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本文引用的文献

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Growth of prochlorococcus, a photosynthetic prokaryote, in the equatorial pacific ocean.海洋中聚球藻(一种光合原核生物)的生长。
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Enumeration and Cell Cycle Analysis of Natural Populations of Marine Picoplankton by Flow Cytometry Using the Nucleic Acid Stain SYBR Green I.利用核酸染料 SYBR Green I 通过流式细胞术对海洋微微型浮游植物自然种群进行计数和细胞周期分析。
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Effects of flow cytometric analysis and cell sorting on photosynthetic carbon uptake by phytoplankton in cultures and from natural populations.流式细胞分析和细胞分选对培养和自然种群浮游植物光合碳吸收的影响。
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Linking the composition of bacterioplankton to rapid turnover of dissolved dimethylsulphoniopropionate in an algal bloom in the North Sea.将北海一次藻华期间浮游细菌的组成与溶解态二甲基磺基丙酸内盐的快速周转联系起来。
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Does the high nucleic acid content of individual bacterial cells allow us to discriminate between active cells and inactive cells in aquatic systems?单个细菌细胞的高核酸含量能否让我们区分水生系统中的活性细胞和非活性细胞?
Appl Environ Microbiol. 2001 Apr;67(4):1775-82. doi: 10.1128/AEM.67.4.1775-1782.2001.
7
Changes in community composition during dilution cultures of marine bacterioplankton as assessed by flow cytometric and molecular biological techniques.通过流式细胞术和分子生物学技术评估海洋浮游细菌稀释培养过程中群落组成的变化。
Environ Microbiol. 2000 Apr;2(2):191-201. doi: 10.1046/j.1462-2920.2000.00092.x.
8
Community composition of marine bacterioplankton determined by 16S rRNA gene clone libraries and fluorescence in situ hybridization.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
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9
Relationships among Bacterial Cell Size, Productivity, and Genetic Diversity in Aquatic Environments using Cell Sorting and Flow Cytometry.利用细胞分选和流式细胞术研究水生环境中细菌细胞大小、生产力和遗传多样性之间的关系。
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10
Unlabeled helper oligonucleotides increase the in situ accessibility to 16S rRNA of fluorescently labeled oligonucleotide probes.未标记的辅助寡核苷酸增加了荧光标记寡核苷酸探针与16S rRNA的原位可及性。
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凯尔特海分层水域中优势浮游细菌类群的细胞和生物量比活性比较。

Comparison of cellular and biomass specific activities of dominant bacterioplankton groups in stratified waters of the Celtic Sea.

作者信息

Zubkov M V, Fuchs B M, Burkill P H, Amann R

机构信息

Plymouth Marine Laboratory, Plymouth PL1 3DH, United Kingdom.

出版信息

Appl Environ Microbiol. 2001 Nov;67(11):5210-8. doi: 10.1128/AEM.67.11.5210-5218.2001.

DOI:10.1128/AEM.67.11.5210-5218.2001
PMID:11679347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC93292/
Abstract

A flow-sorting technique was developed to determine unperturbed metabolic activities of phylogenetically characterized bacterioplankton groups with incorporation rates of [(35)S]methionine tracer. According to fluorescence in situ hybridization with rRNA targeted oligonucleotide probes, a clade of alpha-proteobacteria, related to Roseobacter spp., and a Cytophaga-Flavobacterium cluster dominated the different groups. Cytometric characterization revealed both these groups to have high DNA (HNA) content, while the alpha-proteobacteria exhibited high light scatter (hs) and the Cytophaga-Flavobacterium cluster exhibited low light scatter (ls). A third abundant group with low DNA (LNA) content contained cells from a SAR86 cluster of gamma-proteobacteria. Cellular specific activities of the HNA-hs group were 4- and 1.7-fold higher than the activities in the HNA-ls and LNA groups, respectively. However, the higher cellular protein synthesis by the HNA-hs could simply be explained by their maintenance of a larger cellular protein biomass. Similar biomass specific activities of the different groups strongly support the main assumption that underlies the determination of bacterial production: different bacteria in a complex community incorporate amino acids at a rate proportional to their protein synthesis. The fact that the highest growth-specific rates were determined for the smallest cells of the LNA group can explain the dominance of this group in nutrient-limited waters. The metabolic activities of the three groups accounted for almost the total bacterioplankton activity, indicating their key biogeochemical role in the planktonic ecosystem of the Celtic Sea.

摘要

开发了一种流式细胞分选技术,以通过[(35)S]蛋氨酸示踪剂的掺入率来确定系统发育特征明确的浮游细菌群体的未受干扰的代谢活性。根据与rRNA靶向寡核苷酸探针的荧光原位杂交,与玫瑰杆菌属相关的α-变形杆菌分支和噬纤维菌-黄杆菌簇在不同群体中占主导地位。细胞计数表征显示这两个群体都具有高DNA(HNA)含量,而α-变形杆菌表现出高散射光(hs),噬纤维菌-黄杆菌簇表现出低散射光(ls)。第三个丰富的低DNA(LNA)含量群体包含来自γ-变形杆菌SAR86簇的细胞。HNA-hs组的细胞比活性分别比HNA-ls组和LNA组高4倍和1.7倍。然而,HNA-hs组较高的细胞蛋白质合成可能仅仅是因为它们维持了更大的细胞蛋白质生物量。不同群体相似的生物量比活性有力地支持了细菌生产测定所基于的主要假设:复杂群落中的不同细菌以与其蛋白质合成成比例的速率掺入氨基酸。LNA组最小细胞的生长比速率最高这一事实可以解释该群体在营养受限水域中的优势地位。这三个群体的代谢活性几乎占了浮游细菌总活性的全部,表明它们在凯尔特海浮游生态系统中的关键生物地球化学作用。