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PMID: 2183191 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Purification and characterization of the in vitro activity of I-Sce I, a novel and highly specific endonuclease encoded by a group I intron.

Nucleic acids research ·Vol. 18 ·No. 6 ·1990-03-25 ·Pages 1407-13

Monteilhet C, Perrin A, Thierry A, Colleaux L, Dujon B

Abstract

Group I intron encoded proteins represent a novel class of site specific double strand endonucleases. The endonuclease activity of this class of proteins has been first demonstrated in vivo for I-Sce I which is encoded by a mitochondrial intron of Saccharomyces cerevisiae. Assays using crude cell extracts have shown that I-Sce I can be used in vitro as a restriction endonuclease potentially useful for recombinant DNA technology owing to its large recognition sequence (18 nucleotides). We report here the purification and the first detailed analysis of the in vitro activity and properties of I-Sce I.

MeSH Terms
Base Sequence Chromatography, Gel Chromatography, Ion Exchange Deoxyribonucleases, Type II Site-Specific/genetics,isolation & purification,metabolism Enzyme Stability Escherichia coli/enzymology,genetics Introns Kinetics Molecular Sequence Data Molecular Weight Plasmids Saccharomyces cerevisiae/enzymology,genetics Saccharomyces cerevisiae Proteins
Chemicals
Saccharomyces cerevisiae Proteins SCEI protein, S cerevisiae Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Monteilhet C
Unité de Génétique moléculaire des Levures, Institut Pasteur, Paris, France.
Perrin A
Thierry A
Colleaux L
Dujon B
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1990-03-25
Pages
1407-13
Language
English
Region
England
NLM ID
0411011
PMCID
PMC330504
Subset
IM
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