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本文引用的文献

1
Determination of Active Marine Bacterioplankton: a Comparison of Universal 16S rRNA Probes, Autoradiography, and Nucleoid Staining.海洋活性细菌的测定:通用 16S rRNA 探针、放射自显影和核染色的比较。
Appl Environ Microbiol. 1997 Apr;63(4):1208-13. doi: 10.1128/aem.63.4.1208-1213.1997.
2
Molecular Identification and Localization of Filamentous Symbiotic Bacteria Associated with the Hydrothermal Vent Annelid Alvinella pompejana.与热液喷口环节动物 Alvinella pompejana 相关的丝状共生菌的分子鉴定与定位。
Appl Environ Microbiol. 1997 Mar;63(3):1124-30. doi: 10.1128/aem.63.3.1124-1130.1997.
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Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization.利用原位杂交技术对高山湖泊冬季覆盖层和水层细菌组合进行群落分析。
Appl Environ Microbiol. 1996 Jun;62(6):2138-44. doi: 10.1128/aem.62.6.2138-2144.1996.
4
Culturability and In situ abundance of pelagic bacteria from the North Sea.北海浮游细菌的可培养性及原位丰度
Appl Environ Microbiol. 2000 Jul;66(7):3044-51. doi: 10.1128/AEM.66.7.3044-3051.2000.
5
Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter.消耗低分子量和高分子量溶解有机物的海洋变形菌和噬纤维菌-黄杆菌簇成员的自然组合。
Appl Environ Microbiol. 2000 Apr;66(4):1692-7. doi: 10.1128/AEM.66.4.1692-1697.2000.
6
Identification of polyphosphate-accumulating organisms and design of 16S rRNA-directed probes for their detection and quantitation.聚磷菌的鉴定以及用于其检测和定量的16S rRNA导向探针的设计。
Appl Environ Microbiol. 2000 Mar;66(3):1175-82. doi: 10.1128/AEM.66.3.1175-1182.2000.
7
Molecular characterization of a toluene-degrading methanogenic consortium.一个降解甲苯的产甲烷菌群的分子特征分析
Appl Environ Microbiol. 1999 Dec;65(12):5576-85. doi: 10.1128/AEM.65.12.5576-5585.1999.
8
Visualization and enumeration of marine planktonic archaea and bacteria by using polyribonucleotide probes and fluorescent in situ hybridization.利用多聚核糖核苷酸探针和荧光原位杂交技术对海洋浮游古菌和细菌进行可视化和计数
Appl Environ Microbiol. 1999 Dec;65(12):5554-63. doi: 10.1128/AEM.65.12.5554-5563.1999.
9
Structure and function of the methanogenic archaeal community in stable cellulose-degrading enrichment cultures at two different temperatures (15 and 30 degrees C).两种不同温度(15摄氏度和30摄氏度)下稳定的纤维素降解富集培养物中产甲烷古菌群落的结构与功能
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10
Small ribosomal RNA content in marine Proteobacteria during non-steady-state growth.非稳态生长期间海洋变形菌纲细菌中的小核糖体RNA含量
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通过16S rRNA基因克隆文库和荧光原位杂交确定的海洋浮游细菌群落组成

Community composition of marine bacterioplankton determined by 16S rRNA gene clone libraries and fluorescence in situ hybridization.

作者信息

Cottrell M T, Kirchman D L

机构信息

College of Marine Studies, University of Delaware, Lewes, Delaware 19958, USA.

出版信息

Appl Environ Microbiol. 2000 Dec;66(12):5116-22. doi: 10.1128/AEM.66.12.5116-5122.2000.

DOI:10.1128/AEM.66.12.5116-5122.2000
PMID:11097877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC92431/
Abstract

We determined the compositions of bacterioplankton communities in surface waters of coastal California using clone libraries of 16S rRNA genes and fluorescence in situ hybridization (FISH) in order to compare the community structures inferred from these two culture-independent approaches. The compositions of two clone libraries were quite similar to those of clone libraries of marine bacterioplankton examined by previous studies. Clones from gamma-proteobacteria comprised ca. 28% of the libraries, while approximately 55% of the clones came from alpha-proteobacteria, which dominated the clone libraries. The Cytophaga-Flavobacter group and three others each comprised 10% or fewer of the clone libraries. The community composition determined by FISH differed substantially from the composition implied by the clone libraries. The Cytophaga-Flavobacter group dominated 8 of the 11 communities assayed by FISH, including the two communities assayed using clone libraries. On average only 10% of DAPI (4', 6'-diamidino-2-phenylindole)-stained bacteria were detected by FISH with a probe for alpha-proteobacteria, but 30% of DAPI-stained bacteria appeared to be in the Cytophaga-Flavobacter group as determined by FISH. alpha-Proteobacteria were greatly overrepresented in clone libraries compared to their relative abundance determined by FISH, while the Cytophaga-Flavobacter group was underrepresented in clone libraries. Our data show that the Cytophaga-Flavobacter group can be a numerically dominant component of coastal marine bacterioplankton communities.

摘要

我们利用16S rRNA基因克隆文库和荧光原位杂交(FISH)技术,确定了加利福尼亚沿海表层水体中浮游细菌群落的组成,以便比较从这两种非培养方法推断出的群落结构。两个克隆文库的组成与先前研究中检测的海洋浮游细菌克隆文库的组成非常相似。来自γ-变形菌纲的克隆约占文库的28%,而约55%的克隆来自α-变形菌纲,后者在克隆文库中占主导地位。噬纤维菌-黄杆菌类群和其他三个类群在克隆文库中各自所占比例均不超过10%。通过FISH确定的群落组成与克隆文库所暗示的组成有很大差异。在通过FISH检测的11个群落中,噬纤维菌-黄杆菌类群在8个群落中占主导地位,包括使用克隆文库检测的两个群落。平均而言,用α-变形菌纲的探针通过FISH检测到的仅占DAPI(4′,6′-二脒基-2-苯基吲哚)染色细菌的10%,但通过FISH确定,30%的DAPI染色细菌似乎属于噬纤维菌-黄杆菌类群。与通过FISH确定的相对丰度相比,α-变形菌纲在克隆文库中被大大高估,而噬纤维菌-黄杆菌类群在克隆文库中则被低估。我们的数据表明,噬纤维菌-黄杆菌类群可能是沿海海洋浮游细菌群落中数量上占主导的组成部分。