Bioactive Secondary Metabolites from Symbiotic Marine Dinoflagellates: Symbiodinolide and Durinskiols

被引:25
|
作者
Kita, Masaki [1 ]
Ohno, Osamu [2 ]
Han, Chunguang [2 ]
Uemura, Daisuke [2 ,3 ]
机构
[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki 3058571, Japan
[2] Keio Univ, Dept Biosci & Informat, Yokohama, Kanagawa 2238522, Japan
[3] Nagoya Univ, Inst Adv Res, Chikusa Ku, Nagoya, Aichi 4648602, Japan
来源
CHEMICAL RECORD | 2010年 / 10卷 / 02期
关键词
symbiosis; marine natural products; chemical ecology; long carbon-chain polyol compounds; TRUNCATED POLYHYDROXYL CHAIN; ABSOLUTE-CONFIGURATION; STEREOSELECTIVE-SYNTHESIS; STRUCTURE ELUCIDATION; ZOOXANTHELLATOXIN-A; CHEMICAL-STRUCTURES; C33-C42; FRAGMENT; ACID PORTION; CA2+ INFLUX; COMPOUND;
D O I
10.1002/tcr.200900007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Symbiotic relationships play critical roles in marine ecosystems. Among symbionts, marine dinoflagellates have attracted the attention of natural products chemists, biologists, and ecologists, since they are rich sources of unique bioactive secondary metabolites. The polyol compound symbiodinolide, which was isolated from the symbiotic dinoflagellate Symbiodinium sp., exhibits significant voltage-dependent N-type Ca2+ channel-opening activity and may serve as a defense substance to prevent digestion of the host animals. Durinskiols are also unique long carbon-chain polyol compounds that were isolated from the dinoflagellate Durinskia sp. We found a selective cleavage reaction of allylic 1,2-diol using an olefin metathesis catalyst, and developed a fluorescent-labeling method for MS/MS analysis to achieve the structural elucidation of huge polyol compounds. This review highlights recent advances in structural and biological studies on symbiodinolide, durinskiols, and related polyol compounds. (C) 2010 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 10: 57-69; 2010: Published online in Wiley InterScience (www. interscience.wiley.com) DOI 10.1002/tcr.200900007
引用
收藏
页码:57 / 69
页数:13
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