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. 2003 Jul 15;31(14):e74. doi: 10.1093/nar/gng074

Table 2. Comparison between TspDTI/TspGWI endonuclease ‘twins’ and class-IIS restriction endonucleases with related recognition and cleavage sites.

Restriction endonucleasea Bacterial hosta Recognition sitea Cleavage positionsa Reaction temperaturea Polypeptide sizeb Native molecular sizec Specific DNA methylation Reference
TspDTI Thermus sp. ATGAA N11/9 70°C 114.5 kDa 110–130 kDa +++ This work
TspGWI Thermus sp. ACGGA N11/9 70°C 122.0 kDa 110–130 kDa +/– (32), This work
TaqII Thermus aquaticus GACCGA N11/9 70°C 118.5 kDa 110–130 kDa ++++ (33), (36), This work
    CACCCA N11/9   (125.6 kDad)      
Tth111II Thermus thermophilus CAARCA N11/9 70°C 116.5 kDa 110–130 kDa ND (34), This work
EciI Escherichia coli GGCGGA N11/9 37°C ND ND ND REBASE
BcefI Bacillus cereus ACGGC N12/13 30°C ND ND ND (35)
BceAI Bacillus cereus ACGGC N12/14 30°C ND ND ND REBASE

aThermus sp.-derived and TspDTI/TspGWI-related endonucleases, bases in a recognition sequence, cleavage positions and reaction temperatures are marked in bold.

bAs estimated by SDS/PAGE of homogeneous proteins.

cAs estimated by molecular sieving under native buffer conditions.

dAs calculated from sequencing/genetic analysis data obtained for the taqIIR gene.

ND, not determined.