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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2022, Vol. 16 Issue (8) : 97    https://doi.org/10.1007/s11783-022-1518-7
RESEARCH ARTICLE
An antibiotic composite electrode for improving the sensitivity of electrochemically active biofilm biosensor
Shuyi Wang1, Xiang Qi1, Yong Jiang2(), Panpan Liu3, Wen Hao1, Jinbin Han1, Peng Liang1()
1. State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China
2. Fujian Provincial Key Laboratory of Soil Environmental Health and Regulation, College of Resources and Environment, Fujian Agriculture and Forestry University, Fuzhou 350002, China
3. School of Ecology and Environment, Zhengzhou University, Zhengzhou 450001, China
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Abstract

• Antibiotic azithromycin employed in graphite electrode for EAB biosensor.

• Azithromycin at 0.5% dosage increased the sensitivity for toxic formaldehyde.

• Azithromycin increased the relative abundance of Geobacter.

• Azithromycin regulated thickness of electroactive biofilm.

Extensive research has been carried out for improved sensitivity of electroactive biofilm-based sensor (EAB-sensor), which is recognized as a useful tool in water quality early-warning. Antibiotic that is employed widely to treat infection has been proved feasible in this study to regulate the EAB and to increase the EAB-biosensor’s sensitivity. A novel composite electrode was prepared using azithromycin (AZM) and graphite powder (GP), namely AZM@GP electrode, and was employed as the anode in EAB-biosensor. Different dosages of AZM, i.e., 2 mg, 4 mg, and 8 mg, referred to as 0.25%, 0.5% and 1% AZM@GP were under examination. Results showed that EAB-biosensor was greatly benefited from appropriate dosage of AZM (0.5% AZM@GP) with reduced start-up time period, comparatively higher voltage output, more readable electrical signal and increased inhibition rate (30%-65% higher than control sensor with GP electrode) when exposing to toxic formaldehyde. This may be attributed to the fact that AZM inhibited the growth of non-EAM without much influence on the physiologic or metabolism activities of EAM under proper dosage. Further investigation of the biofilm morphology and microbial community analysis suggested that the biofilm formation was optimized with reduced thickness and enriched Geobacter with 0.5% AZM@GP dosage. This novel electrode is easily fabricated and equipped, and therefore would be a promising way to facilitate the practical application of EAB-sensors.

Keywords AZM@GP composite electrode      EAB-biosensor      Water quality early-warning     
Corresponding Author(s): Yong Jiang,Peng Liang   
About author:

Tongcan Cui and Yizhe Hou contributed equally to this work.

Issue Date: 08 December 2021
 Cite this article:   
Shuyi Wang,Xiang Qi,Yong Jiang, et al. An antibiotic composite electrode for improving the sensitivity of electrochemically active biofilm biosensor[J]. Front. Environ. Sci. Eng., 2022, 16(8): 97.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-022-1518-7
https://academic.hep.com.cn/fese/EN/Y2022/V16/I8/97
Fig.1  (A) Preparation principle of AZM@GP, (B) true-color photographs and SEM images of GP and 1% AZM@GP electrode, (C) CV curves of GP and AZM@GP composite electrode, (D) EIS plots of GP and AZM@GP composite electrode.
Fig.2  (A) Schematic diagram of the built EAB-sensor, (B) Electrical signal output during start-up.
Fig.3  Toxicity tests of formaldehyde under different concentrations. NES changes within 30 min under 0.01% (A), 0.02% (B), 0.03% (C) formaldehyde, respectively and (D) corresponding inhibition rates at 30 min.
Fig.4  (A) Front view of CLSM images, (B) calculated biofilm thickness, (C) SEM images of EABs formed on different electrodes.
Fig.5  Microbial community analyses of EABs. (A) Chao 1 indicator, (B) relative abundance of microbial community.
1 A Adekunle, V Raghavan, B Tartakovsky (2019). On-line monitoring of heavy metals-related toxicity with a microbial fuel cell biosensor. Biosensors & Bioelectronics, 132: 382–390
https://doi.org/10.1016/j.bios.2019.03.011 pmid: 30903911
2 A Antonacci, V Scognamiglio (2020). Biotechnological advances in the design of algae-based biosensors. Trends in Biotechnology, 38(3): 334–347
https://doi.org/10.1016/j.tibtech.2019.10.005 pmid: 31706693
3 A R Attili, S Preziuso, V Ngu Ngwa, A Cantalamessa, M Moriconi, V Cuteri (2016). Clinical evaluation of the use of enrofloxacin against Staphylococcus aureus clinical mastitis in sheep. Small Ruminant Research, 136: 72–77
https://doi.org/10.1016/j.smallrumres.2016.01.004
4 C Catania, A A Karbelkar, A L Furst (2021). Engineering the interface between electroactive bacteria and electrodes. Joule, 5(4): 743–747
https://doi.org/10.1016/j.joule.2021.02.001
5 S Cheng, D Xing, D F Call, B E Logan (2009). Direct biological conversion of electrical current into methane by electromethanogenesis. Environmental Science & Technology, 43(10): 3953–3958
https://doi.org/10.1021/es803531g pmid: 19544913
6 S Dong, C Yin, X Chen (2020). Toxicity-oriented water quality engineering. Frontiers of Environmental Science & Engineering, 14(5): 80
7 F Ejeian, P Etedali, H A Mansouri-Tehrani, A Soozanipour, Z X Low, M Asadnia, A Taheri-Kafrani, A Razmjou (2018). Biosensors for wastewater monitoring: A review. Biosensors & Bioelectronics, 118: 66–79
https://doi.org/10.1016/j.bios.2018.07.019 pmid: 30056302
8 M Hackbarth, T Jung, J E Reiner, J Gescher, H Horn, A Hille-Reichel, M Wagner (2020). Monitoring and quantification of bioelectrochemical Kyrpidia spormannii biofilm development in a novel flow cell setup. Chemical Engineering Journal, 390: 124604
https://doi.org/10.1016/j.cej.2020.124604
9 Y Jiang, N Chu, R J Zeng (2019). Submersible probe type microbial electrochemical sensor for volatile fatty acids monitoring in the anaerobic digestion process. Journal of Cleaner Production, 232: 1371–1378
https://doi.org/10.1016/j.jclepro.2019.06.041
10 Y Jiang, P Liang, P Liu, B Miao, Y Bian, H Zhang, X Huang (2017). Enhancement of the sensitivity of a microbial fuel cell sensor by transient-state operation. Environmental Science. Water Research & Technology, 3(3): 472–479
https://doi.org/10.1039/C6EW00346J
11 T Li, F Chen, Q Zhou, X Wang, C Liao, L Zhou, L Wan, J An, Y Wan, N Li (2020a). Unignorable toxicity of formaldehyde on electroactive bacteria in bioelectrochemical systems. Environmental Research, 183: 109143
https://doi.org/10.1016/j.envres.2020.109143 pmid: 32028180
12 T Li, C Liao, J An, L Zhou, L Tian, Q Zhou, N Li, X Wang (2021). A highly sensitive bioelectrochemical toxicity sensor and its evaluation using immediate current attenuation. Science of the Total Environment, 766: 142646
https://doi.org/10.1016/j.scitotenv.2020.142646 pmid: 33066964
13 T Li, Q Zhou, L Zhou, Y Yan, C Liao, L Wan, J An, N Li, X Wang (2020b). Acetate limitation selects Geobacter from mixed inoculum and reduces polysaccharide in electroactive biofilm. Water Research, 177: 115776
https://doi.org/10.1016/j.watres.2020.115776 pmid: 32294591
14 H Lu, Y Yu, Y Zhou, F Xing (2019). A quantitative evaluation method for wastewater toxicity based on a microbial fuel cell. Ecotoxicology and Environmental Safety, 183(2019): 109589
15 B E Logan, R Rossi, A Ragab, P E Saikaly (2019). Electroactive microorganisms in bioelectrochemical systems. Nature Reviews. Microbiology, 17(5): 307–319
https://doi.org/10.1038/s41579-019-0173-x pmid: 30846876
16 D R Lovley (2008). The microbe electric: Conversion of organic matter to electricity. Current Opinion in Biotechnology, 19(6): 564–571
https://doi.org/10.1016/j.copbio.2008.10.005 pmid: 19000760
17 J Pan, J Hu, B Liu, J Li, D Wang, C Bu, X Wang, K Xiao, S Liang, J Yang, H Hou (2020). Enhanced quorum sensing of anode biofilm for better sensing linearity and recovery capability of microbial fuel cell toxicity sensor. Environmental Research, 181: 108906
https://doi.org/10.1016/j.envres.2019.108906 pmid: 31740039
18 X Peng, H Yu, X Wang, Q Zhou, S Zhang, L Geng, J Sun, Z Cai (2012). Enhanced performance and capacitance behavior of anode by rolling Fe3O4 into activated carbon in microbial fuel cells. Bioresource Technology, 121: 450–453
https://doi.org/10.1016/j.biortech.2012.06.021 pmid: 22863179
19 S Pentassuglia, V Agostino, T Tommasi (2018). Encyclopedia of Interfacial Chemistry. Wandelt, K. (ed). Oxford: Elsevier,110–123
20 X Qi, P Liu, P Liang, W Hao, M Li, X Huang (2019). Dual-signal-biosensor based on luminescent bacteria biofilm for real-time online alert of Cu(II) shock. Biosensors & Bioelectronics, 142: 111500
https://doi.org/10.1016/j.bios.2019.111500 pmid: 31323469
21 X Qi, P Liu, P Liang, W Hao, M Li, Q Li, Y Zhou, X Huang (2020a). Biofilm’s morphology design for high sensitivity of bioelectrochemical sensor: An experimental and modeling study. Science of the Total Environment, 729: 138908
https://doi.org/10.1016/j.scitotenv.2020.138908 pmid: 32361449
22 X Qi, S Wang, T Li, X Wang, Y Jiang, Y Zhou, X Zhou, X Huang, P Liang (2021). An electroactive biofilm-based biosensor for water safety: Pollutants detection and early-warning. Biosensors & Bioelectronics, 173: 112822
https://doi.org/10.1016/j.bios.2020.112822 pmid: 33221512
23 G Reguera, K D McCarthy, T Mehta, J S Nicoll, M T Tuominen, D R Lovley (2005). Extracellular electron transfer via microbial nanowires. Nature, 435(7045): 1098–1101
https://doi.org/10.1038/nature03661 pmid: 15973408
24 L Ren, S R McCuskey, A Moreland, G C Bazan, T Q Nguyen (2019). Tuning Geobacter sulfurreducens biofilm with conjugated polyelectrolyte for increased performance in bioelectrochemical system. Biosensors & Bioelectronics, 144: 111630
https://doi.org/10.1016/j.bios.2019.111630 pmid: 31505403
25 U Schröder, F Harnisch, L T Angenent (2015). Microbial electrochemistry and technology: Terminology and classification. Energy & Environmental Science, 8(2): 513–519
https://doi.org/10.1039/C4EE03359K
26 L Shi, H Dong, G Reguera, H Beyenal, A Lu, J Liu, H Q Yu, J K Fredrickson (2016). Extracellular electron transfer mechanisms between microorganisms and minerals. Nature Reviews. Microbiology, 14(10): 651–662
https://doi.org/10.1038/nrmicro.2016.93 pmid: 27573579
27 M J E Souza, C F Bittencourt, P D S E S Filho (2004). Microbiological assay for enrofloxacin injection. International Journal of Pharmaceutics, 271(1): 287–291
28 M Sui, Y Li, Y Jiang, Y Zhang, L Wang, W Zhang, X Wang (2021). Light exposure interferes with electroactive biofilm enrichment and reduces extracellular electron transfer efficiency. Water Research, 188: 116512
https://doi.org/10.1016/j.watres.2020.116512 pmid: 33161361
29 Z M Summers, H E Fogarty, C Leang, A E Franks, N S Malvankar, D R Lovley (2010). Direct exchange of electrons within aggregates of an evolved syntrophic coculture of anaerobic bacteria. Science, 330(6009): 1413–1415
https://doi.org/10.1126/science.1196526 pmid: 21127257
30 A Tarushi, C P Raptopoulou, V Psycharis, A Terzis, G Psomas, D P Kessissoglou (2010). Zinc(II) complexes of the second-generation quinolone antibacterial drug enrofloxacin: Structure and DNA or albumin interaction. Bioorganic & Medicinal Chemistry, 18(7): 2678–2685
https://doi.org/10.1016/j.bmc.2010.02.021 pmid: 20227280
31 H Wasito, A Fatoni, D Hermawan, S S Susilowati (2019). Immobilized bacterial biosensor for rapid and effective monitoring of acute toxicity in water. Ecotoxicology and Environmental Safety, 170: 205–209
https://doi.org/10.1016/j.ecoenv.2018.11.141 pmid: 30529914
32 Q Wen, F Kong, H Zheng, D Cao, Y Ren, J Yin (2011). Electricity generation from synthetic penicillin wastewater in an air-cathode single chamber microbial fuel cell. Chemical Engineering Journal, 168(2): 572–576
https://doi.org/10.1016/j.cej.2011.01.025
33 D Wu, F Sun, F J D Chua, Y Zhou (2020). Enhanced power generation in microbial fuel cell by an agonist of electroactive biofilm–Sulfamethoxazole. Chemical Engineering Journal, 384: 123238
https://doi.org/10.1016/j.cej.2019.123238
34 X Yi, Z Gao, L Liu, Q Zhu, G Hu, X Zhou (2020). Acute toxicity assessment of drinking water source with luminescent bacteria: Impact of environmental conditions and a case study in Luoma Lake, East China. Frontiers of Environmental Science & Engineering, 14(6): 109
35 D Yu, J Zhai, C Liu, X Zhang, L Bai, Y Wang, S Dong (2017). Small microbial three-electrode cell based biosensor for online detection of acute water toxicity. ACS Sensors, 2(11): 1637–1643
36 L Zhou, T Li, J An, C Liao, N Li, X Wang (2017). Subminimal inhibitory concentration (sub-MIC) of antibiotic induces electroactive biofilm formation in bioelectrochemical systems. Water Research, 125: 280–287
https://doi.org/10.1016/j.watres.2017.08.059 pmid: 28866443
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