首页 | 本学科首页   官方微博 | 高级检索  
     检索      

列当生防菌Br-2的DsRed红色荧光标记及定殖
引用本文:王亚娇,纪莉景,栗秋生,王连生,孔令晓.列当生防菌Br-2的DsRed红色荧光标记及定殖[J].植物保护学报,2017,44(4):664-670.
作者姓名:王亚娇  纪莉景  栗秋生  王连生  孔令晓
作者单位:河北省农林科学院植物保护研究所, 河北省有害生物综合防治工程技术研究中心, 农业部华北北部作物有害生物综合治理重点实验室, 保定 071000,河北省农林科学院植物保护研究所, 河北省有害生物综合防治工程技术研究中心, 农业部华北北部作物有害生物综合治理重点实验室, 保定 071000,河北省农林科学院植物保护研究所, 河北省有害生物综合防治工程技术研究中心, 农业部华北北部作物有害生物综合治理重点实验室, 保定 071000,河北省农林科学院植物保护研究所, 河北省有害生物综合防治工程技术研究中心, 农业部华北北部作物有害生物综合治理重点实验室, 保定 071000,河北省农林科学院植物保护研究所, 河北省有害生物综合防治工程技术研究中心, 农业部华北北部作物有害生物综合治理重点实验室, 保定 071000
基金项目:河北省财政项目(F13R10001),河北省财政基本科研业务费(494-0401-JBN-6440)
摘    要:为探明生防菌Br-2在分枝列当体内及番茄根围的定殖能力,采用PEG-CaCl_2介导的原生质体转化体系将红色荧光蛋白基因DsRed转入到菌株Br-2中,并构建其生长曲线,测定其对分枝列当种子萌发的抑制率,通过共聚焦显微镜观察其在分枝列当茎内及番茄根围的定殖情况。结果表明:通过原生质体转化体系得到了标记菌株Br-2-DsRed,继代培养5代后,其在共聚焦显微镜下仍可观察到亮红色荧光,经PCR检测带有DsRed基因,证明其稳定性好。标记菌株Br-2-DsRed与野生菌株Br-2的生长曲线基本一致,对分枝列当种子萌发的抑制率分别为75.86%和74.14%,无显著差异。显微观察发现,标记菌株Br-2-DsRed接种1 d后即能够侵染分枝列当的茎部表皮,3 d后主要分布在茎表皮和厚壁细胞间隙,5 d后侵染到厚壁细胞及维管束细胞内部并导致茎部腐烂;而标记菌株Br-2-DsRed不能侵染番茄根尖的内部,主要定殖在番茄根尖表面。

关 键 词:列当生防菌  红色荧光蛋白  原生质体转化  定殖
收稿时间:2016/1/29 0:00:00

Broomrape bio-control agent Br-2 labeled by red fluorescent protein and its colonization
Wang Yajiao,Ji Lijing,Li Qiusheng,Wang Liansheng and Kong Lingxiao.Broomrape bio-control agent Br-2 labeled by red fluorescent protein and its colonization[J].Acta Phytophylacica Sinica,2017,44(4):664-670.
Authors:Wang Yajiao  Ji Lijing  Li Qiusheng  Wang Liansheng and Kong Lingxiao
Institution:Key Laboratory of Integrated Pest Management on Crops in Northern Region of North China, Ministry of Agriculture;IPM Center of Hebei Province;Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Baoding 071000, Hebei Province, China,Key Laboratory of Integrated Pest Management on Crops in Northern Region of North China, Ministry of Agriculture;IPM Center of Hebei Province;Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Baoding 071000, Hebei Province, China,Key Laboratory of Integrated Pest Management on Crops in Northern Region of North China, Ministry of Agriculture;IPM Center of Hebei Province;Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Baoding 071000, Hebei Province, China,Key Laboratory of Integrated Pest Management on Crops in Northern Region of North China, Ministry of Agriculture;IPM Center of Hebei Province;Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Baoding 071000, Hebei Province, China and Key Laboratory of Integrated Pest Management on Crops in Northern Region of North China, Ministry of Agriculture;IPM Center of Hebei Province;Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Baoding 071000, Hebei Province, China
Abstract:To investigate the colonization of the broomrape bio-control agent Fusarium oxysporium (Br-2) in the Orobanche aegyptiaca stem and tomato root tip, the gene of red fluorescent protein (RFP/DsRed) was transferred in the strain Br-2 by the PEG-CaCl2-mediated protoplast transformation system. Dynamic growth analyses and inhibiting effect on germination to O. aegyptiaca seed were tested in this study. Br-2-DsRed colonization in the O. aegyptiaca stem and tomato root tip was conducted by the laser scanning confocal microscope. The results showed that the labeled strain Br-2-DsRed was obtained by the protoplast transformation system. After five generations subculturing, bright red fluorescence could still be observed under the confocal microscope and DsRed genes could be detected by PCR in the strain Br-2-DsRed. And the growth curve of labeled strain Br-2-DsRed was basically same as the wild stain Br-2, there was no significant difference in the inhibiting effect on germination to O. aegyptiaca seed between labeled strain Br-2-DsRed and wild strain Br-2 with the inhibition rates were 75.86% and 74.14%, respectively. By the laser scanning confocal microscope, Br-2-DsRed strain infected the epidermis of O. aegyptiaca stem one day after inoculation, infected the intercellular of the epidermis and sclerenchymatous cell three days after inoculation, finally Br-2-DsRed strain infected the cell of the sclerenchymatous and vascular bundle and lead stem to rot after five days. But it mainly distributed on the surface of tomato root couldn''t infect the interior of the root tip.
Keywords:broomrape bio-control agent  DsRed  protoplast transformation system  colonization
本文献已被 CNKI 等数据库收录!
点击此处可从《植物保护学报》浏览原始摘要信息
点击此处可从《植物保护学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号