SibEnzyme restriction enzymes database

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Pkr I

Enzyme name Pkr I
Prototype PkrI
SKU SE-E579
Turbo version Not available
High-concentration version Not available
Recognition site
5'… G(5mC)N▼G(5mC) …3'
3'… (5mC)G▲N(5mC)G …5'
Source Planomicrobium koreense 78k
Optimal buffer SE-buffer Y
Optimal temperature 37 °C
Inactivation temperature 65 °C
Buffer activity
BGOWYROSE
50751025100100
Unit definition One unit is defined as the amount of enzyme required to hydrolyze completely 1 μg of linearized plasmid pFsp4HI3 in 1 hour at 37°C in a total reaction volume of 50 μl (see run 4 in the figure). PkrI activity assay on DNA pFsp4HI3/DriI Lanes: 1 and 6 - 1 Kb SE DNA-markers. 2 - Control DNA pFsp4HI3/DriI, 3 - 0.5 μl Pkr I 4 - 1 μl Pkr I 5 - 2 μl Pkr I Products were separated in 1,4% agarose gel in Buffer TAE..
Assayed on DNA pFsp4HI3/DriI is a linearized plasmid pFsp4HI3, which carries a gene of DNA-methyltransferase M.Fsp4HI and includes three sites 5`-G(5mC)NG(5mC)-3`/3`-CGN(5mC)G-5` [2].
Storage conditions 20 mM Tris-HCl (pH 7.4); 200 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 50% glycerol; Store at -20°C.
Ligation
Nonspecific hydrolysis No detectable degradation of 1μg of Lambda DNA was observed after incubation with 2 units of enzyme for 16 hours at 37°C in a total reaction volume of 50 μl.
Methylation sensitivity The enzyme cleaves C5-methylated DNA and doesn't cut unmodified DNA [1].
Supplied with enzyme 10 X SE-buffer Y
Notes
References
  1. Degtyarev S. Kh., Abdurashitov M.A., Kolyhalov A.A., Rechkunova N.I. Acl I, a new restriction endonuclease from Acinetobacter calcoaceticus recognizing 5'-AA^CGTT -3'. // Nucleic Acids Research, Vol. 20, No. 14, 37-87 (1992) Chmuzh E.V., Kashirina Yu.G., Tomilova Yu.E., Chernukhin V.A., Okhapkina S.S., Gonchar D. A., Dedkov V.S., Abdurashitov M. A., Degtyarev S. Kh. Gene cloning, comparative analysis of the protein structures from Fsp4HI restriction-modification system and biochemical characterization of the recombinant DNA methyltransferase M.Fsp4HI. // Molecular Biology, V.41, No 1, p. 43-50 (2007) 1.V.A. Chernukhin, T. N. Nayakshina, D.A. Gonchar, J.E. Tomilova, M.V. Tarasova, V.S. Dedkov, N.A. Mikhnenkova, S.Kh. Degtyarev A new site-specific methyl-directed DNA endonuclease PkrI recognizes and cuts methylated DNA sequence 5'-GCN^GC-3'/3'-CG^NCG-5' carrying at least three 5-methylcytosines // Translated from "Ovchinnikov bulletin of biotechnology and physical and chemical biology" V.7, No 3, pp 35-42, 2011 Chmuzh E.V., Kashirina Yu.G., Tomilova Yu.E., Chernukhin V.A., Okhapkina S.S., Gonchar D. A., Dedkov V.S., Abdurashitov M. A., Degtyarev S. Kh. Gene cloning, comparative analysis of the protein structures from Fsp4HI restriction-modification system and biochemical characterization of the recombinant DNA methyltransferase M.Fsp4HI. // Molecular Biology, V.41, No 1, p. 43-50 (2007)

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Pkr I

Enzyme name Pkr I
Prototype PkrI
SKU SE-E579
Turbo version Not available
High-concentration version Not available
Recognition site
5'… G(5mC)N▼G(5mC) …3'
3'… (5mC)G▲N(5mC)G …5'
Source Planomicrobium koreense 78k
Optimal buffer SE-buffer Y
Optimal temperature 37 °C
Inactivation temperature 65 °C
Buffer activity
BGOWYROSE
50751025100100
Unit definition One unit is defined as the amount of enzyme required to hydrolyze completely 1 μg of linearized plasmid pFsp4HI3 in 1 hour at 37°C in a total reaction volume of 50 μl (see run 4 in the figure). PkrI activity assay on DNA pFsp4HI3/DriI Lanes: 1 and 6 - 1 Kb SE DNA-markers. 2 - Control DNA pFsp4HI3/DriI, 3 - 0.5 μl Pkr I 4 - 1 μl Pkr I 5 - 2 μl Pkr I Products were separated in 1,4% agarose gel in Buffer TAE..
Assayed on DNA pFsp4HI3/DriI is a linearized plasmid pFsp4HI3, which carries a gene of DNA-methyltransferase M.Fsp4HI and includes three sites 5`-G(5mC)NG(5mC)-3`/3`-CGN(5mC)G-5` [2].
Storage conditions 20 mM Tris-HCl (pH 7.4); 200 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 50% glycerol; Store at -20°C.
Ligation
Nonspecific hydrolysis No detectable degradation of 1μg of Lambda DNA was observed after incubation with 2 units of enzyme for 16 hours at 37°C in a total reaction volume of 50 μl.
Methylation sensitivity The enzyme cleaves C5-methylated DNA and doesn't cut unmodified DNA [1].
Supplied with enzyme 10 X SE-buffer Y
Notes
References
  1. Degtyarev S. Kh., Abdurashitov M.A., Kolyhalov A.A., Rechkunova N.I. Acl I, a new restriction endonuclease from Acinetobacter calcoaceticus recognizing 5'-AA^CGTT -3'. // Nucleic Acids Research, Vol. 20, No. 14, 37-87 (1992) Chmuzh E.V., Kashirina Yu.G., Tomilova Yu.E., Chernukhin V.A., Okhapkina S.S., Gonchar D. A., Dedkov V.S., Abdurashitov M. A., Degtyarev S. Kh. Gene cloning, comparative analysis of the protein structures from Fsp4HI restriction-modification system and biochemical characterization of the recombinant DNA methyltransferase M.Fsp4HI. // Molecular Biology, V.41, No 1, p. 43-50 (2007) 1.V.A. Chernukhin, T. N. Nayakshina, D.A. Gonchar, J.E. Tomilova, M.V. Tarasova, V.S. Dedkov, N.A. Mikhnenkova, S.Kh. Degtyarev A new site-specific methyl-directed DNA endonuclease PkrI recognizes and cuts methylated DNA sequence 5'-GCN^GC-3'/3'-CG^NCG-5' carrying at least three 5-methylcytosines // Translated from "Ovchinnikov bulletin of biotechnology and physical and chemical biology" V.7, No 3, pp 35-42, 2011 Chmuzh E.V., Kashirina Yu.G., Tomilova Yu.E., Chernukhin V.A., Okhapkina S.S., Gonchar D. A., Dedkov V.S., Abdurashitov M. A., Degtyarev S. Kh. Gene cloning, comparative analysis of the protein structures from Fsp4HI restriction-modification system and biochemical characterization of the recombinant DNA methyltransferase M.Fsp4HI. // Molecular Biology, V.41, No 1, p. 43-50 (2007)