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Critical Role of Monooxygenase in Biodegradation of 2,4,6-Trinitrotoluene by Buttiauxella sp. S19-1

Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Xu, Miao;
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
He, Lei;
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Sun, Ping;
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Wu, Ming;
ORCID
0000-0002-5455-205X
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Cui, Xiyan;
Affiliation
Grain School, Jilin Busyness and Technology College, Changchun 130507, China
Liu, Dong;
Affiliation
Institute of Toxicology and Pharmacology, University Medical School Schleswig-Holstein, 24105 Kiel, Germany
Adomako-Bonsu, Amma G.;
Affiliation
School of Food and Biotechnology, Changchun Polytechnic, Changchun 130033, China
Geng, Min;
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Xiong, Guangming;
ORCID
0000-0003-3424-2238
Affiliation
College of Life Science, Jilin Agricultural University, Changchun 130018, China
Guo, Liquan;
ORCID
0000-0003-2405-142X
Affiliation
Institute of Toxicology and Pharmacology, University Medical School Schleswig-Holstein, 24105 Kiel, Germany
Maser, Edmund

2,4,6-Trinitrotoluene (TNT) is an aromatic pollutant that is difficult to be degraded in the natural environment. The screening of efficient degrading bacteria for bioremediation of TNT has received much attention from scholars. In this paper, transcriptome analysis of the efficient degrading bacterium Buttiauxella sp. S19-1 revealed that the monooxygenase gene ( BuMO ) was significantly up-regulated during TNT degradation. S-Δ MO (absence of BuMO gene in S19-1 mutant) degraded TNT 1.66-fold less efficiently than strain S19-1 (from 71.2% to 42.9%), and E- MO mutant ( Escherichia coli BuMO -expressing strain) increased the efficiency of TNT degradation 1.33-fold (from 52.1% to 69.5%) for 9 h at 180 rpm at 27 °C in LB medium with 1.4 µg·mL −1 TNT. We predicted the structure of BuMO and purified recombinant BuMO (rBuMO). Its specific activity was 1.81 µmol·min −1 ·mg −1 protein at pH 7.5 and 35 °C. The results of gas chromatography mass spectrometry (GC–MS) analysis indicated that 4-amino-2,6-dinitrotoluene (ADNT) is a metabolite of TNT biodegradation. We speculate that MO is involved in catalysis in the bacterial degradation pathway of TNT in TNT-polluted environment.

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