首页> 美国卫生研究院文献>3 Biotech >Defense response enhancement in strawberry via elicitors
【2h】

Defense response enhancement in strawberry via elicitors

机译:通过激发子增强草莓的防御反应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this study, cell-suspension culture of strawberry (Fragaria × ananassa), cultivars Camarosa, and Sweet Charlie has been established. Embryogenic callus was induced by incubating the in vitro juvenile leaf explants on medium, containing 2-mg/l picloram at dark. Suspension culture was initiated from 4-week-old embryogenic calli in the liquid MS medium with 1-mg/l 2,4-D and 2-mg/l picloram. Suspension culture was maintained by sub-culturing each 3 weeks into a fresh medium. At week 9 after third sub-cultures, torpedo and cotyledonary embryo stages were observed. Embryos were then developed into shoots on medium 1 mg/l of each BA and IBA. Obtained shoots were successfully rooted on 1-mg/ml GA3, 0.5-mg/ml BA, and 1-mg/ml IBA. To enhance the resistance availability in strawberry plants, elicitation was applied by adding the JA and SA elicitors to the suspension culture with two doses (0.5 and 1 mM) individually and in combination, in addition to the fungal homogenate of Macrophomina phasiolena at concentration of 106 spor/ml. The fawrky-1-Camarosa gene, which has defense-related function, was detected in the different elicited strawberry tissues and isolated via RT-PCR. The isolated gene was submitted to GenBank with accession number ().
机译:在这项研究中,已经建立了草莓(Fragaria×ananassa),Camarosa品种和Sweet Charlie的细胞悬浮培养。胚性愈伤组织是通过在含有2 mg / l吡咯仑的培养基中在黑暗中孵育体外幼叶外植体诱导的。悬浮培养是在具有1 mg / l 2,4-D和2 mg / l吡咯烷的液态MS培养基中从4周大的胚性愈伤组织开始的。通过每3周在新鲜培养基中进行亚培养来维持悬浮培养。在第三次亚培养后的第9周,观察到鱼雷和子叶胚阶段。然后将每种BA和IBA的培养基以1 mg / l的培养基发育成芽。将获得的芽成功生根于1 mg / ml GA3、0.5 mg / ml BA和1mg / ml IBA。为了提高草莓植株的抗药性,通过将JA和SA激发子分别以两种剂量(0.5和1mM)并混合的方式添加到悬浮培养物中来进行诱变,除了浓度为10的大白菜的真菌匀浆外 6 spor / ml。在不同引发的草莓组织中检测到具有防御相关功能的fawrky-1-Camarosa基因,并通过RT-PCR进行分离。分离的基因以登录号()提交给GenBank。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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