Buckley DH, Graber JR, Schmidt TM
Department of Microbiology and Center for Microbial Ecology, Michigan State University, East Lansing, Michigan 48824, USA.
Appl Environ Microbiol. 1998 Nov;64(11):4333-9. doi: 10.1128/AEM.64.11.4333-4339.1998.
Within the last several years, molecular techniques have uncovered numerous 16S rRNA gene (rDNA) sequences which represent a unique and globally distributed lineage of the kingdom Crenarchaeota that is phylogenetically distinct from currently characterized crenarchaeotal species. rDNA sequences of members of this novel crenarchaeotal group have been recovered from low- to moderate-temperature environments (-1.5 to 32 degreesC), in contrast to the high-temperature environments (temperature, >80 degreesC) required for growth of the currently recognized crenarchaeotal species. We determined the diversity and abundance of the nonthermophilic members of the Crenarchaeota in soil samples taken from cultivated and uncultivated fields located at the Kellogg Biological Station's Long-Term Ecological Research site (Hickory Corners, Mich.). Clones were generated from 16S rDNA that was amplified by using broad-specificity archaeal PCR primers. Twelve crenarchaeotal sequences were identified, and the phylogenetic relationships between these sequences and previously described crenarchaeotal 16S rDNA sequences were determined. Phylogenetic analyses included nonthermophilic crenarchaeotal sequences found in public databases and revealed that the nonthermophilic Crenarchaeota group is composed of at least four distinct phylogenetic clusters. A 16S rRNA-targeted oligonucleotide probe specific for all known nonthermophilic crenarchaeotal sequences was designed and used to determine their abundance in soil samples. The nonthermophilic Crenarchaeota accounted for as much as 1.42% +/- 0.42% of the 16S rRNA in the soils analyzed.
在过去几年中,分子技术发现了众多16S rRNA基因(rDNA)序列,这些序列代表了泉古菌门中一个独特的、全球分布的谱系,在系统发育上与目前已鉴定特征的泉古菌物种不同。与目前公认的泉古菌物种生长所需的高温环境(温度>80℃)形成对比的是,这个新型泉古菌群体成员的rDNA序列已从低温至中温环境(-1.5至32℃)中获得。我们测定了从位于凯洛格生物站长期生态研究站点(密歇根州希科里角)的耕地和未耕地采集的土壤样本中,非嗜热泉古菌的多样性和丰度。通过使用具有广泛特异性的古菌PCR引物扩增16S rDNA来生成克隆。鉴定出12个泉古菌序列,并确定了这些序列与先前描述的泉古菌16S rDNA序列之间的系统发育关系。系统发育分析包括在公共数据库中发现的非嗜热泉古菌序列,结果表明非嗜热泉古菌群体至少由四个不同的系统发育簇组成。设计了一种针对所有已知非嗜热泉古菌序列的16S rRNA靶向寡核苷酸探针,并用于测定它们在土壤样本中的丰度。在所分析的土壤中,非嗜热泉古菌占16S rRNA的比例高达1.42%±0.42%。