氧化还原
甲烷厌氧氧化
电子传输链
古细菌
硫酸盐还原菌
微生物燃料电池
化学
生物物理学
环境化学
生物
甲烷
细菌
生物化学
生态学
无机化学
阳极
电极
遗传学
物理化学
作者
Hang Yu,Shuai Xu,Yamini Jangir,Gunter Wegener,Victoria J. Orphan,Mohamed Y. El‐Naggar
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-08-22
卷期号:11 (34): eadw4289-eadw4289
被引量:3
标识
DOI:10.1126/sciadv.adw4289
摘要
Anaerobic methanotrophic archaea (ANME) and sulfate-reducing bacteria (SRB) form syntrophic partnerships in marine sediments to consume greenhouse gas methane. While direct interspecies electron transport is proposed to enable ANME/SRB symbiosis, its electrochemical properties remain uncharacterized. Here, using sediment-free enrichment cultures, we measured the electron transport capabilities of marine consortia under physiological conditions. Diverse ANME/SRB consortia exhibited high dry conductance close to electrogenic biofilms. This conductance diminished upon exposure to heat or oxygen but was preserved following paraformaldehyde fixation, indicating a biomolecular origin for this electric charge transfer. Cyclic voltammetry revealed redox activity centered at 28 ± 11, 94 ± 6, and 24 ± 7 millivolts for ANME-1/Desulfofervidus, ANME-2a/Seep-SRB1, and ANME-2a+2c/Seep-SRB1+2 consortia, respectively. Generator-collector measurements further demonstrated that these redox components facilitate electron transport over micrometer-scale distances, sufficient to link archaeal and bacterial partners. Collectively, our results establish that marine ANME/SRB symbiosis uses redox conduction, consistent with multiheme cytochrome c, for direct interspecies electron transport.
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