Nucleotide sequence of the BsuRI restriction-modification system.
AUTOR(ES)
Kiss, A
RESUMO
The genes of the 5'-GGCC specific BsuRI restriction-modification system of Bacillus subtilis have been cloned and expressed in E. coli and their nucleotide sequence has been determined. The restriction and modification genes code for polypeptides with calculated molecular weights of 66,314 and 49,642, respectively. Both enzymes are coded by the same DNA strand. The restriction gene is upstream of the methylase gene and the coding regions are separated by 780 bp. Analysis of the RNA transcripts by S1-nuclease mapping indicates that the restriction and modification genes are transcribed from different promoters. Comparison of the amino acid sequences revealed no homology between the BsuRI restriction and modification enzymes. There are, however, regions of homology between the BsuRI methylase and two other GGCC specific modification enzymes, the BspRI and SPR methylases.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=321967Documentos Relacionados
- Cloning, nucleotide sequence, and expression of the HincII restriction-modification system.
- Cloning and expression of the BalI restriction-modification system.
- Cloning and characterization of the MboII restriction-modification system.
- Structure and evolution of the XcyI restriction-modification system.
- Cloning, sequencing and expression of the Taq I restriction-modification system.