Antibiotic fermentation residue for biohydrogen production: Inhibitory mechanisms of the inherent antibiotic
Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H2 generation and waste...
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Published in | The Science of the total environment Vol. 944; p. 173986 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
20.09.2024
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Abstract | Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H2 generation and waste management. However, the inherent antibiotic in antibiotic fermentation residue may inhibit its dark fermentation performance, and current understanding on this topic is limited. This investigation examined the impact of the inherent antibiotic on the dark H2 fermentation of Cephalosporin C (CEPC) fermentation residue, and explored the mechanisms from the perspectives of bacterial communities and functional genes. It was found that CEP-C in the antibiotic fermentation residue significantly inhibited the H2 production, with the H2 yield decreasing from 17.2 mL/g-VSadded to 12.5 and 9.6 mL/g-VSadded at CEP-C concentrations of 100 and 200 mg/L, respectively. CEP-C also prolonged the H2-producing lag period. Microbiological analysis indicated that CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria, as well as downregulated the genes involved in hydrogen generation from the“pyruvate pathway” and“NADH pathway”, essentially leading to the decline of H2 productivity. The present work gains insights into how cephalosporin antibiotics influence the dark H2 fermentation, and provide guidance for mitigating the inhibitory effects.
[Display omitted]
•Inhibition of CEP-C on bioH2 production from its fermentation residue was examined.•H2 yield decreased by 44.0 % at CEP-C concentration of 200 mg/L.•The inherent CEP-C inhibited the efficiency of organic utilization.•CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria.•CEP-C down-regulated the genes involved in two crucial H2-producing pathways. |
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AbstractList | Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H
generation and waste management. However, the inherent antibiotic in antibiotic fermentation residue may inhibit its dark fermentation performance, and current understanding on this topic is limited. This investigation examined the impact of the inherent antibiotic on the dark H
fermentation of Cephalosporin C (CEPC) fermentation residue, and explored the mechanisms from the perspectives of bacterial communities and functional genes. It was found that CEP-C in the antibiotic fermentation residue significantly inhibited the H
production, with the H
yield decreasing from 17.2 mL/g-VS
to 12.5 and 9.6 mL/g-VS
at CEP-C concentrations of 100 and 200 mg/L, respectively. CEP-C also prolonged the H
-producing lag period. Microbiological analysis indicated that CEP-C remarkably decreased the abundances of high-yielding H
-producing bacteria, as well as downregulated the genes involved in hydrogen generation from the"pyruvate pathway" and"NADH pathway", essentially leading to the decline of H
productivity. The present work gains insights into how cephalosporin antibiotics influence the dark H
fermentation, and provide guidance for mitigating the inhibitory effects. Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H2 generation and waste management. However, the inherent antibiotic in antibiotic fermentation residue may inhibit its dark fermentation performance, and current understanding on this topic is limited. This investigation examined the impact of the inherent antibiotic on the dark H2 fermentation of Cephalosporin C (CEPC) fermentation residue, and explored the mechanisms from the perspectives of bacterial communities and functional genes. It was found that CEP-C in the antibiotic fermentation residue significantly inhibited the H2 production, with the H2 yield decreasing from 17.2 mL/g-VSadded to 12.5 and 9.6 mL/g-VSadded at CEP-C concentrations of 100 and 200 mg/L, respectively. CEP-C also prolonged the H2-producing lag period. Microbiological analysis indicated that CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria, as well as downregulated the genes involved in hydrogen generation from the"pyruvate pathway" and"NADH pathway", essentially leading to the decline of H2 productivity. The present work gains insights into how cephalosporin antibiotics influence the dark H2 fermentation, and provide guidance for mitigating the inhibitory effects.Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H2 generation and waste management. However, the inherent antibiotic in antibiotic fermentation residue may inhibit its dark fermentation performance, and current understanding on this topic is limited. This investigation examined the impact of the inherent antibiotic on the dark H2 fermentation of Cephalosporin C (CEPC) fermentation residue, and explored the mechanisms from the perspectives of bacterial communities and functional genes. It was found that CEP-C in the antibiotic fermentation residue significantly inhibited the H2 production, with the H2 yield decreasing from 17.2 mL/g-VSadded to 12.5 and 9.6 mL/g-VSadded at CEP-C concentrations of 100 and 200 mg/L, respectively. CEP-C also prolonged the H2-producing lag period. Microbiological analysis indicated that CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria, as well as downregulated the genes involved in hydrogen generation from the"pyruvate pathway" and"NADH pathway", essentially leading to the decline of H2 productivity. The present work gains insights into how cephalosporin antibiotics influence the dark H2 fermentation, and provide guidance for mitigating the inhibitory effects. Antibiotic fermentation residue, which is generated from the microbial antibiotic production process, has been a troublesome waste faced by the pharmaceutical industry. Dark fermentation is a potential technology to treat antibiotic fermentation residue in terms of renewable H2 generation and waste management. However, the inherent antibiotic in antibiotic fermentation residue may inhibit its dark fermentation performance, and current understanding on this topic is limited. This investigation examined the impact of the inherent antibiotic on the dark H2 fermentation of Cephalosporin C (CEPC) fermentation residue, and explored the mechanisms from the perspectives of bacterial communities and functional genes. It was found that CEP-C in the antibiotic fermentation residue significantly inhibited the H2 production, with the H2 yield decreasing from 17.2 mL/g-VSadded to 12.5 and 9.6 mL/g-VSadded at CEP-C concentrations of 100 and 200 mg/L, respectively. CEP-C also prolonged the H2-producing lag period. Microbiological analysis indicated that CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria, as well as downregulated the genes involved in hydrogen generation from the“pyruvate pathway” and“NADH pathway”, essentially leading to the decline of H2 productivity. The present work gains insights into how cephalosporin antibiotics influence the dark H2 fermentation, and provide guidance for mitigating the inhibitory effects. [Display omitted] •Inhibition of CEP-C on bioH2 production from its fermentation residue was examined.•H2 yield decreased by 44.0 % at CEP-C concentration of 200 mg/L.•The inherent CEP-C inhibited the efficiency of organic utilization.•CEP-C remarkably decreased the abundances of high-yielding H2-producing bacteria.•CEP-C down-regulated the genes involved in two crucial H2-producing pathways. |
ArticleNumber | 173986 |
Author | Xu, Youtong Yang, Guang Wang, Jianlong |
Author_xml | – sequence: 1 givenname: Guang surname: Yang fullname: Yang, Guang organization: State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, PR China – sequence: 2 givenname: Youtong surname: Xu fullname: Xu, Youtong organization: China National Chemical Engineering International Corporation Ltd., Beijing 100020, PR China – sequence: 3 givenname: Jianlong surname: Wang fullname: Wang, Jianlong email: wangjl@tsinghua.edu.cn organization: Laboratory of Environmental Technology, INET, Tsinghua University, Beijing 100084, PR China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38876344$$D View this record in MEDLINE/PubMed |
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Keywords | Inhibition Metagenomics analysis Antibiotic fermentation residue Microbial community Biohydrogen production |
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SubjectTerms | Antibiotic fermentation residue Biohydrogen production Inhibition Metagenomics analysis Microbial community |
Title | Antibiotic fermentation residue for biohydrogen production: Inhibitory mechanisms of the inherent antibiotic |
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