Abstract

Polybrominated diphenyl ethers (PBDEs) were applied as flame retardant additives in polymers for many plastic and electronic products. Due to their ubiquitous distribution in the environment, potential toxicity to human and tendency for bioaccumulation, PBDEs have raised public safety concern. In this study we examined the degradation of 4-monobrominated diphenyl ether (4-BDE) in aerobic sludge, as a model for PBDE biodegradation. Degradation of 4-BDE was observed in aerobic sludge. Co-metabolism with toluene or diphenyl ether facilitated 4-BDE biodegradation in terms of kinetics and efficiency. Diphenyl ether seems to perform slightly better as an auxiliary carbon source than toluene in facilitating 4-BDE degradation. During the experiment we identified diphenyl ether by gas chromatography/mass spectrometry(GC/MS), which indicates that an anaerobic debromination has occurred. Bacterial community composition was monitored with denaturing gradient gel electrophoresis. The fragments enriched in 4-BDE-degrading aerobic sludge samples belong to presumably a novel anaerobic Clostridiales species distantly related to all known debrominating microbes. This suggests that 4-BDE biodegradation can occur in anaerobic micro-niche in an apparently aerobic environment, by a previously unknown bacterial species. These findings can provide better understandings of biodegradation of brominated diphenyl ethers and can facilitate the prediction of the fate of PBDEs in the environment.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.