Literature DB >> 7497356

Pseudomonas aeruginosa strain MA01 aerobically metabolizes the aminodinitrotoluenes produced by 2,4,6-trinitrotoluene nitro group reduction.

M A Alvarez1, C L Kitts, J L Botsford, P J Unkefer.   

Abstract

Many microbes reduce the nitro substituents of 2,4,6-trinitrotoluene (TNT), producing aminodinitrotoluenes (ADNTs). These compounds are recalcitrant to further breakdown and are acutely toxic. In a search for organisms capable of metabolizing ADNTs, a bacterial strain was isolated for the ability to use 2-aminobenzoate (anthranilate) as sole C-source. This isolate, Pseudomonas aeruginosa MA01, metabolized TNT by first reducing one nitro group to form either 2-amino-4,6-dinitrotoluene (2ADNT) or 4-amino-2,6-dinitrotoluene (4ADNT). However, strain MA01 was distinct from other TNT-reducing organisms in that it transformed these compounds into highly polar metabolites through an O2-dependent process. Strain MA01 was able to cometabolize TNT, 2ADNT, and 4ADNT in the presence of a variety of carbon and energy sources. During aerobic cometabolism with succinate, 45% of uniformly ring-labeled [14C]TNT was transformed to highly polar compounds. Aerobic cometabolism of purified [14C]2ADNT and [14C]4ADNT with succinate as C-source produced similar amounts of these polar metabolites. During O2-limited cometabolism with succinate as C-source and nitrate as electron acceptor, less than 8% of the [14C]TNT was transformed to polar metabolites. Purified 2,6-diamino-4-nitrotoluene was not metabolized, and while 2,4-diamino-6-nitrotoluene was acetylated, the product (N-acetyl-2,4-diamino-6-nitrotoluene) was not further metabolized. Therefore, strain MA01 metabolized TNT by oxidation of the ADNTs and not by reduction the remaining nitro groups on the ADNTs.

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Year:  1995        PMID: 7497356     DOI: 10.1139/m95-137

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  7 in total

1.  Oxidative transformation of aminodinitrotoluene isomers by multicomponent dioxygenases.

Authors:  G R Johnson; B F Smets; J C Spain
Journal:  Appl Environ Microbiol       Date:  2001-12       Impact factor: 4.792

2.  Biotransformation of 2,4,6-trinitrotoluene with Phanerochaete chrysosporium in agitated cultures at pH 4.5.

Authors:  J Hawari; A Halasz; S Beaudet; L Paquet; G Ampleman; S Thiboutot
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

Review 3.  Biological degradation of 2,4,6-trinitrotoluene.

Authors:  A Esteve-Núñez; A Caballero; J L Ramos
Journal:  Microbiol Mol Biol Rev       Date:  2001-09       Impact factor: 11.056

4.  Formation of hydride-Meisenheimer complexes of picric acid (2,4, 6-trinitrophenol) and 2,4-dinitrophenol during mineralization of picric acid by Nocardioides sp. strain CB 22-2.

Authors:  C Behrend; K Heesche-Wagner
Journal:  Appl Environ Microbiol       Date:  1999-04       Impact factor: 4.792

5.  Transformation of 2,4,6-Trinitrotoluene by Pseudomonas pseudoalcaligenes JS52.

Authors:  P D Fiorella; J C Spain
Journal:  Appl Environ Microbiol       Date:  1997-05       Impact factor: 4.792

6.  Products of Anaerobic 2,4,6-Trinitrotoluene (TNT) Transformation by Clostridium bifermentans.

Authors:  T A Lewis; S Goszczynski; R L Crawford; R A Korus; W Admassu
Journal:  Appl Environ Microbiol       Date:  1996-12       Impact factor: 4.792

7.  Degradation of 2,4,6-trinitrotoluene by P. aeruginosa and characterization of some metabolites.

Authors:  Hatice Aysun Mercimek; Sadik Dincer; Gulcihan Guzeldag; Aysenur Ozsavli; Fatih Matyar; Afet Arkut; Fikret Kayis; Melis Sumengen Ozdenefe
Journal:  Braz J Microbiol       Date:  2015-03-01       Impact factor: 2.476

  7 in total

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