PubMed · 11536708
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E L Shock. 1995-11-23. Methane: an open or shut case?. https://doi.org/10.1038/378338a0
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An anaerobic methylotrophic methanogenic enrichment culture, with sustained metabolic characteristics, including that of methanation for over a decade, was the choice of the present study on interspecies interactions. Growth and methanation by the enrichment were suppressed in the presence of antibiotics, and no methanogen grown on methanol could be isolated using stringent techniques. The present study confirmed syntrophic metabolic interactions in this enrichment with the isolation of a strain of Pseudomonas sp. The organism had characteristic metabolic versatility in metabolizing a variety of substrates including alcohols, aliphatic acids, amino acids, and sugars. Anaerobic growth was favoured with nitrate in the growth medium. Cells grown anaerobically with methanol, revealed maximal nitrate reductase activity. Constitutive oxidative activity of the membrane system emerged from the high-specific oxygen uptake and nitrate reductase activities of the aerobically and anerobically grown cells respectively. Cells grown anaerobically on various alcohols effectively oxidized methanol in the presence of flavins, cofactor FAD and the methanogenic cofactor F420, suggesting a constitutive alcohol oxidizing capacity. In cells grown anaerobically on methanol, the rate of methanol oxidation with F420 was three times that of FAD. Efficient utilization of alcohols in the presence of F420 is a novel feature of the present study. The results suggest that utilization of methanol by the mixed culture would involve metabolic interactions between the Pseudomonas sp. and the methanogen(s). Methylotrophic, methanogenic partnership involving an aerobe is a novel feature hitherto unreported among anaerobic syntrophic associations and is of ecological significance
To evaluate the effect of potential interactions between methanogenic bacteria and iron sulfide minerals during transformation of 1,1,1-trichloroethane (1,1,1-TCA), we measured the kinetics of 1,1,1-TCA transformation by mackinawite (FeS(1 - x), but abbreviated as FeS) and a methanogenic consortium enriched on lactate (termed LEC). Results from batch kinetic experiments show that 1,1,1-TCA transformation by FeS and resting LEC can be described by second-order rate expressions, with rates depending on 1,1,1-TCA concentration (M), FeS surface area concentration (m2 L(-1)), and LEC concentration (as measured by mg L(-1) volatile suspended solids (VSS)). In reactors containing FeS alone, 1,1-dichloroethane (1,1-DCA) and 2-butyne were identified as products, but only accounted for 6% of the 1,1,1-TCA transformed. In reactors containing LEC alone, the only identified product was 1,1-DCA, which accounted for 46 +/- 8% of the 1,1,1-TCA transformed. Supernatant from LEC-alone reactors also transformed 1,1,1-TCA, suggesting that 1,1,1-TCA may be transformed by some non-cell component (such as a extracellular compound excreted by the organisms) that either reacts directly with 1,1,1-TCA or with the abiotic media to form a reactive species. Comparison of 1,1,1-TCA transformation rates from experiments with combinations of FeS (varying surface area concentrations) and LEC (varying VSS concentrations) to those with just FeS alone or LEC alone suggests some synergism occurs between the two reactive species. Observed enhancements took the form of faster 1,1,1-TCA transformation and faster 1,1-DCA appearance but less production of 1,1-DCA per unit of 1,1,1-TCA transformed. These observations suggest that the faster 1,1,1-TCA transformation in the combined systems (compared to the FeS-alone and LEC-alone experiments) is due to increased reactivity of both FeS and LEC, possibly due to production of soluble microbial products that make the FeS more reactive or less inhibition of LEC by 1,1,1-TCA due to FeS transformation of 1,1,1-TCA.