Monitoring co-cultures of Clostridium carboxidivorans and Clostridium kluyveri by fluorescence in situ hybridization with specific 23S rRNA oligonucleotide probes.

23S rRNA Clostridium carboxidivorans Clostridium kluyveri Co-cultivation Fluorescence in situ Hybridization Specific oligonucleotide probe

Journal

Systematic and applied microbiology
ISSN: 1618-0984
Titre abrégé: Syst Appl Microbiol
Pays: Germany
ID NLM: 8306133

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 17 07 2021
revised: 20 08 2021
accepted: 27 08 2021
pubmed: 5 11 2021
medline: 26 11 2021
entrez: 4 11 2021
Statut: ppublish

Résumé

The development of co-cultures of clostridial strains which combine different physiological traits represents a promising strategy to achieve the environmentally friendly production of biofuels and chemicals. For the optimization of such co-cultures it is essential to monitor their composition and stability throughout fermentation. FISH is a quick and sensitive method for the specific labeling and quantification of cells within microbial communities. This technique is neither limited by the anaerobic fermenter environment nor by the need of prior genetic modification of strains. In this study, two specific 23S rRNA oligonucleotide probes, ClosKluy and ClosCarb, were designed for the monitoring of C. kluyveri and C. carboxidivorans, respectively. After the optimization of hybridization conditions for both probes, which was achieved at 30% (v/v) formamide, a high specificity was observed with epifluorescence microscopy using cells from different pure reference strains. The discriminating properties of the ClosKluy and ClosCarb probes was verified with samples from heterotrophic co-cultures in anaerobic flasks as well as autotrophic stirred-tank bioreactor co-cultures of C. kluyveri and C. carboxidivorans. Besides being suited to monitor defined co-cultures of these two species, the new specific FISH oligonucleotide probes for C. kluyveri and C. carboxidivorans additionally have potential to be applied in environmental studies.

Identifiants

pubmed: 34735802
pii: S0723-2020(21)00094-1
doi: 10.1016/j.syapm.2021.126271
pii:
doi:

Substances chimiques

Oligonucleotide Probes 0
RNA, Ribosomal, 16S 0
RNA, Ribosomal, 23S 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126271

Informations de copyright

Copyright © 2021 Elsevier GmbH. All rights reserved.

Auteurs

Martina Schneider (M)

Chair of Microbiology, Technical University of Munich, TUM School of Life Science, Freising, Germany.

Miriam Bäumler (M)

Department of Mechanical Engineering, Institute of Biochemical Engineering, Technical University of Munich, Garching, Germany.

Natuschka M Lee (NM)

Department of Ecology and Environmental Science, Umeå University, Umeå, Sweden; Research Infrastructure Fluorescence in Situ Hybridization (FISH), Chemical Biological Centre, Umeå University, Umeå, Sweden.

Dirk Weuster-Botz (D)

Department of Mechanical Engineering, Institute of Biochemical Engineering, Technical University of Munich, Garching, Germany.

Armin Ehrenreich (A)

Chair of Microbiology, Technical University of Munich, TUM School of Life Science, Freising, Germany. Electronic address: aehrenr@tum.de.

Wolfgang Liebl (W)

Chair of Microbiology, Technical University of Munich, TUM School of Life Science, Freising, Germany.

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Classifications MeSH