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Diversity and abundance of the functional genes and bacteria associated with RDX degradation at a contaminated site pre- and post-biostimulation
Bioremediation is becoming an increasingly popular approach for the remediation of sites contaminated with the explosive hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). Multiple lines of evidence are often needed to assess the success of such approaches, with molecular studies frequently providing im...
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Published in: | Applied microbiology and biotechnology 2021-08, Vol.105 (16-17), p.6463-6475 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Bioremediation is becoming an increasingly popular approach for the remediation of sites contaminated with the explosive hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). Multiple lines of evidence are often needed to assess the success of such approaches, with molecular studies frequently providing important information on the abundance of key biodegrading species. Towards this goal, the current study utilized shotgun sequencing to determine the abundance and diversity of functional genes (
xenA
,
xenB
,
xplA
,
diaA
,
pnrB
,
nfsI
) and species previously associated with RDX biodegradation in groundwater before and after biostimulation at an RDX-contaminated Navy Site. For this, DNA was extracted from four and seven groundwater wells pre- and post-biostimulation, respectively. From a set of 65 previously identified RDX degraders, 31 were found within the groundwater samples, with the most abundant species being
Variovorax
sp. JS1663,
Pseudomonas fluorescens
,
Pseudomonas putida
, and
Stenotrophomonas maltophilia
. Further, 9 RDX-degrading species significantly (
p
30 RDX-degrading species were detected.
• Nine RDX-degrading species increased following biostimulation.
• Sequencing and high-throughput qPCR indicated that xenA and xenB were most abundant. |
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ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-021-11457-x |