T3 DNA Ligase

• Joins blunt-end and cohesive-end termini
• Repair single-stranded nicks in duplex DNA
• Catalyzes the formation of phosphodiester bond between 5ʹ phosphate and a 3ʹ hydroxyl termini in duplex DNA

T3 DNA Ligase catalyzes the formation of a phosphodiester bond between a 5ʹ phosphate and a 3ʹ hydroxyl termini in duplex DNA. The enzyme joins blunt ends and cohesive end termini as well as repairs single-stranded nicks in duplex DNA. In the absence of 20–30% PEG 6000, T3 DNA Ligase displays a very low efficiency for blunt-ended ligation. T3 DNA Ligase displays a higher efficiency for joining A and T overhangs than C- and G matched ends. T3 DNA Ligase retains 95% of its activity in 1.0 M NaCl or KCl, with an optimal concentration of 300 mM.

This enzyme is supplied in 20 mM Tris-HCl, 300 mM NaCl, 1 mM DTT, 0.1 mM EDTA and 50% glycerol; pH 7.5 at 25°C.

2X Rapid Ligation Buffer (B1010) contains the following: 132 mM Tris-HCI, 20 mM MgCl₂, 2 mM DTT, 2 mM ATP at 15% PEG 6000; pH 7.6 at 25°C.

SDS is available on request.

Enzyme properties
• Storage temperature: –25°C to –15°C

OEM by QIAGEN offers bulk manufacturing of T3 DNA Ligase in custom formulations.

Source of recombinant enzyme protein
The protein is produced by a recombinant E. coli strain carrying the T3 DNA Ligase gene.

Unit definition: One unit is defined as the amount of T3 DNA Ligase required to ligate 50% of 100 ng DNA fragments with cohesive termini in 30 minutes at 23°C.

Molecular weight: 37,350 Daltons

The enzyme has also been characterized in the 1X T3 DNA Ligase Buffer, with a 17-fold decrease in specific activity due to the absence of the crowding agent (PEG 6000).

1X T3 DNA Ligase Buffer contains the following: 50 mM Tris-HCl, 300 mM NaCl, 0.5 mM ATP and 1 mM DTT; pH 8.0 at 25°C.

The following information was taken from the Cai reference (Cai, Liang, et al. (2004) J. Biochem. 135:397), which describes the characterization of the T3 DNA Ligase:
• Optimal pH: 8.0
• Optimal reaction temperature: 20°C
• Optimal reaction time: >30 minutes (without PEG 6000)
• Optimal ionic strength: 300 mM NaCl
• Optimal divalent cation/concentration: 2 mM Mg²⁺
• Optimal cofactor: ATP (0.5 mM)

Quality control analysis

Unit activity was measured using a twofold serial dilution method. Dilutions of enzyme were made in 1X Rapid Ligation Buffer and added to 20 µl reactions containing double-stranded DNA fragments and 1X Rapid Ligation Buffer. Reactions were incubated 30 minutes at 23°C (room temp), placed on ice, and analyzed on a 1% agarose gel stained with ethidium bromide.

Protein concentration is determined by OD₂₈₀ absorbance.

Physical purity is evaluated by SDS-PAGE of concentrated and diluted enzyme solutions followed by silver-stain detection. Purity is assessed by comparing the aggregate mass of contaminant bands in the concentrated sample to the mass of the band corresponding to the protein of interest in the diluted sample.

Single-stranded exonuclease is determined in a 50 µl reaction containing a radiolabeled single-stranded DNA substrate and 10 µl of enzyme solution incubated for 4 hours at 37°C.

Double-stranded exonuclease activity is determined in a 50 µl reaction containing a radiolabeled double-stranded DNA substrate and 10 µl of enzyme solution incubated for 4 hours at 37°C.

Double-stranded endonuclease activity is determined in a 50 µl reaction containing 0.5 µg of plasmid DNA and 10 µl of enzyme solution incubated for 4 hours at 37°C.

E. coli contamination is evaluated using 5 µl replicate samples of enzyme solution that are 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.

This OEM by QIAGEN product is available for bulk purchase for the following commercial assay applications.

• Cloning ligation
• Nick-sealing in double-stranded DNA