首页> 外国专利> The new rearrangement baculovirus, the construction manner and the transcription unit where two below constituent

The new rearrangement baculovirus, the construction manner and the transcription unit where two below constituent

机译:新的重排杆状病毒,构建方式和转录单元由两个以下组成

摘要

(57) Abstract bakiyurouirusu porihedorin (PH), rearrangement bakiyurouirusu which produces the rearrangement polyhedron from the Bacillus thuringiensis crystal protein (CP) and the jellyfish Aequorea victoria green fluorescent protein (GFP) being formed introducing the fusion protein where PH, CP and GFP are directly connected continually from N end to C end into the insect cell simultaneously, with gene introduction vector and wild type bakiyurouirusu which include the fused gene which the cord/code is done is constructed by culturing. In this bakiyurouirusu gene introduction vector pColorBtrus, from plasmid pGFP the DNA fragment which GFP the cord/code is done, from the wild type Autographa californica nuclear polyhedrosis virus the PH gene, synthesizing the Cry1Ac gene from the plasmid pPN6.6 which includes the Bacillus thuringiensis Cry1Ac gene with the respective polymerase chain reaction, in order the DNA fragment which first, the cord/code does GFP 5 '' - end the PH gene 3 '' - to be connected to end, inserting DNA fragment and the PH gene which GFP the cord/code are done to bakiyurouirusu manifestation vector pAcUW31, next, with the PH gene and the DNA fragment which GFP the cord/code is done inserting the Cry1Ac geneDepending, it is constructed. As for the rearrangement virus of this invention, it is possible, to become extinct the noxious insect with the insecticidal activity which is superior among brief in addition because the expedient which the infection insect monitoring is done is had, it is possible to prevent excess use.
机译:(57)<摘要> bakiyurouirusu porihedorin(PH),重排bakiyurouirusu由苏云金芽胞杆菌晶体蛋白(CP)和水母维多利亚绿色荧光蛋白(GFP)产生重排多面体,并在其中引入PH,CP和GFP从N端到C端连续不断地直接连接到昆虫细胞中,通过培养构建了基因导入载体和野生型bakiyurouirusu,其中包括完成了编码/编码的融合基因。在该bakiyurouirusu基因导入载体pColorBtrus中,从质粒pGFP得到野生型Autographa californica核多角体病毒PH基因的GFP片段的DNA片段,该DNA片段由包含芽孢杆菌的质粒pPN6.6合成Cry1Ac基因。苏云金芽孢杆菌Cry1Ac基因与各自的聚合酶链反应,以先将DNA片段以GFP / 5'-PH基因的3'末端-末端连接的顺序插入DNA片段和PH基因。对bakiyurouirusu表达载体pAcUW31进行GFP编码,然后,将PH基因和GFP编码的DNA片段插入Cry1Ac基因,完成GFP编码。另外,本发明的重排病毒由于具有进行感染昆虫监视的便利性,因此具有短暂的杀虫活性,并且具有短暂的杀虫活性,从而可以使其灭绝。 。

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