中山大学学报(自然科学版)
中山大學學報(自然科學版)
중산대학학보(자연과학판)
Acta Scientiarum Naturalium Universitatis Sunyatseni
2015年
5期
67-71
,共5页
宋双%薛艳钰%陆勇军%李静%廖宝林%刘岚
宋雙%薛豔鈺%陸勇軍%李靜%廖寶林%劉嵐
송쌍%설염옥%륙용군%리정%료보림%류람
红树林%内生真菌%次级代谢产物%腐皮镰刀菌
紅樹林%內生真菌%次級代謝產物%腐皮鐮刀菌
홍수림%내생진균%차급대사산물%부피렴도균
mangrove%endophytic fungus%secondary metabolites%Fusarium solani
采用色谱技术对 Fusarium solani 387#的次级代谢产物进行分离纯化,根据化合物的理化性质、波谱数据以及与文献谱图、数据对照的方法确定化合物的结构。从南海红树林内生真菌 Fusarium solani 387#的次级代谢产物中分离得到了9个镰红菌素类化合物,分别鉴定为5(R)-deoxyfusarubin (1)、5(S)-deoxyfusarubin (2)、3-methyl ether fusarubin (3)、Fusarubin (4)、Anhydrofusarabin (5)、Anhydro-5-deoxyfusarubin (6)、2-acetonyl-3-methyl-7-methoxy-naphthazarin (7)、Javanicin (8)、2-acetonyl-3-methyl-5-hydrogen-7-methoxy-naphthazarin (9)。通过 X -射线单晶衍射首次确定了化合物1和2的绝对构型及存在形式。
採用色譜技術對 Fusarium solani 387#的次級代謝產物進行分離純化,根據化閤物的理化性質、波譜數據以及與文獻譜圖、數據對照的方法確定化閤物的結構。從南海紅樹林內生真菌 Fusarium solani 387#的次級代謝產物中分離得到瞭9箇鐮紅菌素類化閤物,分彆鑒定為5(R)-deoxyfusarubin (1)、5(S)-deoxyfusarubin (2)、3-methyl ether fusarubin (3)、Fusarubin (4)、Anhydrofusarabin (5)、Anhydro-5-deoxyfusarubin (6)、2-acetonyl-3-methyl-7-methoxy-naphthazarin (7)、Javanicin (8)、2-acetonyl-3-methyl-5-hydrogen-7-methoxy-naphthazarin (9)。通過 X -射線單晶衍射首次確定瞭化閤物1和2的絕對構型及存在形式。
채용색보기술대 Fusarium solani 387#적차급대사산물진행분리순화,근거화합물적이화성질、파보수거이급여문헌보도、수거대조적방법학정화합물적결구。종남해홍수림내생진균 Fusarium solani 387#적차급대사산물중분리득도료9개렴홍균소류화합물,분별감정위5(R)-deoxyfusarubin (1)、5(S)-deoxyfusarubin (2)、3-methyl ether fusarubin (3)、Fusarubin (4)、Anhydrofusarabin (5)、Anhydro-5-deoxyfusarubin (6)、2-acetonyl-3-methyl-7-methoxy-naphthazarin (7)、Javanicin (8)、2-acetonyl-3-methyl-5-hydrogen-7-methoxy-naphthazarin (9)。통과 X -사선단정연사수차학정료화합물1화2적절대구형급존재형식。
The secondary metabolites of Fusarium solani 387 #from the South China Sea were studied. The structures of compounds were analyzed based on physical and chemical properties,and in comparison with the spectroscopic data with literatures published.Nine Fusarbin compounds were isolated from the mangrove endophytic fungus Fusarium solani 387 #from the South China Sea,and their structures were i-dentified as 5 (R)-deoxyfusarubin (1),5 (S)-deoxyfusarubin (2),3-methyl ether fusarubin (3), Fusarubin (4),Anhydrofusarabin (5 ),Anhydro-5-deoxyfusarubin (6 ),2-acetonyl-3-methyl-7-me-thoxy-naphthazarin (7),Javanicin (8 )and 2-acetonyl-3-methyl-5-hydrogen-7-methoxy-naphthazarin (9).The absolute configurations as well as the existing form of compound 1 and 2 were determined by the X-ray crystallography for the first time.