首页> 外国专利> 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

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

机译:通过特异转化目标DNA序列的核酸碱基转化革兰氏阳性菌基因组序列的方法及在其中使用的分子复合物

摘要

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.
机译:本发明提供了修饰双链DNA的革兰氏阳性细菌的靶位点的方法,包括使复合物接触的步骤,其中核酸序列识别模块特异性结合给定双链中的靶核苷酸序列DNA和核酸碱基转化酶与所述双链DNA结合,以将靶位点中的一个或多个核苷酸转化为其他一个或多个核苷酸或删除一个或多个核苷酸,或将一个或多个核苷酸插入所述靶位。 ,而不在靶位点切割所述双链DNA的至少一条链,其中通过将编码复合体的核酸引入革兰氏阳性细菌中,使双链DNA与复合体接触。本发明还提供一种核酸序列识别模块的核酸修饰酶复合物,该核酸复合酶复合物特异性结合革兰氏阳性细菌的双链DNA中的靶核苷酸序列和彼此结合的核酸碱基转化酶。 ,该方法使用哪种复合体。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号