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A new prototype IIS/IIC/IIG endonuclease-methyltransferase TsoI from the thermophile Thermus scotoductus, recognising 5′-TARCCA(N11/9)-3′ sequences
- Jezewska-Frackowiak, Joanna, Lubys, Arvydas, Vitkute, Jolanta, Zakareviciene, Laimute, Zebrowska, Joanna, Krefft, Daria, Skowron, Marta A., Zylicz-Stachula, Agnieszka, Skowron, Piotr M.
- Journal of biotechnology 2015 v.194 pp. 19-26
- S-adenosylmethionine, Thermus scotoductus, bacteriophages, biotechnology, enzyme activity, molecular cloning, nucleotide sequences, nucleotides, plasmids, polymerase chain reaction, proteins, restriction endonucleases, sequence homology, thermal stability, thermophilic microorganisms
- The Thermus sp. family of IIS/IIG/IIC enzymes includes the thermostable, bifunctional, fused restriction endonuclease (REase)-methyltransferases (MTase): TaqII, Tth111II/TthHB27I, TspGWI, TspDTI and TsoI. The enzymes are large proteins (approximately 120kDa), their enzymatic activities are affected by S-adenosylmethionine (SAM), they recognise similar asymmetric cognate sites and cleave at a distance of 11/9 nucleotides (nt). The enzymes exhibit similarities of their amino acid (aa) sequences and DNA catalytic motifs. Thermus sp. enzymes are an example of functional aa sequence homologies among REases recognising different, yet related DNA sequences. The family consists of TspGWI- and TspDTI-subfamilies. TsoI appears to be a non-identical ‘triplet’, related to TspDTI and Tth111II/TthHB27I. The discovery of TsoI, purified from Thermus scotoductus, is described. This prototype, displaying a novel specificity, which was determined by: (i) cleavage of a reference plasmid and bacteriophage DNA, (ii) cleavage of custom PCR DNA substrates, (iii) run-off sequencing of cleavage products and (iv) shotgun cloning and sequencing of bacteriophage lambda (λ) DNA digested with TsoI. The enzyme recognises a degenerated 5′-TARCCA-3′ sequence, whereas DNA strands are cut 11/9 nt downstream. The discovery of the TsoI prototype is of practical importance in biotechnology, as it extends the palette of cleavage specificities for gene cloning.