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通过结合五氯苯酚脱氯培养物和苯酚降解培养物对五氯苯酚(PCP)进行厌氧矿化。

Anaerobic mineralization of pentachlorophenol (PCP) by combining PCP-dechlorinating and phenol-degrading cultures.

作者信息

Yang Suyin, Shibata Atsushi, Yoshida Naoko, Katayama Arata

机构信息

Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan.

出版信息

Biotechnol Bioeng. 2009 Jan 1;102(1):81-90. doi: 10.1002/bit.22032.

Abstract

The dechlorination and mineralization of pentachlorophenol (PCP) was investigated by simultaneously or sequentially combining two different anaerobic microbial populations, a PCP-dechlorinating culture capable of the reductive dechlorination of PCP to phenol and phenol- degrading cultures able to mineralize phenol under sulfate- or iron-reducing conditions. In the simultaneously combined mixture, PCP (about 35 microM) was mostly dechlorinated to phenol after incubation for 17 days under sulfate-reducing conditions or for 22 days under iron-reducing conditions. Thereafter, the complete removal of phenol occurred within 40 days under both conditions. In the sequentially combined mixture, most of the phenol, the end product of PCP dechlorination, was degraded within 12 days of inoculation with the phenol degrader, without a lag phase, under both sulfate- and iron-reducing conditions. In a radioactivity experiment, [14C-U]-PCP was mineralized to 14CO2 and 14CH4 by the combined anaerobic microbial activities. Analysis of electron donor and acceptor utilization and of the production and consumption of H2, CO2, and CH4 suggested that the dechlorinating and degrading microorganisms compete with other microorganisms to perform PCP dechlorination and part of the phenol degradation in complex anoxic environments in the presence of electron donors and acceptors. The presence of a small amount of autoclaved soil slurry in the medium was possibly another advantageous factor in the successful dechlorination and mineralization of PCP by the combined mixtures. This anaerobic-anaerobic combination technology holds great promise as a cost-effective strategy for complete PCP bioremediation in situ.

摘要

通过同时或顺序组合两种不同的厌氧微生物群体,研究了五氯苯酚(PCP)的脱氯和矿化作用。一种是能够将PCP还原脱氯为苯酚的PCP脱氯培养物,另一种是能够在硫酸盐还原或铁还原条件下将苯酚矿化的苯酚降解培养物。在同时组合的混合物中,在硫酸盐还原条件下培养17天或在铁还原条件下培养22天后,PCP(约35微摩尔)大多被脱氯为苯酚。此后,在两种条件下,苯酚在40天内被完全去除。在顺序组合的混合物中,在接种苯酚降解菌后的12天内,PCP脱氯的终产物苯酚在硫酸盐还原和铁还原条件下均无延迟期地大部分被降解。在一项放射性实验中,[14C-U]-PCP通过厌氧微生物的联合活动被矿化为14CO2和14CH4。对电子供体和受体利用以及H2、CO2和CH4的产生和消耗的分析表明,在存在电子供体和受体的复杂缺氧环境中,脱氯和降解微生物与其他微生物竞争进行PCP脱氯和部分苯酚降解。培养基中存在少量经高压灭菌的土壤泥浆可能是联合混合物成功实现PCP脱氯和矿化的另一个有利因素。这种厌氧-厌氧组合技术作为一种具有成本效益的原位完全修复PCP的策略具有很大的前景。

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