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除草菌素F和G,两种新型核苷类抗生素。

Herbicidins F and G, two new nucleoside antibiotics.

作者信息

Takiguchi Y, Yoshikawa H, Terahara A, Torikata A, Terao M

出版信息

J Antibiot (Tokyo). 1979 Sep;32(9):862-7. doi: 10.7164/antibiotics.32.862.

Abstract

A mutant of Streptomyces saganonensis No. 4075, obtained with N-methyl-N'-nitro-N-nitrosoguanidine treatment, produced herbicidins F and G without herbicidins A and B. Isolation of the antibiotics was performed by adsorption on resinous adsorbent followed by elution with aqueous MeOH. Herbicidin F was obtained as colorless needles after extraction of the eluate using methylene dichloride. Purification of herbicidin G was completed with silica-gel chromatography to give a crystalline powder. physico-chemical characterization revealed that herbicidins F and G were new nucleoside antibiotics having an adenine moiety in their structures. There was no inhibition activity at 100 micrograms/ml of herbicidins F and G against all of bacteria and yeast tested. Herbicidin F, as well as herbicidin G, are inhibitory activity against some of fungi such as Tricophyton rubrum (MIC; 6.25 micrograms/ml), T. asteroides (6.25 micrograms/ml), T. mentagrophytes (6.25 approximately 12.5 micrograms/ml), Botrytis cinerea (12.5 micrograms/ml), Blastomyces brasiliensis (12.5 approximately 25 micrograms/ml).

摘要

用N-甲基-N'-硝基-N-亚硝基胍处理获得的萨加诺链霉菌4075突变体,产生了除草菌素F和G,但没有除草菌素A和B。抗生素的分离是通过吸附在树脂吸附剂上,然后用甲醇水溶液洗脱来进行的。用二氯甲烷萃取洗脱液后,除草菌素F以无色针状晶体形式获得。除草菌素G通过硅胶柱色谱法纯化得到结晶粉末。理化性质表征表明,除草菌素F和G是结构中含有腺嘌呤部分的新型核苷类抗生素。除草菌素F和G在100微克/毫升时对所有测试的细菌和酵母均无抑制活性。除草菌素F以及除草菌素G对一些真菌具有抑制活性,如红色毛癣菌(MIC;6.25微克/毫升)、星形奴卡菌(6.25微克/毫升)、须癣毛癣菌(6.25至12.5微克/毫升)、灰葡萄孢(12.5微克/毫升)、巴西芽生菌(12.5至25微克/毫升)。

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