Literature DB >> 34357428

Diversity and abundance of the functional genes and bacteria associated with RDX degradation at a contaminated site pre- and post-biostimulation.

Hongyu Dang1, Alison M Cupples2.   

Abstract

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<0.05) increased in abundance following biostimulation. Both the sequencing data and qPCR indicated that xenA and xenB exhibited the highest relative abundance among the six genes. Several genes (diaA, nsfI, xenA, and pnrB) exhibited higher relative abundance values in some wells following biostimulation. The study provides a comprehensive approach for assessing biomarkers during RDX bioremediation and provides evidence that biostimulation generated a positive impact on a set of key species and genes. KEY POINTS: • A co-occurrence network indicated diverse RDX degraders. • >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.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  RDX; diaA; nfsI; pnrB; xenA; xenB; xplA

Year:  2021        PMID: 34357428     DOI: 10.1007/s00253-021-11457-x

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  34 in total

1.  Isolation and characterization of RDX-degrading Rhodococcus species from a contaminated aquifer.

Authors:  Anat Bernstein; Eilon Adar; Ali Nejidat; Zeev Ronen
Journal:  Biodegradation       Date:  2011-02-17       Impact factor: 3.909

2.  PnrA, a new nitroreductase-family enzyme in the TNT-degrading strain Pseudomonas putida JLR11.

Authors:  Antonio Caballero; Juan J Lázaro; Juan L Ramos; Abraham Esteve-Núñez
Journal:  Environ Microbiol       Date:  2005-08       Impact factor: 5.491

3.  "Dark" Purkinje cells of the cerebellar cortex.

Authors:  C Léránth; J Hámori
Journal:  Acta Biol Acad Sci Hung       Date:  1970

4.  Evaluation of microbial transport during aerobic bioaugmentation of an RDX-contaminated aquifer.

Authors:  Fiona H Crocker; Karl J Indest; Carina M Jung; Dawn E Hancock; Mark E Fuller; Paul B Hatzinger; Simon Vainberg; Jonathan D Istok; Edward Wilson; Mandy M Michalsen
Journal:  Biodegradation       Date:  2015-10-05       Impact factor: 3.909

5.  High throughput quantification of the functional genes associated with RDX biodegradation using the SmartChip real-time PCR system.

Authors:  J M Collier; B Chai; J R Cole; M M Michalsen; Alison M Cupples
Journal:  Appl Microbiol Biotechnol       Date:  2019-07-27       Impact factor: 4.813

6.  Diaphorase catalyzed biotransformation of RDX via N-denitration mechanism.

Authors:  Bharat Bhushan; Annamaria Halasz; Jim C Spain; Jalal Hawari
Journal:  Biochem Biophys Res Commun       Date:  2002-08-30       Impact factor: 3.575

7.  Lateral transfer of genes for hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) degradation.

Authors:  Peter F Andeer; David A Stahl; Neil C Bruce; Stuart E Strand
Journal:  Appl Environ Microbiol       Date:  2009-03-06       Impact factor: 4.792

8.  Cloning and expression of a Clostridium kluyveri gene responsible for diaphorase activity.

Authors:  Saikat Chakraborty; Makiko Sakka; Tetsuya Kimura; Kazuo Sakka
Journal:  Biosci Biotechnol Biochem       Date:  2008-03-07       Impact factor: 2.043

9.  Purification and characterization of an oxygen-insensitive NAD(P)H nitroreductase from Enterobacter cloacae.

Authors:  C Bryant; M DeLuca
Journal:  J Biol Chem       Date:  1991-03-05       Impact factor: 5.157

10.  Cloning, nucleotide sequence, and expression of the nitroreductase gene from Enterobacter cloacae.

Authors:  C Bryant; L Hubbard; W D McElroy
Journal:  J Biol Chem       Date:  1991-03-05       Impact factor: 5.157

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