Sipkema Detmer, Osinga Ronald, Schatton Wolfgang, Mendola Dominick, Tramper Johannes, Wijffels René H
Food and Bioprocess Engineering Group, Wageningen University, P.O. Box 8129, 6700 EV Wageningen, The Netherlands.
Biotechnol Bioeng. 2005 Apr 20;90(2):201-22. doi: 10.1002/bit.20404.
Marine sponges are known to produce an overwhelming array of secondary metabolites with pharmaceutical potential. The technical and economical potential of using marine sponges for large-scale production of these compounds was assessed for two cases: the anticancer molecule halichondrin B from a Lissodendoryx sp., and avarol from Dysidea avara for its antipsoriasis activity. An economic and technical analysis was done for three potential production methods: mariculture, ex situ culture (in tanks), and cell culture. We concluded that avarol produced by mariculture or ex situ culture could become a viable alternative to currently used pharmaceuticals for the treatment of psoriasis. Production of halichondrin B from sponge biomass was found to not be a feasible process, mainly due to the extremely low concentration of the compound in the sponge. Technical feasibility was also analyzed for five alternatives: chemical synthesis, wild harvest, primmorph culture, genetic modification and semi-synthesis. It was concluded that the latter two approaches could prove to be valuable methods for the production of pharmaceuticals, based on chemical structures of secondary metabolites present in trace amounts in marine sponges.
已知海洋海绵能产生大量具有药用潜力的次生代谢产物。针对两种情况评估了利用海洋海绵大规模生产这些化合物的技术和经济潜力:一种是来自 Lissodendoryx 属海绵的抗癌分子海兔毒素 B,另一种是来自淡黄小皮海绵的阿伐他汀,因其具有抗银屑病活性。针对三种潜在生产方法进行了经济和技术分析:海水养殖、异地养殖(在水箱中)和细胞培养。我们得出结论,通过海水养殖或异地养殖生产的阿伐他汀可能成为目前用于治疗银屑病的药物的可行替代品。发现从海绵生物质中生产海兔毒素 B 并非可行的过程,主要是因为该化合物在海绵中的浓度极低。还对五种替代方法进行了技术可行性分析:化学合成、野生采集、原球体培养、基因改造和半合成。结论是,基于海洋海绵中微量存在的次生代谢产物的化学结构,后两种方法可能被证明是生产药物的有价值方法。