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      Prokaryotic Responses to Ammonium and Organic Carbon Reveal Alternative CO 2 Fixation Pathways and Importance of Alkaline Phosphatase in the Mesopelagic North Atlantic

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          Abstract

          To decipher the response of mesopelagic prokaryotic communities to input of nutrients, we tracked changes in prokaryotic abundance, extracellular enzymatic activities, heterotrophic production, dark dissolved inorganic carbon (DIC) fixation, community composition (16S rRNA sequencing) and community gene expression (metatranscriptomics) in 3 microcosm experiments with water from the mesopelagic North Atlantic. Responses in 3 different treatments amended with thiosulfate, ammonium or organic matter (i.e., pyruvate plus acetate) were compared to unamended controls. The strongest stimulation was found in the organic matter enrichments, where all measured rates increased >10-fold. Strikingly, in the organic matter treatment, the dark DIC fixation rates—assumed to be related to autotrophic metabolisms—were equally stimulated as all the other heterotrophic-related parameters. This increase in DIC fixation rates was paralleled by an up-regulation of genes involved in DIC assimilation via anaplerotic pathways. Alkaline phosphatase was the metabolic rate most strongly stimulated and its activity seemed to be related to cross-activation by nonpartner histidine kinases, and/or the activation of genes involved in the regulation of elemental balance during catabolic processes. These findings suggest that episodic events such as strong sedimentation of organic matter into the mesopelagic might trigger rapid increases of originally rare members of the prokaryotic community, enhancing heterotrophic and autotrophic carbon uptake rates, ultimately affecting carbon cycling. Our experiments highlight a number of fairly unstudied microbial processes of potential importance in mesopelagic waters that require future attention.

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          Most cited references72

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          Archaeal nitrification in the ocean.

          Marine Crenarchaeota are the most abundant single group of prokaryotes in the ocean, but their physiology and role in marine biogeochemical cycles are unknown. Recently, a member of this clade was isolated from a sea aquarium and shown to be capable of nitrification, tentatively suggesting that Crenarchaeota may play a role in the oceanic nitrogen cycle. We enriched a crenarchaeote from North Sea water and showed that its abundance, and not that of bacteria, correlates with ammonium oxidation to nitrite. A time series study in the North Sea revealed that the abundance of the gene encoding for the archaeal ammonia monooxygenase alfa subunit (amoA) is correlated with a decline in ammonium concentrations and with the abundance of Crenarchaeota. Remarkably, the archaeal amoA abundance was 1-2 orders of magnitude higher than those of bacterial nitrifiers, which are commonly thought to mediate the oxidation of ammonium to nitrite in marine environments. Analysis of Atlantic waters of the upper 1,000 m, where most of the ammonium regeneration and oxidation takes place, showed that crenarchaeotal amoA copy numbers are also 1-3 orders of magnitude higher than those of bacterial amoA. Our data thus suggest a major role for Archaea in oceanic nitrification.
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            Microbial community gene expression in ocean surface waters.

            Metagenomics is expanding our knowledge of the gene content, functional significance, and genetic variability in natural microbial communities. Still, there exists limited information concerning the regulation and dynamics of genes in the environment. We report here global analysis of expressed genes in a naturally occurring microbial community. We first adapted RNA amplification technologies to produce large amounts of cDNA from small quantities of total microbial community RNA. The fidelity of the RNA amplification procedure was validated with Prochlorococcus cultures and then applied to a microbial assemblage collected in the oligotrophic Pacific Ocean. Microbial community cDNAs were analyzed by pyrosequencing and compared with microbial community genomic DNA sequences determined from the same sample. Pyrosequencing-based estimates of microbial community gene expression compared favorably to independent assessments of individual gene expression using quantitative PCR. Genes associated with key metabolic pathways in open ocean microbial species-including genes involved in photosynthesis, carbon fixation, and nitrogen acquisition-and a number of genes encoding hypothetical proteins were highly represented in the cDNA pool. Genes present in the variable regions of Prochlorococcus genomes were among the most highly expressed, suggesting these encode proteins central to cellular processes in specific genotypes. Although many transcripts detected were highly similar to genes previously detected in ocean metagenomic surveys, a significant fraction ( approximately 50%) were unique. Thus, microbial community transcriptomic analyses revealed not only indigenous gene- and taxon-specific expression patterns but also gene categories undetected in previous DNA-based metagenomic surveys.
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              Microbial ecology of organic aggregates in aquatic ecosystems

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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                21 October 2016
                2016
                : 7
                : 1670
                Affiliations
                [1] 1Centre for Ecology and Evolution in Microbial Model Systems, EEMiS, Linnaeus University Kalmar, Sweden
                [2] 2Department of Marine Sciences, University of Otago Dunedin, New Zealand
                [3] 3National Institute of Water and Atmospheric Research (NIWA)/University of Otago Research Centre for Oceanography Dunedin, New Zealand
                [4] 4Division of Bio-Oceanography, Department of Limnology and Oceanography, University of Vienna Vienna, Austria
                [5] 5Institut Català de Recerca de l'Aigua Girona, Spain
                [6] 6Department of Marine Microbiology and Biogeochemistry, NIOZ Royal Netherlands Institute for Sea Research, Utrecht University Den Burg, Netherlands
                Author notes

                Edited by: Marcelino T. Suzuki, Sorbonne Universities, France

                Reviewed by: Christian Jeanthon, Roscoff Marine Station (CNRS), France; Ian Salter, Alfred Wegener Institute for Polar and Marine Research, Germany

                *Correspondence: Federico Baltar federico.baltar@ 123456otago.ac.nz

                This article was submitted to Aquatic Microbiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2016.01670
                5073097
                27818655
                f4185aab-b4d6-4a7a-a03f-b551e502138b
                Copyright © 2016 Baltar, Lundin, Palovaara, Lekunberri, Reinthaler, Herndl and Pinhassi.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 June 2016
                : 06 October 2016
                Page count
                Figures: 6, Tables: 3, Equations: 0, References: 90, Pages: 19, Words: 12665
                Funding
                Funded by: Crafoordska Stiftelsen 10.13039/501100003173
                Funded by: Svenska Forskningsrådet Formas 10.13039/501100001862
                Funded by: University of Otago 10.13039/100008247
                Funded by: Austrian Science Fund 10.13039/501100002428
                Award ID: I486-B09
                Award ID: P23234-B11
                Award ID: P23221-B11
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                prokaryotic community structure,functional diversity,co2 fixation,alkaline phosphatase,mesopelagic

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