The SalI (SalGI) restriction-modification system of Streptomyces albus G

Gene. 1988 Dec 25;74(1):39-42. doi: 10.1016/0378-1119(88)90246-6.

Abstract

The salIR and salM genes of Streptomyces albus G specify the SalGI (SalI) restriction enzyme and its cognate methyltransferase, respectively. These enzymes are responsible for restriction and modification of bacteriophages. Some phages carry genes that interfere with SalI-specific modification. The sal genes have been cloned in a Streptomyces host-vector system. Use of the cloned DNA as a hybridization probe reveals that sal mutants frequently arise from transposition of a DNA segment of approx. 1 kb into the sal genes. Some, but not all, other bacteria that produce SalGI isoschizomers contain nucleotide sequences that hybridize with sal DNA.

Publication types

  • Review

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • DNA, Bacterial / metabolism
  • DNA, Viral / metabolism
  • Deoxyribonucleases, Type II Site-Specific / genetics
  • Deoxyribonucleases, Type II Site-Specific / metabolism*
  • Genes, Bacterial
  • Recombinant Proteins / genetics
  • Site-Specific DNA-Methyltransferase (Adenine-Specific) / genetics
  • Site-Specific DNA-Methyltransferase (Adenine-Specific) / metabolism
  • Streptomyces / enzymology*
  • Streptomyces / genetics

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • DNA, Viral
  • Recombinant Proteins
  • DNA modification methylase SalGI
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)
  • Deoxyribonucleases, Type II Site-Specific
  • GTCGAC-specific type II deoxyribonucleases