Evaluation of bacterial biodegradation and accumulation of phenanthrene in the presence of humic acid

被引:32
|
作者
Xie, Yun [1 ,2 ]
Gu, Zhenggui [1 ]
Herath, H. M. S. K. [3 ]
Gu, Minfen [1 ]
He, Chang [1 ]
Wang, Fang [2 ]
Jiang, Xin [2 ]
Zhang, Jie [1 ]
Zhang, Yinping [1 ,2 ]
机构
[1] Nanjing Normal Univ, Sch Chem & Mat Sci, Ctr Anal & Testing, Nanjing 210046, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Inst Soil Sci, Key Lab Soil Environm & Pollut Remediat, Nanjing 210008, Jiangsu, Peoples R China
[3] Uva Wellassa Univ, Fac Anim Sci & Export Agr, Dept Export Agr, Passara Rd, Badulla 90000, Sri Lanka
基金
中国国家自然科学基金;
关键词
Polycyclic aromatic hydrocarbons (PAHs); Humic acid (HA); Bacteria; Biodegradation; Bioaccumulation; POLYCYCLIC AROMATIC-HYDROCARBONS; DISSOLVED ORGANIC-MATTER; ENERGY-DEPENDENT UPTAKE; FATTY-ACIDS; BIOAVAILABILITY; FRACTIONS; MEMBRANE; MECHANISM; POLLUTION; STRESS;
D O I
10.1016/j.chemosphere.2017.06.026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study evaluated the effect of humic acid (HA) on physicochemical properties of bacterial surfaces and on mass transfer of polycyclic aromatic hydrocarbons (PAHs) from aqueous phase into intracellular bacteria. Due to this process' potential for bacterial degradation, using Sphingobium sp. PHE3, degradation of phenanthrene (PHE) was compared in HA and non-HA sets. The results showed that approximately 51.1% of PHE at a concentration of 102.0 mg L-1 was biodegraded in the non-HA sets, whereas almost all PHE was biodegraded with HA after 72 h. Interestingly, PHE that accumulated in the intracellular bacteria reached 3.80 mg L-1 for the HA sets, which was significantly higher than that of non-HA. Lipid inclusion bodies appeared when Sphingobium sp. PHE3 was treated with HA. The results were further confirmed by the enhanced bacterial surface sorption capacity for the HA sets. Therefore, we concluded that added HA not only act as carriers and biosurfactants facilitating PHE uptake but also adjust bacteria cell wall properties for internalizing PHE, which ultimately overcame the PHE bioavailability resulting in enhanced biodegradation. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:482 / 488
页数:7
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