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PMID: 10880511 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Novel subtype of type IIs restriction enzymes. BfiI endonuclease exhibits similarities to the EDTA-resistant nuclease Nuc of Salmonella typhimurium.

The Journal of biological chemistry ·Vol. 275 ·No. 40 ·2000-10-06 ·Pages 30878-85

Sapranauskas R, Sasnauskas G, Lagunavicius A, Vilkaitis G, Lubys A, Siksnys V

Abstract

The type IIs restriction enzyme BfiI recognizes the non-palindromic nucleotide sequence 5'-ACTGGG-3' and cleaves complementary DNA strands 5/4 nucleotides downstream of the recognition sequence. The genes coding for the BfiI restriction-modification (R-M) system were cloned/sequenced and biochemical characterization of BfiI restriction enzyme was performed. The BfiI R-M system contained three proteins: two N4-methylcytosine methyltransferases and a restriction enzyme. Sequencing of bisulfite-treated methylated DNA indicated that each methyltransferase modifies cytosines on opposite strands of the recognition sequence. The N-terminal part of the BfiI restriction enzyme amino acid sequence revealed intriguing similarities to an EDTA-resistant nuclease of Salmonella typhimurium. Biochemical analyses demonstrated that BfiI, like the nuclease of S. typhimurium, cleaves DNA in the absence of Mg(2+) ions and hydrolyzes an artificial substrate bis(p-nitrophenyl) phosphate. However, unlike the nonspecific S. typhimurium nuclease, BfiI restriction enzyme cleaves DNA specifically. We propose that the DNA-binding specificity of BfiI stems from the C-terminal part of the protein. The catalytic N-terminal subdomain of BfiI radically differs from that of type II restriction enzymes and is presumably similar to the EDTA-resistant nonspecific nuclease of S. typhimurium; therefore, BfiI did not require metal ions for catalysis. We suggest that BfiI represents a novel subclass of type IIs restriction enzymes that differs from the archetypal FokI endonuclease by the fold of its cleavage domain, the domain location, and reaction mechanism.

MeSH Terms
Amino Acid Sequence Bacterial Proteins Catalytic Domain Cloning, Molecular Cytosine/metabolism DNA Methylation DNA Restriction Enzymes/chemistry,classification DNA, Complementary/metabolism DNA-Cytosine Methylases/metabolism Deoxyribonucleases, Type II Site-Specific/chemistry,metabolism Dose-Response Relationship, Drug Edetic Acid/pharmacology Endonucleases/chemistry Hydrogen-Ion Concentration Hydrolysis Kinetics Magnesium/metabolism Micrococcal Nuclease Molecular Sequence Data Mutagenesis, Site-Directed Nitrophenols/metabolism Oligonucleotides/metabolism Plasmids/metabolism Protein Folding Protein Structure, Tertiary Salmonella typhimurium/enzymology Sequence Analysis, DNA Sequence Homology, Amino Acid Sulfites/pharmacology Time Factors
Chemicals
Bacterial Proteins DNA, Complementary Nitrophenols Oligonucleotides Sulfites nuc protein, staphylococcus bis(4-nitrophenyl)phosphate Cytosine Edetic Acid DNA-Cytosine Methylases Endonucleases DNA Restriction Enzymes endodeoxyribonuclease BfiI endodeoxyribonuclease FokI Deoxyribonucleases, Type II Site-Specific Micrococcal Nuclease Magnesium sodium bisulfite
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sapranauskas R
Institute of Biotechnology, Graiciuno 8, Vilnius 2028, Lithuania.
Sasnauskas G
Lagunavicius A
Vilkaitis G
Lubys A
Siksnys V
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-10-06
Pages
30878-85
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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