Marine Bioproducts Engineering Group, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, Liaoning, China.
Mar Biotechnol (NY). 2011 Oct;13(5):868-82. doi: 10.1007/s10126-010-9347-2. Epub 2011 Jan 19.
Sponges (Porifera), as the best known source of bioactive marine natural products in metazoans, play a significant role in marine drug discovery and development. As sessile filter-feeding animals, a considerable portion of the sponge biomass can be made of endosymbiotic and associated microorganisms. Understanding the cellular origin of targeted bioactive compounds from sponges is therefore important not only for providing chemotaxonomic information but also for defining the bioactive production strategy in terms of sponge aquaculture, cell culture, or fermentation of associated bacteria. The two alkaloids debromohymenialdisine (DBH) and hymenialdisine (HD), which are cyclin-dependent kinase inhibitors with pharmacological activities for treating osteoarthritis and Alzheimer's disease, have been isolated from the sponge Axinella sp. In this study, the cellular localization of these two alkaloids was determined through the quantification of these alkaloids in different cell fractions by high-performance liquid chromatography (HPLC). First, using a differential centrifugation method, the dissociated cells were separated into different groups according to their sizes. The two bioactive alkaloids were mainly found in sponge cells obtained from low-speed centrifugation. Further cell purifications were accomplished by a newly developed multi-step protocol. Four enriched cell fractions (C1, C2, C3, and C4) were obtained and subjected to light and transmission electron microscopy, cytochemical staining, and HPLC quantification. Compared to the low concentrations in other cell fractions, DBH and HD accounted for 10.9% and 6.1%, respectively, of dry weight in the C1 fraction. Using the morphological characteristics and cytochemical staining results, cells in the C1 fraction were speculated to be spherulous cells. This result shows that DBH and HD in Axinella sp. are located in sponge cells and mostly stored in spherulous cells.
海绵(多孔动物门)作为后生动物中最著名的生物活性海洋天然产物来源,在海洋药物发现和开发中发挥着重要作用。作为固着滤食动物,相当一部分海绵生物量由内共生和相关微生物组成。因此,了解海绵中目标生物活性化合物的细胞起源不仅对于提供化学分类学信息很重要,而且对于定义海绵养殖、细胞培养或相关细菌发酵的生物活性生产策略也很重要。两种生物碱 debromohymenialdisine (DBH) 和 hymenialdisine (HD) 是具有治疗骨关节炎和阿尔茨海默病的药理活性的细胞周期蛋白依赖性激酶抑制剂,已从海绵 Axinella sp. 中分离得到。在这项研究中,通过高效液相色谱 (HPLC) 对不同细胞组分中这些生物碱的定量,确定了这两种生物碱的细胞定位。首先,使用差速离心法,根据细胞大小将解离细胞分离成不同的组。两种生物活性生物碱主要存在于低速离心获得的海绵细胞中。进一步的细胞纯化通过新开发的多步方案完成。获得了四个富含细胞的级分 (C1、C2、C3 和 C4),并进行了光镜和透射电镜、细胞化学染色和 HPLC 定量。与其他细胞级分中的低浓度相比,DBH 和 HD 分别占 C1 级分干重的 10.9%和 6.1%。根据形态特征和细胞化学染色结果,推测 C1 级分中的细胞为球状细胞。该结果表明,DBH 和 HD 存在于 Axinella sp. 的海绵细胞中,并且主要储存在球状细胞中。