Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Gene ; 129(1): 77-81, 1993 Jul 15.
Article in English | MEDLINE | ID: mdl-8335262

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.


Subject(s)
Citrobacter freundii/genetics , DNA Restriction-Modification Enzymes/genetics , Genes, Bacterial , Amino Acid Sequence , Base Sequence , Citrobacter freundii/enzymology , Cloning, Molecular , DNA Restriction-Modification Enzymes/chemistry , Methylation , Molecular Sequence Data , Molecular Weight , Restriction Mapping , Sequence Alignment
SELECTION OF CITATIONS
SEARCH DETAIL
...