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利用来自RS1的抗真菌蛋白对兰花致病霉菌进行生物防治

Biocontrol of Orchid-pathogenic Mold, , by Antifungal Proteins from RS1.

作者信息

Sowanpreecha Rapeewan, Rerngsamran Panan

机构信息

Department of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.

出版信息

Mycobiology. 2018 May 30;46(2):129-137. doi: 10.1080/12298093.2018.1468055. eCollection 2018.

Abstract

Black rot disease in orchids is caused by the water mold . To gain better biocontrol performance, several factors affecting growth and antifungal substance production by RS1 were verified. These factors include type and pH of media, temperature, and time for antifungal production. The results showed that the best conditions for RS1 to produce the active compounds was cultivating the bacteria in Luria-Bertani medium at pH 7.0 for 21 h at 37 °C. The culture filtrate was subjected to stepwise ammonium sulfate precipitation. The precipitated proteins from the 40% to 80% fraction showed antifungal activity and were further purified by column chromatography. The eluted proteins from fractions 9-10 and 33-34 had the highest antifungal activity at about 75% and 82% inhibition, respectively. SDS-PAGE revealed that the 9-10 fraction contained mixed proteins with molecular weights of 54 kDa, 32 kDa, and 20 kDa, while the 33-34 fraction contained mixed proteins with molecular weights of 40 kDa, 32 kDa, and 29 kDa. Each band of the proteins was analyzed by LC/MS to identify the protein. The result from Spectrum Modeler indicated that these proteins were closed similarly to three groups of the following proteins; catalase, chitin binding protein, and protease. Morphological study under scanning electron microscopy demonstrated that the partially purified proteins from RS1 caused abnormal growth and hypha elongation in . The bacteria and/or these proteins may be useful for controlling black rot disease caused by in orchid orchards.

摘要

兰花黑腐病由水霉菌引起。为了获得更好的生物防治效果,对影响RS1生长和抗真菌物质产生的几个因素进行了验证。这些因素包括培养基的类型和pH值、温度以及抗真菌物质产生的时间。结果表明,RS1产生活性化合物的最佳条件是在pH值为7.0的Luria-Bertani培养基中于37℃培养21小时。将培养滤液进行分步硫酸铵沉淀。40%至80%组分中沉淀的蛋白质具有抗真菌活性,并通过柱色谱进一步纯化。第9-10和33-34组分洗脱的蛋白质具有最高的抗真菌活性,抑制率分别约为75%和82%。SDS-PAGE显示,第9-10组分包含分子量为54 kDa、32 kDa和20 kDa的混合蛋白质,而第33-34组分包含分子量为40 kDa、32 kDa和29 kDa的混合蛋白质。对蛋白质的每条带进行LC/MS分析以鉴定蛋白质。光谱建模器的结果表明,这些蛋白质与以下三组蛋白质相似;过氧化氢酶、几丁质结合蛋白和蛋白酶。扫描电子显微镜下的形态学研究表明,RS1部分纯化的蛋白质导致[此处原文缺失相关内容]生长异常和菌丝伸长。这些细菌和/或这些蛋白质可能有助于控制兰花果园中由[此处原文缺失相关内容]引起的黑腐病。

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