Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-4582
Main Title: Development of a flow-fluorescence in situ hybridization protocol for the analysis of microbial communities in anaerobic fermentation liquor
Author(s): Nettmann, Edith
Fröhling, Antje
Heeg, Kathrin
Klocke, Michael
Schlüter, Oliver
Mumme, Jan
Type: Article
Language: English
Language Code: en
Abstract: Background: The production of bio-methane from renewable raw material is of high interest because of the increasing scarcity of fossil fuels. The process of biomethanation is based on the inter- and intraspecific metabolic activity of a highly diverse and dynamic microbial community. The community structure of the microbial biocenosis varies between different biogas reactors and the knowledge about these microbial communities is still fragmentary. However, up to now no approaches are available allowing a fast and reliable access to the microbial community structure. Hence, the aim of this study was to originate a Flow-FISH protocol, namely a combination of flow cytometry and fluorescence in situ hybridization, for the analysis of the metabolically active microorganisms in biogas reactor samples. With respect to the heterogenic texture of biogas reactor samples and to collect all cells including those of cell aggregates and biofilms the development of a preceding purification procedure was indispensable. Results: Six different purification procedures with in total 29 modifications were tested. The optimized purification procedure combines the use of the detergent sodium hexametaphosphate with ultrasonic treatment and a final filtration step. By this treatment, the detachment of microbial cells from particles as well as the disbandment of cell aggregates was obtained at minimized cell loss. A Flow-FISH protocol was developed avoiding dehydration and minimizing centrifugation steps. In the exemplary application of this protocol on pure cultures as well as biogas reactor samples high hybridization rates were achieved for commonly established domain specific oligonucleotide probes enabling the specific detection of metabolically active bacteria and archaea. Cross hybridization and autofluorescence effects could be excluded by the use of a nonsense probe and negative controls, respectively. Conclusions: The approach described in this study enables for the first time the analysis of the metabolically active fraction of the microbial communities within biogas reactors by Flow-FISH.
URI: urn:nbn:de:kobv:83-opus4-69412
http://depositonce.tu-berlin.de/handle/11303/4879
http://dx.doi.org/10.14279/depositonce-4582
Issue Date: 2013
Date Available: 29-Jul-2015
DDC Class: 570 Biowissenschaften; Biologie
610 Medizin und Gesundheit
Subject(s): Anaerobic digestion
Biogas reactor
Flow cytometry
Flow-FISH
Fluorescence in situ hybridization
Upflow anaerobic solid state (UASS) reactor
Creative Commons License: https://creativecommons.org/licenses/by/2.0/
Journal Title: BMC Microbiology
Publisher: BioMed Central
Publisher Place: London
Volume: 13
Article Number: 278
Publisher DOI: 10.1186/1471-2180-13-278
Notes: First published by BioMed Central Nettmann, Edith ; Fröhling, Antje ; Heeg, Kathrin ; Klocke, Michael; Schlüter, Oliver ; Mumme, Jan : Development of a flow fluorescence in situ hybridization protocol for the analysis of microbial communities in anaerobic fermentation liquor. - In: BMC Microbiology. - ISSN 1471-2180 (online). - 13 (2013), art. 278. - doi:10.1186/1471-2180-13-278.
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