Literature DB >> 16329859

The abundance of nahAc genes correlates with the 14C-naphthalene mineralization potential in petroleum hydrocarbon-contaminated oxic soil layers.

Pirjo M Tuomi1, Jani M Salminen, Kirsten S Jørgensen.   

Abstract

In this study, we evaluated whether the abundance of the functional gene nahAc reflects aerobic naphthalene degradation potential in subsurface and surface samples taken from three petroleum hydrocarbon contaminated sites in southern Finland. The type of the contamination at the sites varied from lightweight diesel oil to high molecular weight residuals of crude oil. Samples were collected from both oxic and anoxic soil layers. The naphthalene dioxygenase gene nahAc was quantified using a replicate limiting dilution-polymerase chain reaction (RLD-PCR) method with a degenerate primer pair. In the non-contaminated samples nahAc genes were not detected. In the petroleum hydrocarbon-contaminated oxic soil samples nahAc gene abundance [range 3 x 10(1)-9 x 10(4) copies (g dry wt soil)(-1)] was correlated (Kendall non-parametric correlation r2=0.459, p<0.01) with the aerobic 14C-naphthalene mineralization potential (range 1 x 10(-5)-0.1 d(-1)) measured in microcosms at in situ temperatures (8 degrees C for subsurface and 20 degrees C for surface soil samples). In these samples nahAc gene abundance was also correlated with total microbial cell counts (r2=0.471, p<0.01), respiration rate (r2=0.401, p<0.01) and organic matter content (r2=0.341, p<0.05). NahAc genes were amplified from anoxic soil layers indicating that, although involved in aerobic biodegradation of naphthalene, these genes or related sequences were also present in the anoxic subsurface. In the samples taken from the anoxic layers, the aerobic 14C-naphthalene mineralization rates were not correlated with nahAc gene abundance. In conclusion, current sequence information provides the basis for a robust tool to estimate the naphthalene degradation potential at oxic zones of different petroleum hydrocarbon-contaminated sites undergoing in situ bioremediation.

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Year:  2004        PMID: 16329859     DOI: 10.1016/j.femsec.2004.07.011

Source DB:  PubMed          Journal:  FEMS Microbiol Ecol        ISSN: 0168-6496            Impact factor:   4.194


  15 in total

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2.  Microbial dioxygenase gene population shifts during polycyclic aromatic hydrocarbon biodegradation.

Authors:  Sinéad M Ní Chadhain; R Sean Norman; Karen V Pesce; Jerome J Kukor; Gerben J Zylstra
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3.  A targeted real-time PCR assay for studying naphthalene degradation in the environment.

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4.  Diversity, abundance, and consistency of microbial oxygenase expression and biodegradation in a shallow contaminated aquifer.

Authors:  Jane M Yagi; Eugene L Madsen
Journal:  Appl Environ Microbiol       Date:  2009-08-21       Impact factor: 4.792

Review 5.  Comparison of the specificities and efficacies of primers for aromatic dioxygenase gene analysis of environmental samples.

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Journal:  Appl Environ Microbiol       Date:  2011-04-15       Impact factor: 4.792

6.  Advances in monitoring of catabolic genes during bioremediation.

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7.  Spatial patterns of microbial diversity and activity in an aged creosote-contaminated site.

Authors:  Shinjini Mukherjee; Heli Juottonen; Pauli Siivonen; Cosme Lloret Quesada; Pirjo Tuomi; Pertti Pulkkinen; Kim Yrjälä
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8.  pahE, a Functional Marker Gene for Polycyclic Aromatic Hydrocarbon-Degrading Bacteria.

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Journal:  Appl Environ Microbiol       Date:  2019-01-23       Impact factor: 4.792

9.  Degradation rates of aged petroleum hydrocarbons are likely to be mass transfer dependent in the field.

Authors:  Katarina Björklöf; Jani Salminen; Pirjo Sainio; Kirsten Jørgensen
Journal:  Environ Geochem Health       Date:  2008-02-08       Impact factor: 4.609

10.  Novel aromatic ring-hydroxylating dioxygenase genes from coastal marine sediments of Patagonia.

Authors:  Mariana Lozada; Juan P Riva Mercadal; Leandro D Guerrero; Walter D Di Marzio; Marcela A Ferrero; Hebe M Dionisi
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