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本文引用的文献

1
Mapping gene clusters within arrayed metagenomic libraries to expand the structural diversity of biomedically relevant natural products.在排列的宏基因组文库中定位基因簇,以扩展与医学相关天然产物的结构多样性。
Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11797-802. doi: 10.1073/pnas.1222159110. Epub 2013 Jul 3.
2
phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data.phyloseq:一个用于重现交互式分析和微生物组普查数据分析的图形的 R 包。
PLoS One. 2013 Apr 22;8(4):e61217. doi: 10.1371/journal.pone.0061217. Print 2013.
3
Deep sequencing of non-ribosomal peptide synthetases and polyketide synthases from the microbiomes of Australian marine sponges.从澳大利亚海洋海绵微生物组中对非核糖体肽合成酶和聚酮合酶进行深度测序。
ISME J. 2013 Sep;7(9):1842-51. doi: 10.1038/ismej.2013.65. Epub 2013 Apr 18.
4
Natural products: a continuing source of novel drug leads.天然产物:新型药物先导物的持续来源。
Biochim Biophys Acta. 2013 Jun;1830(6):3670-95. doi: 10.1016/j.bbagen.2013.02.008. Epub 2013 Feb 18.
5
Cross-biome metagenomic analyses of soil microbial communities and their functional attributes.跨生态系统土壤微生物群落及其功能特性的宏基因组分析。
Proc Natl Acad Sci U S A. 2012 Dec 26;109(52):21390-5. doi: 10.1073/pnas.1215210110. Epub 2012 Dec 10.
6
The natural product domain seeker NaPDoS: a phylogeny based bioinformatic tool to classify secondary metabolite gene diversity.天然产物领域探索者 NaPDoS:一种基于系统发育的生物信息学工具,用于分类次生代谢物基因多样性。
PLoS One. 2012;7(3):e34064. doi: 10.1371/journal.pone.0034064. Epub 2012 Mar 29.
7
Natural product biosynthetic gene diversity in geographically distinct soil microbiomes.地理上不同土壤微生物组中的天然产物生物合成基因多样性。
Appl Environ Microbiol. 2012 May;78(10):3744-52. doi: 10.1128/AEM.00102-12. Epub 2012 Mar 16.
8
Combinatorial biosynthesis of polyketides--a perspective.聚酮化合物的组合生物合成——一个展望。
Curr Opin Chem Biol. 2012 Apr;16(1-2):117-23. doi: 10.1016/j.cbpa.2012.01.018. Epub 2012 Feb 16.
9
Natural products as sources of new drugs over the 30 years from 1981 to 2010.天然产物:1981 年至 2010 年 30 年间的新药来源。
J Nat Prod. 2012 Mar 23;75(3):311-35. doi: 10.1021/np200906s. Epub 2012 Feb 8.
10
Recent application of metagenomic approaches toward the discovery of antimicrobials and other bioactive small molecules.近年来,宏基因组学方法在发现抗生素和其他生物活性小分子方面的应用。
Curr Opin Microbiol. 2010 Oct;13(5):603-9. doi: 10.1016/j.mib.2010.08.012. Epub 2010 Sep 29.

土壤次生代谢产物的化学生态地理学调查。

Chemical-biogeographic survey of secondary metabolism in soil.

机构信息

Laboratory of Genetically Encoded Small Molecules, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065.

出版信息

Proc Natl Acad Sci U S A. 2014 Mar 11;111(10):3757-62. doi: 10.1073/pnas.1318021111. Epub 2014 Feb 18.

DOI:10.1073/pnas.1318021111
PMID:24550451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3956145/
Abstract

In this study, we compare biosynthetic gene richness and diversity of 96 soil microbiomes from diverse environments found throughout the southwestern and northeastern regions of the United States. The 454-pyroseqencing of nonribosomal peptide adenylation (AD) and polyketide ketosynthase (KS) domain fragments amplified from these microbiomes provide a means to evaluate the variation of secondary metabolite biosynthetic diversity in different soil environments. Through soil composition and AD- and KS-amplicon richness analysis, we identify soil types with elevated biosynthetic potential. In general, arid soils show the richest observed biosynthetic diversity, whereas brackish sediments and pine forest soils show the least. By mapping individual environmental amplicon sequences to sequences derived from functionally characterized biosynthetic gene clusters, we identified conserved soil type-specific secondary metabolome enrichment patterns despite significant sample-to-sample sequence variation. These data are used to create chemical biogeographic distribution maps for biomedically valuable families of natural products in the environment that should prove useful for directing the discovery of bioactive natural products in the future.

摘要

在这项研究中,我们比较了美国西南部和东北部不同环境中 96 个土壤微生物组的生物合成基因丰富度和多样性。从这些微生物组中扩增的非核糖体肽腺苷酸化 (AD) 和聚酮合酶 (KS) 结构域片段的 454 焦磷酸测序为评估不同土壤环境中次生代谢物生物合成多样性的变化提供了一种手段。通过土壤成分和 AD 和 KS 扩增子丰富度分析,我们确定了具有较高生物合成潜力的土壤类型。总的来说,干旱土壤表现出最丰富的观察到的生物合成多样性,而半咸沉积物和松林土壤则表现出最少的生物合成多样性。通过将单个环境扩增子序列映射到功能表征的生物合成基因簇中获得的序列,我们确定了尽管存在显著的样本间序列变异,但仍存在保守的土壤类型特异性次生代谢物富集模式。这些数据用于创建环境中具有医学价值的天然产物生物地理分布图谱,这对于指导未来生物活性天然产物的发现应该是有用的。