首页> 外国专利> NONPATHOGENICIZED PLASMID AND NONPATHOGENIC TRANSFORMANT

NONPATHOGENICIZED PLASMID AND NONPATHOGENIC TRANSFORMANT

机译:非致病性质粒和非致病性转化子

摘要

PURPOSE: To provide the subject easily and safely available plasmid for controlling plant pathogenic bacteria, derived from a nonpathogenic mutant, M4S, of Pseudomonas solanacearum and capable of nonpathogenicizing Pseudomonas pathogenic bacteria. ;CONSTITUTION: M4S (FERM P-700), a nonpathogenic mutant of Pseudomonas solanacearum is inoculated into a medium followed by shaking culture at 30°C for ca. 18hr and then subcultured. The resulting culture solution is centrifugated to collect microbial cells, which are, in turn, suspended in physiological saline followed by addition of a surfactant-contg. solution to effect bacteriolysis, and then plasmid is separated from the system by a conventional technique. The plasmid is then put to restriction enzyme treatment and incorporated with a drug-resistant gene and a promoter gene, thus obtaining the objective plasmid having 6.62kbp of molecular weight and broken sites due to EcoRI, StuI, XhoI, PstI, ApaI, HindIII or EcoRV, which can trans form pseudomonas pathogenic bacteria into nonpathogenic and nontoxic ones.;COPYRIGHT: (C)1993,JPO&Japio
机译:目的:提供易于和安全地获得的用于控制植物病原菌的质粒,该质粒衍生自青枯假单胞菌的非致病性突变体M4S,并且能够使非致病性假单胞菌致病菌。 ;组成:M4S(FERM P-700),一种无致病性青枯假单胞菌的突变株,接种到培养基中,然后在30°C摇动培养大约20分钟。 18小时,然后传代培养。离心所得的培养液以收集微生物细胞,然后将其悬浮在生理盐水中,然后加入浓缩表面活性剂。溶液进行溶菌,然后通过常规技术将质粒从系统中分离出来。然后将质粒置于限制性内切酶处理中,并掺入抗药性基因和启动子基因,从而获得具有6.62kbp分子量且由于EcoRI,StuI,XhoI,PstI,ApaI,HindIII或HindIII而断裂的位点的目的质粒。 EcoRV,可将假单胞菌致病菌转化为非致病性和无毒的细菌。;版权所有:(C)1993,日本特许厅和日本

著录项

  • 公开/公告号JPH0541987A

    专利类型

  • 公开/公告日1993-02-23

    原文格式PDF

  • 申请/专利权人 JAPAN TOBACCO INC;

    申请/专利号JP19910328393

  • 申请日1991-11-18

  • 分类号C12N15/11;C12N1/21;

  • 国家 JP

  • 入库时间 2022-08-22 05:15:06

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