Abstract
In the last decade, biological degradation and mineralization of antibiotics have been increasingly reported feats of environmental bacteria. The most extensively described example is that of sulfonamides that can be degraded by several members of Actinobacteria and Proteobacteria. Previously, we reported sulfamethoxazole (SMX) degradation and partial mineralization by Achromobacter denitrificans strain PR1, isolated from activated sludge. However, further studies revealed an apparent instability of this metabolic trait in this strain. Here, we investigated this instability and describe the finding of a low-abundance and slow-growing actinobacterium, thriving only in co-culture with strain PR1. This organism, named GP, shared highest 16S rRNA gene sequence similarity (94.6–96.9%) with the type strains of validly described species of the genus Leucobacter. This microbial consortium was found to harbor a homolog to the sulfonamide monooxygenase gene (sadA) also found in other sulfonamide-degrading bacteria. This gene is overexpressed in the presence of the antibiotic, and evidence suggests that it codes for a group D flavin monooxygenase responsible for the ipso-hydroxylation of SMX. Additional side reactions were also detected comprising an NIH shift and a Baeyer–Villiger rearrangement, which indicate an inefficient biological transformation of these antibiotics in the environment. This work contributes to further our knowledge in the degradation of this ubiquitous micropollutant by environmental bacteria.
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Acknowledgments
The authors wish to thank Anna Weston (FHNW, Switzerland) for the advice on the optimization of the qPCR assays, Jonas Romer (FHNW, Switzerland) for the assistance with the TiO2/UV experiments, Prof. Dr. Hans-Peter Kohler (EWAG, Switzerland) for the helpful insights about the metabolic pathway, and Dr. Ana Rita Lopes (FEUP, Portugal) for the relevant comments about the structure of the manuscript and presentation of results. The authors wish to acknowledge the Swiss National Science Foundation, Comissão de Coordenação e Desenvolvimento Regional do Norte and Fundação para a Ciência e a Tecnologia for the funding. Ana Reis further acknowledges the Fundação para a Ciência e a Tecnologia (FCT) for her PhD scholarship.
Funding
This work was financially supported by the Swiss National Science Foundation (grant no. 160332), Comissão de Coordenação e Desenvolvimento Regional do Norte (project reference NORTE-01-0145-FEDER-000005), and Fundação para a Ciência e a Tecnologia and Technology (FCT) through the project UID/EQU/00511/2013—POCI-01-0145-FEDER-006939 and Ana Reis PhD grant (reference SFRH/BD/95814/2013).
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Reis, A.C., Čvančarová, M., Liu, Y. et al. Biodegradation of sulfamethoxazole by a bacterial consortium of Achromobacter denitrificans PR1 and Leucobacter sp. GP. Appl Microbiol Biotechnol 102, 10299–10314 (2018). https://doi.org/10.1007/s00253-018-9411-9
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DOI: https://doi.org/10.1007/s00253-018-9411-9
Keywords
- Bacterial consortium
- Sulfonamide
- Mass spectra
- Metabolic pathway
- Ipso-hydroxylation
- 16S rRNA gene Nanopore sequencing