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未培养原核生物的特征分析:从浮游海洋古菌中分离并分析一个40千碱基对的基因组片段

Characterization of uncultivated prokaryotes: isolation and analysis of a 40-kilobase-pair genome fragment from a planktonic marine archaeon.

作者信息

Stein J L, Marsh T L, Wu K Y, Shizuya H, DeLong E F

机构信息

Recombinant BioCatalysis, Inc., La Jolla, California 92037, USA.

出版信息

J Bacteriol. 1996 Feb;178(3):591-9. doi: 10.1128/jb.178.3.591-599.1996.

Abstract

One potential approach for characterizing uncultivated prokaryotes from natural assemblages involves genomic analysis of DNA fragments retrieved directly from naturally occurring microbial biomass. In this study, we sought to isolate large genomic fragments from a widely distributed and relatively abundant but as yet uncultivated group of prokaryotes, the planktonic marine Archaea. A fosmid DNA library was prepared from a marine picoplankton assemblage collected at a depth of 200 m in the eastern North Pacific. We identified a 38.5-kbp recombinant fosmid clone which contained an archaeal small subunit ribosomal DNA gene. Phylogenetic analyses of the small subunit rRNA sequence demonstrated it close relationship to that of previously described planktonic archaea, which form a coherent group rooted deeply within the Crenarchaeota branch of the domain Archaea. Random shotgun sequencing of subcloned fragments of the archaeal fosmid clone revealed several genes which bore highest similarity to archaeal homologs, including large subunit ribosomal DNA and translation elongation factor 2 (EF2). Analyses of the inferred amino acid sequence of archaeoplankton EF2 supported its affiliation with the Crenarchaeote subdivision of Archaea. Two gene fragments encoding proteins not previously found in Archaea were also identified: RNA helicase, responsible for the ATP-dependent alteration of RNA secondary structure, and glutamate semialdehyde aminotransferase, an enzyme involved in initial steps of heme biosynthesis. In total, our results indicate that genomic analysis of large DNA fragments retrieved from mixed microbial assemblages can provide useful perspective on the physiological potential of abundant but as yet uncultivated prokaryotes.

摘要

一种用于表征自然群落中未培养原核生物的潜在方法是对直接从天然存在的微生物生物质中获取的DNA片段进行基因组分析。在本研究中,我们试图从一组分布广泛、相对丰富但尚未培养的原核生物——浮游海洋古菌中分离出大的基因组片段。从北太平洋东部200米深处采集的海洋微微型浮游生物群落制备了一个fosmid DNA文库。我们鉴定出一个38.5千碱基对的重组fosmid克隆,它包含一个古菌小亚基核糖体DNA基因。对小亚基rRNA序列的系统发育分析表明,它与先前描述的浮游古菌密切相关,这些浮游古菌形成了一个紧密的群体,深深地扎根于古菌域的泉古菌分支内。对古菌fosmid克隆的亚克隆片段进行随机鸟枪法测序,发现了几个与古菌同源物相似度最高的基因,包括大亚基核糖体DNA和翻译延伸因子2(EF2)。对推断的古菌浮游生物EF2氨基酸序列的分析支持了它与古菌泉古菌亚群的归属关系。还鉴定出两个以前在古菌中未发现的编码蛋白质的基因片段:负责ATP依赖的RNA二级结构改变的RNA解旋酶,以及参与血红素生物合成初始步骤的谷氨酸半醛转氨酶。总的来说,我们的结果表明,从混合微生物群落中获取的大DNA片段的基因组分析可以为丰富但尚未培养的原核生物的生理潜力提供有用的视角。

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