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Four new type I restriction enzymes identified in Escherichia coli clinical isolates
Using a plasmid transformation method and the RM search computer program, four type I restriction enzymes with new recognition sites and two isoschizomers (EcoBI and Eco377I) were identified in a collection of clinical Escherichia coli isolates. These new enzymes were designated Eco394I, Eco826I, Ec...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1178010/ https://www.ncbi.nlm.nih.gov/pubmed/16040596 http://dx.doi.org/10.1093/nar/gni114 |
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author | Kasarjian, Julie K. A. Kodama, Yoshiaki Iida, Masatake Matsuda, Katsura Ryu, Junichi |
author_facet | Kasarjian, Julie K. A. Kodama, Yoshiaki Iida, Masatake Matsuda, Katsura Ryu, Junichi |
author_sort | Kasarjian, Julie K. A. |
collection | PubMed |
description | Using a plasmid transformation method and the RM search computer program, four type I restriction enzymes with new recognition sites and two isoschizomers (EcoBI and Eco377I) were identified in a collection of clinical Escherichia coli isolates. These new enzymes were designated Eco394I, Eco826I, Eco851I and Eco912I. Their recognition sequences were determined to be GAC(5N)RTAAY, GCA(6N)CTGA, GTCA(6N)TGAY and CAC(5N)TGGC, respectively. A methylation sensitivity assay, using various synthetic oligonucleotides, was used to identify the adenines that prevent cleavage when methylated (underlined). These results suggest that type I enzymes are abundant in E.coli and many other bacteria, as has been inferred from bacterial genome sequencing projects. |
format | Text |
id | pubmed-1178010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-11780102005-07-21 Four new type I restriction enzymes identified in Escherichia coli clinical isolates Kasarjian, Julie K. A. Kodama, Yoshiaki Iida, Masatake Matsuda, Katsura Ryu, Junichi Nucleic Acids Res Methods Online Using a plasmid transformation method and the RM search computer program, four type I restriction enzymes with new recognition sites and two isoschizomers (EcoBI and Eco377I) were identified in a collection of clinical Escherichia coli isolates. These new enzymes were designated Eco394I, Eco826I, Eco851I and Eco912I. Their recognition sequences were determined to be GAC(5N)RTAAY, GCA(6N)CTGA, GTCA(6N)TGAY and CAC(5N)TGGC, respectively. A methylation sensitivity assay, using various synthetic oligonucleotides, was used to identify the adenines that prevent cleavage when methylated (underlined). These results suggest that type I enzymes are abundant in E.coli and many other bacteria, as has been inferred from bacterial genome sequencing projects. Oxford University Press 2005 2005-07-21 /pmc/articles/PMC1178010/ /pubmed/16040596 http://dx.doi.org/10.1093/nar/gni114 Text en © The Author 2005. Published by Oxford University Press. All rights reserved |
spellingShingle | Methods Online Kasarjian, Julie K. A. Kodama, Yoshiaki Iida, Masatake Matsuda, Katsura Ryu, Junichi Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title | Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title_full | Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title_fullStr | Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title_full_unstemmed | Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title_short | Four new type I restriction enzymes identified in Escherichia coli clinical isolates |
title_sort | four new type i restriction enzymes identified in escherichia coli clinical isolates |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1178010/ https://www.ncbi.nlm.nih.gov/pubmed/16040596 http://dx.doi.org/10.1093/nar/gni114 |
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