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Characterization of an antibiotic produced by a strain of Pseudomonas fluorescens inhibitory to Gaeumannomyces graminis var. tritici and Pythium spp.

机译:荧光假单胞菌菌株产生的对制革假单胞菌的抑制作用的抗生素的表征。小麦和腐霉属。

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摘要

The production, isolation, and characterization of an antibiotic substance from cultures of Pseudomonas fluorescens 2-79 (NRRL B-15132) is described. P. fluorescens 2-79 originally was isolated from the roots of wheat and is suppressive to the wheat root disease take-all caused by Gaeumannomyces graminis var. tritici. The antibiotic was isolated from potato glucose broth cultures of strain 2-79 by solvent extraction. It was purified by silica gel column chromatography and was a greenish yellow, needle-shaped crystal with a melting point of 242 degrees C (decomposition). It was soluble in methylene chloride, chloroform, acetone, 2 N sodium hydroxide, and 2 N hydrochloric acid and was insoluble in water, methanol, ethyl acetate, tetrahydrofuran, diethyl ether, carbon tetrachloride, hexane, and petroleum ether. On the basis of UV, infrared, 1H-nuclear magnetic resonance, 13C-nuclear magnetic resonance, mass spectral analysis, and elemental analysis, the structure of the antibiotic is proposed to be a dimer of phenazine carboxylic acid. Lithium aluminum hydride reduction of the antibiotic yielded hydroxymethyl phenazine as a major product which retained most of the biological characteristics of the parent molecule. There were no toxic symptoms when mice received this antibiotic by oral doses up to 464 mg/kg. The antibiotic showed excellent activity against several species of fungi, including the wheat pathogens Gaeumannomyces graminis var. tritici, Rhizoctonia solani, and Pythium aristosporum; and it may have a role in suppression of take-all in vivo by strain 2-79.
机译:描述了荧光假单胞菌2-79(NRRL B-15132)培养物中抗生素物质的生产,分离和表征。荧光假单胞菌2-79最初是从小麦的根中分离出来的,并且抑制了由Gaeumannomyces graminis var引起的小麦根部疾病的全吸收。小麦。通过溶剂提取从菌株2-79的马铃薯葡萄糖肉汤培养物中分离抗生素。用硅胶柱色谱法纯化,为淡黄色针状结晶,熔点为242℃(分解)。它可溶于二氯甲烷,氯仿,丙酮,2 N氢氧化钠和2 N盐酸,不溶于水,甲醇,乙酸乙酯,四氢呋喃,乙醚,四氯化碳,己烷和石油醚。在紫外,红外,1H-核磁共振,13C-核磁共振,质谱分析和元素分析的基础上,该抗生素的结构被认为是吩嗪羧酸的二聚体。氢化锂铝对抗生素的还原产生羟甲基吩嗪作为主要产物,其保留了母体分子的大部分生物学特性。当小鼠口服这种剂量高达464 mg / kg的抗生素时,没有任何毒性症状。该抗生素对几种真菌显示出优异的活性,其中包括小麦病原菌Gaeumannomyces graminis var。 Tritici,Rhizoctonia solani和Pythium aristosporum;并且它可能在抑制2-79菌​​株对体内的吸收方面发挥作用。

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