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对土壤宏基因组文库中聚酮合酶I结构域进行系统发育分析有助于筛选出有前景的克隆。

Phylogenetic analysis of polyketide synthase I domains from soil metagenomic libraries allows selection of promising clones.

作者信息

Ginolhac Aurélien, Jarrin Cyrille, Gillet Benjamin, Robe Patrick, Pujic Petar, Tuphile Karine, Bertrand Hélène, Vogel Timothy M, Perrière Guy, Simonet Pascal, Nalin Renaud

机构信息

LibraGen S.A., BAtiment Canal Biotech 1, 3 rue des Satellites, 31400 Toulouse, France.

出版信息

Appl Environ Microbiol. 2004 Sep;70(9):5522-7. doi: 10.1128/AEM.70.9.5522-5527.2004.

DOI:10.1128/AEM.70.9.5522-5527.2004
PMID:15345440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC520897/
Abstract

The metagenomic approach provides direct access to diverse unexplored genomes, especially from uncultivated bacteria in a given environment. This diversity can conceal many new biosynthetic pathways. Type I polyketide synthases (PKSI) are modular enzymes involved in the biosynthesis of many natural products of industrial interest. Among the PKSI domains, the ketosynthase domain (KS) was used to screen a large soil metagenomic library containing more than 100,000 clones to detect those containing PKS genes. Over 60,000 clones were screened, and 139 clones containing KS domains were detected. A 700-bp fragment of the KS domain was sequenced for 40 of 139 randomly chosen clones. None of the 40 protein sequences were identical to those found in public databases, and nucleic sequences were not redundant. Phylogenetic analyses were performed on the protein sequences of three metagenomic clones to select the clones which one can predict to produce new compounds. Two PKS-positive clones do not belong to any of the 23 published PKSI included in the analysis, encouraging further analyses on these two clones identified by the selection process.

摘要

宏基因组学方法可直接获取各种未被探索的基因组,尤其是来自特定环境中未培养细菌的基因组。这种多样性可能隐藏着许多新的生物合成途径。I型聚酮合酶(PKSI)是参与许多具有工业价值天然产物生物合成的模块化酶。在PKSI结构域中,酮合成酶结构域(KS)被用于筛选一个包含超过10万个克隆的大型土壤宏基因组文库,以检测那些含有PKS基因的克隆。筛选了超过6万个克隆,检测到139个含有KS结构域的克隆。对139个随机选择的克隆中的40个克隆的KS结构域的700 bp片段进行了测序。40个蛋白质序列中没有一个与公共数据库中发现的序列相同,并且核酸序列也不冗余。对三个宏基因组克隆的蛋白质序列进行了系统发育分析,以选择那些可以预测会产生新化合物的克隆。两个PKS阳性克隆不属于分析中包含的23个已发表的PKSI中的任何一个,这促使对通过选择过程鉴定出的这两个克隆进行进一步分析。

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本文引用的文献

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