Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Mar Biotechnol (NY). 2011 Jun;13(3):423-32. doi: 10.1007/s10126-010-9313-z. Epub 2010 Aug 11.
We describe here a method for the micropropagation of coral that creates progeny from tissue explants derived from a single polyp or colonial corals. Coral tissue explants of various sizes (0.5-2.5 mm in diameter) were manually microdissected from the solitary coral Fungia granulosa. Explants could be maintained in an undeveloped state or induced to develop into polyps by manipulating environmental parameters such as light and temperature regimes, as well as substrate type. Fully developed polyps were able to be maintained for a long-term in a closed sea water system. Further, we demonstrate that mature explants are also amenable to this technique with the micropropagation of second-generation explants and their development into mature polyps. We thereby experimentally have established coral clonal lines that maintain their ability to differentiate without the need for chemical induction or genetic manipulation. The versatility of this method is also demonstrated through its application to two other coral species, the colonial corals Oculina patigonica and Favia favus.
我们在这里描述了一种珊瑚的微繁殖方法,该方法可以从单个珊瑚虫或群体珊瑚虫的组织外植体中产生后代。我们从孤立的珊瑚 Fungia granulosa 中手动分离出各种大小(直径 0.5-2.5 毫米)的珊瑚组织外植体。通过操纵光照和温度条件以及基质类型等环境参数,可以使外植体保持未发育状态或诱导其发育成珊瑚虫。完全发育的珊瑚虫可以在封闭的海水系统中长期维持。此外,我们还证明成熟的外植体也可以通过第二代外植体的微繁殖及其发育成成熟的珊瑚虫来进行该技术。因此,我们通过实验建立了珊瑚无性系,这些无性系无需化学诱导或遗传操作即可保持分化能力。该方法的多功能性还通过其在两种其他珊瑚物种(群体珊瑚 Oculina patigonica 和 Favia favus)中的应用得到了证明。