五氯苯酚
化学
生物转化
环境化学
生物地球化学循环
脱氯作用
胞外聚合物
细胞外
环境修复
辅因子
氧化还原
生物化学
酶
细菌
生物降解
有机化学
污染
生物膜
生物
遗传学
生态学
作者
Baogang Zhang,Yutong Cheng,Jiaxin Shi,Xing Xuan,Yuling Zhu,Nan Xu,Jianxin Xia,Alistair G.L. Borthwick
标识
DOI:10.1016/j.cej.2019.121965
摘要
Aquifer co-contamination by vanadium (V) and pentachlorophenol (PCP) involves complicated biogeochemical processes that remain poorly understood, particularly from the perspective of microbial metabolism. Batch experiment results demonstrated that V(V) and PCP could be competitively bio-reduced, with 96.0 ± 1.8% of V(V) and 43.4 ± 4.6% of PCP removed during 7 d operation. V(V) was bio-transformed to vanadium (IV), which could precipitate naturally under circumneutral conditions, facilitating the removal of up to 78.2 ± 3.1% dissolved total V. The PCP reductive dechlorination products were mainly 2,4,6-trichlorophenol and 4-monochlorophenol with lower toxicity. High-throughput 16S rRNA gene sequencing indicated that Pseudomonas, Soehngenia, and Anaerolinea might be responsible for the two bio-transformations, with detected functional genes of nirS and cprA. Extracellular reduction by cytochrome c and intracellular conversion by nicotinamide adenine dinucleotide (NADH) occurred for both V(V) and PCP. Extracellular proteins in microbial-secreted extracellular polymeric substances (EPS) might also be involved in these enzymatic bioprocesses. EPS could protect microbial cells through V(V) binding by the chemically reactive carboxyl (COO−), and hydroxyl (–OH) groups. These findings elucidate the metabolic processes during anaerobic V(V) and PCP biotransformation, advance understanding of their biogeochemical fates, and provide a foundation on which to develop novel strategies for remediation of co-contaminated aquifers.
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