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Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors
Biofilm formation on the filtration membrane and the subsequent clogging of membrane pores (called biofouling) is one of the most persistent problems in membrane bioreactors for wastewater treatment and reclamation. Here, we investigated the structure and microbiome of fouling-related biofilms in th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445582/ https://www.ncbi.nlm.nih.gov/pubmed/28649406 http://dx.doi.org/10.1038/s41522-016-0010-1 |
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author | Inaba, Tomohiro Hori, Tomoyuki Aizawa, Hidenobu Ogata, Atsushi Habe, Hiroshi |
author_facet | Inaba, Tomohiro Hori, Tomoyuki Aizawa, Hidenobu Ogata, Atsushi Habe, Hiroshi |
author_sort | Inaba, Tomohiro |
collection | PubMed |
description | Biofilm formation on the filtration membrane and the subsequent clogging of membrane pores (called biofouling) is one of the most persistent problems in membrane bioreactors for wastewater treatment and reclamation. Here, we investigated the structure and microbiome of fouling-related biofilms in the membrane bioreactor using non-destructive confocal reflection microscopy and high-throughput Illumina sequencing of 16S rRNA genes. Direct confocal reflection microscopy indicated that the thin biofilms were formed and maintained regardless of the increasing transmembrane pressure, which is a common indicator of membrane fouling, at low organic-loading rates. Their solid components were primarily extracellular polysaccharides and microbial cells. In contrast, high organic-loading rates resulted in a rapid increase in the transmembrane pressure and the development of the thick biofilms mainly composed of extracellular lipids. High-throughput sequencing revealed that the biofilm microbiomes, including major and minor microorganisms, substantially changed in response to the organic-loading rates and biofilm development. These results demonstrated for the first time that the architectures, chemical components, and microbiomes of the biofilms on fouled membranes were tightly associated with one another and differed considerably depending on the organic-loading conditions in the membrane bioreactor, emphasizing the significance of alternative indicators other than the transmembrane pressure for membrane biofouling. |
format | Online Article Text |
id | pubmed-5445582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54455822017-06-23 Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors Inaba, Tomohiro Hori, Tomoyuki Aizawa, Hidenobu Ogata, Atsushi Habe, Hiroshi NPJ Biofilms Microbiomes Article Biofilm formation on the filtration membrane and the subsequent clogging of membrane pores (called biofouling) is one of the most persistent problems in membrane bioreactors for wastewater treatment and reclamation. Here, we investigated the structure and microbiome of fouling-related biofilms in the membrane bioreactor using non-destructive confocal reflection microscopy and high-throughput Illumina sequencing of 16S rRNA genes. Direct confocal reflection microscopy indicated that the thin biofilms were formed and maintained regardless of the increasing transmembrane pressure, which is a common indicator of membrane fouling, at low organic-loading rates. Their solid components were primarily extracellular polysaccharides and microbial cells. In contrast, high organic-loading rates resulted in a rapid increase in the transmembrane pressure and the development of the thick biofilms mainly composed of extracellular lipids. High-throughput sequencing revealed that the biofilm microbiomes, including major and minor microorganisms, substantially changed in response to the organic-loading rates and biofilm development. These results demonstrated for the first time that the architectures, chemical components, and microbiomes of the biofilms on fouled membranes were tightly associated with one another and differed considerably depending on the organic-loading conditions in the membrane bioreactor, emphasizing the significance of alternative indicators other than the transmembrane pressure for membrane biofouling. Nature Publishing Group UK 2017-02-23 /pmc/articles/PMC5445582/ /pubmed/28649406 http://dx.doi.org/10.1038/s41522-016-0010-1 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Inaba, Tomohiro Hori, Tomoyuki Aizawa, Hidenobu Ogata, Atsushi Habe, Hiroshi Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title | Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title_full | Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title_fullStr | Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title_full_unstemmed | Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title_short | Architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
title_sort | architecture, component, and microbiome of biofilm involved in the fouling of membrane bioreactors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445582/ https://www.ncbi.nlm.nih.gov/pubmed/28649406 http://dx.doi.org/10.1038/s41522-016-0010-1 |
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