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本文引用的文献

1
ARB: a software environment for sequence data.ARB:一种用于序列数据的软件环境。
Nucleic Acids Res. 2004 Feb 25;32(4):1363-71. doi: 10.1093/nar/gkh293. Print 2004.
2
The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy.核糖体数据库项目(RDP-II):预览一种允许定期更新的新型自动比对工具和新的原核生物分类法。
Nucleic Acids Res. 2003 Jan 1;31(1):442-3. doi: 10.1093/nar/gkg039.
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Is it better to add taxa or characters to a difficult phylogenetic problem?对于一个棘手的系统发育问题,增加分类单元还是特征更好呢?
Syst Biol. 1998 Mar;47(1):9-17. doi: 10.1080/106351598260996.
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Taxonomic sampling, phylogenetic accuracy, and investigator bias.分类学采样、系统发育准确性和研究者偏差。
Syst Biol. 1998 Mar;47(1):3-8. doi: 10.1080/106351598260987.
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Sensitivity of phylogeny estimation to taxonomic sampling.系统发育估计对分类群抽样的敏感性。
Syst Biol. 1998 Mar;47(1):18-31. doi: 10.1080/106351598261003.
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Bacterial diversity in human subgingival plaque.人类龈下菌斑中的细菌多样性
J Bacteriol. 2001 Jun;183(12):3770-83. doi: 10.1128/JB.183.12.3770-3783.2001.
7
A multiple-outgroup approach to resolving division-level phylogenetic relationships using 16S rDNA data.一种使用16S rDNA数据解析科级系统发育关系的多外类群方法。
Int J Syst Evol Microbiol. 2001 Mar;51(Pt 2):385-391. doi: 10.1099/00207713-51-2-385.
8
Expanding the known diversity and environmental distribution of an uncultured phylogenetic division of bacteria.扩大未培养细菌系统发育类群的已知多样性和环境分布范围。
Appl Environ Microbiol. 2000 Apr;66(4):1617-21. doi: 10.1128/AEM.66.4.1617-1621.2000.
9
Microbial diversity in a hydrocarbon- and chlorinated-solvent-contaminated aquifer undergoing intrinsic bioremediation.正在进行自然生物修复的受碳氢化合物和氯化溶剂污染的含水层中的微生物多样性。
Appl Environ Microbiol. 1998 Oct;64(10):3869-77. doi: 10.1128/AEM.64.10.3869-3877.1998.
10
Impact of culture-independent studies on the emerging phylogenetic view of bacterial diversity.非培养研究对细菌多样性新系统发育观点的影响。
J Bacteriol. 1998 Sep;180(18):4765-74. doi: 10.1128/JB.180.18.4765-4774.1998.

未培养细菌系统发育分支OP11的新视角。

New perspective on uncultured bacterial phylogenetic division OP11.

作者信息

Harris J Kirk, Kelley Scott T, Pace Norman R

机构信息

Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado 80309-0347, USA.

出版信息

Appl Environ Microbiol. 2004 Feb;70(2):845-9. doi: 10.1128/AEM.70.2.845-849.2004.

DOI:10.1128/AEM.70.2.845-849.2004
PMID:14766563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC348892/
Abstract

Organisms belonging to the OP11 candidate phylogenetic division of Bacteria have been detected only in rRNA-based sequence surveys of environmental samples. Preliminary studies indicated that such organisms represented by the sequences are abundant and widespread in nature and highly diverse phylogenetically. In order to document more thoroughly the phylogenetic breadth and environmental distribution of this diverse group of organisms, we conducted further molecular analyses on environmental DNAs. Using PCR techniques and primers directed toward each of the five described subdivisions of OP11, we surveyed 17 environmental DNAs and analyzed rRNA gene sequences in 27 clonal libraries from 14 environments. Ninety-nine new and unique sequences were determined completely, and approximately 200 additional clones were subjected to partial sequencing. Extensive phylogenetic comparisons of the new sequences to those representing other bacterial divisions further resolved the phylogeny of the bacterial candidate division OP11 and identified two new candidate bacterial divisions, OP11-derived 1 (OD1) and Sulphur River 1 (SR1). The widespread environmental distribution of representatives of the bacterial divisions OD1, OP11, and SR1 suggests potentially conspicuous biogeochemical roles for these organisms in their respective environments. The information on environmental distribution offers clues for attempts to culture landmark representatives of these novel bacterial divisions, and the sequences are specific molecular signatures that provide for their identification in other contexts.

摘要

仅在基于rRNA的环境样本序列调查中检测到属于细菌OP11候选系统发育分支的生物。初步研究表明,此类由序列代表的生物在自然界中数量丰富、分布广泛且系统发育高度多样。为了更全面地记录这一多样生物群体的系统发育广度和环境分布,我们对环境DNA进行了进一步的分子分析。使用针对OP11五个已描述亚群各自的PCR技术和引物,我们调查了17种环境DNA,并分析了来自14个环境的27个克隆文库中的rRNA基因序列。完全确定了99个新的独特序列,另外约200个克隆进行了部分测序。将新序列与代表其他细菌分支的序列进行广泛的系统发育比较,进一步解析了细菌候选分支OP11的系统发育,并确定了两个新的候选细菌分支,即OP11衍生1(OD1)和硫磺河1(SR1)。细菌分支OD1、OP11和SR1代表的广泛环境分布表明这些生物在其各自环境中可能具有显著的生物地球化学作用。关于环境分布的信息为尝试培养这些新型细菌分支的标志性代表提供了线索,并且这些序列是特定的分子特征,可用于在其他情况下对它们进行识别。