Piel J
Kekulé-Institute of Organic Chemistry and Biochemistry, University of Bonn, Gerhard-Domagk-Str. 1, D-53121 Bonn, Germany.
Curr Med Chem. 2006;13(1):39-50.
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.
无脊椎动物,如海绵动物、被囊动物和苔藓虫,是生物医学相关天然产物的最重要来源之一。然而,由于这些动物通常仅含有少量此类化合物,在大多数情况下,进一步的药物开发具有难度。越来越多的证据表明,许多代谢产物,特别是聚酮化合物和非核糖体合成肽,并非由动物自身产生,而是由相关的细菌共生体产生。这种共生体假说目前引起了相当大的关注,因为这意味着可以创建基于细菌发酵过程的独立于动物的生产系统。本综述概述了天然产物共生研究的最新进展。将讨论已用于确定实际生产者的不同技术。由于细菌共生体要求苛刻,且通常对培养尝试具有抗性,因此将重点介绍不依赖培养的策略,如细胞分离方法和生物合成基因的克隆。这些策略为几种天然产物的可能来源提供了见解,例如苔藓抑素、佩德菌素、奥纳米德、斯氏大环内酯A和奥帕劳酰胺。最后,将讨论生成共生体衍生候选药物可再生供应的潜在技术。培养方法以及从未培养共生体克隆的生物合成基因的异源表达,未来可能会提供获得几种重要海洋候选药物的途径,包括苔藓抑素1、海兔毒素或ET - 743。