Schmidt T M, DeLong E F, Pace N R
Department of Biology, Indiana University, Bloomington 47405.
J Bacteriol. 1991 Jul;173(14):4371-8. doi: 10.1128/jb.173.14.4371-4378.1991.
The phylogenetic diversity of an oligotrophic marine picoplankton community was examined by analyzing the sequences of cloned ribosomal genes. This strategy does not rely on cultivation of the resident microorganisms. Bulk genomic DNA was isolated from picoplankton collected in the north central Pacific Ocean by tangential flow filtration. The mixed-population DNA was fragmented, size fractionated, and cloned into bacteriophage lambda. Thirty-eight clones containing 16S rRNA genes were identified in a screen of 3.2 x 10(4) recombinant phage, and portions of the rRNA gene were amplified by polymerase chain reaction and sequenced. The resulting sequences were used to establish the identities of the picoplankton by comparison with an established data base of rRNA sequences. Fifteen unique eubacterial sequences were obtained, including four from cyanobacteria and eleven from proteobacteria. A single eucaryote related to dinoflagellates was identified; no archaebacterial sequences were detected. The cyanobacterial sequences are all closely related to sequences from cultivated marine Synechococcus strains and with cyanobacterial sequences obtained from the Atlantic Ocean (Sargasso Sea). Several sequences were related to common marine isolates of the gamma subdivision of proteobacteria. In addition to sequences closely related to those of described bacteria, sequences were obtained from two phylogenetic groups of organisms that are not closely related to any known rRNA sequences from cultivated organisms. Both of these novel phylogenetic clusters are proteobacteria, one group within the alpha subdivision and the other distinct from known proteobacterial subdivisions. The rRNA sequences of the alpha-related group are nearly identical to those of some Sargasso Sea picoplankton, suggesting a global distribution of these organisms.
通过分析克隆核糖体基因的序列,研究了贫营养海洋微微型浮游生物群落的系统发育多样性。该策略不依赖于对驻留微生物的培养。通过切向流过滤从北太平洋中部采集的微微型浮游生物中分离出大量基因组DNA。混合群体的DNA被片段化、按大小分级,并克隆到噬菌体λ中。在对3.2×10⁴个重组噬菌体的筛选中,鉴定出38个含有16S rRNA基因的克隆,并通过聚合酶链反应扩增rRNA基因的部分片段并进行测序。通过与已建立的rRNA序列数据库进行比较,将所得序列用于确定微微型浮游生物的身份。获得了15个独特的真细菌序列,包括4个来自蓝细菌和11个来自变形菌。鉴定出一个与甲藻相关的单一真核生物;未检测到古细菌序列。蓝细菌序列均与培养的海洋聚球藻菌株的序列以及从大西洋(马尾藻海)获得的蓝细菌序列密切相关。几个序列与变形菌γ亚群的常见海洋分离株相关。除了与已描述细菌的序列密切相关的序列外,还从两个与培养生物的任何已知rRNA序列都不密切相关的生物系统发育组中获得了序列。这两个新的系统发育簇都是变形菌,一组在α亚群内,另一组与已知的变形菌亚群不同。与α相关组的rRNA序列与一些马尾藻海微微型浮游生物的序列几乎相同,表明这些生物具有全球分布。