Pkr I

6,000.00 24,000.00 

  • CNY: 478.32 ¥ - 1,913.28 ¥

MD DNA endonuclease Pkr I.
The enzyme cleaves C5-methylated DNA and doesn’t cut unmodified DNA.

  • Концентрация: 1000 е.а./мл
  • Recognition site: G(5mC)N↑G(5mC) / (5mC)G↓N(5mC)G
  • Источник: Planomicrobium koreense 78k
  • Оптимальный буфер: SE-буфер Y
  • Оптимальная температура: 37
  • Температура инактивации, 20 мин при: 65

Available Options

SKUРackagePackagePrice 
E579S50 u6,000.00 
  • CNY: 478.32 ¥
E580L250 u24,000.00 
  • CNY: 1,913.28 ¥

Description

Recognition site and hydrolysis position:

DNA sequence with at least three 5mC: DNA sequence with at least three 5mC:
GCN↑GC GCN↑GC
CG↓NCG

Source: Planomicrobium koreense 78k
Substrate specificity:
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.

PkrI activity assay on DNA pFsp4HI3/DriI

.
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].
Optimal SE-buffer: SE-buffer Y
Enzyme activity (%):

B G O W Y ROSE
50 75 10 25 100 100

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: –
Non-specific hydrolisis: 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. Reagents Supplied with Enzyme 10 X SE-buffer Y
Methylation sensitivity: The enzyme cleaves C5-methylated DNA and doesn’t cut unmodified DNA [1].
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)
2. 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
2. 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)