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作 者:衡周 孙小晴 黄俊霖 孙保娟[1] 李植良[1] 李颖[1] 李涛[1] HENG Zhou;SUN Xiaoqing;HUANG Junlin;SUN Baojuan;LI Zhi-liang;LI Ying;LI Tao(Vegetable Research Institute,Guangdong Academy of Agricultural Sciences/Guangdong Key Laboratory for New Technology Research of Vegetables,Guangzhou 510640,China;College of Horticulture&Forestry Sciences,Huazhong Agricultural University,Wuhan 430070,China)
机构地区:[1]广东省农业科学院蔬菜研究所/广东省蔬菜新技术重点实验室,广东广州510640 [2]华中农业大学园艺林学学院,湖北武汉430070
出 处:《广东农业科学》2020年第6期56-62,共7页Guangdong Agricultural Sciences
基 金:广东省自然科学基金(2020A151501337);广东省农业科学院“十三五”学科团队项目(201630TD);广东省农业科学院院长基金(201812);广东省农业厅岗位专家项目(2018kczx06,2019KJ106,2019KJ110);肇庆市科信局项目(2019N008)。
摘 要:【目的】由茄褐纹拟茎点霉(Phomopsis vexans Harter)引起的褐纹病是当前茄子产业的重要病害,孢子富集是深入研究褐纹病菌孢子萌发及其致病机理的基础。进一步简化当前复杂的产孢过程,提高产孢效率。【方法】采用组织分离法开展病原菌的分离纯化,利用形态学特征观察及rDNA-ITS序列分析对病原菌进行鉴定;使用液体培养的方式,对茄子褐纹病菌的产孢条件进行优化。【结果】分离获得的病原菌rDNA-ITS序列经NCBI序列比对,与茄子褐纹病菌遗传关系最近,同源性达99%;相同培养条件下培养1 d后,液体培养基中的菌丝生长量较大;28℃培养1 d 24℃培养3 d后的产孢量为1.2×1010个/mL,大于24℃培养4 d的产孢量(6×107个/mL);不同培养温度产孢量分别为2.5×107(20℃)、1.2×1010(22℃)、9.4×109(24℃)、8.5×108(26℃)个/mL;相同培养条件下,25%葡萄糖马铃薯液体(PDB)培养基产孢量最高(1.2×1010个/mL)。【结论】分离并鉴定了茄褐纹病病原菌,优化了褐纹病菌产孢条件。优化后的产孢条件为:在150 r/min摇床中,使用25%葡萄糖PDB培养基28℃培养1 d后24℃培养3 d。【Objective】Phomopsis blight of eggplant caused by Phomopsis vexans Harter is an important disease in the current eggplant industry.A sufficient amount of spores is the material basis for studying the spore germination of P.vexans and its pathogenic mechanism.This research is aimed to further simplify the current complex sporulation process and improve the sporulation efficiency.【Method】The tissue separation method was used to isolate and purify the pathogen.The morphological characteristics observation and rDNA-ITS sequence analysis were used to identify the pathogen.The liquid culture method was used to optimize the sporulation conditions of P.vexans.【Result】The rDNA-ITS sequence of P.vexans was obtained.The sequence had the closest genetic relationship with P.vexans through NCBI and sequence alignment,with a homology of 99%.After cultivation for one day under the same condition,the mycelial growth in the liquid medium was better.The spore production after culture at 28℃for one day then 24℃for three days was 1.2×1010 spores/mL,which was larger than the spore production(6×107 spores/mL)after culture at 24℃for four days.The spore production at different culture temperatures were 2.5×107(20℃),1.2×1010(22℃),9.4×109(24℃)and 8.5×108(26℃)spores/mL,respectively.Under the same culture condition,the 25%glucose PDB medium had the highest spore production(1.2×1010 spores/mL).【Conclusion】The pathogens of P.vexans were isolated and identified,and the sporulation conditions were optimized.The optimized sporulation conditions were as follows:in a 150 r/min shaker,using the 25%glucose PDB medium to culture at 28℃for one day,and then culture at 24℃for three days.
分 类 号:S432.44[农业科学—植物病理学]
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