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Molecular Analysis of the Nitrate-Reducing Community from Unplanted and Maize-Planted Soils

机译:未种植和玉米种植土壤中硝酸盐还原群落的分子分析

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摘要

Microorganisms that use nitrate as an alternative terminal electron acceptor play an important role in the global nitrogen cycle. The diversity of the nitrate-reducing community in soil and the influence of the maize roots on the structure of this community were studied. The narG gene encoding the membrane bound nitrate reductase was selected as a functional marker for the nitrate-reducing community. The use of narG is of special interest because the phylogeny of the narG gene closely reflects the 16S ribosomal DNA phylogeny. Therefore, targeting the narG gene provided for the first time a unique insight into the taxonomic composition of the nitrate-reducing community in planted and unplanted soils. The PCR-amplified narG fragments were cloned and analyzed by restriction fragment length polymorphism (RFLP). In all, 60 RFLP types represented by two or more clones were identified in addition to the 58 RFLP types represented by only one clone. At least one clone belonging to each RFLP type was then sequenced. Several of the obtained sequences were not related to the narG genes from cultivated bacteria, suggesting the existence of unidentified nitrate-reducing bacteria in the studied soil. However, environmental sequences were also related to NarG from many bacterial divisions, i.e., Actinobacteria and α, β, and γ Proteobacteria. The presence of the plant roots resulted in a shift in the structure of the nitrate-reducing community between the unplanted and planted soils. Sequencing of RFLP types dominant in the rhizosphere or present only in the rhizosphere revealed that they are related to NarG from the Actinobacteria in an astonishingly high proportion.
机译:使用硝酸盐作为替代性末端电子受体的微生物在全球氮循环中起着重要作用。研究了土壤中减少硝酸盐的群落的多样性以及玉米根系对该群落结构的影响。选择编码膜结合硝酸盐还原酶的narG基因作为硝酸盐还原群落的功能标记。 narG的使用特别受关注,因为narG基因的系统发育紧密反映了16S核糖体DNA系统发育。因此,以narG基因为靶标,首次为在种植和未种植的土壤中减少硝酸盐的群落的生物分类组成提供了独特的见解。克隆PCR扩增的narG片段,并通过限制性片段长度多态性(RFLP)进行分析。除了仅由一个克隆代表的58种RFLP类型外,总共鉴定了由两个或多个克隆代表的60种RFLP类型。然后对属于每种RFLP类型的至少一个克隆进行测序。某些获得的序列与栽培细菌的narG基因无关,这表明在研究的土壤中存在未知的还原硝酸盐的细菌。然而,环境序列也与来自许多细菌部门的NarG有关,即放线菌以及α,β和γ变形杆菌。植物根的存在导致未种植土壤和已种植土壤之间硝酸盐还原群落的结构发生了变化。在根际占主导地位或仅在根际存在的RFLP类型的测序表明,它们与放线菌中的NarG的比例惊人地高。

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