...
首页> 外文期刊>Plant Biotechnology >Agrobacterium-mediated genetic transformation of Cattleya with an Odontoglossum ringspot virus replicase gene sequence
【24h】

Agrobacterium-mediated genetic transformation of Cattleya with an Odontoglossum ringspot virus replicase gene sequence

机译:农杆菌介导的齿牙rings环斑病毒复制酶基因序列对卡特兰的遗传转化

获取原文
获取原文并翻译 | 示例

摘要

Protocorm-like bodies (PLBs) of Cattleya orchid CM2450 cultured either under constant illumination with cool-white-fluorescent lamps or in the dark were cocultivated with Agrobacterium tumefaciens strain EHA105 carrying plasmid pSMAHdN627-ORSV harboring genes coding for Odontoglossum ringspot virus (ORSV) replicase and hygromycin phosphotransferase. PLBs were maintained in liquid New Dogashima (ND) medium and then added to a bacterial suspension culture (OD600 approximate to 0.6) yielding medium dilution ratio of 1 : 10 and incubated for either 30 minutes or 3 h. Hygromycin-resistant secondary PLBs were induced after 4 weeks of culture on 2.5 g l(-1) gellan gum-solidified ND medium containing 1 mg l(-1) naphthaleneacetic acid (NAA), 0.1 mg l(-1) benzyladenine (BA), 10 mg l(-1) hygromycin, 20 mg l(-1) meropenem, 10 g l(-1) sucrose in both light-and dark-cultured PLBs. The number of resistant PLBs generated using dark-cultured PLBs was higher than those cultured under constant illumination. Presence of acetosyringone (AS) in the pre-culture medium was also effective for the transformation. The highest frequency of transformation was obtained when dark-cultured PLBs were pre-cultured with 100 mu M AS for 3 days and inoculated with Agrobacterium liquid culture for 3 h. Transformation of hygromycin-resistant plantlets regenerated from different sites of inoculated PLBs was confirmed by Southern blot hybridization. Transcription of ORSV replicase gene in transgenic lines was successfully confirmed by Northern blot hybridization.
机译:将卡特兰兰花CM2450的原球茎样体(PLB)在冷白色荧光灯下恒定照明下或在黑暗中培养,然后与携带质粒pSMAHdN627-ORSV的根癌农杆菌菌株EHA105共同培养,该质粒带有编码齿牙垢环斑病毒(ORSV)复制酶的基因和潮霉素磷酸转移酶。将PLB保持在液体新多吉岛(ND)培养基中,然后添加至细菌悬浮培养物(OD600约为0.6)中,产生1:10的培养基稀释比,并孵育30分钟或3小时。在含有1 mg l(-1)萘乙酸(NAA),0.1 mg l(-1)苄基腺嘌呤(BA)的2.5 gl(-1)吉兰糖胶固化的ND培养基上培养4周后,诱导出潮霉素抗性次级PLB。 ,浅色和深色培养的小球中10 mg l(-1)潮霉素,20 mg l(-1)美罗培南,10 gl(-1)蔗糖。使用深色培养的PLB产生的抗性PLB的数量要多于在恒定光照下培养的抗性PLB。预培养基中乙酰丁香酮(AS)的存在也对转化有效。将深色培养的PLB与100μMAS一起预培养3天,并用农杆菌液体培养物接种3 h,可获得最高的转化率。通过Southern印迹杂交证实了从接种的PLB的不同位点再生的潮霉素抗性小植株的转化。通过Northern印迹杂交成功证实了ORSV复制酶基因在转基因系中的转录。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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