Ammonia-oxidizing archaea release a suite of organic compounds potentially fueling prokaryotic heterotrophy in the ocean

被引:70
作者
Bayer, Barbara [1 ]
Hansman, Roberta L. [1 ,2 ]
Bittner, Meriel J. [1 ]
Noriega-Ortega, Beatriz E. [3 ]
Niggemann, Jutta [3 ]
Dittmar, Thorsten [3 ]
Herndl, Gerhard J. [1 ,4 ,5 ]
机构
[1] Univ Vienna, Ctr Funct Ecol, Dept Limnol & Biooceanog, Div Biooceanog, A-1090 Vienna, Austria
[2] Intemat Atom Energy Agcy, Radioecol Lab, Environm Labs, MC-98000 Monaco, Monaco
[3] Carl von Ossietzky Univ Oldenburg, ICBM MPI Bridging Grp Marine Geochem, D-26129 Oldenburg, Germany
[4] NIOZ Royal Netherlands Inst Sea Res, Dept Marine Microbiol & Biogeochem, NL-1790 AB Den Burg, Texel, Netherlands
[5] Univ Utrecht, NL-1790 AB Den Burg, Texel, Netherlands
基金
奥地利科学基金会;
关键词
FREE AMINO-ACIDS; MARINE; MATTER; CARBON; PHYTOPLANKTON; BACTERIA; GROWTH; BACTERIOPLANKTON; CONSUMPTION; METABOLITES;
D O I
10.1111/1462-2920.14755
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ammonia-oxidizing archaea (AOA) constitute a considerable fraction of microbial biomass in the global ocean, comprising 20%-40% of the ocean's prokaryotic plankton. However, it remains enigmatic to what extent these chemolithoautotrophic archaea release dissolved organic carbon (DOC). A combination of targeted and untargeted metabolomics was used to characterize the exometabolomes of three model AOA strains of the Nitrosopumilus genus. Our results indicate that marine AOA exude a suite of organic compounds with potentially varying reactivities, dominated by nitrogen-containing compounds. A significant fraction of the released dissolved organic matter (DOM) consists of labile compounds, which typically limit prokaryotic heterotrophic activity in open ocean waters, including amino acids, thymidine and B vitamins. Amino acid release rates corresponded with ammonia oxidation activity and the three Nitrosopumilus strains predominantly released hydrophobic amino acids, potentially as a result of passive diffusion. Despite the low contribution of DOC released by AOA (similar to 0.08%-1.05%) to the heterotrophic prokaryotic carbon demand, the release of physiologically relevant metabolites could be crucial for microbes that are auxotrophic for some of these compounds, including members of the globally abundant and ubiquitous SAR11 clade.
引用
收藏
页码:4062 / 4075
页数:14
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