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Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems

BACKGROUND: Soil microbial fuel cells (MFCs) can remove antibiotics and antibiotic resistance genes (ARGs) simultaneously, but their removal mechanism is unclear. In this study, metagenomic analysis was employed to reveal the functional genes involved in degradation, electron transfer and the nitrog...

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Autores principales: Zhao, Xiaodong, Qin, Xiaorui, Jing, Xiuqing, Wang, Teng, Qiao, Qingqing, Li, Xiaojing, Yan, Pingmei, Li, Yongtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652473/
https://www.ncbi.nlm.nih.gov/pubmed/37974273
http://dx.doi.org/10.1186/s13068-023-02430-z
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author Zhao, Xiaodong
Qin, Xiaorui
Jing, Xiuqing
Wang, Teng
Qiao, Qingqing
Li, Xiaojing
Yan, Pingmei
Li, Yongtao
author_facet Zhao, Xiaodong
Qin, Xiaorui
Jing, Xiuqing
Wang, Teng
Qiao, Qingqing
Li, Xiaojing
Yan, Pingmei
Li, Yongtao
author_sort Zhao, Xiaodong
collection PubMed
description BACKGROUND: Soil microbial fuel cells (MFCs) can remove antibiotics and antibiotic resistance genes (ARGs) simultaneously, but their removal mechanism is unclear. In this study, metagenomic analysis was employed to reveal the functional genes involved in degradation, electron transfer and the nitrogen cycle in the soil MFC. RESULTS: The results showed that the soil MFC effectively removed tetracycline in the overlapping area of the cathode and anode, which was 64% higher than that of the control. The ARGs abundance increased by 14% after tetracycline was added (54% of the amplified ARGs belonged to efflux pump genes), while the abundance decreased by 17% in the soil MFC. Five potential degraders of tetracycline were identified, especially the species Phenylobacterium zucineum, which could secrete the 4-hydroxyacetophenone monooxygenase encoded by EC 1.14.13.84 to catalyse deacylation or decarboxylation. Bacillus, Geobacter, Anaerolinea, Gemmatirosa kalamazoonesis and Steroidobacter denitrificans since ubiquinone reductase (encoded by EC 1.6.5.3), succinate dehydrogenase (EC 1.3.5.1), Coenzyme Q-cytochrome c reductase (EC 1.10.2.2), cytochrome-c oxidase (EC 1.9.3.1) and electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1) served as complexes I, II, III, IV and ubiquinone, respectively, to accelerate electron transfer. Additionally, nitrogen metabolism-related gene abundance increased by 16% to support the microbial efficacy in the soil MFC, and especially EC 1.7.5.1, and coding the mutual conversion between nitrite and nitrate was obviously improved. CONCLUSIONS: The soil MFC promoted functional bacterial growth, increased functional gene abundance (including nitrogen cycling, electron transfer, and biodegradation), and facilitated antibiotic and ARG removal. Therefore, soil MFCs have expansive prospects in the remediation of antibiotic-contaminated soil. This study provides insight into the biodegradation mechanism at the gene level in soil bioelectrochemical remediation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-023-02430-z.
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spelling pubmed-106524732023-11-16 Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems Zhao, Xiaodong Qin, Xiaorui Jing, Xiuqing Wang, Teng Qiao, Qingqing Li, Xiaojing Yan, Pingmei Li, Yongtao Biotechnol Biofuels Bioprod Research BACKGROUND: Soil microbial fuel cells (MFCs) can remove antibiotics and antibiotic resistance genes (ARGs) simultaneously, but their removal mechanism is unclear. In this study, metagenomic analysis was employed to reveal the functional genes involved in degradation, electron transfer and the nitrogen cycle in the soil MFC. RESULTS: The results showed that the soil MFC effectively removed tetracycline in the overlapping area of the cathode and anode, which was 64% higher than that of the control. The ARGs abundance increased by 14% after tetracycline was added (54% of the amplified ARGs belonged to efflux pump genes), while the abundance decreased by 17% in the soil MFC. Five potential degraders of tetracycline were identified, especially the species Phenylobacterium zucineum, which could secrete the 4-hydroxyacetophenone monooxygenase encoded by EC 1.14.13.84 to catalyse deacylation or decarboxylation. Bacillus, Geobacter, Anaerolinea, Gemmatirosa kalamazoonesis and Steroidobacter denitrificans since ubiquinone reductase (encoded by EC 1.6.5.3), succinate dehydrogenase (EC 1.3.5.1), Coenzyme Q-cytochrome c reductase (EC 1.10.2.2), cytochrome-c oxidase (EC 1.9.3.1) and electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1) served as complexes I, II, III, IV and ubiquinone, respectively, to accelerate electron transfer. Additionally, nitrogen metabolism-related gene abundance increased by 16% to support the microbial efficacy in the soil MFC, and especially EC 1.7.5.1, and coding the mutual conversion between nitrite and nitrate was obviously improved. CONCLUSIONS: The soil MFC promoted functional bacterial growth, increased functional gene abundance (including nitrogen cycling, electron transfer, and biodegradation), and facilitated antibiotic and ARG removal. Therefore, soil MFCs have expansive prospects in the remediation of antibiotic-contaminated soil. This study provides insight into the biodegradation mechanism at the gene level in soil bioelectrochemical remediation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-023-02430-z. BioMed Central 2023-11-16 /pmc/articles/PMC10652473/ /pubmed/37974273 http://dx.doi.org/10.1186/s13068-023-02430-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhao, Xiaodong
Qin, Xiaorui
Jing, Xiuqing
Wang, Teng
Qiao, Qingqing
Li, Xiaojing
Yan, Pingmei
Li, Yongtao
Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title_full Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title_fullStr Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title_full_unstemmed Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title_short Key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
title_sort key genes of electron transfer, the nitrogen cycle and tetracycline removal in bioelectrochemical systems
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652473/
https://www.ncbi.nlm.nih.gov/pubmed/37974273
http://dx.doi.org/10.1186/s13068-023-02430-z
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