Cloning and characterization of the TneDI restriction: modification system of Thermotoga neapolitana

Extremophiles. 2011 Nov;15(6):665-72. doi: 10.1007/s00792-011-0397-9. Epub 2011 Sep 15.

Abstract

A putative Type II restriction-modification system of Thermotoga neapolitana, TneDI, was cloned into Escherichia coli XL1-Blue MRF' and characterized. Gene CTN_0339 specifies the endonuclease R.TneDI, while CTN_0340 encodes the cognate DNA methyltransferase M.TneDI. Both enzymes were purified simply by heating the cell lysates of E. coli followed by centrifugation. The enzymes were active over a broad range of temperatures, from 42°C to at least 77°C, with the highest activities observed at 77°C. R.TneDI cleaved at the center of the recognition sequence (CG↓CG) and generated blunt-end cuts. Overexpression of R.TneDI in BL21(DE3) was confirmed by both SDS-PAGE and Western blotting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Western
  • Cloning, Molecular
  • DNA Modification Methylases / metabolism*
  • DNA Primers
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli / genetics
  • Escherichia coli / growth & development
  • Recombination, Genetic
  • Thermotoga neapolitana / enzymology
  • Thermotoga neapolitana / genetics*

Substances

  • DNA Primers
  • DNA Modification Methylases