METHOD FOR CONVERTING GENOME SEQUENCE OF GRAM-POSITIVE BACTERIUM BY SPECIFICALLY CONVERTING NUCLEIC ACID BASE OF TARGETED DNA SEQUENCE, AND MOLECULAR COMPLEX USED IN SAME
The present invention provide a method of modifying a targeted site of gram-positive bacterium of a double stranded DNA, including a step of contacting a complex wherein a nucleic acid sequence-recognizing module that specifically binds to a target nucleotide sequence in a given double stranded DNA...
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Format | Patent |
Language | English French German |
Published |
13.03.2019
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Abstract | The present invention provide a method of modifying a targeted site of gram-positive bacterium of a double stranded DNA, including a step of contacting a complex wherein a nucleic acid sequence-recognizing module that specifically binds to a target nucleotide sequence in a given double stranded DNA and a nucleic acid base converting enzyme are bonded, with said double stranded DNA, to convert one or more nucleotides in the targeted site to other one or more nucleotides or delete one or more nucleotides, or insert one or more nucleotides into said targeted site, without cleaving at least one strand of said double stranded DNA in the targeted site, wherein the double stranded DNA is contacted with the complex by introducing the nucleic acid encoding the complex into the gram-positive bacterium. The present invention also provide a nucleic acid-modifying enzyme complex of a nucleic acid sequence-recognizing module that specifically binds to a target nucleotide sequence in a double stranded DNA of a gram-positive bacterium and a nucleic acid base converting enzyme bonded to each other, which complex is used for the method. |
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AbstractList | The present invention provide a method of modifying a targeted site of gram-positive bacterium of a double stranded DNA, including a step of contacting a complex wherein a nucleic acid sequence-recognizing module that specifically binds to a target nucleotide sequence in a given double stranded DNA and a nucleic acid base converting enzyme are bonded, with said double stranded DNA, to convert one or more nucleotides in the targeted site to other one or more nucleotides or delete one or more nucleotides, or insert one or more nucleotides into said targeted site, without cleaving at least one strand of said double stranded DNA in the targeted site, wherein the double stranded DNA is contacted with the complex by introducing the nucleic acid encoding the complex into the gram-positive bacterium. The present invention also provide a nucleic acid-modifying enzyme complex of a nucleic acid sequence-recognizing module that specifically binds to a target nucleotide sequence in a double stranded DNA of a gram-positive bacterium and a nucleic acid base converting enzyme bonded to each other, which complex is used for the method. |
Author | KONDO, Akihiko ICHIGE, Eita NISHIDA, Keiji MUKOYAMA, Masaharu |
Author_xml | – fullname: ICHIGE, Eita – fullname: KONDO, Akihiko – fullname: NISHIDA, Keiji – fullname: MUKOYAMA, Masaharu |
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DocumentTitleAlternate | PROCÉDÉ DE CONVERSION D'UNE SÉQUENCE GÉNOMIQUE D'UNE BACTÉRIE À GRAM POSITIF PAR CONVERSION SPÉCIFIQUE D'UNE BASE D'ACIDE NUCLÉIQUE D'UNE SÉQUENCE D'ADN CIBLÉE, ET COMPLEXE MOLÉCULAIRE UTILISÉ DANS CELUI-CI VERFAHREN ZUR KONVERTIERUNG VON GENOMSEQUENZEN EINES GRAM-POSITIVEN BAKTERIUMS DURCH SPEZIFISCHE UMWANDLUNG VON NUKLEINSÄUREBASEN EINER GEZIELTEN DNA-SEQUENZ SOWIE MOLEKULARKOMPLEX ZUR VERWENDUNG DARIN |
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Notes | Application Number: EP20160844517 |
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Snippet | The present invention provide a method of modifying a targeted site of gram-positive bacterium of a double stranded DNA, including a step of contacting a... |
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Title | METHOD FOR CONVERTING GENOME SEQUENCE OF GRAM-POSITIVE BACTERIUM BY SPECIFICALLY CONVERTING NUCLEIC ACID BASE OF TARGETED DNA SEQUENCE, AND MOLECULAR COMPLEX USED IN SAME |
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