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枯草芽胞杆菌NCD-2菌株抑菌蛋白的分离及鉴定
引用本文:张晓云,郭庆港,鹿秀云,赵卫松,王培培,李社增,马平.枯草芽胞杆菌NCD-2菌株抑菌蛋白的分离及鉴定[J].植物病理学报,2018,48(3):395-401.
作者姓名:张晓云  郭庆港  鹿秀云  赵卫松  王培培  李社增  马平
作者单位:河北省农林科学院植物保护研究所,河北省农业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:国家重点研发计划项目(2017YFD0201101);国家自然科学基金(31501697);公益性行业科研专项(201503109);国家现代棉花产业技术体系(CARS-18-15)。
摘    要:枯草芽胞杆菌NCD-2菌株对灰葡萄孢菌具有较强的抑菌活性,抑菌蛋白是其产生的抑菌物质之一。本研究为明确NCD-2菌株所产抑菌蛋白的作用方式和特性,采用牛津杯法测定抑菌蛋白的抑菌活性及其对病原菌菌丝生长的影响,采用混合培养法测定其对病原菌分生孢子萌发的影响,同时采用阴离子交换层析和非变性聚丙烯酰胺凝胶电泳技术对其进行分离纯化,并利用MALDI-TOF-MS进行鉴定。结果表明,NCD-2菌株产生的粗蛋白能够显著抑制灰葡萄孢菌分生孢子的萌发和菌丝生长,并导致病原菌菌丝分枝增多、局部膨大肿胀。通过分离纯化获得具抑菌活性的蛋白组分D1-3,经鉴定该蛋白的肽指纹图谱与leucyl aminopeptidaseBacillus subtilis](WP_041057629.1)的氨基酸序列匹配率最高,达到65%,相对分子质量为53.936 k Da,功能分析表明组分D1-3可能是一种新的抑菌蛋白。

关 键 词:枯草芽胞杆菌    抑菌蛋白    抑菌机制    鉴定  

Isolation and identification of an antifungal protein produced by Bacillus subtilis NCD-2
ZHANG Xiao-yun,GUO Qing-gang,LU Xiu-yun,ZHAO Wei-song,WANG Pei-pei,LI She-zeng,MA Ping.Isolation and identification of an antifungal protein produced by Bacillus subtilis NCD-2[J].Acta Phytopathologica Sinica,2018,48(3):395-401.
Authors:ZHANG Xiao-yun  GUO Qing-gang  LU Xiu-yun  ZHAO Wei-song  WANG Pei-pei  LI She-zeng  MA Ping
Institution:Institute of Plant Protection, Hebei Academy of Agricultural and Forestry Sciences, Integrated Pest Management Center of Hebei Province, Key Laboratory of IPM on Crops in Northern Region of North China, Ministry of Agriculture, Baoding 071000, China
Abstract:Bacillus subtilis NCD-2 exhibits an effective inhibitory activity against mycelial growth of Botrytis cinerea, which caused tomato gray mold. The antifungal protein was one of the major antifungal active compounds produced by this strain. To clarify the action mode and the characteristics of the antifungal protein, the inhibitory activity of the crude protein against mycelial growth and conidial germination of B. cinerea were eva-luated with the Oxford-cup test method and the dual culture method, respectively. The anion exchange chromatography and native PAGE were employed for further purification of the protein, and the active fraction of purified proteins against B. cinerea was identified by MALDI-TOF-MS. The crude proteins showed the significant inhibition against mycelial growth and conidial germination of B. cinerea and led to the abnormal growth of the mycelia with ramification and swellings. Among the fractions of the purified proteins, only the fraction D1-3 showed antifungal activity against this pathogen. MALDI-TOF-MS revealed that fraction D1-3 with a relative molecular mass of 53.936 kDa had a high homology (> 65%) with the leucyl aminopeptidase produced by Bacillus subtilis (WP_041057629.1). It is suggested that fraction D1-3 is a novel antifungal protein.
Keywords:Bacillus subtilis  antifungal protein  inhibition mechanism  identification  
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