The Ecl18kI restriction‐modification system: cloning, expression, properties of the purified enzymes

FEBS Letters

Petrauskene, O.V.¹  Repyk, A.V.²  Zakharova, M.V.²  Gromova, E.S.¹  Solonin, A.S.²  Brevnov, M.G.¹  Denjmukhametov, M.M.² 

[1] Department of Chemistry and Belozersky Institute of Physico-Chemical Biology, Moscow State University, 119899 Moscow, Russia;Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pushchino, Moscow Region, Russia

关键词: Ecl18kI DNA methyltransferase;    Ecl18kI restriction endonuclease;    Purification;    Abasic substrate analog;   

DOI  :  10.1016/S0014-5793(98)00921-1

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

Ecl18kI is a type II restriction-modification system isolated from Enterobacter cloaceae 18kI strain. Genes encoding Ecl18kI methyltransferase (M.Ecl18kI) and Ecl18kI restriction endonuclease (R.Ecl18kI) have been cloned and expressed in Escherichia coli. These enzymes recognize the 5′….↓CCNGG….′ sequence in DNA; M.Ecl18kI methylates the C5 carbon atom of the inner dC residue and R.Ecl18kI cuts DNA as shown by the arrow. The restriction endonuclease and the methyltransferase were purified from E. coli B834 [p18Ap1] cells to near homogeneity. The restriction endonuclease is present in the solution as a tetramer, while the methyltransferase is a monomer. The interactions of M.Ecl18kI and R.Ecl18kI with 1,2-dideoxy-d-ribofuranose containing DNA duplexes were investigated. The target base flipping-out mechanism is applicable in the case of M.Ecl18kI. Correct cleavage of the abasic substrates by R.Ecl18kI is accompanied by non-canonical hydrolysis of the modified strand.

【 授权许可】

Unknown