J J Pelletier; E J Hess; J Benner; G G Wilson; S Y Xu
Journal:  Mol Gen Genet       Date:  1996-10-28

8.  Genetic analysis of the requirements for SOS induction by nalidixic acid in Escherichia coli.

Authors:  Kathryn G Newmark; Erin K O'Reilly; Jennifer Reineke Pohlhaus; Kenneth N Kreuzer
Journal:  Gene       Date:  2005-08-15       Impact factor: 3.688

9.  Functional recA, lexA, umuD, umuC, polA, and polB genes are not required for the Escherichia coli UVM response.

Authors:  V A Palejwala; G E Wang; H S Murphy; M Z Humayun
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

10.  Inhibition and restart of initiation of chromosome replication: effects on exponentially growing Escherichia coli cells.

Authors:  R Bernander; T Akerlund; K Nordström
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

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