Back to Search Start Over

Biodegradation of C7 and C8 iso-alkanes under methanogenic conditions.

Authors :
Abu Laban N
Dao A
Semple K
Foght J
Source :
Environmental microbiology [Environ Microbiol] 2015 Dec; Vol. 17 (12), pp. 4898-915. Date of Electronic Publication: 2014 Dec 11.
Publication Year :
2015

Abstract

Iso-alkanes comprise a substantial proportion of petroleum and refined products that impact the environment, but their fate is cryptic under methanogenic conditions. We investigated methanogenic biodegradation of C7 and C8 iso-alkanes found in naphtha, specifically 2-methylhexane, 3-methylhexane, 2-methylheptane, 4-methylheptane and 3-ethylhexane. These were incubated as a mixture or individually with enrichment cultures derived from oil sands tailings ponds that generate methane from naphtha components; substrate depletion and methane production were monitored for up to 663 days. 3-Methylhexane and 4-methylheptane were degraded both singly and in the mixture, whereas 2-methylhexane and 2-methylheptane resisted degradation as single substrates but were depleted in the iso-alkane mixture, suggesting co-metabolism. 3-Ethylhexane was degraded neither singly nor with co-substrates. Putative metabolites consistent with succinylated C7 and C8 were detected, suggesting activation by addition of iso-alkanes to fumarate and corresponding to detection of alkylsuccinate synthase-like genes. 454 pyrotag sequencing, cloning and terminal restriction fragment length polymorphism of 16S rRNA genes revealed predominance of a novel member of the family Peptococcaceae (order Clostridiales) and Archaea affiliated with Methanoregula and Methanosaeta. We report here isomer-specific metabolism of C7 -C8 iso-alkanes under methanogenic conditions and propose their activation by a novel Peptococcaceae via addition to fumarate.<br /> (© 2014 Society for Applied Microbiology and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1462-2920
Volume :
17
Issue :
12
Database :
MEDLINE
Journal :
Environmental microbiology
Publication Type :
Academic Journal
Accession number :
25331365
Full Text :
https://doi.org/10.1111/1462-2920.12643