Regulation of microbial enzymatic degradation of organic matter in deep-sea sediments
نویسندگان
چکیده
The enzymatic response of a natural deep-sea microbial community to input of organic matter was investigated by substrate enrichment experiments. Sediments from the BIOTRANS area at 47"N 20°W in the NE Atlantic (4500 m depth) were supplied with particulate and dissolved organic matter from stenhzed net plankton and incubated under in situ pressure and temperature. Changes in the potential hydrolytic activities of the extracellular enzymes aand P-glucosidase, chitobiase, lipase and aminopeptidase were observed over a 15 d incubation period. Direct microscopic counts and phospholipid concentrations were used as measures of microbial biomass. Induction of enzyme production proportional to the supply of organic matter was found for enzymes degrading structural polysaccharides (P-glucosidase, chitobiase), while aminopeptidase activity was Inhibited and no clear effect was found for enzymes degrading storage compounds (a-glucosidase and lipase). Particulate organic matter induced higher enzyme production than equivalent amounts of dissolved organic matter. Only a slight increase in microbial biomass was observed until the end of the experiment after 15 d indicating that changes in enzyme activity were not due to bacterial growth. The observations give evidence that the production of enzymes in natural mixed microbial communities is directly regulated by the supply of appropriate food.
منابع مشابه
Potential Mechanisms for Microbial Energy Acquisition in Oxic Deep-Sea Sediments
UNLABELLED The South Pacific Gyre (SPG) possesses the lowest rates of sedimentation, surface chlorophyll concentration, and primary productivity in the global oceans. As a direct result, deep-sea sediments are thin and contain small amounts of labile organic carbon. It was recently shown that the entire SPG sediment column is oxygenated and may be representative of up to a third of the global m...
متن کاملMicrobial Communities and Organic Matter Composition in Surface and Subsurface Sediments of the Helgoland Mud Area, North Sea
The role of microorganisms in the cycling of sedimentary organic carbon is a crucial one. To better understand relationships between molecular composition of a potentially bioavailable fraction of organic matter and microbial populations, bacterial and archaeal communities were characterized using pyrosequencing-based 16S rRNA gene analysis in surface (top 30 cm) and subsurface/deeper sediments...
متن کاملGenomic insights into potential interdependencies in microbial hydrocarbon and nutrient cycling in hydrothermal sediments
BACKGROUND Deep-sea hydrothermal vents are hotspots for productivity and biodiversity. Thermal pyrolysis and circulation produce fluids rich in hydrocarbons and reduced compounds that stimulate microbial activity in surrounding sediments. Several studies have characterized the diversity of Guaymas Basin (Gulf of California) sediment-inhabiting microorganisms; however, many of the identified tax...
متن کاملBacterial dominance in subseafloor sediments characterized by methane hydrates.
The degradation of organic carbon in subseafloor sediments on continental margins contributes to the largest reservoir of methane on Earth. Sediments in the Andaman Sea are composed of ~ 1% marine-derived organic carbon and biogenic methane is present. Our objective was to determine microbial abundance and diversity in sediments that transition the gas hydrate occurrence zone (GHOZ) in the Anda...
متن کاملShort Communication Phylogenetic Characterization of Phosphatase-Expressing Bacterial Communities in Baltic Sea Sediments
Phosphate release from sediments hampers the remediation of aquatic systems from a eutrophic state. Microbial phosphatases in sediments release phosphorus during organic matter degradation. Despite the important role of phosphatase-expressing bacteria, the identity of these bacteria in sediments is largely unknown. We herein presented a culture-independent method to phylogenetically characteriz...
متن کامل