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Blondal, Thorarinn; Thorisdottir, Audur; Unnsteinsdottir, Unnur; Hjorleifsdottir, Sigridur; Ævarsson, Arnthor; Ernstsson, Sveinn; Fridjonsson, Olafur H.; Skirnisdottir, Sigurlaug; Wheat, Jon Oskar; Hermannsdottir, Anna Gudny; Sigurdsson, Snorri Th; Hreggvidsson, Gudmundur O.; Smith, Albert Vernon; Kristjansson, Jakob K.
Nucleic acids research, 01/2005, Letnik: 33, Številka: 1Journal Article
We have recently sequenced the genome of a novel thermophilic bacteriophage designated as TS2126 that infects the thermophilic eubacterium Thermus scotoductus. One of the annotated open reading frames (ORFs) shows homology to T4 RNA ligase 1, an enzyme of great importance in molecular biology, owing to its ability to ligate single-stranded nucleic acids. The ORF was cloned, and recombinant protein was expressed, purified and characterized. The recombinant enzyme ligates single-stranded nucleic acids in an ATP-dependent manner and is moderately thermostable. The recombinant enzyme exhibits extremely high activity and high ligation efficiency. It can be used for various molecular biology applications including RNA ligase-mediated rapid amplification of cDNA ends (RLM-RACE). The TS2126 RNA ligase catalyzed both inter- and intra-molecular single-stranded DNA ligation to >50% completion in a matter of hours at an elevated temperature, although favoring intra-molecular ligation on RNA and single-stranded DNA substrates. The properties of TS2126 RNA ligase 1 makes it very attractive for processes like adaptor ligation, and single-stranded solid phase gene synthesis.
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