{"title":"菜花镰刀菌对植物抗菌素菜花异黄酮的代谢","authors":"E.A. Wietor-Orlandi , D.A. Smith","doi":"10.1016/0048-4059(85)90067-0","DOIUrl":null,"url":null,"abstract":"<div><p>Phascollinisoflavan, an isoflavonoid phytoalexin produced by <em>Phaseolus vulgaris</em>, was metabolized by <em>Fusarium solani</em> f. sp. <em>phaseoli</em>. A major product of this reaction, designated metabolite-1 (M-1), was isolated from fungal cultures; whereas phaseollinisoflavan could not be recovered from the fungal culture medium 21 h after its addition, the level of M-1 rose steadily between nine and 24 h. Bioassays of radial mycelial growth or of dry matter accumulation involving <em>F. solani</em> f. sp. <em>phaseoli, Pythium myrioylum, Phytophthora cryptogea</em> and/or <em>Rhizoctonia solani</em> indicated that M-1 was less fungitoxic than phaseollinisoflavan. In addition to its production in liquid cultures treated with phaseollinisolflavan, M-1 was also isolated from Fusarium-infected bean tissues; trace amounts of M-1 were detected two days after inoculation and levels rose to at least I mg g<sup>−1</sup> dry weight 8 days later. Purification of M-1 involved solvent partitioning, TLC, gel filtration and gas chromatography. Partial characterization indicated that the molecular weight of this metabolite was 342, 18 mass units greater than that of phaseollinisoflavan, suggesting the addition of the elements of water to the phytoalexin.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"27 2","pages":"Pages 197-207"},"PeriodicalIF":0.0000,"publicationDate":"1985-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90067-0","citationCount":"6","resultStr":"{\"title\":\"Metabolism of the phytoalexin, phaseollinisoflavan, by Fusarium solani f. sp. phaseoli\",\"authors\":\"E.A. Wietor-Orlandi , D.A. Smith\",\"doi\":\"10.1016/0048-4059(85)90067-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Phascollinisoflavan, an isoflavonoid phytoalexin produced by <em>Phaseolus vulgaris</em>, was metabolized by <em>Fusarium solani</em> f. sp. <em>phaseoli</em>. A major product of this reaction, designated metabolite-1 (M-1), was isolated from fungal cultures; whereas phaseollinisoflavan could not be recovered from the fungal culture medium 21 h after its addition, the level of M-1 rose steadily between nine and 24 h. Bioassays of radial mycelial growth or of dry matter accumulation involving <em>F. solani</em> f. sp. <em>phaseoli, Pythium myrioylum, Phytophthora cryptogea</em> and/or <em>Rhizoctonia solani</em> indicated that M-1 was less fungitoxic than phaseollinisoflavan. In addition to its production in liquid cultures treated with phaseollinisolflavan, M-1 was also isolated from Fusarium-infected bean tissues; trace amounts of M-1 were detected two days after inoculation and levels rose to at least I mg g<sup>−1</sup> dry weight 8 days later. Purification of M-1 involved solvent partitioning, TLC, gel filtration and gas chromatography. Partial characterization indicated that the molecular weight of this metabolite was 342, 18 mass units greater than that of phaseollinisoflavan, suggesting the addition of the elements of water to the phytoalexin.</p></div>\",\"PeriodicalId\":101028,\"journal\":{\"name\":\"Physiological Plant Pathology\",\"volume\":\"27 2\",\"pages\":\"Pages 197-207\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1985-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0048-4059(85)90067-0\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physiological Plant Pathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0048405985900670\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological Plant Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0048405985900670","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
摘要
菜豆素异黄酮是一种由菜豆素产生的异黄酮类植物抗菌素,可被番茄镰刀菌代谢。该反应的主要产物,称为代谢物-1 (M-1),从真菌培养物中分离出来;而在添加后21 h无法从真菌培养基中恢复相油葵异黄酮,而M-1的水平在9 ~ 24 h之间稳步上升。对番茄枯萎菌(F. solani F. sp. phaseoli)、蘑菇霉(Pythium myrioylum)、隐疫霉(Phytophthora cryptoa)和番茄根丝核菌(Rhizoctonia solani)的径向菌丝生长或干物质积累的生物测定表明,M-1的真菌毒性低于相油葵异黄酮。M-1除了在经豆油异黄酮处理的液体培养物中产生外,还从镰刀菌感染的豆类组织中分离出来;接种后2天检测到微量M-1, 8天后含量上升至至少1 mg g -1干重。M-1的纯化过程包括溶剂分割、薄层色谱、凝胶过滤和气相色谱。部分表征表明,该代谢产物的分子量为342,比菜籽油异黄酮的分子量大18个质量单位,表明该植物抗毒素中加入了水元素。
Metabolism of the phytoalexin, phaseollinisoflavan, by Fusarium solani f. sp. phaseoli
Phascollinisoflavan, an isoflavonoid phytoalexin produced by Phaseolus vulgaris, was metabolized by Fusarium solani f. sp. phaseoli. A major product of this reaction, designated metabolite-1 (M-1), was isolated from fungal cultures; whereas phaseollinisoflavan could not be recovered from the fungal culture medium 21 h after its addition, the level of M-1 rose steadily between nine and 24 h. Bioassays of radial mycelial growth or of dry matter accumulation involving F. solani f. sp. phaseoli, Pythium myrioylum, Phytophthora cryptogea and/or Rhizoctonia solani indicated that M-1 was less fungitoxic than phaseollinisoflavan. In addition to its production in liquid cultures treated with phaseollinisolflavan, M-1 was also isolated from Fusarium-infected bean tissues; trace amounts of M-1 were detected two days after inoculation and levels rose to at least I mg g−1 dry weight 8 days later. Purification of M-1 involved solvent partitioning, TLC, gel filtration and gas chromatography. Partial characterization indicated that the molecular weight of this metabolite was 342, 18 mass units greater than that of phaseollinisoflavan, suggesting the addition of the elements of water to the phytoalexin.