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Nucleic Acids Research, 1994, Vol. 22, No. 22 4583-4590
© 1994


MOLECULAR BIOLOGY

DNA substrate specificity and cleavage kinetics of an archaeal homing-type endonuclease from Pyrobaculum organotrophum

Jens Lykke-Andersen, Hoa Phan Thi-Ngoc and Roger A. Garrett*

Institute of Molecular Biology, Copenhagen Uniersity Sølvgade 83H, DK-1307 Copendhagen K, Denmark

*To whom correspondence should be addressed

Received August 25, 1994. Accepted October 10, 1994.

The protein encoded by intron 1 of the single 23S rRNA gene of the archaeal hyperthermophile Pyrobaculum organotrophum was isolated and shown to constitute a homing-type DNA endonuclease, l-Porl. It cleaves the intron- 23S rDNA of the closely related organism Pyrobaculum islandicum near the site of intron insertion in Pb.organotrophum. In contrast, no endonuclease activity was detected for the protein product of intron 2 of the same gene of Pb.organotrophum which, like l-Porl, carries the LAGLI-DADG motif, common to group I intron-encoded homing enzymes. I-Porl cleaves optimally at 80°C, with kcat and Kmvalues of about 2 min-1 and 4 nM, respectively, and generates four nucleotide 3'-overhangs and 5'-phosphates. It can cleave a 25 base pair DNA fragment encompassing the intron insertion site. A mutationselection study established the base pair specificity of the endonuclease within a 17 bp region, from positions –6 to +11 with respect to the intron-insertion site. Four of the essential base pairs encode the sequence involved in the intron-exon interaction in the pre-rRNA that is required for recognition by the RNA splicing enzymes. Properties of the enzyme are compared andcontrasted with those of eucaryotic homing endonucleases.


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