Simon N, Campbell L, Ornolfsdottir E, Groben R, Guillou L, Lange M, Medlin L K
Department of Oceanography, Texas A&M University, College Station 77843-3146, USA.
J Eukaryot Microbiol. 2000 Jan-Feb;47(1):76-84. doi: 10.1111/j.1550-7408.2000.tb00014.x.
Photosynthetic pico- and nanoplankton dominate phytoplankton biomass and primary production in the oligotrophic open ocean. Species composition, community structure, and dynamics of the eukaryotic components of these size classes are poorly known primarily because of the difficulties associated with their preservation and identification. Molecular techniques utilizing 18S rRNA sequences offer a number of new and rapid means of identifying the picoplankton. From the available 18S rRNA sequence data for the algae, we designed new group-specific oligonucleotide probes for the division Chlorophyta, the division Haptophyta, and the class Pelagophyceae (division Heterokonta). Dot blot hybridization with polymerase chain reaction amplified target rDNA and whole-cell hybridization assays with fluorescence microscopy and flow cytometry were used to demonstrate probe specificity. Hybridization results with representatives from seven algal classes supported the phylogenetic affinities of the cells. Such group- or taxon-specific probes will be useful in examining community structure, for identifying new algal isolates, and for in situ detection of these three groups, which are thought to be the dominant algal taxa in the oligotrophic regions of the ocean.
光合微微型和微型浮游生物在贫营养开阔海洋中主导着浮游植物生物量和初级生产力。这些大小类别的真核生物成分的物种组成、群落结构和动态鲜为人知,主要是因为与其保存和鉴定相关的困难。利用18S rRNA序列的分子技术提供了许多鉴定微微型浮游生物的新的快速方法。根据藻类现有的18S rRNA序列数据,我们为绿藻门、定鞭藻门和褐藻纲(不等鞭毛藻门)设计了新的组特异性寡核苷酸探针。用聚合酶链反应扩增的目标rDNA进行斑点印迹杂交,并用荧光显微镜和流式细胞术进行全细胞杂交试验,以证明探针的特异性。与七个藻类类别的代表进行杂交的结果支持了细胞的系统发育亲缘关系。这种组特异性或分类群特异性探针将有助于研究群落结构、鉴定新的藻类分离物以及对这三个类群进行原位检测,这三个类群被认为是海洋贫营养区域的主要藻类分类群。