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Cell cultures from the symbiotic soft coral Sinularia flexibilis

机译:共生软珊瑚Sinularia flexibilis的细胞培养

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摘要

The symbiotic octocoral Sinularia flexibilis is a producer of potential pharmaceuticals. Sustainable mass production of these corals as a source of such compounds demands innovative approaches, including coral cell culture. We studied various cell dissociation methodologies and the feasibility of cultivation of S. flexibilis cells on different media and cell dissociation methodologies. Mechanical dissociation of coral tissue always yielded the highest number of cells and allowed subsequent cellular growth in all treatments. The best results from chemical dissociation reagents were found with trypsin-ethylene diamine tetraacetic acid. Coral cells obtained from spontaneous dissociation did not grow. Light intensity was found to be important for coral cell culture showing an enduring symbiosis between the cultured cells and their intracellular algae. The Grace's insect medium and Grace's modified insect medium were found to be superior substrates. To confirm the similarity of the cultured cells and those in the coral tissue, a molecular test with Internal Transcribed Spacer primers was performed. Thereby, the presence of similar cells of both the coral cells and zooxanthella in different culture media was confirmed.
机译:八齿共生的Sinularia flexibilis是潜在药物的生产商。作为这些化合物的来源,这些珊瑚的可持续大规模生产需要创新方法,包括珊瑚细胞培养。我们研究了各种细胞解离方法以及在不同培养基和细胞解离方法上培养柔韧性链球菌的可行性。珊瑚组织的机械解离总是产生最高数量的细胞,并在所有处理中均允许随后的细胞生长。用胰蛋白酶-乙二胺四乙酸可以发现化学解离试剂的最佳结果。自发解离获得的珊瑚细胞没有生长。发现光强度对于珊瑚细胞培养很重要,显示出培养的细胞与其细胞内藻类之间的持久共生。发现格雷斯的昆虫培养基和格雷斯的改性昆虫培养基是优良的底物。为了确认培养的细胞和珊瑚组织中细胞的相似性,使用内部转录间隔子引物进行了分子测试。由此,确认了在不同培养基中存在珊瑚细胞和虫黄藻的相似细胞。

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