Coal-bed methane is one of the largest unconventional natural gas resources. Although microbial activity may greatly contribute to coal-bed methane formation, it is unclear whether the complex aromatic organic compounds present in coal can be used for methanogenesis. We show that deep subsurface-derived Methermicoccus methanogens can produce methane from more than 30 types of methoxylated aromatic compounds (MACs) as well as from coals containing MACs. In contrast to known methanogenesis pathways involving one- and two-carbon compounds, this "methoxydotrophic" mode of methanogenesis couples O-demethylation, CO reduction, and possibly acetyl-coenzyme A metabolism. Because MACs derived from lignin may occur widely in subsurface sediments, methoxydotrophic methanogenesis would play an important role in the formation of natural gas not limited to coal-bed methane and in the global carbon cycle.

The methanogenic communities and pathways in a high-temperature petroleum reservoir were investigated through incubations of the production water and crude oil, combined with radiotracer experiments and molecular biological analyses. The incubations were conducted without any substrate amendment and under high-temperature and pressurized conditions that mimicked the in situ environment (55°C, 5 MPa). Changes in methane and acetate concentrations during the incubations indicated stoichiometric production of methane from acetate. Rates of hydrogenotrophic methanogenesis measured using [(14)C]-bicarbonate were 42-68 times those of acetoclastic methanogenesis measured using [2-(14) C]-acetate, implying the dominance of methane production by syntrophic acetate oxidation coupled to hydrogenotrophic methanogenesis in the environment. 16S rRNA gene sequence analyses of the incubated production water showed bacterial communities dominated by the genus Thermacetogenium, known as a thermophilic syntrophic acetate-oxidizing bacterium, and archaeal communities dominated by thermophilic hydrogenotrophic methanogens belonging to the genus Methanothermobacter. Furthermore, group-specific real-time PCR assays revealed that 16S rRNA gene copy numbers of the hydrogenotrophic methanogens affiliated with the order Methanobacteriales were almost identical to those of archaeal 16S rRNA genes. This study demonstrates that syntrophic acetate oxidation is the main methanogenic pathway in a high-temperature petroleum reservoir.

Methanogen diversity and methanogenic potential in formation water obtained from the Minami-kanto gas field in Japan were investigated by using 16S rRNA gene libraries and culture-based enrichment methods, respectively. This region is the largest gas field that produces natural gases of dissolved-in-water type in Japan. Although the microbial population density was below statistical quantification limits (1 × 10 4 cells ml −1 ), autofluorescent coccoid and rod-shaped cells indicative of methanogens were observed. The represented genera in the archaeal 16S rRNA genes libraries were comprised of Methanobacterium, Methanospirillum, Methanocalculus, Methanococcus, Methanolobus and Methanosaeta. The dominant archaeal sequences were related to the hydrogenotrophic methanogens in the genus Methanobacterium. Of the methanogenic substrates tested using the formation water-based medium, H 2 -CO 2 yielded the highest methane production. These results strongly suggest that the formation water of the Pleistocene strata in the gas fields harbor viable hydrogenotrophic methanogens and have possibly been making a contribution to ongoing methanogenesis.