Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells
Microbial fuel cells (MFCs) can generate electricity simultaneously with wastewater treatment. For MFCs to be considered a cost-effective treatment technology, they should quickly re-establish a stable electroactive microbial community in the case of system failure. In order to shorten startup times...
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doaj-f264c66e5a25411e9d32128dcb91318a2020-12-01T00:02:22ZengMDPI AGApplied Sciences2076-34172020-11-01108570857010.3390/app10238570Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel CellsKeren Yanuka-Golub0Leah Reshef1Judith Rishpon2Uri Gophna3The Porter School of Environmental Studies, Tel Aviv University, P.O. Box 39040, Tel Aviv 6997801, IsraelSchool of Molecular Cell Biology and Biotechnology, Tel Aviv University, P.O. Box 39040, Tel Aviv 6997801, IsraelThe Porter School of Environmental Studies, Tel Aviv University, P.O. Box 39040, Tel Aviv 6997801, IsraelThe Porter School of Environmental Studies, Tel Aviv University, P.O. Box 39040, Tel Aviv 6997801, IsraelMicrobial fuel cells (MFCs) can generate electricity simultaneously with wastewater treatment. For MFCs to be considered a cost-effective treatment technology, they should quickly re-establish a stable electroactive microbial community in the case of system failure. In order to shorten startup times, temporal studies of anodic biofilm development are required, however, frequent sampling can reduce the functionality of the system due to electroactive biomass loss; therefore, on-line monitoring of the microbial community without interfering with the system’s stability is essential. Although all anodic biofilms were composed of <i>Desulfuromonadaceae</i>, MFCs differed in startup times. Generally, a <i>Desulfuromonadaceae</i>-dominated biofilm was associated with faster startup MFCs. A positive PCR product of a specific 16S rRNA gene PCR primer set for detecting the acetate-oxidizing, Eticyclidine (PCE)-dechlorinating <i>Desulfuromonas</i> group was associated with efficient MFCs in our samples. Therefore, this observation could serve as a biomarker for monitoring the formation of an efficient anodic biofilm. Additionally, we successfully enriched an electroactive consortium from an active anode, also resulting in a positive amplification of the specific primer set. Direct application of this enrichment to a clean MFC anode showed a substantial reduction of startup times from 18 to 3 days.https://www.mdpi.com/2076-3417/10/23/8570microbial fuel cells (MFCs)startup time<i>Desulfuromonadaceae</i>anodic biofilmspecific 16S-<i>Desulfuromonas</i> primer set |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Keren Yanuka-Golub Leah Reshef Judith Rishpon Uri Gophna |
spellingShingle |
Keren Yanuka-Golub Leah Reshef Judith Rishpon Uri Gophna Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells Applied Sciences microbial fuel cells (MFCs) startup time <i>Desulfuromonadaceae</i> anodic biofilm specific 16S-<i>Desulfuromonas</i> primer set |
author_facet |
Keren Yanuka-Golub Leah Reshef Judith Rishpon Uri Gophna |
author_sort |
Keren Yanuka-Golub |
title |
Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells |
title_short |
Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells |
title_full |
Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells |
title_fullStr |
Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells |
title_full_unstemmed |
Specific <i>Desulfuromonas</i> Strains Can Determine Startup Times of Microbial Fuel Cells |
title_sort |
specific <i>desulfuromonas</i> strains can determine startup times of microbial fuel cells |
publisher |
MDPI AG |
series |
Applied Sciences |
issn |
2076-3417 |
publishDate |
2020-11-01 |
description |
Microbial fuel cells (MFCs) can generate electricity simultaneously with wastewater treatment. For MFCs to be considered a cost-effective treatment technology, they should quickly re-establish a stable electroactive microbial community in the case of system failure. In order to shorten startup times, temporal studies of anodic biofilm development are required, however, frequent sampling can reduce the functionality of the system due to electroactive biomass loss; therefore, on-line monitoring of the microbial community without interfering with the system’s stability is essential. Although all anodic biofilms were composed of <i>Desulfuromonadaceae</i>, MFCs differed in startup times. Generally, a <i>Desulfuromonadaceae</i>-dominated biofilm was associated with faster startup MFCs. A positive PCR product of a specific 16S rRNA gene PCR primer set for detecting the acetate-oxidizing, Eticyclidine (PCE)-dechlorinating <i>Desulfuromonas</i> group was associated with efficient MFCs in our samples. Therefore, this observation could serve as a biomarker for monitoring the formation of an efficient anodic biofilm. Additionally, we successfully enriched an electroactive consortium from an active anode, also resulting in a positive amplification of the specific primer set. Direct application of this enrichment to a clean MFC anode showed a substantial reduction of startup times from 18 to 3 days. |
topic |
microbial fuel cells (MFCs) startup time <i>Desulfuromonadaceae</i> anodic biofilm specific 16S-<i>Desulfuromonas</i> primer set |
url |
https://www.mdpi.com/2076-3417/10/23/8570 |
work_keys_str_mv |
AT kerenyanukagolub specificidesulfuromonasistrainscandeterminestartuptimesofmicrobialfuelcells AT leahreshef specificidesulfuromonasistrainscandeterminestartuptimesofmicrobialfuelcells AT judithrishpon specificidesulfuromonasistrainscandeterminestartuptimesofmicrobialfuelcells AT urigophna specificidesulfuromonasistrainscandeterminestartuptimesofmicrobialfuelcells |
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