Literature DB >> 7698663

Cloning and expression of the NaeI restriction endonuclease-encoding gene and sequence analysis of the NaeI restriction-modification system.

C H Taron1, E M Van Cott, G G Wilson, L S Moran, B E Slatko, L J Hornstra, J S Benner, R B Kucera, E P Guthrie.   

Abstract

NaeI, a type-II restriction-modification (R-M) system from the bacterium Nocardia aerocolonigenes, recognizes the sequence 5'-GCCGGC. The NaeI DNA methyltransferase (MTase)-encoding gene, naeIM, had been cloned previously in Escherichia coli [Van Cott and Wilson, Gene 74 (1988) 55-59]. However, none of these clones expressed detectable levels of the restriction endonuclease (ENase). The absence of the intact ENase-encoding gene (naeIR) within the isolated MTase clones was confirmed by recloning the MTase clones into Streptomyces lividans. The complete NaeI system was finally cloned using E. coli AP1-200 [Piekarowicz et al., Nucleic Acids Res. 19 (1991) 1831-1835] and less stringent MTase-selection conditions. The naeIR gene was expressed first by cloning into S. lividans, and later by cloning under control of a regulated promoter in an E. coli strain preprotected by the heterologous MspI MTase (M.MspI). The DNA sequence of the NaeI R-M system has been determined, analyzed and compared to previously sequenced R-M systems.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7698663     DOI: 10.1016/0378-1119(94)00806-4

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


  6 in total

1.  Isolation of segments of homologous genes with only one conserved amino acid region via PCR.

Authors:  M Laging; B Fartmann; W Kramer
Journal:  Nucleic Acids Res       Date:  2001-01-15       Impact factor: 16.971

2.  Crystal structure of NaeI-an evolutionary bridge between DNA endonuclease and topoisomerase.

Authors:  Q Huai; J D Colandene; Y Chen; F Luo; Y Zhao; M D Topal; H Ke
Journal:  EMBO J       Date:  2000-06-15       Impact factor: 11.598

Review 3.  Behavior of restriction-modification systems as selfish mobile elements and their impact on genome evolution.

Authors:  I Kobayashi
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

4.  The domain organization of NaeI endonuclease: separation of binding and catalysis.

Authors:  J D Colandene; M D Topal
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-31       Impact factor: 11.205

5.  The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA.

Authors:  K Drotschmann; A Aronshtam; H J Fritz; M G Marinus
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

6.  A genomic sample sequence of the entomopathogenic bacterium Photorhabdus luminescens W14: potential implications for virulence.

Authors:  R H Ffrench-Constant; N Waterfield; V Burland; N T Perna; P J Daborn; D Bowen; F R Blattner
Journal:  Appl Environ Microbiol       Date:  2000-08       Impact factor: 4.792

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.