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本文引用的文献

1
Development and quantitative analyses of a universal rRNA-subtraction protocol for microbial metatranscriptomics.开发并定量分析用于微生物宏转录组学的通用 rRNA 消减方案。
ISME J. 2010 Jul;4(7):896-907. doi: 10.1038/ismej.2010.18. Epub 2010 Mar 11.
2
Aerobic and anaerobic ammonia oxidizing bacteria--competitors or natural partners?好氧和厌氧氨氧化细菌——竞争者还是天然伙伴?
FEMS Microbiol Ecol. 2002 Mar 1;39(3):175-81. doi: 10.1111/j.1574-6941.2002.tb00920.x.
3
N2O emission hotspots at different spatial scales and governing factors for small scale hotspots.不同空间尺度下的一氧化二氮排放热点及小尺度热点的控制因素。
Sci Total Environ. 2009 Mar 15;407(7):2325-32. doi: 10.1016/j.scitotenv.2008.11.010. Epub 2008 Dec 13.
4
Detection of large numbers of novel sequences in the metatranscriptomes of complex marine microbial communities.在复杂海洋微生物群落的宏转录组中检测到大量新序列。
PLoS One. 2008 Aug 22;3(8):e3042. doi: 10.1371/journal.pone.0003042.
5
Isolation and analysis of mRNA from environmental microbial communities.从环境微生物群落中分离和分析信使核糖核酸
J Microbiol Methods. 2008 Oct;75(2):172-6. doi: 10.1016/j.mimet.2008.05.019. Epub 2008 Jun 25.
6
Simultaneous assessment of soil microbial community structure and function through analysis of the meta-transcriptome.通过宏转录组分析同时评估土壤微生物群落结构和功能。
PLoS One. 2008 Jun 25;3(6):e2527. doi: 10.1371/journal.pone.0002527.
7
Distantly sampled soils carry few species in common.远距离采集的土壤样本中,共有物种很少。
ISME J. 2008 Sep;2(9):901-10. doi: 10.1038/ismej.2008.55. Epub 2008 Jun 5.
8
Temporal transcriptomic microarray analysis of "Dehalococcoides ethenogenes" strain 195 during the transition into stationary phase.“嗜盐脱卤球菌”菌株195进入稳定期转变过程中的时间转录组微阵列分析。
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9
Development and application of a PCR-denaturing gradient gel electrophoresis tool to study the diversity of Nitrobacter-like nxrA sequences in soil.用于研究土壤中类硝化杆菌nxrA序列多样性的PCR-变性梯度凝胶电泳工具的开发与应用
FEMS Microbiol Ecol. 2008 Feb;63(2):261-71. doi: 10.1111/j.1574-6941.2007.00416.x.
10
Changes in bacterial and archaeal community structure and functional diversity along a geochemically variable soil profile.沿地球化学性质多变的土壤剖面细菌和古菌群落结构及功能多样性的变化
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开发用于土壤微生物群落的环境功能基因微阵列。

Development of an environmental functional gene microarray for soil microbial communities.

机构信息

School of Biological Sciences, University of Queensland, St. Lucia, Queensland 4072, Australia.

出版信息

Appl Environ Microbiol. 2010 Nov;76(21):7161-70. doi: 10.1128/AEM.03108-09. Epub 2010 Sep 17.

DOI:10.1128/AEM.03108-09
PMID:20851978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976231/
Abstract

Functional attributes of microbial communities are difficult to study, and most current techniques rely on DNA- and rRNA-based profiling of taxa and genes, including microarrays containing sequences of known microorganisms. To quantify gene expression in environmental samples in a culture-independent manner, we constructed an environmental functional gene microarray (E-FGA) consisting of 13,056 mRNA-enriched anonymous microbial clones from diverse microbial communities to profile microbial gene transcripts. A new normalization method using internal spot standards was devised to overcome spotting and hybridization bias, enabling direct comparisons of microarrays. To evaluate potential applications of this metatranscriptomic approach for studying microbes in environmental samples, we tested the E-FGA by profiling the microbial activity of agricultural soils with a low or high flux of N₂O. A total of 109 genes displayed expression that differed significantly between soils with low and high N₂O emissions. We conclude that mRNA-based approaches such as the one presented here may complement existing techniques for assessing functional attributes of microbial communities.

摘要

微生物群落的功能属性很难研究,目前大多数技术都依赖于基于 DNA 和 rRNA 的分类群和基因分析,包括包含已知微生物序列的微阵列。为了在非培养的方式下定量环境样本中的基因表达,我们构建了一个由来自不同微生物群落的 13056 个富含 mRNA 的匿名微生物克隆组成的环境功能基因微阵列(E-FGA),以分析微生物基因转录本。我们设计了一种新的使用内部点标准的归一化方法,以克服点样和杂交偏倚,从而能够直接比较微阵列。为了评估这种宏转录组学方法在研究环境样品中微生物的潜在应用,我们通过对 N₂O 通量低或高的农业土壤中的微生物活性进行分析,测试了 E-FGA。共有 109 个基因的表达在低 N₂O 排放和高 N₂O 排放土壤之间存在显著差异。我们得出结论,基于 mRNA 的方法,如本文所述的方法,可能会补充现有的评估微生物群落功能属性的技术。