Description
T4 Polynucleotide Kinase (PNK) is widely used to phosphorylate the 5’ end of both DNA and RNA in labeling and ligation experiments. T4 PNK catalyzes the transfer and exchange of the terminal gamma position phosphate of ATP to the 5′-hydroxyl terminus of double- and single-stranded DNA, RNA and nucleoside 3′-monophosphate molecules. T4 PNK also catalyzes the hydrolytic removal of 3′-PO 4 termini from DNA, RNA and deoxynucleoside 3′-monophosphates. The enzyme is used to remove 3′-phosphoryl groups from nucleotide/nucleoside or DNA and RNA in studies of gene expression and gene function. In addition to its importance in molecular biology and biochemistry research, T4 PNK exemplifies a family of bifunctional enzymes with 5′-kinase and 3′-phosphatase activities that play key roles in RNA and DNA repair. The enzyme is supplied in 10 mM Tris-HCl, 50 mM KCl, 0.1 µM ATP, 1 mM DTT, 0.1 mM EDTA, 50% glycerol; pH 7.4 at 25°C. The enzyme is supplied with a 10X PNK Buffer (B9040) containing 700 mM Tris-HCl, 100 mM MgCl 2, 50 mM DTT; pH 7.6 at 25°C.
Test Specification Purity >99% Specific activity 133,333 U/mg Single-stranded exonuclease 2000 U <5.0% released Double-stranded exonuclease 2000 U <1.0% released Double-stranded endonuclease 2000 U = No conversion E. coli DNA contamination 2000 U; <10 copies
T4 Polynucleotide Kinase (PNK) catalyzes the transfer and exchange of the terminal gamma position phosphate of ATP to the 5′-hydroxyl terminus of double-and single-stranded DNA, RNA and nucleoside 3′-monophosphate molecules. T4 PNK also exhibits 3′-phosphatase and 2′, 3′-cyclicphosphodiesterase activities.
Instructions for using T4 Polynucleotide Kinase are provided in the corresponding kit protocol in the resources below. Quality Control Unit activity was measured using a 2-fold serial dilution method. Dilutions of enzyme were made in 1X Reaction Buffer and added to 50 µL reactions containing 10 µM Oligo(dT) single-stranded DNA, 1X PNK Reaction Buffer, and 66 µM ATP and [γ 32 P]-ATP. Reactions were incubated for 30 minutes at 37°C, plunged on ice, and analyzed using the method of Sambrook and Russell (Molecular Cloning, v3, 2001, pp. A8.25-A8.26). Protein concentration was determined by OD 280 absorbance A 2.0 μL sample of enzyme was analyzed at OD 280 using a spectrophotometer standardized using a 2.0 mg/mL BSA sample and blanked with product storage solution. Physical purity was evaluated by SDS-PAGE of concentrated and diluted enzyme solutions followed by silver-stain detection. Purity was assessed by comparing the aggregate mass of contaminant bands in the concentrated sample to the mass of the protein of interest band in the diluted sample. Single-stranded exonuclease activity was determined in a 50 μL reaction containing 10,000 cpm of radiolabeled single-stranded DNA and 10 μL of enzyme solution. Incubation for 4 hours at 37°C resulted in less than 5.0% release of TCA-soluble counts. Double-stranded exonuclease activity was determined in a 50 μL reaction containing 5,000 cpm of a radiolabeled double-stranded DNA substrate and 10 μL of enzyme solution. Incubation for 4 hours at 37°C resulted in less than 1.0% release of TCA-soluble counts. Double-stranded endonuclease activity was determined in a 50 μL reaction containing 0.5 μg of pBR322 DNA and 10 μL of enzyme solution. Incubation for 4 hours at 37°C resulted in no visually discernible conversion to nicked circular DNA as determined by agarose gel electrophoresis. E. coli contamination was evaluated using 5 μL replicate samples of enzyme solution denatured and screened in a TaqMan qPCR assay for the presence of contaminating E. coli genomic DNA using oligonucleotide primers corresponding to the 16S rRNA locus.
