Department of Oceanography, Florida State University, Tallahassee, FL 32306-4470, USA.
Appl Environ Microbiol. 2010 May;76(10):3244-54. doi: 10.1128/AEM.03069-09. Epub 2010 Mar 19.
In terrestrial subsurface environments where nitrate is a critical groundwater contaminant, few cultivated representatives are available to verify the metabolism of organisms that catalyze denitrification. In this study, five species of denitrifying bacteria from three phyla were isolated from subsurface sediments exposed to metal radionuclide and nitrate contamination as part of the U.S. Department of Energy's Oak Ridge Integrated Field Research Challenge (OR-IFRC). Isolates belonged to the genera Afipia and Hyphomicrobium (Alphaproteobacteria), Rhodanobacter (Gammaproteobacteria), Intrasporangium (Actinobacteria), and Bacillus (Firmicutes). Isolates from the phylum Proteobacteria were complete denitrifiers, whereas the Gram-positive isolates reduced nitrate to nitrous oxide. rRNA gene analyses coupled with physiological and genomic analyses suggest that bacteria from the genus Rhodanobacter are a diverse population of denitrifiers that are circumneutral to moderately acidophilic, with a high relative abundance in areas of the acidic source zone at the OR-IFRC site. Based on genome analysis, Rhodanobacter species contain two nitrite reductase genes and have not been detected in functional-gene surveys of denitrifying bacteria at the OR-IFRC site. Nitrite and nitrous oxide reductase gene sequences were recovered from the isolates and from the terrestrial subsurface by designing primer sets mined from genomic and metagenomic data and from draft genomes of two of the isolates. We demonstrate that a combination of cultivation and genomic and metagenomic data is essential to the in situ characterization of denitrifiers and that current PCR-based approaches are not suitable for deep coverage of denitrifiers. Our results indicate that the diversity of denitrifiers is significantly underestimated in the terrestrial subsurface.
在以硝酸盐为关键地下水污染物的陆地地下环境中,可用于验证催化反硝化作用的生物体代谢的培养物代表很少。在这项研究中,从暴露于金属放射性核素和硝酸盐污染的地下沉积物中分离出 5 种来自 3 个门的反硝化细菌,这是美国能源部橡树岭综合现场研究挑战(OR-IFRC)的一部分。分离株属于 Afipia 和 Hyphomicrobium(α变形菌)、Rhodanobacter(γ变形菌)、Intrasporangium(放线菌)和 Bacillus(Firmicutes)属。来自变形菌门的分离株是完全反硝化细菌,而革兰氏阳性分离株将硝酸盐还原为一氧化二氮。rRNA 基因分析结合生理和基因组分析表明,Rhodanobacter 属的细菌是一个多样化的反硝化种群,它们对中性到中度嗜酸,在 OR-IFRC 现场酸性源区的某些区域相对丰度较高。基于基因组分析,Rhodanobacter 物种含有两个亚硝酸盐还原酶基因,并且在 OR-IFRC 现场反硝化细菌的功能基因调查中未检测到。从分离物和陆地地下环境中通过设计从基因组和宏基因组数据以及两个分离物的草图基因组中挖掘的引物对来回收亚硝酸盐和一氧化二氮还原酶基因序列。我们证明了培养物结合基因组和宏基因组数据对于原位反硝化细菌的特征描述至关重要,并且当前基于 PCR 的方法不适合反硝化细菌的深度覆盖。我们的结果表明,陆地地下环境中反硝化细菌的多样性被严重低估。