Microbial interactions in the anaerobic oxidation of methane: model simulations constrained by process rates and activity patterns

被引:8
作者
He, Xiaojia [1 ]
Chadwick, Grayson [2 ]
Kempes, Christopher [3 ]
Shi, Yimeng [1 ,5 ]
McGlynn, Shawn [2 ,4 ]
Orphan, Victoria [2 ]
Meile, Christof [1 ]
机构
[1] Univ Georgia, Dept Marine Sci, Athens, GA 30602 USA
[2] CALTECH, Div Geol & Planetary Sci, Pasadena, CA 91125 USA
[3] Santa Fe Inst, Santa Fe, NM 87501 USA
[4] Tokyo Inst Technol, Earth Life Sci Inst, Meguro Ku, Tokyo, Japan
[5] Rutgers State Univ, Dept Stat & Biostat, New Brunswick, NJ USA
关键词
SULFATE-REDUCING BACTERIA; ELECTRON-TRANSFER; METHANOTROPHIC ARCHAEA; NITROGEN-FIXATION; ANME-2; ARCHAEA; GROWTH; TRANSPORT; CONSORTIA; NANOWIRES; ENERGY;
D O I
10.1111/1462-2920.14507
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Proposed syntrophic interactions between the archaeal and bacterial cells mediating anaerobic oxidation of methane coupled with sulfate reduction include electron transfer through (1) the exchange of H-2 or small organic molecules between methane-oxidizing archaea and sulfate-reducing bacteria, (2) the delivery of disulfide from methane-oxidizing archaea to bacteria for disproportionation and (3) direct interspecies electron transfer. Each of these mechanisms was implemented in a reactive transport model. The simulated activities across different arrangements of archaeal and bacterial cells and aggregate sizes were compared to empirical data for AOM rates and intra-aggregate spatial patterns of cell-specific anabolic activity determined by FISH-nanoSIMS. Simulation results showed that rates for chemical diffusion by mechanism (1) were limited by the build-up of metabolites, while mechanisms (2) and (3) yielded cell specific rates and archaeal activity distributions that were consistent with observations from single cell resolved FISH-nanoSIMS analyses. The novel integration of both intra-aggregate and environmental data provided powerful constraints on the model results, but the similarities in model outcomes for mechanisms (2) and (3) highlight the need for additional observational data (e.g. genomic or physiological) on electron transfer and metabolic functioning of these globally important methanotrophic consortia.
引用
收藏
页码:631 / 647
页数:17
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