Electron flow in hydrogenotrophic methanogens under nickel limitation
成果类型:
Article
署名作者:
Nomura, Shunsuke; San Segundo-Acosta, Pablo; Protasov, Evgenii; Kaneko, Masanori; Kahnt, Joerg; Murphy, Bonnie J.; Shima, Seigo
署名单位:
Max Planck Society; Max Planck Society; Centro Nacional de Investigaciones Oncologicas (CNIO); National Institute of Advanced Industrial Science & Technology (AIST); Max Planck Society
刊物名称:
NATURE
ISSN/ISSBN:
0028-0836; 1476-4687
DOI:
10.1038/s41586-025-09229-y
发表日期:
2025-08-01
关键词:
H-2-FORMING METHYLENETETRAHYDROMETHANOPTERIN DEHYDROGENASE
methanobacterium-thermoautotrophicum
cryo-em
methyltransferase complex
hydrogenase
reductase
enzyme
gene
POLYFERREDOXIN
bifurcation
摘要:
Methanogenic archaea are the main producers of the potent greenhouse gas methane(1,2). In the methanogenic pathway from CO2 and H-2 studied under laboratory conditions, low-potential electrons for CO2 reduction are generated by a flavin-based electron-bifurcation reaction catalysed by heterodisulfide reductase (Hdr) complexed with the associated [NiFe]-hydrogenase (Mvh)(3-5). F-420-reducing [NiFe]-hydrogenase (Frh) provides electrons to the methanogenic pathway through the electron carrier F-420 (ref.(6)). Here we report that under strictly nickel-limited conditions, in which the nickel concentration is similar to those often observed in natural habitats(7-11), the production of both [NiFe]-hydrogenases in Methanothermobacter marburgensis is strongly downregulated. The Frh reaction is substituted by a coupled reaction with [Fe]-hydrogenase (Hmd), and the role of Mvh is taken over by F-420-dependent electron-donating proteins (Elp). Thus, Hmd provides all electrons for the reducing metabolism under these nickel-limited conditions. Biochemical and structural characterization of Elp-Hdr complexes confirms the electronic interaction between Elp and Hdr. The conservation of the genes encoding Elp and Hmd in CO2-reducing hydrogenotrophic methanogens suggests that the Hmd system is an alternative pathway for electron flow in CO2-reducing hydrogenotrophic methanogens under nickel-limited conditions.
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