Pyridine, a highly toxic nitrogen-containing heterocyclic compound, is recalcitrant in the conventional biodegradation process. In this study, BiVO4/FeOOH semiconductor-microbe interface was developed for enhanced visible-light-driven biodegradation of pyridine, where the efficiencies of pyridine removal (100%), total organic carbon (TOC) removal (88.06±3.76%) and NH4+-N formation (84.51±8.95%) were remarkably improved, compared to the biodegradation system and photodegradation system. The electron transport system activity and photoelectrochemical analysis implied the significant improvement of photogenerated carriers transfer between microbes and semiconductors. High-throughput sequencing analysis suggested functional species related to pyridine biodegradation (Shewanella, Bacillus and Lysinibacillus) and electron transfer (Shewanella and Tissierella) were enriched at the semiconductor-microbe interface. The light-excited holes played a crucial role in promoting pyridine mineralization. This study demonstrated that this bio-photodegradation system would be a potential alternative for the efficient treatment of wastewater containing recalcitrant pollutant such as pyridine.
Keywords: Electron acceptor; Photoelectron transfer; Photohole; Pyridine; Semiconductor-microbe interface.
Copyright © 2020 Elsevier Ltd. All rights reserved.