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Inorganic nutrients, bacteria, and the microbial loop.无机营养素、细菌和微生物环。
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2
Molecular analysis of the in situ growth rates of subsurface Geobacter species.地下 Geobacter 种原位生长速率的分子分析。
Appl Environ Microbiol. 2013 Mar;79(5):1646-53. doi: 10.1128/AEM.03263-12. Epub 2012 Dec 28.
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Characterization and transcription of arsenic respiration and resistance genes during in situ uranium bioremediation.原位铀生物修复过程中砷呼吸和抗性基因的特性与转录。
ISME J. 2013 Feb;7(2):370-83. doi: 10.1038/ismej.2012.109. Epub 2012 Oct 4.
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Spatial and temporal dynamics of the microbial community in the Hanford unconfined aquifer.汉福德无约束含水层中微生物群落的时空动态。
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Geobacter: the microbe electric's physiology, ecology, and practical applications.产电菌:微生物电化学的生理、生态及实际应用。
Adv Microb Physiol. 2011;59:1-100. doi: 10.1016/B978-0-12-387661-4.00004-5.
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Molecular analysis of the metabolic rates of discrete subsurface populations of sulfate reducers.对硫酸盐还原菌离散地下种群代谢率的分子分析。
Appl Environ Microbiol. 2011 Sep;77(18):6502-9. doi: 10.1128/AEM.00576-11. Epub 2011 Jul 15.
7
Coupling a genome-scale metabolic model with a reactive transport model to describe in situ uranium bioremediation.将基因组规模的代谢模型与反应性传输模型相耦合,以描述原位铀生物修复。
Microb Biotechnol. 2009 Mar;2(2):274-86. doi: 10.1111/j.1751-7915.2009.00087.x.
8
Direct coupling of a genome-scale microbial in silico model and a groundwater reactive transport model.直接耦合基因组规模的微生物计算模型和地下水反应传输模型。
J Contam Hydrol. 2011 Mar 25;122(1-4):96-103. doi: 10.1016/j.jconhyd.2010.11.007. Epub 2010 Nov 28.
9
In situ to in silico and back: elucidating the physiology and ecology of Geobacter spp. using genome-scale modelling.从原位到计算模拟再到原位:利用基因组尺度建模阐明 Geobacter spp 的生理学和生态学。
Nat Rev Microbiol. 2011 Jan;9(1):39-50. doi: 10.1038/nrmicro2456. Epub 2010 Dec 6.
10
Genome-scale dynamic modeling of the competition between Rhodoferax and Geobacter in anoxic subsurface environments.在缺氧地下环境中 Rhodoferax 和 Geobacter 竞争的基因组规模动态建模。
ISME J. 2011 Feb;5(2):305-16. doi: 10.1038/ismej.2010.117. Epub 2010 Jul 29.

原位生物修复铀污染地下水过程中特定原生动物种群的富集。

Enrichment of specific protozoan populations during in situ bioremediation of uranium-contaminated groundwater.

机构信息

Department of Microbiology, Morrill Science Center IVN, University of Massachusetts Amherst, Amherst, MA 01003, USA.

出版信息

ISME J. 2013 Jul;7(7):1286-98. doi: 10.1038/ismej.2013.20. Epub 2013 Feb 28.

DOI:10.1038/ismej.2013.20
PMID:23446832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3695288/
Abstract

The importance of bacteria in the anaerobic bioremediation of groundwater polluted with organic and/or metal contaminants is well recognized and in some instances so well understood that modeling of the in situ metabolic activity of the relevant subsurface microorganisms in response to changes in subsurface geochemistry is feasible. However, a potentially significant factor influencing bacterial growth and activity in the subsurface that has not been adequately addressed is protozoan predation of the microorganisms responsible for bioremediation. In field experiments at a uranium-contaminated aquifer located in Rifle, CO, USA, acetate amendments initially promoted the growth of metal-reducing Geobacter species, followed by the growth of sulfate reducers, as observed previously. Analysis of 18S rRNA gene sequences revealed a broad diversity of sequences closely related to known bacteriovorous protozoa in the groundwater before the addition of acetate. The bloom of Geobacter species was accompanied by a specific enrichment of sequences most closely related to the ameboid flagellate, Breviata anathema, which at their peak accounted for over 80% of the sequences recovered. The abundance of Geobacter species declined following the rapid emergence of B. anathema. The subsequent growth of sulfate-reducing Peptococcaceae was accompanied by another specific enrichment of protozoa, but with sequences most similar to diplomonadid flagellates from the family Hexamitidae, which accounted for up to 100% of the sequences recovered during this phase of the bioremediation. These results suggest a prey-predator response with specific protozoa responding to increased availability of preferred prey bacteria. Thus, quantifying the influence of protozoan predation on the growth, activity and composition of the subsurface bacterial community is essential for predictive modeling of in situ uranium bioremediation strategies.

摘要

细菌在受有机和/或金属污染物污染的地下水的厌氧生物修复中的重要性已得到充分认识,在某些情况下,对相关地下微生物在地下地球化学变化下的原位代谢活性进行建模是可行的。然而,一个潜在的重要因素影响着地下细菌的生长和活性,但尚未得到充分解决,那就是原生动物对负责生物修复的微生物的捕食。在美国科罗拉多州里弗尔铀污染含水层的现场实验中,最初添加乙酸盐促进了金属还原菌 Geobacter 物种的生长,随后是硫酸盐还原菌的生长,这与之前的观察结果一致。18S rRNA 基因序列分析表明,在添加乙酸盐之前,地下水中存在与已知食细菌原生动物密切相关的广泛多样性序列。Geobacter 物种的大量繁殖伴随着与阿米巴鞭毛虫 Breviata anathema 最密切相关的序列的特定富集,其峰值时占回收序列的 80%以上。Geobacter 物种的丰度在 Breviata anathema 的快速出现后下降。随后硫酸盐还原菌 Peptococcaceae 的生长伴随着另一种原生动物的特定富集,但与六鞭毛虫Hexamitidae 家族的双鞭毛原生动物的序列最相似,在生物修复的这一阶段,它们占回收序列的 100%。这些结果表明存在一种猎物-捕食者的反应,特定的原生动物对增加的首选猎物细菌的可用性作出反应。因此,量化原生动物捕食对地下细菌群落生长、活性和组成的影响,对于原位铀生物修复策略的预测建模至关重要。