Lim E L
Biology Department, Woods Hole Oceanographic Institution, Massachusetts 02543, USA.
J Eukaryot Microbiol. 1996 Mar-Apr;43(2):101-6. doi: 10.1111/j.1550-7408.1996.tb04488.x.
Nanoplanktonic protists are comprised of a diverse assemblage of species which are responsible for a variety of trophic processes in marine and freshwater ecosystems. Current methods for identifying small protists by electron microscopy do not readily permit both identification and enumeration of nanoplanktonic protists in field samples. Thus, one major goal in the application of molecular approaches in protistan ecology has been the detection and quantification of individual species in natural water samples. Sequences of small subunit ribosomal RNA (SSU rRNA) genes have proven to be useful towards achieving this goal. Comparison of sequences from clone libraries of protistan SSU rRNA genes amplified from natural assemblages of protists by the polymerase chain reaction (PCR) can be used to examine protistan diversity. Furthermore, oligonucleotide probes complementary to short sequence regions unique to species of small protists can be designed by comparative analysis of rRNA gene sequences. These probes may be used to either detect the RNA of particular species of protists in total nucleic acid extracts immobilized on membranes, or the presence of target species in water samples via in situ hybridization of whole cells. Oligonucleotide probes may also serve as primers for the selective amplification of target sequences from total population DNA by PCR. Thus, molecular sequence information is becoming increasingly useful for identifying and enumerating protists, and for studying their spatial and temporal distribution in nature. Knowledge of protistan species composition, abundance and variability in an environment can ultimately be used to relate community structure to various aspects of community function and biogeochemical activity.
微型浮游生物由多种不同的物种组成,它们在海洋和淡水生态系统中负责各种营养过程。目前通过电子显微镜鉴定小型原生生物的方法,不容易同时对野外样本中的微型浮游生物进行鉴定和计数。因此,在原生生物生态学中应用分子方法的一个主要目标,是检测和定量天然水样中的单个物种。小亚基核糖体RNA(SSU rRNA)基因序列已被证明有助于实现这一目标。通过聚合酶链反应(PCR)从原生生物的自然群落中扩增出的原生生物SSU rRNA基因克隆文库中的序列比较,可用于研究原生生物的多样性。此外,通过对rRNA基因序列的比较分析,可以设计与小型原生生物物种特有的短序列区域互补的寡核苷酸探针。这些探针可用于检测固定在膜上的总核酸提取物中特定原生生物物种的RNA,或通过全细胞原位杂交检测水样中目标物种的存在。寡核苷酸探针也可作为引物,通过PCR从总群体DNA中选择性扩增目标序列。因此,分子序列信息在识别和计数原生生物以及研究它们在自然界中的空间和时间分布方面变得越来越有用。了解环境中原生生物的物种组成、丰度和变异性,最终可用于将群落结构与群落功能和生物地球化学活动的各个方面联系起来。