Removals of Gentamicin and Benzo[a]Pyrene in an Anaerobic Multichamber Bed Reactor
PDF

Keywords

AMCBR, Benzo (a) pyrene, Inhibiton, Gentamicin, Petrochemical, Substrate.

How to Cite

1.
Delia Teresa Sponza, Hakan Celebi, Oguzhan Gok. Removals of Gentamicin and Benzo[a]Pyrene in an Anaerobic Multichamber Bed Reactor. Glob. Environ. Eng. [Internet]. 2019 Dec. 30 [cited 2024 Sep. 19];6(1):16-33. Available from: https://avantipublisher.com/index.php/tgevnie/article/view/927

Abstract

 The petrochemical industry wastewaters were not treated effectively due to high concentrations of Polycyclic aromatic hydrocarbon (PAH) benzo [a] pyren (BaP) and an aminoglucoside antibiotic gentamicin (GNT) in an aerobic treatment plant in Turkey. The high GNT concentration in this industry wastewater mainly originated from the toilets of the working people and from the medical care facilities since an intestinal epidemic occurrred for a period of approximately 1.5 years. The High BaP concentrations release into the wastewater originated from the high BaP production in this industry. In order to improve the biodegradability of petrochemical industry wastewaters containing excess BaP and GNT, different mixtures of BaP and GNT were biodegraded in a high rate anaerobic multichamber bed (AMCBR) reactor. The maximum anaerobic yields for 10 mg/L BaP and 1 mg/ L GNT alone were 45% and 12%, respectively. The addition of primary susbstrate increased the 200 mg/L BaP and 50 mg/ L GNT removals to 97% and 89%, respectively. BaP was biodegraded at short operation times compared to GNT. At low BaP (10-200 mg/ L) and GNT (10-35 mg/ L) concentrations, a non-competitive inhibition does not affect the binding of the substrate and KS were not affected. At high BaP (500-900 mg/ L) and GNT (75-100 mg/ L) concentrations, the BaP and GNT were biodegraded according to competitive inhibition with increased KS. BaP and GNT were biodegraded according to Haldane equations at high concentrations where they were used as the sole substrate.
https://doi.org/10.15377/2410-3624.2019.06.2
PDF

References

Quality Criteria for Water. U.S Environmental Protection Agency, 1987; EPA440-5-86-001, Washington, DC, 2013.

Zheng XJ, et al. PAH removal from spiked municipal wastewater sewage sludge using biological, chemical and electrochemical treatments. Chemosphere 2007; 68:1143-1152. https://doi.org/10.1016/j.chemosphere.2007.01.052

Sponza DT, Gok O. Effects of sludge retention time (SRT) and biosurfactant on the removal of polyaromatic compounds and toxicity. J Hazard Mater 2011; 197: 404-416. https://doi.org/10.1016/j.jhazmat.2011.09.101

Chang BV, Chang JS, Yuan SY. Anaerobic degradation of phenanthrene in riversediment under nitrate-reducing conditions. Bull Environ Contam Toxicol 2001; 67: 898-905. https://doi.org/10.1007/s001280206

Sponza DT and Gok O. Aerobic biodegradation and inhibition kinetics of poly-aromatic hydrocarbons (PAHs) in a petrochemical industry wastewater in the presence of biosurfactants. J Chem Technol Biotechnol 2012; 87: 658-672. https://doi.org/10.1002/jctb.2762

Loffler D, Ternes TA. Analytical method for the determination of the aminoglycoside gentamicin in hospital wastewater via liquid chromatography-electrospray-tandem mass spectrometry. J Chromatogr A 2003; 1000: 583-558. https://doi.org/10.1016/S0021-9673(03)00059-1

Diaz-Cruz MS, Barcelo D. LC-MS2 trace analysis of antimicrobials in water, sediment and soil. Trend Anal Chem 2005; 24: 645-657. https://doi.org/10.1016/j.trac.2005.05.005

Alexy R, Kümpel T, Kümmerer K. Assessment of degradation of 18 antibiotics in the Closed Bottle Test. Chemosphere 2004; 57: 505-512. https://doi.org/10.1016/j.chemosphere.2004.06.024

Graham AE, Speicher E, Williamson B. Analysis of gentamicin sulfate and a study of its degradation in dextrose solution. J Pharm Biomed Anal 1997; 15:537-543. https://doi.org/10.1016/S0731-7085(96)01852-3

Kümmerer et al. Biodegradability of some antibiotics, elimination of the genotoxicity and affection of wastewater bacteria in a sample test. Chemosphere 2008; 40: 701-710. https://doi.org/10.1016/S0045-6535(99)00439-7

Sponza DT, Gok O. Effect of rhamnolipid on the aerobic removal of polyaromatic hydrocarbons (PAHs) and COD components from petrochemical wastewater. Bioresour Technol 2010; 101: 914-924. https://doi.org/10.1016/j.biortech.2009.09.022

Amin MM, Zilles JL, Greiner J, Charbonneau S, Raskin L and Morgenroth E. Influence of the antibiotic erythromycin on anaerobic treatment of a pharmaceutical wastewater. Environ Sci Technol 2006; 40: 3971-3977. https://doi.org/10.1021/es060428j

Kummerer K. Significance of antibiotics in the environment. J Antimicrob Chemos 2003; 52: 5-7. https://doi.org/10.1093/jac/dkg293

Chang BV, Chang I Yuan S. Anaeobic degradation of phenanthrene and pyrene in mangrove sediment. Bull Environ Contam Toxicol 2008; 80: 145-149. https://doi.org/10.1007/s00128-007-9333-1

Brandt BW, van Leeuwen IMM, Kooijman Salm, A. general model for multiple substrate biodegradation, Application to co-metabolism of structurally non-analogous compounds. Water Res 2003; 37: 4843-4854. https://doi.org/10.1016/j.watres.2003.08.006

Slana M, Dolenc MS. Environmental Risk Assessment of antimicrobials applied in veterinary medicine-A field study and laboratory approach. Environ Toxicol Pharmacol 2013; 35: 131-141. https://doi.org/10.1016/j.etap.2012.11.017

Liu R, Tian Q, Chen J. The developments of anaerobic baffled reactor for wastewater treatment: A Review. Afr J Biotechnol 2010; 9: 1535-1542. https://doi.org/10.5897/AJB10.036

Celebi H, Gok O, Sponza D. Removals of Oxytetracycline (antibiotic) and Benzo[a]pyrene (polycyclic aromatic hydrocarbon) in anaerobic multichamber bed reactor (AMCBR). Proceedings of the 12th International Conference on Environmental Science and Technology, Rhodes, Greece 2011; pp. 279-286.

Nielsen DR, Daugulis AJ, McLellan PJ. Dynamic simulation of benzene vapor treatment by a two-phase partitioning bioscrubber: part II: model calibration, validation, and predictions. Biochem Eng J 2007; 36: 250-261. https://doi.org/10.1016/j.bej.2007.02.027

Wu J, et al. Acute toxicities of BaP and GNT. Chemosphere 2016; 144: 2183-2188. https://doi.org/10.1016/j.chemosphere.2015.10.099

Lomba L, et al. Ecotoxicological study of six drugs in Aliivibrio fischeri, Daphnia magna and Raphidocelis subcapitata. Environmental Science and Pollution Research 2020; 27: 9891-9900. https://doi.org/10.1007/s11356-019-07592-8

Mohamed AF, et al. Pharmacokinetic-pharmacodynamic model for gentamicin and its adaptive resistance with predictions of dosing schedules in newborn infants. Antimicrob Agents Chemother 2012; 56: 179-188. https://doi.org/10.1128/AAC.00694-11

Littlejohns JV, Daugulis AJ. Kinetics and interactions of BTEX compounds during degradation by a bacterial consortium. Process Biochem 2008; 43: 1068-1076. https://doi.org/10.1016/j.procbio.2008.05.010

Rockne KJ, et al. Anaerobic naphthalene degradation by microbial pure cultures under nitrate reducing conditions. Appl Environ Microbiol 2000; 66: 1595-1601. https://doi.org/10.1128/AEM.66.4.1595-1601.2000

McNally DL, Mihelcic JR. Lueking DR Biodegradation of three- and four-ring polycyclic aromatic hydrocarbons under aerobic and denitrifying conditions. Environ Sci Technol 1998; 32: 2633-2639. https://doi.org/10.1021/es980006c

Sponza DT, Celebi H. Removal of oxytetracycline (OTC) in a synthetic pharmaceutical wastewater by sequential anaerobic multichamber bed reactor (AMCBR)/completely stirred tank reactor (CSTR) system: biodegradation and inhibition kinetics. J Chem Technol Biotechnol 2012; 87: 961-975. https://doi.org/10.1002/jctb.3706

APHA-AWWA-WEF. Standard Methods for the Examination of Water and Wastewater. 24th edition, American Public Health Association/American Water Works Association/Water Environment Federation, Washington, DC, USA 2018; pp. 340-390.

Stringfellow WT, Aitken MD. Competitive metabolism of naphthalene, methylphthalenes, and fluorene by phenanthrene-degrading Pseudomonas. Appl Environ Microbiol 1995; 61: 357-362. https://doi.org/10.1128/AEM.61.1.357-362.1995

Haritash AK, Kaushik CP. Biodegradation aspects of Polycyclic Aromatic Hydrocarbons (PAHs): A review. J Hazard Mater 2009; 169: 1-15. https://doi.org/10.1016/j.jhazmat.2009.03.137

Yuan SY, Shiung LC, Chang BV. Biodegradation of polycyclic aromatic hydrocarbons by inoculated microorganisms in soil. Bull Environ Conatm Toxicol 2002; 69: 66-73. https://doi.org/10.1007/s00128-002-0011-z

Zang S, et al. Influence of Chemical Oxidant on Degradation of Benzo[a]pyrene Metabolites by the Bacterium-Zoogloea sp. Environ Engineer Sci 2008; 25: 247-254. https://doi.org/10.1089/ees.2006.0209

Juhasz AL, Stanley GA, Britz ML. Metabolite repression inhibits degradation of benzo[a]pyrene and dibenz[a,h]anthracene by Stenotrophomonas maltophilia VUN 10,003. J Ind Microbiol Biotechnol 2002; 28: 88-96. https://doi.org/10.1038/sj/jim/7000216

Shuler ML, Kargi F. Bioprocess Engineering 2nd ed., New Jersey: Prentice Hall; 2002; pp. 123-145

Boonchan S, Britz FL, Stanley GA. Degradation and mineralization of high molecular-weight polycyclic aromatic hydrocarbons by defined fungal-bacterial cocultures. Appl Environ Microbiol 2000; 66: 1007-1019. https://doi.org/10.1128/AEM.66.3.1007-1019.2000

Liu WD, Lee CY. Practical identification analysis of haldane kinetic parameters describing phenol biodegradation in batch operations. J Environ Eng Manage 2007; 17: 71-80.

Pishgara R, et al. Phenol biodegradation kinetics in the presence of supplimentary substrate. Int J Engineer 2012; 25: 181-191. https://doi.org/10.5829/idosi.ije.2012.25.03b.05

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright (c) 2019 Delia Teresa Sponza, Hakan Celebi, Oguzhan Gok