缺氧水域
环境化学
发酵
生物
无氧呼吸
反硝化
细菌
呼吸
微生物代谢
生态学
化学
植物
氮气
食品科学
遗传学
有机化学
作者
Adam J. Kessler,Ya-Jou Chen,David W. Waite,Tess Hutchinson,Sharlynn Koh,María Elena Popa,John Beardall,Philip Hugenholtz,Perran L. M. Cook,Chris Greening
出处
期刊:Nature microbiology
日期:2019-03-11
卷期号:4 (6): 1014-1023
被引量:75
标识
DOI:10.1038/s41564-019-0391-z
摘要
Permeable (sandy) sediments cover half of the continental margin and are major regulators of oceanic carbon cycling. The microbial communities within these highly dynamic sediments frequently shift between oxic and anoxic states, and hence are less stratified than those in cohesive (muddy) sediments. A major question is, therefore, how these communities maintain metabolism during oxic–anoxic transitions. Here, we show that molecular hydrogen (H2) accumulates in silicate sand sediments due to decoupling of bacterial fermentation and respiration processes following anoxia. In situ measurements show that H2 is 250-fold supersaturated in the water column overlying these sediments and has an isotopic composition consistent with fermentative production. Genome-resolved shotgun metagenomic profiling suggests that the sands harbour diverse and specialized microbial communities with a high abundance of [NiFe]-hydrogenase genes. Hydrogenase profiles predict that H2 is primarily produced by facultatively fermentative bacteria, including the dominant gammaproteobacterial family Woeseiaceae, and can be consumed by aerobic respiratory bacteria. Flow-through reactor and slurry experiments consistently demonstrate that H2 is rapidly produced by fermentation following anoxia, immediately consumed by aerobic respiration following reaeration and consumed by sulfate reduction only during prolonged anoxia. Hydrogenotrophic sulfur, nitrate and nitrite reducers were also detected, although contrary to previous hypotheses there was limited capacity for microalgal fermentation. In combination, these experiments confirm that fermentation dominates anoxic carbon mineralization in these permeable sediments and, in contrast to the case in cohesive sediments, is largely uncoupled from anaerobic respiration. Frequent changes in oxygen availability in these sediments may have selected for metabolically flexible bacteria while excluding strict anaerobes. In sandy, permeable sediments, which frequently cycle between oxic and anoxic conditions, there is an uncoupling of fermentative and respiratory bacteria, and bacterial, rather than microalgal, fermentation drives the accumulation of hydrogen in this environment.
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