Palenik B
Marine Biology Research Division, Scripps Institution of Oceanography, University of California, San Diego, La Jolla 92093-0202.
Appl Environ Microbiol. 1994 Sep;60(9):3212-9. doi: 10.1128/aem.60.9.3212-3219.1994.
PCR was used to amplify DNA-dependent RNA polymerase gene sequences specifically from the cyanobacterial population in a seawater sample from the Sargasso Sea. Sequencing and analysis of the cloned fragments suggest that the population in the sample consisted of two distinct clusters of Prochlorococcus-like cyanobacteria and four clusters of Synechococcus-like cyanobacteria. The diversity within these clusters was significantly different, however. Clones within each Synechococcus-like cluster were 99 to 100% identical, while each Prochlorococcus-like cluster was only 91% identical at the nucleotide level. One Prochlorococcus-like cluster was significantly more closely related to a Mediterranean Sea (surface) Prochlorococcus isolate than to the other cluster, showing the highly divergent nature of this group even in one sample. The approach described here can be used as a general method for examining cyanobacterial diversity, while an oligotrophic ocean ecosystem such as the Sargasso Sea may be an ideal model for examining diversity in relation to environmental parameters.
采用聚合酶链反应(PCR)从马尾藻海海水样本中的蓝藻菌群中特异性扩增出依赖DNA的RNA聚合酶基因序列。对克隆片段的测序和分析表明,样本中的菌群由两类不同的类原绿球藻蓝藻菌群和四类类聚球藻蓝藻菌群组成。然而,这些菌群内部的多样性存在显著差异。每个类聚球藻菌群内的克隆在核苷酸水平上的相似度为99%至100%,而每个类原绿球藻菌群仅为91%。一个类原绿球藻菌群与一株地中海(表层)原绿球藻分离株的亲缘关系明显比与另一类原绿球藻菌群更近,这表明即使在一个样本中,该菌群也具有高度的分化特性。这里描述的方法可作为检测蓝藻多样性的通用方法,而像马尾藻海这样的贫营养海洋生态系统可能是研究与环境参数相关的多样性的理想模型。