Literature DB >> 8335262

Cloning and sequences of the genes encoding the CfrBI restriction-modification system from Citrobacter freundii.

M V Zakharova1, A N Kravetz, I V Beletzkaja, A V Repyk, A S Solonin.   

Abstract

The genes encoding the CfrBI restriction and modification (R-M) systems from Citrobacter freundii and recognizing the sequence 5'-CCWWGG-3' (W = A or T) were cloned in Escherichia coli McrBC- cells. The nucleotide (nt) sequences of the genes were determined. Two large open reading frames were found. Deletion analysis showed that one of them [1128 nt coding for 376 amino acids (aa)] corresponds to a methyltransferase (MTase)-encoding gene and the other (1065 nt coding for 355 aa) to a restriction endonuclease-encoding gene. The genes are oriented divergently and separated by 76 bp. A CfrBI site (5'-m4CCATGG) was found in the intergenic region of the cfrBIRM genes. Analysis of the deduced aa sequence of M.CfrBI made it possible to determine the typical features of a m4C-specific MTase. Limited homology between the M.CfrBI and R.CfrBI proteins was also found.

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Year:  1993        PMID: 8335262     DOI: 10.1016/0378-1119(93)90698-3

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


  3 in total

1.  DNA methylation at the CfrBI site is involved in expression control in the CfrBI restriction-modification system.

Authors:  I V Beletskaya; M V Zakharova; M G Shlyapnikov; L M Semenova; A S Solonin
Journal:  Nucleic Acids Res       Date:  2000-10-01       Impact factor: 16.971

2.  REBASE--restriction enzymes and methylases.

Authors:  R J Roberts; D Macelis
Journal:  Nucleic Acids Res       Date:  1994-09       Impact factor: 16.971

3.  An alternative approach to study the enzymatic specificities of the CfrBI restriction-modification system.

Authors:  Marina V Zakharova; Irina V Beletskaya; Elena M Ibryashkina; Alexander S Solonin
Journal:  Heliyon       Date:  2019-06-08
  3 in total

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