Quaiser Achim, Ochsenreiter Torsten, Klenk Hans-Peter, Kletzin Arnulf, Treusch Alexander H, Meurer Guido, Eck Jürgen, Sensen Christoph W, Schleper Christa
Institute of Microbiology and Genetics, Darmstadt University of Technology, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.
Environ Microbiol. 2002 Oct;4(10):603-11. doi: 10.1046/j.1462-2920.2002.00345.x.
Molecular phylogenetic surveys based on the characterization of 16S rRNA genes have revealed that soil is an environment particularly rich in microbial diversity. A clade of crenarchaeota (archaea) has frequently been detected among many other novel lineages of uncultivated bacteria. In this study we have initiated a genomic approach for the characterization of uncultivated microorganisms from soil. We have developed a procedure based on a two-phase electrophoresis technique that allows the fast and reliable purification of concentrated and clonable, high molecular weight DNA. From this DNA we have constructed complex large-insert genomic libraries. Using archaea-specific 16S rRNA probes we have isolated a 34 kbp fragment from a 900 Mbp fosmid library of soil DNA. The clone contained a complete 16S/23S rRNA operon and 17 genes encoding putative proteins. Phylogenetic analyses of the rRNA genes and of several protein encoding genes (e.g. DNA polymerase, FixAB, glycosyl transferase) confirmed the specific affiliation of the genomic fragment with the non-thermophilic clade of the crenarchaeota. Content and structure of the genomic fragment indicated that the archaea from soil differ significantly from their previously studied uncultivated marine relatives. The protein encoding genes gave the first insights into the physiological potential of these organisms and can serve as a basis for future genomic and functional genomic studies.
基于16S rRNA基因特征的分子系统发育调查表明,土壤是一个微生物多样性特别丰富的环境。在许多未培养细菌的新谱系中,经常检测到泉古菌门(古菌)的一个进化枝。在本研究中,我们启动了一种基因组方法来表征土壤中未培养的微生物。我们开发了一种基于两相电泳技术的程序,该程序能够快速、可靠地纯化浓缩且可克隆的高分子量DNA。利用这种DNA,我们构建了复杂的大插入片段基因组文库。使用古菌特异性16S rRNA探针,我们从土壤DNA的900 Mbp fosmid文库中分离出一个34 kbp的片段。该克隆包含一个完整的16S/23S rRNA操纵子和17个编码假定蛋白质的基因。对rRNA基因和几个编码蛋白质的基因(如DNA聚合酶、FixAB、糖基转移酶)的系统发育分析证实了该基因组片段与泉古菌门非嗜热进化枝的特定亲缘关系。基因组片段的内容和结构表明,土壤中的古菌与其先前研究的未培养海洋亲缘种有显著差异。编码蛋白质的基因首次揭示了这些生物的生理潜能,并可为未来的基因组和功能基因组研究提供基础。