Bacterial symbionts: Prospects for the sustainable production of invertebrate-derived pharmaceuticals

被引:92
作者
Piel, J [1 ]
机构
[1] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
关键词
symbiosis; polyketides; nonribosomal peptides; metagenomic studies; marine invertebrates; bacteria; drug supply; biosynthesis;
D O I
10.2174/092986706775197971
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Invertebrate animals, such as sponges, tunicates and bryozoans, are among the most important sources of biomedically relevant natural products. However, as these animals generally contain only low quantities. of the compounds, further pharmacological development is in most cases difficult. There is increasing evidence that many metabolites, in particular polyketides and nonribosomally synthesized peptides, are not produced by the animals themselves but by associated bacterial symbionts. This symbiont hypothesis currently attracts considerable interest, since it implicates that animal-independent production systems based on bacterial fermentation processes could be created. This review gives an overview about recent developments in the research on natural product symbiosis. Different techniques will be discussed that have been employed to pinpoint the actual producer. Since bacterial symbionts are highly fastidious and have been generally resistant to cultivation attempts, emphasis will be laid on culture-independent strategies, such as cell separation approaches and the cloning of biosynthetic genes. These strategies have provided insights into possible sources of several natural products, e.g. the bryostatins, pederin, the onnamides, swinholide A and theopalauamide. Finally, potential techniques for the generation of renewable supplies of symbiont-derived drug candidates will be discussed. Cultivation approaches and the heterologous expression of cloned biosynthesis genes from uncultured symbionts could in future provide access to several important marine drug candidates, including bryostatin 1, halichondrin or ET-743.
引用
收藏
页码:39 / 50
页数:12
相关论文
共 100 条
[11]   Salicylihalamides A and B, novel cytotoxic macrolides from the marine sponge Haliclona sp. [J].
Erickson, KL ;
Beutler, JA ;
Cardellina, JH ;
Boyd, MR .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (23) :8188-8192
[12]  
Faulkner DJ, 2000, NAT PROD REP, V17, P1, DOI 10.1039/a909113k
[13]  
Fernández-Busquets X, 1999, MICROSC RES TECHNIQ, V44, P204, DOI 10.1002/(SICI)1097-0029(19990215)44:4<204::AID-JEMT2>3.0.CO
[14]  
2-I
[15]   Discovery of the novel candidate phylum "Poribacteria" in marine sponges [J].
Fieseler, L ;
Horn, M ;
Wagner, M ;
Hentschel, U .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (06) :3724-3732
[16]   Cellular origin of chlorinated diketopiperazines in the dictyoceratid sponge Dysidea herbacea (Keller) [J].
Flowers, AE ;
Garson, MJ ;
Webb, RI ;
Dumdei, EJ ;
Charan, RD .
CELL AND TISSUE RESEARCH, 1998, 292 (03) :597-607
[17]   TERPENES IN SPONGE CELL-MEMBRANES - CELL-SEPARATION AND MEMBRANE FRACTIONATION STUDIES WITH THE TROPICAL MARINE SPONGE AMPHIMEDON-SP [J].
GARSON, MJ ;
THOMPSON, JE ;
LARSEN, RM ;
BATTERSHILL, CN ;
MURPHY, PT ;
BERGQUIST, PR .
LIPIDS, 1992, 27 (05) :378-388
[18]   A sponge/dinoflagellate association in the haplosclerid sponge Haliclona sp.:: cellular origin of cytotoxic alkaloids by Percoll density gradient fractionation [J].
Garson, MJ ;
Flowers, AE ;
Webb, RI ;
Charan, RD ;
McCaffrey, EJ .
CELL AND TISSUE RESEARCH, 1998, 293 (02) :365-373
[19]   THE DISTRIBUTION OF BROMINATED LONG-CHAIN FATTY-ACIDS IN SPONGE AND SYMBIONT CELL-TYPES FROM THE TROPICAL MARINE SPONGE AMPHIMEDON TERPENENSIS [J].
GARSON, MJ ;
ZIMMERMANN, MP ;
BATTERSHILL, CN ;
HOLDEN, JL ;
MURPHY, PT .
LIPIDS, 1994, 29 (07) :509-516
[20]   Immunolocalization of the toxin latrunculin B within the Red Sea sponge Negombata magnifica (Demospongiae, Latrunculiidae) [J].
Gillor, O ;
Carmeli, S ;
Rahamim, Y ;
Fishelson, Z ;
Ilan, M .
MARINE BIOTECHNOLOGY, 2000, 2 (03) :213-223