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首页> 外文期刊>Notulae Botanicae Horti Agrobotanici Cluj-Napoca >Extraction, Isolation and Identification of Antimicrobial Substances from Bacillus amyloliquefaciens CMN1308
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Extraction, Isolation and Identification of Antimicrobial Substances from Bacillus amyloliquefaciens CMN1308

机译:淀粉芽孢杆菌CMN1308的抗菌物质的提取,分离与鉴定

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Four separation methods of antimicrobial substances produced by CMN1308 (Bacillus amyloliquefaciens) were evaluated and selected according to number of antimicrobial substances and its activity in vitro. The results showed that extraction by acid precipitation of the fermentation supernatant of CMN1308 was the best with a diameter of inhibition zone of pathogen fungi P. expansum of 12.3 mm in a laboratory bioassay. Applying a silica thin layer chromatography (TLC), SDS-PAGE and other separation technologies we isolate antimicrobial substances, and the separated band were cut off for mass spectrometry analysis. The TLC of crude extract of CMN1308 show a topical band corresponding with the surfactin standard (Rf value =0.75), proved that the strain CMN1308 can produce this surface active compound. The mycoprotein extracted from CMN1308 was separated by Tricine-SDS-PAGE modified with the addition of urea in the separation gel. After mass spectrometric analysis and protein characterization, the isolated mycoprotein showed a maximum ion peak at M/Z of 2679 and molecular weight of 29.5 kDa, matching with protein flagellin. The extracellular antimicrobial protein of strain CMN1308 display four bands after urea-Tricine-SDS-PAGE, but after mass spectrometry analysis only two bands were identified. Band “A” with a maximum ion peak at M/Z of 1926 and molecular weight of 49.8 kDa, aligned with NCBI database, matching with DLDH (dihydrolipoamide dehydrogenase enzyme). Band “D” show the maximum ion peak at M/Z of 2936 and molecular weight of 22.4 kD, matching with a chitin binding protein. Thus, the strain CMN1308 has the potential to be developed as a commercial biological control agent for chestnut common pathogenic fungi.
机译:根据抗菌素的数量及其在体外的活性,对CMN1308(解淀粉芽孢杆菌)生产的四种抗菌素的分离方法进行了评价和选择。结果表明,在实验室生物测定中,用酸沉淀法提取CMN1308发酵上清液的效果最好,其病原真菌扩张性毕赤酵母的抑制区直径为12.3 mm。应用硅胶薄层色谱(TLC),SDS-PAGE和其他分离技术,我们分离了抗菌物质,并切断了分离的谱带用于质谱分析。 CMN1308粗提物的薄层色谱显示出与表面活性素标准品相对应的局部谱带(Rf值= 0.75),证明菌株CMN1308可以产生这种表面活性化合物。通过在分离凝胶中添加尿素修饰的Tricine-SDS-PAGE分离从CMN1308提取的真菌蛋白。经过质谱分析和蛋白质表征后,分离的霉菌蛋白在M / Z处显示最大离子峰为2679,分子量为29.5 kDa,与鞭毛蛋白相匹配。尿素-Tricine-SDS-PAGE后,菌株CMN1308的细胞外抗菌蛋白显示4条带,但在质谱分析后仅鉴定出2条带。带“ A”的谱带在M / Z处的最大离子峰为1926,分子量为49.8 kDa,与NCBI数据库对齐,与DLDH(二氢脂酰胺脱氢酶)匹配。带“ D”显示在M / Z处的最大离子峰为2936,分子量为22.4 kD,与几丁质结合蛋白相匹配。因此,菌株CMN1308具有被开发为栗常见病原性真菌的商业生物防治剂的潜力。

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