Removal of tetrachlorobisphenol A and the effects on bacterial communities in a hybrid sequencing biofilm batch reactor-constructed wetland system

Xiaohui Wang, Shuai Du, Tao Ya, Zhiqiang Shen, Jing Dong, Xiaobiao Zhu

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Front. Environ. Sci. Eng. ›› 2019, Vol. 13 ›› Issue (1) : 14. DOI: 10.1007/s11783-019-1097-4
RESEARCH ARTICLE
RESEARCH ARTICLE

Removal of tetrachlorobisphenol A and the effects on bacterial communities in a hybrid sequencing biofilm batch reactor-constructed wetland system

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Highlights

SBBR-CW system was proposed to effectively treat wastewater containing TCBPA.

CW unit contributed more than SBBR to the removal of TCBPA.

TCBPA changed the composition and structure of bacterial community in the system.

GAOs massively grew in SBBR, but did not deteriorate TP removal efficiency.

Abstract

Tetrachlorobisphenol A (TCBPA) released into the sewage may cause environmental pollution and health risk to human beings. The objective of this study was to investigate the removal of TCBPA and bacterial community structures in a laboratory-scale hybrid sequencing biofilm batch reactor (SBBR)-constructed wetland (CW) system. The results showed that the removal efficiency of chemical oxidation demand (COD), ammonia, total nitrogen and total phosphorus in the SBBR-CW system was 96.7%, 97.3%, 94.4%, and 88.6%, respectively. At the stable operation stage, the system obtained a 71.7%±1.8% of TCBPA removal efficiency with the influent concentration at 200 mg/L. Illumina MiSeq sequencing of 16S rRNA gene revealed that the presence of TCBPA not only reduced the bacterial diversity in the SBBR-CW system, but also altered the composition and structure of bacterial community. After the addition of TCBPA, Proteobacteria increased from 31.3% to 38.7%, while Acidobacteria and Parcubacteria decreased greatly in the SBBR. In contrast, Acidobacteria replaced Proteobacteria as the dominant phylum in the upper soils of CW. The results indicated that TCBPA stimulated the growth of GAOs in the SBBR without deteriorating the phosphorus removal due to the presence of sufficient carbon sources. The ammonia oxidizing bacteria, Nitrosomonas, and denitrification bacteria, Hyphomicrobium and Pseudomonas, were inhibited by TCBPA, resulting in a decreasing the removal efficiency of TN and ammonia.

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Keywords

SBBR / Constructed wetland / Tetrachlorobisphenol A / Microbial community structure

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Xiaohui Wang, Shuai Du, Tao Ya, Zhiqiang Shen, Jing Dong, Xiaobiao Zhu. Removal of tetrachlorobisphenol A and the effects on bacterial communities in a hybrid sequencing biofilm batch reactor-constructed wetland system. Front. Environ. Sci. Eng., 2019, 13(1): 14 https://doi.org/10.1007/s11783-019-1097-4

References

[1]
APHA AWWA, WEF (1998). Standard methods for the examination of water and wastewater. 20th ed. Washington: American Public Health Association
[2]
Arias D M, Uggetti E, García-Galán M J, García J (2017). Cultivation and selection of cyanobacteria in a closed photobioreactor used for secondary effluent and digestate treatment. Science of the Total Environment, 587-588: 157–167
CrossRef Pubmed Google scholar
[3]
Aruoja V, Sihtmäe M, Dubourguier H C, Kahru A (2011). Toxicity of 58 substituted anilines and phenols to algae Pseudokirchneriella subcapitata and bacteria Vibrio fischeri: Comparison with published data and QSARs. Chemosphere, 84(10): 1310–1320
CrossRef Pubmed Google scholar
[4]
Carvalheira M, Oehmen A, Carvalho G, Eusébio M, Reis M A M (2014a). The impact of aeration on the competition between polyphosphate accumulating organisms and glycogen accumulating organisms. Water Research, 66: 296–307
CrossRef Pubmed Google scholar
[5]
Carvalheira M, Oehmen A, Carvalho G, Reis M A M (2014b). Survival strategies of polyphosphate accumulating organisms and glycogen accumulating organisms under conditions of low organic loading. Bioresource Technology, 172: 290–296
CrossRef Pubmed Google scholar
[6]
Chang B V, Liu J H, Liao C S (2014). Aerobic degradation of bisphenol-A and its derivatives in river sediment. Environmental Technology, 35(1-4): 416–424
CrossRef Pubmed Google scholar
[7]
Chen M, Fan Z, Zhao F, Gao F, Mu D, Zhou Y, Shen H, Hu J (2016). Occurrence and maternal transfer of chlorinated bisphenol A and nonylphenol in pregnant women and their matching embryos. Environmental Science & Technology, 50(2): 970–977
CrossRef Pubmed Google scholar
[8]
Crocetti G R, Banfield J F, Keller J, Bond P L, Blackall L L (2002). Glycogen-accumulating organisms in laboratory-scale and full-scale wastewater treatment processes. Microbiology, 148(Pt 11): 3353–3364
CrossRef Pubmed Google scholar
[9]
Ge G, Zhao J, Chen A, Hu B, Chen Y, Gao K, Li X, Ding X (2018). Nitrogen removal and nitrous oxide emission in an anaerobic/oxic/anoxic sequencing biofilm batch reactor. Environmental Engineering Science, 35(1): 19–26
CrossRef Google scholar
[10]
Horikoshi S, Miura T, Kajitani M, Horikoshi N, Serpone N (2008). Photodegradation of tetrahalobisphenol-A (X= Cl, Br) flame retardants and delineation of factors affecting the process. Applied Catalysis B: Environmental, 84(3–4): 797–802
CrossRef Google scholar
[11]
Hu Z, Ferraina R A, Ericson J F, Mackay A A, Smets B F (2005). Biomass characteristics in three sequencing batch reactors treating a wastewater containing synthetic organic chemicals. Water Research, 39(4): 710–720
CrossRef Pubmed Google scholar
[12]
Mao Y, Xia Y, Zhang T (2013). Characterization of Thauera-dominated hydrogen-oxidizing autotrophic denitrifying microbial communities by using high-throughput sequencing. Bioresource Technology, 128: 703–710
CrossRef Pubmed Google scholar
[13]
McIlroy S, Seviour R J (2009). Elucidating further phylogenetic diversity among the Defluviicoccus-related glycogen-accumulating organisms in activated sludge. Environmental Microbiology Reports, 1(6): 563–568
CrossRef Pubmed Google scholar
[14]
McIlroy S J, Albertsen M, Andresen E K, Saunders A M, Kristiansen R, Stokholm-Bjerregaard M, Nielsen K L, Nielsen P H (2014). ‘Candidatus Competibacter’-lineage genomes retrieved from metagenomes reveal functional metabolic diversity. ISME Journal, 8(3): 613–624
CrossRef Pubmed Google scholar
[15]
Miao L, Zhang Q, Wang S, Li B, Wang Z, Zhang S, Zhang M, Peng Y (2018). Characterization of EPS compositions and microbial community in an Anammox SBBR system treating landfill leachate. Bioresource Technology, 249: 108–116
CrossRef Pubmed Google scholar
[16]
Molina-Molina J M, Amaya E, Grimaldi M, Sáenz J M, Real M, Fernández M F, Balaguer P, Olea N (2013). In vitro study on the agonistic and antagonistic activities of bisphenol-S and other bisphenol-A congeners and derivatives via nuclear receptors. Toxicology and Applied Pharmacology, 272(1): 127–136
CrossRef Pubmed Google scholar
[17]
Philips J, Haest P J, Springael D, Smolders E (2013). Inhibition of Geobacter dechlorinators at elevated trichloroethene concentrations is explained by a reduced activity rather than by an enhanced cell decay. Environmental Science & Technology, 47(3): 1510–1517
Pubmed
[18]
Riu A, le Maire A, Grimaldi M, Audebert M, Hillenweck A, Bourguet W, Balaguer P, Zalko D (2011). Characterization of novel ligands of ERa, Erb, and PPARg: the case of halogenated bisphenol A and their conjugated metabolites. Toxicological Sciences, 122(2): 372–382
CrossRef Pubmed Google scholar
[19]
Ronen Z, Abeliovich A (2000). Anaerobic-aerobic process for microbial degradation of tetrabromobisphenol A. Applied and Environmental Microbiology, 66(6): 2372–2377
CrossRef Pubmed Google scholar
[20]
Rosenkranz F, Cabrol L, Carballa M, Donoso-Bravo A, Cruz L, Ruiz-Filippi G, Chamy R, Lema J M (2013). Relationship between phenol degradation efficiency and microbial community structure in an anaerobic SBR. Water Research, 47(17): 6739–6749
CrossRef Pubmed Google scholar
[21]
Sellström U, Bo J (1995). Analysis of tetrabromobisphenol A in a product and environmental samples. Chemosphere, 31(4): 3085–3092
CrossRef Google scholar
[22]
Simon M I, Seviour R J (2009). Elucidating further phylogenetic diversity among the Defluviicoccus-related glycogen-accumulating organisms in activated sludge. Environmental Microbiology Reports, 1(6): 563–568
[23]
Singh M, Srivastava R K (2011). Sequencing batch reactor technology for biological wastewater treatment: A review. Asia-Pacific Journal of Chemical Engineering, 6(1): 3–13
CrossRef Google scholar
[24]
Song M, Liang D, Liang Y, Chen M, Wang F, Wang H, Jiang G (2014). Assessing developmental toxicity and estrogenic activity of halogenated bisphenol A on zebrafish (Danio rerio). Chemosphere, 112: 275–281
CrossRef Pubmed Google scholar
[25]
Spieck E, Hartwig C, McCormack I, Maixner F, Wagner M, Lipski A, Daims H (2006). Selective enrichment and molecular characterization of a previously uncultured Nitrospira-like bacterium from activated sludge. Environmental Microbiology, 8(3): 405–415
CrossRef Pubmed Google scholar
[26]
Sun H, Shen O X, Wang X R, Zhou L, Zhen S Q, Chen X D (2009). Anti-thyroid hormone activity of bisphenol A, tetrabromobisphenol A and tetrachlorobisphenol A in an improved reporter gene assay. Toxicology In Vitro, 23(5): 950–954
CrossRef Pubmed Google scholar
[27]
Tang C C, Tian Y, Liang H, Zuo W, Wang Z W, Zhang J, He Z W (2018). Enhanced nitrogen and phosphorus removal from domestic wastewater via algae-assisted sequencing batch biofilm reactor. Bioresource Technology, 250: 185–190
CrossRef Pubmed Google scholar
[28]
Terasaki M, Kosaka K, Kunikane S, Makino M, Shiraishi F (2011). Assessment of thyroid hormone activity of halogenated bisphenol A using a yeast two-hybrid assay. Chemosphere, 84(10): 1527–1530
CrossRef Pubmed Google scholar
[29]
Thomsen C, Lundanes E, Becher G (2015). A simplified method for determination of tetrabromobisphenol A and polybrominated diphenyl ethers in human plasma and serum. Journal of Separation Science, 24(4): 282–290
CrossRef Google scholar
[30]
Yang Y, Lu L, Zhang J, Yang Y, Wu Y, Shao B (2014). Simultaneous determination of seven bisphenols in environmental water and solid samples by liquid chromatography-electrospray tandem mass spectrometry. Journal of Chromatography. A, 1328: 26–34
CrossRef Pubmed Google scholar
[31]
Yang Y, Zhang L, Cheng J, Zhang S, Li X, Peng Y (2018). Microbial community evolution in partial nitritation/anammox process: From sidestream to mainstream. Bioresource Technology, 251: 327–333
CrossRef Pubmed Google scholar
[32]
Ye G, Chen Y, Wang H O, Ye T, Lin Y, Huang Q, Chi Y, Dong S (2016). Metabolomics approach reveals metabolic disorders and potential biomarkers associated with the developmental toxicity of tetrabromobisphenol A and tetrachlorobisphenol A. Scientific Reports, 6(1): 35257
CrossRef Pubmed Google scholar
[33]
Yin N, Liang S, Liang S, Yang R, Hu B, Qin Z, Liu A, Faiola F (2018). TBBPA and its alternatives disturb the early stages of neural development by interfering with the NOTCH and WNT pathways. Environmental Science & Technology, 52(9): 5459–5468
CrossRef Pubmed Google scholar
[34]
Yuan S Y, Chen S J, Chang B V (2011). Anaerobic degradation of tetrachlorobisphenol-A in river sediment. International Biodeterioration & Biodegradation, 65(1): 185–190
CrossRef Google scholar
[35]
Zeng R J, van Loosdrecht M C, Yuan Z, Keller J (2003). Metabolic model for glycogen-accumulating organisms in anaerobic/aerobic activated sludge systems. Biotechnology and Bioengineering, 81(1): 92–105
CrossRef Pubmed Google scholar
[36]
Zhang J, Liu S C, Li L L, Ren Y, Feng C H, Wei C H, Li Y P, Huang Z L (2017). Anaerobic dechlorination of tetrachlorobisphenol A in river sediment and associated changes in bacterial communities. Water, Air, and Soil Pollution, 228(2): 78
CrossRef Google scholar
[37]
Zhang T, Liu Y, Fang H H P (2005). Effect of pH change on the performance and microbial community of enhanced biological phosphate removal process. Biotechnology and Bioengineering, 92(2): 173–182
CrossRef Pubmed Google scholar
[38]
Zhang Y, Cong J, Lu H, Li G, Qu Y, Su X, Zhou J, Li D (2014). Community structure and elevational diversity patterns of soil Acidobacteria. Journal of Environmental Sciences (China), 26(8): 1717–1724
CrossRef Pubmed Google scholar
[39]
Zheng D, Chang Q, Gao M, She Z, Jin C, Guo L, Zhao Y, Wang S, Wang X (2016). Performance evaluation and microbial community of a sequencing batch biofilm reactor (SBBR) treating mariculture wastewater at different chlortetracycline concentrations. Journal of Environmental Management, 182: 496–504
CrossRef Pubmed Google scholar

Acknowledgements

This work was supported by the National Key Research and Development Program of China (Grant No. 2016YFC0401105), National Natural Science Foundation of China (Grant Nos. 51508538 and 51308319) and Beijing Talented Backbones Program (No. 2015000021733G171).

Electronic Supplementary Material

Supplementary material is available in the online version of this article at https://doi.org/10.1007/s11783-019-1097-4 and is accessible for authorized users.

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2019 Higher Education Press and Springer-Verlag GmbH Germany, part of Springer Nature
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