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Diversity Abundance and Consistency of Microbial Oxygenase Expression and Biodegradation in a Shallow Contaminated Aquifer

机译:浅层含水层中微生物氧化酶表达和生物降解的多样性丰度和一致性

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摘要

The diversity of Rieske dioxygenase genes and short-term temporal variability in the abundance of two selected dioxygenase gene sequences were examined in a naphthalene-rich, coal tar waste-contaminated subsurface study site. Using a previously published PCR-based approach (S. M. Ní Chadhain, R. S. Norman, K. V. Pesce, J. J. Kukor, and G. J. Zylstra, Appl. Environ. Microbiol. 72:4078-4087, 2006) a broad suite of genes was detected, ranging from dioxygenase sequences associated with Rhodococcus and Sphingomonas to 32 previously uncharacterized Rieske gene sequence clone groups. The nag genes appeared frequently (20% of the total) in two groundwater monitoring wells characterized by low (∼102 ppb; ∼1 μM) ambient concentrations of naphthalene. A quantitative competitive PCR assay was used to show that abundances of nag genes (and archetypal nah genes) fluctuated substantially over a 9-month period. To contrast short-term variation with long-term community stability, in situ community gene expression (dioxygenase mRNA) and biodegradation potential (community metabolism of naphthalene in microcosms) were compared to measurements from 6 years earlier. cDNA sequences amplified from total RNA extracts revealed that nah- and nag-type genes were expressed in situ, corresponding well with structural gene abundances. Despite evidence for short-term (9-month) shifts in dioxygenase gene copy number, agreement in field gene expression (dioxygenase mRNA) and biodegradation potential was observed in comparisons to equivalent assays performed 6 years earlier. Thus, stability in community biodegradation characteristics at the hemidecadal time frame has been documented for these subsurface microbial communities.
机译:在富含萘,受煤焦油废物污染的地下研究场所,研究了Rieske双加氧酶基因的多样性和两个选定的双加氧酶基因序列的短期短期变化。使用先前发表的基于PCR的方法(SMNíChadhain,RS Norman,KV Pesce,JJ Kukor和GJ Zylstra,Appl。Environ。Microbiol。72:4078-4087,2006),检测到了一系列基因,范围从与红球菌和鞘氨醇单胞菌相关的双加氧酶序列与32个以前未表征的Rieske基因序列克隆组有关。在两个地下水监测井中,nag基因频繁出现(占总数的20%),其特征在于萘的环境浓度较低(〜10 2 ppb;〜1μM)。定量竞争PCR分析法用于显示nag基因(和原型nah基因)的丰度在9个月内大幅波动。为了将短期变化与长期社区稳定性进行对比,将原位社区基因表达(双加氧酶mRNA)和生物降解潜力(微观世界中萘的社区代谢)与6年前的测量结果进行了比较。从总RNA提取物中扩增的cDNA序列显示nah和nag型基因在原位表达,与结构基因丰度相对应。尽管有证据表明双加氧酶基因拷贝数有短期(9个月)的变化,但与6年前进行的同等分析相比,仍观察到田间基因表达(双加氧酶mRNA)和生物降解潜力一致。因此,已经记录了这些地下微生物群落在半水准时间范围内的群落生物降解特征的稳定性。

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