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Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence
BACKGROUND: The widely established production of CH(4) from renewable biomass in industrial scale anaerobic reactors may play a major role in the future energy supply. It relies on methanogenic archaea as key organisms which represent the bottleneck in the process. The quantitative analysis of these...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663091/ https://www.ncbi.nlm.nih.gov/pubmed/29084543 http://dx.doi.org/10.1186/s12934-017-0793-7 |
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author | Lambrecht, Johannes Cichocki, Nicolas Hübschmann, Thomas Koch, Christin Harms, Hauke Müller, Susann |
author_facet | Lambrecht, Johannes Cichocki, Nicolas Hübschmann, Thomas Koch, Christin Harms, Hauke Müller, Susann |
author_sort | Lambrecht, Johannes |
collection | PubMed |
description | BACKGROUND: The widely established production of CH(4) from renewable biomass in industrial scale anaerobic reactors may play a major role in the future energy supply. It relies on methanogenic archaea as key organisms which represent the bottleneck in the process. The quantitative analysis of these organisms can help to maximize process performance, uncover disturbances before failure, and may ultimately lead to community-based process control schemes. Existing qPCR and fluorescence microscopy-based methods are very attractive but can be cost-intensive and laborious. RESULTS: In this study we present an autofluorescence-based, flow cytometric method for the fast low-cost quantification of methanogenic archaea in complex microbial communities and crude substrates. The method was applied to a methanogenic enrichment culture (MEC) and digester samples (DS). The methanogenic archaea were quantified using the distinct fluorescence of their cofactor F(420) in a range from 3.7 × 10(8) (± 3.3 × 10(6)) cells mL(−1) and 1.8 x 10(9) (± 1.1 × 10(8)) cells mL(−1). We evaluated different fixation methods and tested the sample stability. Stable abundance and fluorescence intensity were recorded up to 26 days during aerobic storage in PBS at 6 °C. The discrimination of the whole microbial community from the ubiquitous particle noise was facilitated by SYBR Green I staining and enabled calculation of relative abundances of methanogenic archaea of up to 9.64 ± 0.23% in the MEC and up to 4.43 ± 0.74% in the DS. The metaprofiling of the mcrA gene reinforced the results. CONCLUSIONS: The presented method allows for fast and reliable quantification of methanogenic archaea in microbial communities under authentic digester conditions and can thus be useful for process monitoring and control in biogas digesters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-017-0793-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5663091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56630912017-11-01 Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence Lambrecht, Johannes Cichocki, Nicolas Hübschmann, Thomas Koch, Christin Harms, Hauke Müller, Susann Microb Cell Fact Technical Notes BACKGROUND: The widely established production of CH(4) from renewable biomass in industrial scale anaerobic reactors may play a major role in the future energy supply. It relies on methanogenic archaea as key organisms which represent the bottleneck in the process. The quantitative analysis of these organisms can help to maximize process performance, uncover disturbances before failure, and may ultimately lead to community-based process control schemes. Existing qPCR and fluorescence microscopy-based methods are very attractive but can be cost-intensive and laborious. RESULTS: In this study we present an autofluorescence-based, flow cytometric method for the fast low-cost quantification of methanogenic archaea in complex microbial communities and crude substrates. The method was applied to a methanogenic enrichment culture (MEC) and digester samples (DS). The methanogenic archaea were quantified using the distinct fluorescence of their cofactor F(420) in a range from 3.7 × 10(8) (± 3.3 × 10(6)) cells mL(−1) and 1.8 x 10(9) (± 1.1 × 10(8)) cells mL(−1). We evaluated different fixation methods and tested the sample stability. Stable abundance and fluorescence intensity were recorded up to 26 days during aerobic storage in PBS at 6 °C. The discrimination of the whole microbial community from the ubiquitous particle noise was facilitated by SYBR Green I staining and enabled calculation of relative abundances of methanogenic archaea of up to 9.64 ± 0.23% in the MEC and up to 4.43 ± 0.74% in the DS. The metaprofiling of the mcrA gene reinforced the results. CONCLUSIONS: The presented method allows for fast and reliable quantification of methanogenic archaea in microbial communities under authentic digester conditions and can thus be useful for process monitoring and control in biogas digesters. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-017-0793-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-30 /pmc/articles/PMC5663091/ /pubmed/29084543 http://dx.doi.org/10.1186/s12934-017-0793-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Technical Notes Lambrecht, Johannes Cichocki, Nicolas Hübschmann, Thomas Koch, Christin Harms, Hauke Müller, Susann Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title | Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title_full | Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title_fullStr | Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title_full_unstemmed | Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title_short | Flow cytometric quantification, sorting and sequencing of methanogenic archaea based on F(420) autofluorescence |
title_sort | flow cytometric quantification, sorting and sequencing of methanogenic archaea based on f(420) autofluorescence |
topic | Technical Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663091/ https://www.ncbi.nlm.nih.gov/pubmed/29084543 http://dx.doi.org/10.1186/s12934-017-0793-7 |
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