Abstract
An obligate methanotrophic bacterium, strain MTS, was isolated from a methane-fed microaerobic denitrifying bioreactor. 16S rRNA and DNA–DNA hybridization analysis revealed that this organism was most closely related to Methylocystis parvus, a Type II methanotroph, belonging to the a-subclass of the Proteobacteria. The metabolism of the bacterium under microaerobic and anaerobic conditions was studied by 13C-NMR. 13C-labelled poly-ß-hydroxybutyrate (PHB) formation occurred in cell suspensions incubated with 13C-labelled methane at low (5–10%) oxygen concentration. Under these conditions low levels of succinate, acetate and 2,3-butanediol were formed and excreted into the culture medium. Intracellular PHB degradation was observed in intact cells under anaerobic conditions in the absence of an exogenous carbon source during a long-term incubation of 90 days. Multiple 13C-labelled ß-hydroxybutyrate, butyrate, acetate, acetone, isopropanol, 2,3-butanediol and succinate were identified as products in in vivo13C-NMR spectra and in the spectra of culture medium during the dynamic PHB degradation. The isolated obligate methanotroph clearly shows a fermentative metabolism of PHB under anaerobic conditions. The excreted products may serve as substrates for denitrifying bacteria
Original language | English |
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Pages (from-to) | 442-449 |
Journal | Environmental Microbiology Reports |
Volume | 1 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- methane-dependent denitrification
- external carbon source
- methanotrophic bacteria
- renaturation rates
- dna hybridization
- acid
- community
- sequence
- sediments
- oxygen