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
相关论文
共 50 条
  • [41] Bioactive Secondary Metabolites from Higher Fungi in China
    Liu, Ji-Kai
    IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2010, 46 : S43 - S44
  • [42] Bioactive Secondary Metabolites from the Endophytic Aspergillus Genus
    Zhang, Huawei
    Tang, Yifei
    Ruan, Chuanfen
    Bai, Xuelian
    RECORDS OF NATURAL PRODUCTS, 2016, 10 (01) : 1 - 16
  • [43] Isolation of bioactive secondary metabolites from terrestrial myxobacteria
    Millard, Lexie
    White, Kimberly N.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 247
  • [44] Secondary metabolites of fungi from marine habitats
    Rateb, Mostafa E.
    Ebel, Rainer
    NATURAL PRODUCT REPORTS, 2011, 28 (02) : 290 - 344
  • [45] SECONDARY METABOLITES FROM MARINE BRYOZOANS - A REVIEW
    CHRISTOPHERSEN, C
    ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1985, 39 (07): : 517 - 529
  • [46] SECONDARY METABOLITES FROM MARINE-ALGAE
    ERICKSON, KL
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1979, (APR): : 277 - 277
  • [47] Anticancer secondary metabolites from marine sponges
    Uras, Ibrahim Seyda
    Konuklugil, Belma
    SU URUNLERI DERGISI, 2021, 38 (01): : 101 - 106
  • [48] Secondary metabolites from marine penicillium brevicompactum
    Rovirosa, J
    Diaz-Marrero, A
    Darias, J
    Painemal, K
    San Martin, A
    JOURNAL OF THE CHILEAN CHEMICAL SOCIETY, 2006, 51 (01): : 775 - 778
  • [49] BIOACTIVE MARINE METABOLITES .52. SIMPLE ANTIFUNGAL METABOLITES FROM A MARINE SPONGE, HALICHONDRIA SP
    LI, HY
    MATSUNAGA, S
    FUSETANI, N
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1994, 107 (02): : 261 - 264
  • [50] Secondary Structure Models for the Internal Transcribed Spacer (ITS) Region 1 from Symbiotic Dinoflagellates
    Thornhill, Daniel J.
    Lord, Jenna B.
    PROTIST, 2010, 161 (03) : 434 - 451